Recent from talks
Nothing was collected or created yet.
Body odor
View on Wikipedia
Body odor or body odour (BO) is present in all animals and its intensity can be influenced by many factors (behavioral patterns, survival strategies). Body odor has a strong genetic basis, but can also be strongly influenced by various factors, such as sex, diet, health, and medication.[1] The body odor of human males plays an important role in human sexual attraction, as a powerful indicator of MHC/HLA heterozygosity.[2][1] Significant evidence suggests that women are attracted to men whose body odor is different from theirs, indicating that they have immune genes that are different from their own, which may produce healthier offspring.[3]
Causes
[edit]In humans, the formation of body odors is caused by factors such as diet, sex, health, and medication, but the major contribution comes from bacterial activity on skin gland secretions.[1] Humans have three types of sweat glands: eccrine sweat glands, apocrine sweat glands and sebaceous glands. Eccrine sweat glands are present from birth, while the latter two become activated during puberty. Among the different types of human skin glands, body odor is primarily the result of the apocrine sweat glands, which secrete the majority of chemical compounds that the skin flora metabolize into odorant substances.[1] This happens mostly in the axillary (armpit) region, although the gland can also be found in the areola, anogenital region, and around the navel.[4] In humans, the armpit regions seem more important than the genital region for body odor, which may be related to human bipedalism. The genital and armpit regions also contain springy hairs which help diffuse body odors.[5]
The main components of human axillary odor are unsaturated or hydroxylated branched fatty acids with E-3-methylhex-2-enoic acid (E-3M2H) and 3-hydroxy-3-methylhexanoic acid (HMHA), sulfanylalkanols and particularly 3-methyl-3-sulfanylhexan-1-ol (3M3SH), and the odoriferous steroids androstenone (5α-androst-16-en-3-one) and androstenol (5α-androst-16-en-3α-ol).[6] E-3M2H is bound and carried by two apocrine secretion odor-binding proteins, ASOB1 and ASOB2, to the skin surface.[7]
Body odor is influenced by the actions of the skin flora, including members of Corynebacterium, which manufacture enzymes called lipases that break down the lipids in sweat to create smaller molecules like butyric acid. Greater bacteria populations of Corynebacterium jeikeium are found more in the armpits of men, whereas greater population numbers of Staphylococcus haemolyticus are found in the armpits of women. This causes male armpits to give off a rancid/cheese-like smell, whereas female armpits give off a more fruity/onion-like smell.[8] Staphylococcus hominis is also known for producing thioalcohol compounds that contribute to odors.[9] These smaller molecules smell, and give body odor its characteristic aroma.[10] Propionic acid (propanoic acid) is present in many sweat samples. This acid is a breakdown product of some amino acids by propionibacteria, which thrive in the ducts of adolescent and adult sebaceous glands. Because propionic acid is chemically similar to acetic acid, with similar characteristics including odor, body odors may be identified as having a pungent, cheesy and vinegar-like smell although certain people might find it pleasant at lower concentrations.[11] Isovaleric acid (3-methyl butanoic acid) is the other source of body odor as a result of actions of the bacteria Staphylococcus epidermidis,[12] which is also present in several types of strong cheese.
Factors such as food, drink, gut microbiome,[13] and genetics can affect body odor.[5]
Function
[edit]Animals
[edit]In many animals, body odor plays an important survival function. Strong body odor can be a warning signal for predators to stay away (such as porcupine stink), or it can also be a signal that the prey animal is unpalatable.[14] For example, some animal species that feign death to survive (like opossums), in this state produce a strong body odor to deceive a predator that the prey animal has been dead for a long time and is already in the advanced stage of decomposing. Some animals with strong body odor are rarely attacked by most predators, although they can still be killed and eaten by birds of prey, which are tolerant of carrion odors.[citation needed]
Body odor is an important feature of animal physiology. It plays a different role in different animal species. For example, in some predator species that hunt by stalking (such as big and small cats), the absence of body odor is important, and they spend plenty of time and energy to keep their body free of odor. For other predators, such as those that hunt by visually locating prey and running for long distances after it (such as dogs and wolves), the absence of body odor is not critical. In most animals, body odor intensifies in moments of stress and danger.[15]
Humans
[edit]In humans, body odor serves as a means of chemosensory signal communication between members of the species. These signals are called pheromones and they can be transmitted through a variety of mediums. The most common way that human pheromones are transmitted is through bodily fluids. Human pheromones are contained in sweat, semen, vaginal secretions, breast milk, and urine.[1] The signals carried in these fluids serve a range of functions from reproductive signaling to infant socialization.[16] Each person produces a unique spread of pheromones that can be identified by others.[2] This differentiation allows the formation of sexual attraction and kinship ties to occur.[2][17]
Sebaceous and apocrine glands become active at puberty. This, as well as many apocrine glands being close to the sex organs, points to a role related to mating.[5] Sebaceous glands line the human skin while apocrine glands are located around body hairs.[1] Compared to other primates, humans have extensive axillary hair and have many odor producing sources, in particular many apocrine glands.[18] In humans, the apocrine glands have the ability to secrete pheromones. These steroid compounds are produced within the peroxisomes of the apocrine glands by enzymes such as mevalonate kinases.[19]
Sexual selection
[edit]Pheromones are a factor seen in the mating selection and reproduction in humans. In women, the sense of olfaction is strongest around the time of ovulation, significantly stronger than during other phases of the menstrual cycle and also stronger than the sense in males.[20][21] Pheromones can be used to deliver information about the major histocompatibility complex (MHC).[2] The MHC in humans is referred to as the Human Leukocyte Antigen (HLA).[22] Each type has a unique scent profile that can be utilized during the mating selection process. When selecting mates, women tend to be attracted to those that have different HLA-types than their own.[2][22] This is thought to increase the strength of the family unit and increase the chances of survival for potential offspring.[2]
Studies have suggested that people might be using odor cues associated with the immune system to select mates. Using a brain-imaging technique, Swedish researchers have shown that homosexual and heterosexual males' brains respond in different ways to two odors that may be involved in sexual arousal, and that homosexual men respond in the same way as heterosexual women, though it could not be determined whether this was cause or effect. When the study was expanded to include lesbian women, the results were consistent with previous findings – meaning that lesbian women were not as responsive to male-identified odors, while responding to female odors in a similar way as heterosexual males.[23] According to the researchers, this research suggests a possible role for human pheromones in the biological basis of sexual orientation.[24]
Kinship communication
[edit]Humans can olfactorily detect blood-related kin.[17] Mothers can identify by body odor their biological children, but not their stepchildren. Preadolescent children can olfactorily detect their full siblings, but not half-siblings or step-siblings, and this might explain incest avoidance and the Westermarck effect.[25] Babies can recognize their mothers by smell while mothers, fathers, and other relatives can identify a baby by smell.[5] This connection between genetically similar family members is due to the habituation of familial pheromones. In the case of babies and mothers, this chemosensory information is primarily contained within breastmilk and the mother's sweat. When compared to that of strangers, babies are observed to have stronger neural connections with their mothers.[26] This strengthened neurological connection allows for the biological development and socialization of the infant by their mother. Using these connections, the mother transmits olfactory signals to the infant which are then perceived and integrated.[26]
In terms of biological functioning, olfactory signaling allows for functional breastfeeding to occur. In cases of effective latching, breastfed infants are able to locate their mother's nipples for feeding using the sensory information enclosed in their mother's body odor.[27] While no specific human breast pheromones have been identified, studies compare the communication to that of the rabbit mammary pheromone 2MB2.[28][29] The perception and integration of these signals is an evolutionary response that allows newborns to locate their source of nutrition. Signaling contains a level of precision that allows babies to differentiate their mother's breasts from that of other women. Once the baby recognizes the familiar olfactory signal, the behavioral response of latching follows. Over time the infant becomes habituated to their mother's breast pheromones which increases latch efficiency.[27]
Beyond a biological function, a mother's body odor plays a role in developing a baby's social capabilities. The ability of an infant to evaluate the properties of human faces stems from the olfactory cues given from their mother.[16] Frequent exposure to the pheromones exuded by their mother allows the connection between vision and smell to form in infants.[26] This type of connection is only found between mothers and babies and over time it socializes the ability to recognize the features that distinguish human faces from inanimate objects.[16]
Environmental threats
[edit]The connection between olfactory and visual cues has also been observed outside of familial relationships. Evolutionarily, body odor has been used to communicate messages about potentially dangerous stimuli in the environment.[1] Body odor produced during particularly stressful situations can produce a cascade of reactions in the brain. Once the olfactory system is activated by a threatening stimuli, heightened activity in the amygdala and occipital cortex is triggered.[30][1] This chain reaction serves to help assess the nature of the threat and increase chance of survival.
Humans have few olfactory receptor cells compared to dogs and few functional olfactory receptor genes compared to rats. This is in part due to a reduction of the size of the snout in order to achieve depth perception as well as other changes related to bipedalism. However, it has been argued that humans may have larger brain areas associated with olfactory perception compared to other species.[18]
Genes affecting body odor
[edit]
MHC
[edit]Body odor is influenced by major histocompatibility complex (MHC) molecules. These are genetically determined and play an important role in immunity of the organism. The vomeronasal organ contains cells sensitive to MHC molecules in a genotype-specific way.[citation needed]
Experiments on animals and volunteers have shown that potential sexual partners tend to be perceived more attractive if their MHC composition is substantially different. Married couples are more different regarding MHC genes than would be expected by chance. This behavior pattern promotes variability of the immune system of individuals in the population, thus making the population more robust against new diseases. Another reason may be to prevent inbreeding.[5]
ABCC11
[edit]The ABCC11 gene determines axillary body odor and earwax type.[6][31][32][33] The loss of a functional ABCC11 gene is caused by a 538G>A single-nucleotide polymorphism, resulting in a loss of body odor in people who are specifically homozygous for it.[33][34] Firstly, it affects apocrine sweat glands by reducing secretion of odorous molecules and its precursors.[6] The lack of ABCC11 function results in a decrease of the odorant compounds 3M2H, HMHA, and 3M3SH via a strongly reduced secretion of the precursor amino-acid conjugates 3M2H–Gln, HMHA–Gln, and Cys–Gly–(S) 3M3SH; and a decrease of the odoriferous steroids androstenone and androstenol, possibly due to the reduced secretion of dehydroepiandrosterone sulfate (DHEAS) and dehydroepiandrosterone (DHEA), thought to be precursors for skin bacterial metabolism leading to the steroids' formation.[6] Secondly, it is associated with a strongly reduced and atrophic size of apocrine sweat glands.[6] Thirdly, it is associated with a decreased concentration of proteins, such as apocrine secretion odor-binding protein 2, in axillary sweat.[6]
The non-functional ABCC11 allele is predominant among East Asians (80–95%), but very low among European and African populations (0–3%).[6] Most of the world's population has the gene that codes for the wet-type earwax and average body odor; however, East Asians are more likely to inherit the allele associated with the dry-type earwax and a reduction in body odor.[6][31][33] The reduction in body odor may be due to adaptation to colder climates by their ancient Northeast Asian ancestors.[31]
Research suggests that ethnicity significantly influences human axillary odor production quantitatively, but the ABCC11 genotype alone does not account for the ethnic differences in scent, even though it plays a major role.[35] For example, a 2016 study found that individuals with the same ABCC11 genotype exhibited differences in the levels of characteristic axillary odorants between ethnic groups (African American versus Caucasian), such as variations in the amounts of E-3M2H and 3H3M.[35]
Research has indicated a strong association between people with axillary osmidrosis, a condition characterized by axillary odor, and the ABCC11-genotypes GG or GA in comparison to the genotype AA.[33]
| Ethnic groups | Tribes or inhabitants | AA | GA | GG |
|---|---|---|---|---|
| Korean | Daegu city inhabitants | 100% | 0% | 0% |
| Chinese | Northern and southern Han Chinese | 80.8% | 19.2% | 0% |
| Mongolian | Khalkha tribe | 75.9% | 21.7% | 2.4% |
| Japanese | Nagasaki people | 69% | 27.8% | 3.2% |
| Thai | Central Thai in Bangkok | 63.3% | 20.4% | 16.3% |
| Vietnamese | People from multiple regions | 53.6% | 39.2% | 7.2% |
| Dravidian | Inhabitants of southern India | 54.0% | 17% | 29% |
| Native American | 30% | 40% | 30% | |
| Filipino | Palawan | 22.9% | 47.9% | 29.2% |
| Kazakh | 20% | 36.7 | 43.3% | |
| Russian | 4.5% | 40.2% | 55.3% | |
| White Americans | From CEPH families without the French and Venezuelans | 1.2% | 19.5% | 79.3% |
| African | From various sub-Saharan nations | 0% | 8.3% | 91.7% |
| African Americans | 0% | 0% | 100% |
| Genotype ABCC11 |
Sex | Ethnic population | Age | Net weight sweat (g)/2 pads |
HMHA–Gln (μmol/2 pads) |
3M2H–Gln (μmol/2 pads) |
Cys–Gly conjugate
of 3M3SH (μmol/2 pads) |
|---|---|---|---|---|---|---|---|
| AA | F | Chinese | 27 | 2.05 | ND | ND | ND |
| AA | F | Filipino | 33 | 2.02 | ND | ND | ND |
| AA | F | Korean | 35 | 1.11 | ND | ND | ND |
| GA | F | Filipino | 31 | 1.47 | 1.23 | 0.17 | Detectable, < 0.03 μmol |
| GA | F | Thai | 25 | 0.90 | 0.89 | 0.14 | Detectable, < 0.03 μmol |
| GA | F | German | 25 | 1.64 | 0.54 | 0.10 | Detectable, < 0.03 μmol |
| GG | F | Filipino | 45 | 1.74 | 0.77 | 0.13 | Detectable, < 0.03 μmol |
| GG | F | German | 28 | 0.71 | 1.30 | 0.19 | 0.041 |
| GG | F | German | 33 | 1.23 | 1.12 | 0.16 | 0.038 |
* ND indicates that no detectable peak is found on the [M+H]+ ion trace of the selected analyte at the correct retention time.
* HMHA: 3-hydroxy-3-methyl-hexanoic acid; 3M2H: (E)-3-methyl-2-hexenoic acid; 3M3SH: 3-methyl-3-sulfanylhexan-1-ol.
Other factors affecting body odor
[edit]Age
[edit]As seen in non-human animals such as mice, black-tailed deer, rabbits, otters, and owl monkeys, body odor contains age-related signals that these animals can detect and process. Similarly, humans have been seen to distinguish age-related information from body odor, particularly relating to odors of those of old age. In a study determining if there is a difference between the body odor of individuals of various ages, three groups were studied: those aged 20-30, aged 45-55, and aged 75-95, corresponding to young age, middle-aged, and old age, respectively. This study determined that individuals could distinguish between odors of various ages and group odors of old age, suggesting that there are certain chemical differences in age resulting in "age-dependent odor characteristics".[39]
Another study evaluated the components of body odor in participants aged 26 through 75 using headspace gas chromatography and mass spectroscopy. This study demonstrated that in individuals 40 years or older, 2-Nonenal, an unsaturated aldehyde producing a greasy and grassy odor, was detected in increasing concentrations of those individuals. The detection of increasing amounts of 2-Nonenal in individuals 40 years or older suggested that 2-Nonenal contributes to the deteriorating body odor seen with aging.[40]
Diseases
[edit]In mammals, body odor can also be used as a symptom of disease. One's body odor is completely unique to themselves, similar to a fingerprint, and can change due to sexual life, genetics, age and diet. Body odor, however, can be used as an indication for disease. For example, typically, human urine contains 95% water,[41] however, for a person with an abnormal amount of blood sugar, their urine becomes more concentrated with glucose.[42] Therefore, if a person's body odor or urine smells unusually fruity or sweet, that can be a sign of diabetes. Additionally, an ammonia smell that occurs in one's body, urine, or breath could also be an indicator of kidney disease. Typically, the liver converts ammonia to urea because ammonia has a high level of toxicity. The kidneys are responsible for removing waste, such as urea, out from the body. However, if the kidneys are not functioning properly, this urea is kept as ammonia, causing the urine and even one's breath to smell like ammonia.[43] In conclusion, body odor could be used as a helpful indicator of disease, especially when it suddenly deviates from normal.
Alterations
[edit]Body odor may be reduced or prevented or even aggravated by using deodorants, antiperspirants, disinfectants, underarm liners, triclosan, special soaps or foams with antiseptic plant extracts such as ribwort and liquorice, chlorophyllin ointments and sprays topically, and chlorophyllin supplements internally. Although body odor is commonly associated with hygiene practices, its presentation can be affected by changes in diet as well as the other factors.[44] Skin spectrophotometry analysis found that males who consumed more fruits and vegetables were significantly associated with more pleasant smelling sweat, which was described as "floral, fruity, sweet and medicinal qualities".[45]
Industry
[edit]As many as 90% of Americans and 92% of teenagers use antiperspirants or deodorants.[46][47] In 2014, the global market for deodorants was estimated at US$13 billion with a compound annual growth rate of 5.62% between 2015 and 2020.[48]
Medical conditions
[edit]Osmidrosis or bromhidrosis is defined by a foul odor due to a water-rich environment that supports bacteria, which is caused by an abnormal increase in perspiration (hyperhidrosis).[32] This can be particularly strong when it happens in the axillary region (underarms). In this case, the condition may be referred to as axillary osmidrosis.[32] The condition can also be known medically as apocrine bromhidrosis, ozochrotia, fetid sweat, body smell, or malodorous sweating.[49][50]
Treatment
[edit]If body odor is affecting a person's quality of life, then seeing a primary care physician may be helpful. A doctor could recommend prescription antiperspirants containing aluminum-chloride.[51] This chemical agent helps temporarily block sweat pores which reduces the amount a person will sweat. Deodorant is another remedy for body odor. It specifically targets odor but will not reduce sweat. Deodorants are usually alcohol-based which fights off bacteria.[52] Most deodorants contain perfumes which also help with masking odor. If someone is experiencing severe body odor, a doctor may recommend a surgical procedure called endoscopic thoracic sympathectomy.[53] This surgery will cut nerves that control sweating. This surgery poses the risk of harming other nerves in the body.
Prevention
[edit]This section contains instructions or advice. (December 2024) |
Bathing daily with antibacterial soap reduces the amount of bacteria found on the skin.[54] Shaving armpit hair allows for sweat to evaporate more quickly so it won't produce an odor. Applying deodorant or antiperspirant after showering which helps kill bacteria and prevent someone from sweating is helpful.
Trimethylaminuria (TMAU), also known as fish odor syndrome or fish malodor syndrome, is a rare metabolic disorder where trimethylamine is released in the person's sweat, urine, and breath, giving off a strong fishy odor or strong body odor.[55]
See also
[edit]References
[edit]- ^ a b c d e f g h Lundström JN, Olsson MJ (2010). "Functional Neuronal Processing of Human Body Odors". Vitamins & Hormones. 83: 1–23. doi:10.1016/S0083-6729(10)83001-8. ISBN 978-0-12-381516-3. PMC 3593650. PMID 20831940.
- ^ a b c d e f Grammer K, Fink B, Neave N (February 2005). "Human pheromones and sexual attraction". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 118 (2): 135–142. doi:10.1016/j.ejogrb.2004.08.010. PMID 15653193.
- ^ Everts S (July 21, 2021). "What Your Body Odor Says About You". Time.
In one study about smell and romance, straight women preferred the body odor of straight men whose immune systems were different enough that any offspring would have healthy immune systems. For most of human history, infectious disease has been our greatest threat. In modern times we may seek life-partners that satisfy a multitude of needs, but more fundamentally, if you could produce babies with immune systems able to fight a potpourri of pathogens, then your progeny—and your genes—stand a better chance at survival.
- ^ Turkington C, Dover JS (2007). The encyclopedia of skin and skin disorders (3rd ed.). New York: Facts on File. pp. 363. ISBN 978-0-8160-6403-8.
- ^ a b c d e Wedekind C (2007). "Body Odours and Body Odour Preferences in Humans". Oxford Handbook of Evolutionary Psychology. pp. 315–320. doi:10.1093/oxfordhb/9780198568308.013.0022. ISBN 978-0-19-174365-8.
- ^ a b c d e f g h Martin A, Saathoff M, Kuhn F, Max H, Terstegen L, Natsch A (February 2010). "A functional ABCC11 allele is essential in the biochemical formation of human axillary odor". The Journal of Investigative Dermatology. 130 (2): 529–540. doi:10.1038/jid.2009.254. PMID 19710689.
- ^ Zeng C, Spielman AI, Vowels BR, Leyden JJ, Biemann K, Preti G (June 1996). "A human axillary odorant is carried by apolipoprotein D". Proceedings of the National Academy of Sciences of the United States of America. 93 (13): 6626–6630. Bibcode:1996PNAS...93.6626Z. doi:10.1073/pnas.93.13.6626. PMC 39076. PMID 8692868.
- ^ Kort R (September 2017). De microbemens: Het belang van het onzichtbare leven [The microbes: The importance of the invisible life.] (in Dutch). Amsterdam: Athenaeum, Polak & Van Gennep. ISBN 978-90-253-0692-2.
- ^ "Bacterial genetic pathway involved in body odor production discovered" (Press release). Society for General Microbiology. March 30, 2015.
- ^ Buckman R (2003). Human Wildlife: The Life That Lives On Us. Baltimore, Md.: The Johns Hopkins University Press. pp. 93–94. ISBN 978-0-8018-7407-9.
- ^ Charles M, Martin B, Ginies C, Etievant P, Coste G, Guichard E (2000). "Potent aroma compounds of two red wine vinegars". Journal of Agricultural and Food Chemistry. 48 (1): 70–77. Bibcode:2000JAFC...48...70C. doi:10.1021/jf9905424. PMID 10637054.
- ^ Ara K, Hama M, Akiba S, Koike K, Okisaka K, Hagura T, et al. (April 2006). "Foot odor due to microbial metabolism and its control". Canadian Journal of Microbiology. 52 (4): 357–364. CiteSeerX 10.1.1.1013.4047. doi:10.1139/w05-130. PMID 16699586.
- ^ Gabashvili IS (2020). "Cutaneous Bacteria in the Gut Microbiome as Biomarkers of Systemic Malodor and People Are Allergic to Me (PATM) Conditions: Insights from a Virtually Conducted Clinical Trial". JMIR Dermatology. 3 e10508. doi:10.2196/10508. S2CID 226280399.
- ^ Ruxton GD, Allen WL, Sherratt TN, Speed MP (2018). Avoiding Attack: The Evolutionary Ecology of Crypsis, Aposematism, and Mimicry. Oxford University Press. ISBN 978-0-19-186849-8.[page needed]
- ^ Takahashi LK (March 11, 2014). "Olfactory systems and neural circuits that modulate predator odor fear". Frontiers in Behavioral Neuroscience. 8: 72. doi:10.3389/fnbeh.2014.00072. PMC 3949219. PMID 24653685.
- ^ a b c Damon F, Mezrai N, Magnier L, Leleu A, Durand K, Schaal B (October 5, 2021). "Olfaction in the Multisensory Processing of Faces: A Narrative Review of the Influence of Human Body Odors". Frontiers in Psychology. 12 750944. doi:10.3389/fpsyg.2021.750944. PMC 8523678. PMID 34675855.
- ^ a b Porter RH, Cernoch JM, Balogh RD (March 1985). "Odor signatures and kin recognition". Physiology & Behavior. 34 (3): 445–448. doi:10.1016/0031-9384(85)90210-0. PMID 4011726. S2CID 42316168.
- ^ a b Roberts SC, Havlicek J (2011). "Evolutionary psychology and perfume design". Applied Evolutionary Psychology. pp. 330–348. doi:10.1093/acprof:oso/9780199586073.003.0020. ISBN 978-0-19-958607-3.
- ^ Rothardt G, Beier K (August 2001). "Peroxisomes in the apocrine sweat glands of the human axilla and their putative role in pheromone production". Cellular and Molecular Life Sciences. 58 (9): 1344–1349. doi:10.1007/PL00000946. PMC 11337405. PMID 11577991. S2CID 28790000.
- ^ Lundström & Olsson 2010:"In addition, the impact that biological factors have on our percept of body odors has recently been indirectly demonstrated by several experiments. Our percept of body odors is dependent on the sexual orientations of both the donor and the perceiver (Martins et al., 2005), and heterosexual women's percept of men's body odor varies over their menstrual cycle (Roberts et al., 2004)."
- ^ Navarrete-Palacios E, Hudson R, Reyes-Guerrero G, Guevara-Guzmán R (July 2003). "Lower olfactory threshold during the ovulatory phase of the menstrual cycle". Biological Psychology. 63 (3): 269–279. doi:10.1016/s0301-0511(03)00076-0. PMID 12853171. S2CID 46065468.
- ^ a b Kromer J, Hummel T, Pietrowski D, Giani AS, Sauter J, Ehninger G, et al. (August 2016). "Influence of HLA on human partnership and sexual satisfaction". Scientific Reports. 6 32550. Bibcode:2016NatSR...632550K. doi:10.1038/srep32550. PMC 5006172. PMID 27578547.
- ^ Berglund H, Lindström P, Savic I (May 2006). "Brain response to putative pheromones in lesbian women". Proceedings of the National Academy of Sciences of the United States of America. 103 (21): 8269–8274. Bibcode:2006PNAS..103.8269B. doi:10.1073/pnas.0600331103. PMC 1570103. PMID 16705035.
- ^ Wade N (May 9, 2005). "Gay Men Are Found to Have Different Scent of Attraction". The New York Times.
- ^ Weisfeld GE, Czilli T, Phillips KA, Gall JA, Lichtman CM (July 2003). "Possible olfaction-based mechanisms in human kin recognition and inbreeding avoidance". Journal of Experimental Child Psychology. 85 (3): 279–295. doi:10.1016/s0022-0965(03)00061-4. PMID 12810039.
- ^ a b c Endevelt-Shapira Y, Djalovski A, Dumas G, Feldman R (December 2021). "Maternal chemosignals enhance infant-adult brain-to-brain synchrony". Science Advances. 7 (50) eabg6867. Bibcode:2021SciA....7.6867E. doi:10.1126/sciadv.abg6867. PMC 8664266. PMID 34890230.
- ^ a b Varendi H, Porter RH, Winberg J (October 1994). "Does the newborn baby find the nipple by smell?". Lancet. 344 (8928): 989–990. doi:10.1016/S0140-6736(94)91645-4. PMID 7934434. S2CID 35029502.
- ^ Schaal B (2014), Mucignat-Caretta C (ed.), "Pheromones for Newborns", Neurobiology of Chemical Communication, Frontiers in Neuroscience, Boca Raton (FL): CRC Press/Taylor & Francis, ISBN 978-1-4665-5341-5, PMID 24830031, retrieved November 27, 2022
- ^ "Pheromone From Mother's Milk May Rapidly Promote Learning In Newborn Mammals". ScienceDaily. Retrieved November 27, 2022.
- ^ Mujica-Parodi LR, Strey HH, Frederick B, Savoy R, Cox D, Botanov Y, et al. (July 2009). "Chemosensory cues to conspecific emotional stress activate amygdala in humans". PLOS ONE. 4 (7) e6415. Bibcode:2009PLoSO...4.6415M. doi:10.1371/journal.pone.0006415. PMC 2713432. PMID 19641623.
- ^ a b c Yoshiura K, Kinoshita A, Ishida T, Ninokata A, Ishikawa T, Kaname T, et al. (March 2006). "A SNP in the ABCC11 gene is the determinant of human earwax type". Nature Genetics. 38 (3): 324–330. doi:10.1038/ng1733. PMID 16444273. S2CID 3201966.
- ^ a b c Kanlayavattanakul M, Lourith N (August 2011). "Body malodours and their topical treatment agents". International Journal of Cosmetic Science. 33 (4): 298–311. doi:10.1111/j.1468-2494.2011.00649.x. PMID 21401651.
- ^ a b c d Nakano M, Miwa N, Hirano A, Yoshiura K, Niikawa N (August 2009). "A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene". BMC Genetics. 10 (1) 42. doi:10.1186/1471-2156-10-42. PMC 2731057. PMID 19650936.
- ^ Preti G, Leyden JJ (February 2010). "Genetic influences on human body odor: from genes to the axillae". The Journal of Investigative Dermatology. 130 (2): 344–346. doi:10.1038/jid.2009.396. PMID 20081888.
- ^ a b Prokop-Prigge KA, Greene K, Varallo L, Wysocki CJ, Preti G (January 2016). "The Effect of Ethnicity on Human Axillary Odorant Production". Journal of Chemical Ecology. 42 (1): 33–39. Bibcode:2016JCEco..42...33P. doi:10.1007/s10886-015-0657-8. PMC 4724538. PMID 26634572.
- ^ Ishikawa T, Toyoda Y, Yoshiura K, Niikawa N (2012). "Pharmacogenetics of human ABC transporter ABCC11: new insights into apocrine gland growth and metabolite secretion". Frontiers in Genetics. 3: 306. doi:10.3389/fgene.2012.00306. PMC 3539816. PMID 23316210.
- ^ Miura K, Yoshiura Ki, Miura S, Shimada T, Yamasaki K, Yoshida A, et al. (June 2007). "A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland". Human Genetics. 121 (5): 631–633. doi:10.1007/s00439-007-0356-9. ISSN 0340-6717. PMID 17394018. S2CID 575882.
- ^ Martin A, Saathoff M, Kuhn F, Max H, Terstegen L, Natsch A (February 2010). "A functional ABCC11 allele is essential in the biochemical formation of human axillary odor". The Journal of Investigative Dermatology. 130 (2): 529–540. doi:10.1038/jid.2009.254. PMID 19710689. S2CID 36754463.
- ^ Mitro S, Gordon AR, Olsson MJ, Lundström JN (May 30, 2012). "The Smell of Age: Perception and Discrimination of Body Odors of Different Ages". PLOS ONE. 7 (5) e38110. Bibcode:2012PLoSO...738110M. doi:10.1371/journal.pone.0038110. PMC 3364187. PMID 22666457.
- ^ Haze S, Gozu Y, Nakamura S, Kohno Y, Sawano K, Ohta H, et al. (December 8, 2015). "2-Nonenal Newly Found in Human Body Odor Tends to Increase with Aging". Journal of Investigative Dermatology. 116 (4): 520–524. doi:10.1046/j.0022-202x.2001.01287.x. PMID 11286617.
- ^ Sarigul N (2019). "A New Artificial Urine Protocol to Better Imitate Human Urine". Scientific Reports. 9 (1) 20159. Bibcode:2019NatSR...920159S. doi:10.1038/s41598-019-56693-4. PMC 6934465. PMID 31882896.
- ^ Siyang S (2012). "Diabetes diagnosis by direct measurement from urine odor using electronic nose". The 5th 2012 Biomedical Engineering International Conference. IEEE. pp. 1–4. doi:10.1109/BMEiCon.2012.6465441. ISBN 978-1-4673-4892-8 – via IEEE conference publication.
- ^ Chan MJ (2020). "Breath Ammonia Is a Useful Biomarker Predicting Kidney Function in Chronic Kidney Disease Patients". Biomedicines. 8 (11): 468. doi:10.3390/biomedicines8110468. PMC 7692127. PMID 33142890.
- ^ "Learn How to Fight Body Odor". MD Health Network. Archived from the original on March 24, 2010. Retrieved July 5, 2007.
- ^ Zuniga A, Stevenson RJ, Mahmut MK, Stephen ID (January 2017). "Diet quality and the attractiveness of male body odor". Evolution and Human Behavior. 38 (1): 136–143. Bibcode:2017EHumB..38..136Z. doi:10.1016/j.evolhumbehav.2016.08.002. ISSN 1090-5138.
- ^ Pomeroy R (August 10, 2014). "Antiperspirants Alter Your Armpit Bacteria and Could Actually Make You Smell Worse". RealClearScience.
- ^ Considine A (January 17, 2013). "Genetically, Some of Us Never Have Body Odor, But We Still Think We're Smelly". Vice.
- ^ "Global Deodorants Market is Expected to Reach USD 17.55 Billion by 2020". gosreports.com. Archived from the original on October 28, 2016. Retrieved July 29, 2016.
- ^ William J, Berger T, Elston D (2005). Andrews' Diseases of the Skin: Clinical Dermatology (10th ed.). Saunders. p. 779. ISBN 978-0-7216-2921-6.
- ^ Freedberg IM, Eisen AZ, Austen KF, Goldsmith LA, Katz SI (2003). Fitzpatrick's Dermatology in General Medicine (6th ed.). McGraw-Hill. p. 707. ISBN 978-0-07-138076-8.
- ^ Felman A (November 29, 2017). "What to know about body odor". Medical News Today.
- ^ "Sweating and body odor". Mayo Clinic.
- ^ "Endoscopic thoracic sympathectomy". Medlineplus medical encyclopedia.
- ^ Brennan D. "Tips for Reducing Body Odor". WebMD.
- ^ "Body Odor: Causes, Prevention, Treatments". Medical News Today. Retrieved March 4, 2017.
External links
[edit]- Flores G (November 4, 2004). "Immunity, smell linked". The Scientist Magazine.
- Dunning B (October 25, 2022). "Skeptoid #855: Sniffing for Human Sex Pheromones". Skeptoid.
Body odor
View on GrokipediaBiological Mechanisms
Sweat Production and Glands
Human sweat is produced by two primary types of glands: eccrine and apocrine, each contributing differently to the precursors of body odor. Eccrine glands are distributed across nearly the entire body surface, with an estimated 2 to 4 million glands per person, concentrated in areas like the palms, soles, and forehead.[15] These glands secrete a clear, watery fluid that is approximately 99% water, along with small amounts of electrolytes such as sodium, chloride, and potassium, forming a hypotonic solution relative to plasma.[16] Their primary function is thermoregulation, achieved through the evaporation of sweat, which cools the body during heat stress or physical activity; this secretion is odorless and contributes minimally to body odor.[17] Apocrine glands, in contrast, are fewer in number and localized to specific hairy regions, including the axillae (armpits), groin, perianal area, and areolae of the breasts.[18] These glands are present from birth but remain inactive until puberty, when they are stimulated by androgens to begin secretion.[19] Apocrine sweat is viscous and nutrient-rich, containing lipids, proteins, steroids, and ammonia, which provide substrates that can develop into odorous compounds upon interaction with skin bacteria.[20] Key odor precursors in apocrine secretions include volatile fatty acids, such as 3-methyl-2-hexenoic acid, which imparts a characteristic goat-like scent.[21] Sebaceous glands, associated with hair follicles throughout the body but particularly dense in the face, scalp, and upper trunk, produce sebum—a mixture of oils, waxes, and squalene that lubricates the skin and hair.[22] In axillary regions, sebum can mix with apocrine and eccrine secretions, potentially enhancing the volatility of odor precursors, though its direct contribution to body odor is minor compared to sweat gland outputs.[23] Overall, while eccrine sweat dominates in volume for cooling, apocrine and sebaceous secretions serve as the main physiological sources of body odor precursors in humans. Notably, the axillary regions (armpits) are the primary site of human body odor production, where specialized apocrine glands and associated microbial activity dominate the formation of characteristic odors.[24]Microbial Interactions
The skin microbiome plays a pivotal role in body odor formation, particularly in moist areas such as the axillae and pubic regions, where bacteria metabolize odorless sweat precursors into volatile compounds. Dominant genera include Corynebacterium (approximately 28% abundance), Staphylococcus (21%), and Cutibacterium, which collectively comprise 45–80% of the microbial community in these sites and thrive due to the nutrient-rich, occluded environment provided by apocrine sweat secretions.[25] These bacteria act as commensals but contribute to odor through enzymatic breakdown of sweat components originating from apocrine glands.[9] Biochemical processes involve bacterial enzymes that transform apocrine precursors into odorous volatiles, including thioalcohols, short- and medium-chain fatty acids, and amines derived from protein degradation. Corynebacterium species primarily utilize C–S β-lyases to cleave S-hydroxyalkyl-L-cysteine or L-cysteinylglycine conjugates, yielding thioalcohols such as 3-methyl-3-sulfanylhexan-1-ol (3M3SH), which imparts a pungent, onion-like scent at concentrations of μg–mg L⁻¹.[26] Meanwhile, Staphylococcus metabolizes branched amino acids like L-leucine into short-chain fatty acids (e.g., isovaleric acid, C5), and Corynebacterium employs Nα-acylglutamine aminoacylase to generate medium-chain fatty acids like 3-methyl-2-hexenoic acid (3M2H, C6) from Nα-acyl-L-glutamine conjugates.[26] Amines arise secondarily from bacterial proteases acting on sweat proteins, though they contribute less intensely to overall malodor compared to fatty acids and thioalcohols.[26] The pH of axillary skin, typically ranging from 6.1 to 6.5 under baseline conditions, favors the proliferation of odor-producing bacteria like Corynebacterium and Staphylococcus, as higher pH values enhance microbial enzymatic activity and precursor degradation.[27] Lowering pH below this range, such as to 5.3–5.7, inhibits these bacteria and reduces odor formation.[27] Post-2020 research highlights variations in skin microbiome diversity influenced by age and ethnicity, impacting body odor profiles. Aging is associated with increased alpha diversity (e.g., Shannon index, p=0.043) on facial skin and shifts in axillary composition, including a decline in Cutibacterium acnes (-16.1%, p=0.024) and a rise in Staphylococcus hominis (+9.03%), which produces thioalcohols and contributes to age-specific odors.[28] Ethnic differences show higher Proteobacteria abundance in East Asians compared to Caucasians and Hispanics (p<0.001), with Cutibacterium more prevalent across most groups except African and Latin American populations, potentially altering volatile compound production.[29] These variations emerge post-infancy and stabilize in adulthood, influencing individual odor distinctiveness without direct ties to lifestyle.[29] Environmental factors like moisture and temperature promote microbial growth in odor-prone areas. Warm, humid, and occluded conditions—such as in the axillae, the interdigital spaces of the hands, and the feet—enhance Corynebacterium and Staphylococcus proliferation by providing optimal substrates from sweat, dead skin cells, and oils. In particular, the spaces between the fingers commonly develop noticeable odor in the morning due to the overnight accumulation of sweat, dead skin cells, and oils in these warm, moist, low-ventilation areas, where bacteria metabolize these substances into volatile odorous compounds. This is a common and usually normal occurrence, similar to foot odor, and may be more pronounced if the hands are sweaty or not thoroughly washed before bed. Such dynamics amplify volatile compound release but are independent of modifiable lifestyle elements.[30] Deodorants and antiperspirants alter the armpit microbiome by shifting bacterial composition and reducing the density of odor-causing species. Antiperspirants strongly reduce overall bacterial abundance, which can increase microbial diversity, while favoring families like Staphylococcaceae over Corynebacterium. Regular deodorants have milder impacts, similarly reducing odor-producing bacteria but with less pronounced effects on abundance. Natural aluminum-free deodorants cause temporary adjustments to the microbiome, less aggressive than alcohol-heavy formulas.[31]Evolutionary Functions
In Non-Human Animals
In non-human animals, body odor plays a crucial role in communication and survival through specialized scent glands that produce volatile compounds for marking territories and signaling social status. Many mammals possess anal glands, as seen in dogs (Canis familiaris), which secrete odorous substances used to delineate personal space and convey information about identity and dominance during interactions. Similarly, deer species like the white-tailed deer (Odocoileus virginianus) utilize musk glands located in the abdomen to deposit scents on vegetation, aiding in territorial defense and advertisement of reproductive status to conspecifics. These glandular secretions, often rich in lipids and proteins, persist in the environment to reinforce boundaries and reduce conflicts within populations.[32][33] Pheromonal functions of body odor extend to alarm signaling and attraction across taxa. In insects, such as ants of the genus Tapinoma, the compound 2-methyl-4-heptanone serves as an alarm pheromone released from the anal glands to recruit nestmates during threats, triggering rapid defensive behaviors like biting or fleeing. In rodents, major urinary proteins (MUPs) in male house mice (Mus musculus) bind and slowly release volatile ligands, functioning as attractants that draw females to potential mates by enhancing the salience of urinary scents over distances. These pheromones facilitate coordinated group responses and mate location, underscoring odor's role in social cohesion.[34][35] Evolutionary adaptations amplify body odor's utility in detection and defense. The vomeronasal organ (VNO), a specialized chemosensory structure present in many mammals and reptiles, detects pheromones with high sensitivity, enabling responses to conspecific scents that influence aggression or affiliation without reliance on the main olfactory system. For predator avoidance, skunks (Mephitis mephitis) employ anal gland spray containing thiols as a potent deterrent, repelling attackers through intense, lingering odor and irritation that signals unprofitability. Studies on gray wolves (Canis lupus) reveal that scent marking contributes to pack hierarchy by allowing subordinates to recognize dominant individuals' odors, thereby maintaining order and minimizing intra-group strife through olfactory cues alone.[36][37][38] Body odor also enables kin recognition, fostering familial bonds essential for cooperative behaviors. In mice, urinary volatiles influenced by major histocompatibility complex (MHC) genes provide distinct odor profiles that allow individuals to discriminate relatives from non-kin, promoting nepotistic aid in nesting or foraging without direct visual cues. This olfactory kinship signaling, conserved across vertebrates, supports inclusive fitness by directing resources toward genetic relatives.[39][40]In Humans
In humans, body odor serves primarily vestigial functions compared to its more pronounced roles in non-human animals, where apocrine glands facilitate overt chemical communication for territory marking and mate attraction. Although human apocrine glands are fewer and less distributed—concentrated mainly in the axillae and pubic regions—their secretions retain a capacity for subtle signaling, contributing to interpersonal cues amid the dominance of eccrine glands for thermoregulation.[41] Body odor acts as a social signal conveying information about an individual's health, hygiene, and emotional state. For instance, apocrine sweat produced under stress contains compounds like androstadienone, which can influence observers' mood, focus, and behavioral responses, such as increasing individualistic tendencies while reducing cooperation.[42] These chemosignals from stress sweat, distinct from thermal eccrine sweat, may alert others to potential threats or emotional arousal, fostering adaptive social interactions.[43] Anthropological studies in hunter-gatherer societies, such as the Jahai of Malaysia, indicate that body odor contributes to mate choice by signaling genetic compatibility and vitality, with participants in traditional settings rating unmasked odors as key factors in attraction.[44] Neuroimaging research from the 2010s further reveals that human body odors are processed in brain regions associated with emotion and social cognition, such as the insula and fusiform gyrus, rather than primary olfactory areas, underscoring their role in subconscious emotional evaluation.[45][46] Developmentally, human body odor undergoes significant changes, remaining minimal in infancy due to inactive apocrine glands and reliance on eccrine secretions, which are largely odorless until microbial breakdown.[5] At puberty, typically around ages 10-14, apocrine glands activate under hormonal influence, leading to increased volatile compound production and the onset of characteristic axillary and genital odors that persist into adulthood.[47] This transition not only marks physiological maturation but also enhances the potential for odor-based social signaling in reproductive contexts.[9]Genetic Influences
Major Histocompatibility Complex
The Major Histocompatibility Complex (MHC) in humans, known as the human leukocyte antigen (HLA) system, consists of a cluster of genes on chromosome 6 that encode cell-surface proteins essential for the adaptive immune response, particularly in antigen presentation to T cells. These genes exhibit extreme polymorphism, with over 42,000 known alleles across HLA loci such as HLA-A, HLA-B, and HLA-DR as of 2024, making each individual's MHC profile highly unique and influencing the diversity of immune recognition. This genetic variability extends to body odor, as MHC alleles correlate with distinct volatile compounds in sweat and skin secretions, contributing to individualized odor profiles that may serve as olfactory signals.[48][49] Pioneering research has demonstrated that MHC dissimilarity influences odor preferences, particularly in mate selection, to promote genetic diversity in offspring immunity. In the 1995 "sweaty T-shirt" experiment, women exposed to T-shirts worn by men for two nights rated odors from MHC-dissimilar men as more pleasant and less intense, suggesting an subconscious drive to avoid inbreeding and enhance hybrid vigor in immune function; this preference was modulated by hormonal status, with oral contraceptive users showing reversed patterns. Subsequent studies have replicated these findings, confirming that MHC-heterozygous individuals produce odors perceived as more attractive, linking odor cues to evolutionary advantages in partner choice. However, while genetic factors like MHC can contribute to perceptions of body odor as mildly pleasant, true natural body fragrances that are distinctly floral or fruity, akin to perfumes, are rare and almost nonexistent in humans. Most perceived pleasant scents are attributable to external products such as soaps, lotions, or detergents, or are subjective due to factors like affection. Genetic variations in odorant receptors can cause some individuals to perceive certain body odor compounds, such as androstenone, as sweet or floral, but this variability does not typically result in aromatic natural scents for the majority. Mild pleasantness may also arise from interactions with diet or hygiene, but remains subtle rather than strongly aromatic.[50][51][52][53] One hypothesized mechanism involves MHC-associated volatiles, such as branched-chain carboxylic acids (e.g., 3-methyl-2-hexenoic acid), potentially varying by HLA genotype through the binding of peptides or their metabolites to MHC molecules, which may then be released via apocrine sweat glands and modulated by skin microbiota. However, empirical evidence for specific genotype-linked volatile patterns remains limited, with studies indicating no clear HLA associations for key odorous carboxylic acids in axillary secretions. The precise biochemical pathways linking MHC to odor profiles are still under investigation, with recent reviews suggesting that MHC-derived peptides may play a more direct role in olfactory signaling than volatiles.[54][55][49][56] Body odor can signal health status, particularly infection or inflammation, as immune activation alters volatile emissions in sweat within hours, allowing potential mates to assess immunocompetence and avoid disease transmission risk. This olfactory health signaling integrates with broader immune dynamics, potentially aiding in kin recognition and disease avoidance, though direct ties to MHC-specific volatiles are not established.[57][58] While MHC influences individual odor profiles and there may be variations in microbiome composition across ethnic groups, perceptions of body odor differences across cultural groups are not racially determined but are often influenced by factors such as diet (e.g., consumption of garlic, onions, and spices), environmental exposures like increased sweating from manual labor, and socio-economic factors affecting access to hygiene products; hygiene varies person-to-person, not by race.[59][60][61]ABCC11 Gene
The ABCC11 gene encodes a member of the ATP-binding cassette (ABC) transporter family, specifically ABCC11 (also known as MRP8), which functions as an apical efflux pump responsible for transporting lipids and other precursors essential for apocrine sweat secretion in glands such as those in the axillae and ceruminous glands of the ear.[62] This transporter facilitates the secretion of odor precursors that, upon bacterial metabolism, contribute to axillary body odor.[63] A key single nucleotide polymorphism (SNP), 538G>A (rs17822931), results in a glycine-to-arginine substitution at amino acid position 180 (G180R), leading to a loss-of-function variant that impairs the protein's transport activity.[64] The homozygous AA genotype of this SNP is associated with significant phenotypic effects, including the production of dry, flaky earwax (instead of wet, sticky earwax) and a marked reduction in axillary body odor due to decreased apocrine sweat lipid content and altered microbial substrate availability.[65] Individuals with the AA genotype exhibit less apocrine sweat secretion and odorless axillary secretions, as the dysfunctional ABCC11 protein fails to export necessary lipid precursors for bacterial odor formation.[66] This genotype predominates in East Asian populations, with allele frequencies reaching 80-95%, contrasting with much lower frequencies (0-3%) in European and African populations.[67] The link between ABCC11 and reduced body odor was established in 2009 through studies demonstrating a strong association between the 538G>A SNP and axillary osmidrosis (excessive underarm odor), where the GG and GA genotypes correlate with wet earwax and higher odor intensity, while AA homozygotes show minimal odor.[68] Genetic variations in ABCC11 affect sweat composition by determining the amount of lipid precursors secreted in apocrine sweat, which skin bacteria metabolize into volatile organic compounds (VOCs) such as (E)-3-methyl-2-hexenoic acid and 3-methyl-3-sulfanylhexan-1-ol. Individuals with the functional G allele produce higher levels of these precursors, leading to greater production of odorous VOCs and stronger body odor intensity. Genetic factors also influence axillary skin microbiota composition, modulating the efficiency and type of volatile compound production from sweat precursors.[69] Population genetic analyses reveal a clinal distribution of the A allele, with high frequencies in East Asia decreasing progressively westward through Central and South Asia (30-50% in some groups) to near absence in Europe, suggesting historical migration patterns from Northeast Asia.[65] Evolutionary analyses indicate that the A allele has undergone positive selection in East Asian populations, potentially conferring advantages such as reduced body odor in cold climates by minimizing heat loss through apocrine secretions or aligning with cultural hygiene practices that favor lower odor profiles.[70] This selection signal is evident in extended haplotype homozygosity around the ABCC11 locus, highlighting its adaptive significance without interaction from other major genetic factors like the major histocompatibility complex.[63] While the ABCC11 gene contributes to population-level variations in body odor, perceptions of differences across cultural groups are not racially determined but influenced by non-genetic factors including diet (e.g., garlic, onions, and spices in cuisines like Mexican, which can affect sweat scent through volatile compounds), environmental factors such as increased sweating in manual labor occupations common in certain immigrant groups, and class-based biases linked to poverty and limited access to hygiene products; ultimately, hygiene varies person-to-person rather than by race.[59][60][61][71]Factors Modifying Odor
Body odor intensity varies among individuals, and in some cases, it can be strong enough to be detectable from a distance. This often results from higher production of volatile organic compounds produced by bacteria breaking down apocrine sweat, particularly in areas like the armpits and groin. Contributing factors include genetics (influencing sweat composition and skin microbiota), diet (especially sulfur-rich foods), hormonal changes (such as puberty, stress, and menopause), excessive sweating (from heat, exercise, hyperhidrosis, or other causes), poor hygiene, and certain medical conditions like bromhidrosis or infections. Environmental conditions such as heat, humidity, and poor ventilation can enhance odor intensity by promoting sweat production, bacterial growth, and the evaporation and dispersion of volatile molecules.[7][3][9]Diet and Lifestyle
Dietary choices significantly influence body odor through the production of volatile compounds that are metabolized and excreted via sweat, breath, and other secretions. Consumption of sulfur-rich foods such as garlic and onions leads to the formation of allyl methyl sulfide (AMS), a volatile metabolite that is exhaled in breath and secreted in sweat, contributing to a persistent pungent odor that can increase intensity and be more noticeable. This compound arises from the breakdown of organosulfur precursors like allicin in Allium vegetables, which are absorbed into the bloodstream and eliminated through sweat. A healthy diet low in such strong spices, combined with adequate water intake, can help dilute sweat and reduce the intensity of these odor-causing volatile compounds.[60][72] Red meat intake has been shown to alter axillary body odor, making it less attractive to others. In a controlled study involving male participants on meat versus non-meat diets for two weeks, odor samples from the meat diet group were rated as less pleasant and more intense.[73] Certain spices, including cumin, can impart a distinctive aroma to body odor. These effects stem from phenolic and sulfur-containing compounds in spices that are metabolized and released through perspiration, often amplified by skin microbiota.[74] Alcohol consumption modifies body odor via its metabolic byproducts. During metabolism, ethanol is converted to acetaldehyde, which can be detected in perspiration and contributes to a fruity or vinegary scent, particularly in heavy drinkers.[75] While certain dietary choices, such as increased consumption of fruits and vegetables, have been associated with more pleasant body odors, often described as having mild floral, fruity, or sweet qualities, true natural aromatic body fragrances resembling rose or fruit-like scents are rare in humans. Most perceptions of pleasant body scents are attributable to external products such as soaps, lotions, and perfumes, or to subjective factors influenced by personal affection, genetics, diet, or hygiene, but these mild pleasant scents are not typically strongly aromatic.[53][76][77] Lifestyle habits further modulate body odor intensity and quality. Smoking introduces a smoky scent through the excretion of tobacco alkaloids and their metabolites, such as cotinine, in sweat and sebum, leading to a characteristic stale odor on the skin and clothing.[78] Exercise exacerbates body odor by increasing sweat volume from eccrine and apocrine glands, providing more substrate for bacterial decomposition into odorous compounds like 3-methyl-2-hexenoic acid. Excessive sweating, such as in hyperhidrosis, can further intensify body odor by increasing the amount of sweat available for bacterial breakdown.[79][7] Close physical contact with another person, such as hugging, kissing, or sexual intercourse, can result in the temporary transfer of another person's scent through sweat, skin bacteria, and microbiota, causing their scent to linger on the body. For general contact like hugging or kissing, the effect is typically short-lived, lasting hours to about a day, and is readily removed by showering and changing clothes. In intimate contact, particularly involving genital areas, microbial changes can persist longer, for several days (up to approximately 3 days in some studies). These effects are transient, and body odor itself is not permanently transmitted.[80][81] Sexual activity can also temporarily alter or intensify body odor. The physical exertion and physiological arousal associated with intercourse increase sweat production, similar to other forms of vigorous exercise, thereby enhancing bacterial metabolism of sweat into odorous volatiles. In addition, intimate contact facilitates the exchange of microbiota between partners, which can temporarily modify skin and genital microbial communities and influence odor profiles. The odor associated with sexual activity is subjective and varies among individuals, but is commonly described as musky, sweaty, or earthy, resulting from a mixture of perspiration (especially apocrine sweat), genital fluids, pheromones, and bodily secretions. Semen is often described as having a bleach-, chlorine-, or ammonia-like smell due to its alkaline nature. Healthy vaginal odors are typically tangy, sour, or slightly metallic, but may intensify after sex due to temporary pH changes from the mixing of semen and vaginal fluids. Anecdotal reports commonly describe a distinct "post-sex" or intensified odor following sexual activity, often attributed to the mixing of bodily fluids (particularly genital secretions), hormonal shifts, and microbial transfer; these changes are frequently more pronounced in localized genital areas than in general axillary body odor. Such alterations are generally considered normal and transient, varying by individual, but persistent or unusually foul odors may warrant improved hygiene practices or medical evaluation to rule out underlying conditions.[82][1] Body odor in apocrine-rich areas such as the groin can become particularly pronounced during or after exercise due to increased sweat production and the resulting moist, warm environment that promotes bacterial breakdown of apocrine sweat, which is rich in proteins and lipids, into volatile odorous compounds. This process can lead to strong or foul odors in the groin and genital regions. Contributing factors include poor hygiene, which allows greater bacterial accumulation; tight or non-breathable clothing, which traps moisture and restricts airflow; obesity, which creates additional skin folds that retain moisture; certain dietary patterns, such as high intake of proteins or sulfur-containing foods that may influence sweat composition; and conditions like intertrigo, an inflammatory skin disorder in moist skin folds that can lead to secondary bacterial or fungal overgrowth and foul-smelling odors.[7][83][3][84] Hygiene practices, such as regular shaving of axillary hair, reduce bacterial colonization by minimizing the habitat for odor-producing microbes like Corynebacterium, thereby decreasing overall odor intensity. Clinical evaluations confirm that shaved underarms exhibit lower bacterial loads and more favorable odor profiles compared to unshaved ones.[85] In populations with spice-heavy diets, body odor often reflects these culinary traditions through the excretion of aromatic metabolites in sweat. Perceptions of body odor differences across cultural groups are frequently attributed to such dietary variations, for example, the consumption of garlic, onions, and spices in Mexican cuisine, which can lead to distinct sweat scents via volatile sulfur compounds. Additionally, lifestyle factors like increased sweating from manual labor jobs, often more prevalent among immigrant populations due to socio-economic circumstances, contribute to these perceptions. Class-based biases may associate poverty with limited access to hygiene products, exacerbating stereotypes. However, hygiene practices and body odor intensity vary significantly from person to person, influenced by individual genetics and microbiome, rather than by race.[75][74][86][9]Gender and Hormonal Variations in Body Odor
Body odor exhibits variations between genders and is influenced by hormonal fluctuations including puberty, stress, the menstrual cycle, pregnancy, or menopause, as well as diet, hygiene practices, and skin microbiota. These are normal physiological differences, with hormonal changes contributing to fluctuations in odor profiles. In women, natural body odors vary across body regions:- The vaginal/vulvar area often produces a tangy, sour, or slightly metallic scent, similar to yogurt or sourdough bread, primarily due to lactobacilli bacteria maintaining an acidic vaginal environment. Mildly musky or earthy odors are also common and normal. These odors may temporarily intensify after sexual activity due to pH changes from the introduction of alkaline semen. During menstruation, the presence of menstrual blood can contribute to a more pronounced metallic odor due to iron in the blood. Many reports from online communities like Reddit indicate that it is possible to smell when someone is menstruating, with common descriptions including metallic, musky, sweet-meaty, or fishy odors from period blood or changes in body/vaginal scent. These are often noticeable in close proximity, during heavy flow, or if hygiene products are not changed frequently, with some users reporting detection on others or themselves, or concerns about being detected.[87][1][88][89]
- Axillary (armpit) regions typically have a musky scent, sometimes onion-like or grapefruit-like, resulting from bacterial metabolism of sweat compounds such as 3-methyl-3-sulfanylhexan-1-ol. This differs from men, where axillary odors are more commonly cheesy due to compounds like 3-hydroxy-3-methylhexanoic acid.[2]
- The groin area can exhibit stronger, sweatier, or musky odors, arising from apocrine gland secretions and bacterial activity in the moist, warm environment.[90]
