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Prehypertension
Prehypertension
Prehypertension
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Prehypertension
Other namesHigh normal blood pressure, borderline hypertensive (BH)
SpecialtyCardiology

Prehypertension, also known as high normal blood pressure and borderline hypertensive (BH),[1] is a medical classification for cases where a person's blood pressure is elevated above optimal or normal, but not to the level considered hypertension (high blood pressure). Prehypertension is now referred to as "elevated blood pressure" by the American College of Cardiology (ACC) and the American Heart Association (AHA).[2] The ACC/AHA define elevated blood pressure as readings with a systolic pressure from 120 to 129 mm Hg and a diastolic pressure under 80 mm Hg.[3] Readings greater than or equal to 130/80 mm Hg are considered hypertension by ACC/AHA and if greater than or equal to 140/90 mm Hg by ESC/ESH.[4] and the European Society of Hypertension defines "high normal blood pressure" as readings with a systolic pressure from 130 to 139 mm Hg and a diastolic pressure 85-89 mm Hg.[5]

Classification of blood pressure is based upon two or more readings at two or more separate occasions, and compared to out-of-office blood pressure readings if possible.[6][7]

Signs and symptoms

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Prehypertension is often asymptomatic (without symptoms) at the time of diagnosis. Only extremely elevated blood pressure (malignant hypertension) can, in rare cases, cause headaches, visual changes, fatigue, or dizziness, but these are nonspecific symptoms which can occur with many other conditions. Thus, blood pressures above normal can go undiagnosed for a long period of time.

Causes

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Elevated blood pressure develops gradually over many years usually without a specific identifiable cause. However, possible medical causes, such as medications, kidney disease, adrenal problems or thyroid problems, must first be excluded. High blood pressure that develops over time without a specific cause is considered benign or essential hypertension. Blood pressure also tends to increase as a person ages.

Management

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To lower the risk of prehypertension progressing to hypertension, modification of lifestyle or behaviors is necessary.

Lifestyle modifications

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Diet

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A low-sodium, high potassium diet is recommended, along with increasing physical activity to at least thirty minutes a day most days of the week, quitting smoking, reducing alcohol consumption, and maintaining a healthy weight.[8]

Specifically, a diet that is high in fruits and vegetables (aim for half of your meal including non-starchy vegetables, like leafy greens, beans, carrots, cucumbers, tomatoes, etc.), whole grains, low in refined grains (e.g., white breads and baked goods made from white flour), low in saturated fats ( e.g., fatty cuts of meat or fried foods) and low in sodium (homemade or minimally processed) have been demonstrated through randomized controlled studies to significantly lower blood pressure. These types of diet changes alone can lower blood pressure greater than any single drug therapy. The effects of both diet and sodium reduction work together, meaning the more you improve your diet to include less saturated fat and more fruits and vegetables OR lower your sodium intake significantly below what is typical in industrialized nations, like the United States, the greater the benefit will be seen. Similarly, the better the quality of diet, the more the results will be seen. Significant results have been seen in 30 days.[9]

Foods rich in potassium include banana, papaya, sweet potato, dark leafy greens, avocado, prune juice, tomato juice, oranges, milk, yogurt, dried beans such as navy, pinto and black beans, chickpeas, lentils, beef, pork, fish, nuts and seeds such as pistachio, almonds, pumpkin, flax and sunflower seeds.[10]

Exercise

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Exercise including aerobic exercise,[11][12]  isometric exercise,[11][12]  dynamic resistance training,[11][13] Tai Chi,[12]  Qigong,[12]  and Yoga[12][14]  can reduce blood pressure in prehypertensive individuals.

Sleep

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Lack of sleep can increase blood pressure, and longer sleep cycles may reduce blood pressure in prehypertensive individuals.[15]

Stress

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Stress reducing techniques can improve elevated blood pressure.[16]

Monitoring

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Careful monitoring for signs of end-organ damage or progression to hypertension is an important part of the follow-up of patients with prehypertension. Any change in blood pressure classification should be confirmed on at least one subsequent visit.

The major indication for pharmacologic antihypertensive therapy is progression to hypertension. The threshold is lower in patients with diabetes, chronic kidney failure, or cardiovascular disease.[17] The target blood pressure for these conditions is currently less than 120/80 mm Hg.

Home monitoring

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Home monitoring of blood pressure can be used to monitor and track prehypertensive patients. This can help to raise the awareness of the patient and his / her doctor if blood pressure levels rise to hypertensive levels. Home monitoring can help to avoid white coat hypertension which results in blood pressure levels being elevated due to the presence of a doctor or physician in a "white coat". Monitoring at home or work at regular times each day helps to diagnose a patient with prehypertension or hypertension.

The American Heart Association website[18] says, "You may have what's called 'white coat hypertension'; that means your blood pressure goes up when you're at the doctor's surgery. Monitoring at home will help you measure your true blood pressure and can provide your doctor with a log of blood pressure measurements over time. This is helpful in diagnosing and preventing potential health problems."

People using home blood pressure monitoring devices are increasingly also using blood pressure charting software. These charting methods provide print outs for the patient's physician and reminders to check blood pressure.

Medication

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Patients with other health conditions and elevated blood pressure, especially those with diabetes, kidney disease or heart disease, may be advised to take blood pressure medication.[19]

Prognosis

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The extent to which prehypertension constitutes a serious health concern remains controversial.[20] Several long-term studies have suggested no significant increase in all-cause mortality over long periods of time for individuals falling within the prehypertensive range.[21][22] Many studies further indicate a J-shaped relationship between blood pressure and mortality, whereby both very high and very low levels are associated with notable increases in mortality.[23] On the other hand, the National Heart, Lung, and Blood Institute suggests that people with prehypertension are at a higher risk for developing hypertension, or high blood pressure, compared to people with normal blood pressure.[24]

A 2014 meta-analysis concluded that prehypertension increases the risk of stroke, and that even low-range prehypertension significantly increases stroke risk[25] and a 2019 meta-analysis found elevated blood pressure increases the risk of heart attack by 86% and stroke by 66%.[26]

Epidemiology

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Data from the 1999 and 2000 National Health and Nutrition Examination Survey (NHANES III) estimated that the prevalence of prehypertension among adults in the United States was approximately 31 percent and decreased to 28 percent in the 2011–2012 National Health and Nutrition Examination Survey.[27] The prevalence was higher among men than women.[27]

Risk factors

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A primary risk factor for prehypertension is being overweight. Other risk factors include a family history of hypertension, a sedentary lifestyle, eating high sodium foods, smoking, and excessive alcohol or caffeine intake.[28]

See also

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia

Prehypertension

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Prehypertension, a term introduced in 2003 by the Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7), describes readings that are higher than normal but not yet in the hypertensive range, specifically systolic of 120 to 139 mm Hg or diastolic of 80 to 89 mm Hg. This classification aimed to identify individuals at increased risk for developing and (CVD) before clinical manifests. However, the term has largely been phased out in favor of more nuanced categories in subsequent guidelines. In the 2017 / (ACC/AHA) guidelines, prehypertension was reclassified into two groups: elevated blood pressure (systolic 120–129 mm Hg and diastolic <80 mm Hg) and stage 1 hypertension (systolic 130–139 mm Hg or diastolic 80–89 mm Hg), reflecting evidence that even these levels confer elevated CVD risk. The 2025 ACC/AHA guideline maintains this framework, defining normal blood pressure as <120/<80 mm Hg, elevated as 120–129/<80 mm Hg, and stage 1 hypertension as 130–139/80–89 mm Hg, with diagnosis based on the average of at least two readings on at least two separate occasions in a clinical setting, confirmed by out-of-office monitoring such as ambulatory or home blood pressure measurement to account for white-coat or masked effects. These categories, primarily from U.S. guidelines, underscore that blood pressure in the prehypertension range—now split—signals a continuum of risk, with historical U.S. prevalence estimates around 30% before reclassification. Key risk factors for progressing from prehypertension to hypertension include advancing age, genetic predisposition, obesity (body mass index ≥30 kg/m²), excessive sodium intake (>2,300 mg/day), physical inactivity, and high alcohol consumption (>14 drinks/week for men or >7 for women). Secondary causes, though less common, encompass , , and . Individuals with in this range face approximately a 2-fold higher of CVD events, such as , , and , compared to those with normal , with the escalating if accompanied by comorbidities like or . improves with early intervention, as lifestyle modifications can significantly reduce progression , though untreated cases often advance to , with studies showing about 20–30% progression over 4 years. Diagnosis involves comprehensive evaluation beyond , including history, physical exam, laboratory tests (e.g., serum electrolytes, , fasting glucose), electrocardiogram, and CVD using tools like the PREVENT equations to estimate 10-year risk. Differential diagnoses include white-coat hypertension, , and acute stressors like anxiety or medication effects. Management prioritizes nonpharmacological interventions for all with elevated or stage 1 without high CVD risk: the (Dietary Approaches to Stop ) diet, which emphasizes fruits, , and low-fat ; sodium restriction to <1,500–2,300 mg/day; regular aerobic exercise (90–150 minutes/week of moderate intensity); weight loss (5–10% of body weight if overweight); and smoking cessation, potentially lowering systolic by 4–8 mm Hg collectively. Pharmacotherapy, such as thiazide diuretics, ACE inhibitors, or calcium channel blockers, is recommended for stage 1 if 10-year CVD risk is ≥7.5% (per 2025 guidelines, lowered from 10% in 2017), existing CVD, diabetes, or chronic kidney disease, with a target of <130/80 mm Hg to optimize outcomes while minimizing adverse effects. Team-based care, including telehealth monitoring, enhances adherence and long-term control.

Definition and Classification

Historical Definition

Prehypertension was formally introduced as a distinct blood pressure category in the Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC 7), published in 2003 by the National Heart, Lung, and Blood Institute (NHLBI). This report defined prehypertension in adults without hypertension as a systolic blood pressure of 120–139 mm Hg or a diastolic blood pressure of 80–89 mm Hg. The term was created to bridge the gap between normal blood pressure (less than 120 mm Hg systolic and 80 mm Hg diastolic) and hypertension (140 mm Hg systolic or 90 mm Hg diastolic or higher), highlighting a continuum of risk rather than a binary state. The primary purpose of establishing prehypertension was to identify individuals at elevated short-term risk for progressing to hypertension and developing cardiovascular disease (CVD), enabling earlier preventive measures before blood pressure reaches hypertensive thresholds. The JNC 7 guidelines emphasized that this category underscores the importance of lifestyle interventions, such as weight control, increased physical activity, and dietary modifications, to avert or delay the onset of frank hypertension and associated complications. By adopting this classification, the NHLBI aimed to shift clinical focus toward proactive risk stratification in primary care settings. This introduction marked a significant evolution in hypertension guidelines, which were reclassified in subsequent updates, such as the 2017 ACC/AHA guidelines, into terms like elevated blood pressure and stage 1 hypertension.

Current Terminology and Relation to Hypertension Stages

The term "prehypertension," previously used to describe blood pressure levels between 120 and 139 mm Hg systolic or 80 and 89 mm Hg diastolic, was eliminated in the 2017 American Heart Association (AHA)/American College of Cardiology (ACC) guidelines, with these ranges reclassified to emphasize early intervention and risk stratification. Instead, blood pressure in the 120-129 mm Hg systolic and less than 80 mm Hg diastolic range was designated as "elevated blood pressure," while 130-139 mm Hg systolic or 80-89 mm Hg diastolic was categorized as stage 1 hypertension. Normal blood pressure remains below 120 mm Hg systolic and 80 mm Hg diastolic. This redefinition aimed to better align terminology with the continuous risk gradient of blood pressure elevations for cardiovascular disease (CVD). The 2025 AHA/ACC guidelines confirm and retain these blood pressure classifications, maintaining normal blood pressure as less than 120/80 mm Hg, elevated blood pressure as 120-129/<80 mm Hg, and stage 1 hypertension as 130-139/80-89 mm Hg. Elevated blood pressure is explicitly recognized as a precursor to CVD, reflecting its role in the progression toward hypertension and associated complications. Stage 1 hypertension now encompasses the upper range of what was formerly termed prehypertension, underscoring the need for proactive management in this group. Key to contemporary management is the use of the PREVENT calculator, introduced by the AHA, to estimate 10-year CVD risk and guide decisions for individuals with elevated blood pressure or stage 1 hypertension. A 10-year CVD risk of 7.5% or greater, as determined by PREVENT, prompts consideration of pharmacotherapy alongside lifestyle interventions, particularly for stage 1 hypertension. The 2025 guidelines further emphasize team-based care, involving multidisciplinary teams such as physicians, nurses, and pharmacists, to enhance risk assessment, adherence, and overall CVD prevention. Elevated blood pressure is associated with a 1.1- to 1.5-fold increased risk of CVD events, such as coronary heart disease and stroke, compared to normal blood pressure levels. For stage 1 hypertension, this risk escalates to 1.5- to 2.0-fold, necessitating individualized risk stratification using tools like PREVENT to tailor interventions.

Epidemiology

Prevalence and Distribution

Prehypertension, historically defined as blood pressure readings of 120–139 mmHg systolic or 80–89 mmHg diastolic, affected approximately 20–30% of adults worldwide based on studies prior to the 2017 guideline updates. With the reclassification under the 2017 ACC/AHA guidelines, this spectrum is now divided into elevated blood pressure (120–129 mmHg systolic and <80 mmHg diastolic) and stage 1 hypertension (130–139 mmHg systolic or 80–89 mmHg diastolic), reflecting a continuum of risk rather than a distinct diagnostic entity. Estimates indicate that elevated blood pressure affects about 25–30% of adults in high-income settings like the United States, while stage 1 hypertension contributes to the overall hypertension prevalence of 46.7% (as of 2017–2020). In the United States, National Health and Nutrition Examination Survey (NHANES) data from 2017–2020 reveal an overall hypertension prevalence of 45.4% among adults (age-adjusted), with higher rates among men (51.0%) compared to women (39.7%). Distribution patterns show higher rates among middle-aged adults aged 40–59 years, where prevalence exceeds 50%, and among specific ethnic groups, such as non-Hispanic Black adults at approximately 57%. These disparities underscore the influence of age and socioeconomic factors on blood pressure elevation. Globally, hypertension prevalence is estimated at 33% among adults aged 30–79 years (1.4 billion people as of 2024), with higher rates in low- and middle-income countries driven by urbanization and dietary shifts. Trends indicate a rising burden, linked to the ongoing obesity epidemic; the American Heart Association's 2025 guidelines highlight that nearly half of U.S. adults have hypertension, emphasizing the need for early intervention to curb progression to frank hypertension.

Risk Factors

Prehypertension, now often referred to as elevated blood pressure in contemporary guidelines, is influenced by a range of modifiable risk factors that contribute to its development and progression. Obesity, particularly with a body mass index (BMI) greater than 30 kg/m², significantly elevates the risk, accounting for 65-78% of essential hypertension cases and approximately doubling the likelihood of prehypertension compared to normal-weight individuals. A high-sodium diet exceeding 2,300 mg per day promotes blood pressure elevation, while low potassium intake exacerbates this effect by impairing vascular function. Physical inactivity, defined as less than 150 minutes of moderate aerobic exercise per week, is associated with higher systolic blood pressure levels and increased incidence. Excessive alcohol consumption, more than 1-2 standard drinks per day, raises risk through direct vascular effects, and contributes by promoting endothelial dysfunction. Non-modifiable risk factors play a foundational role in susceptibility. Advancing age, particularly beyond 45 years, is linked to a 2-3-fold increase in prehypertension prevalence due to progressive arterial stiffening and reduced vascular compliance. Family history confers genetic predisposition, with heritability estimates ranging from 30-50%, reflecting polygenic influences that explain up to 10% of blood pressure variance. Ethnic disparities are evident, with non-Hispanic Black adults facing higher rates—approximately 57% prevalence of hypertension—compared to other groups, as highlighted in the 2025 AHA/ACC guidelines. Emerging factors further modulate risk, including poor sleep duration of less than 7 hours per night, which disrupts hormonal regulation and elevates sympathetic activity, and chronic stress, which heightens incident hypertension particularly in Black adults. The 2025 guidelines emphasize components of metabolic syndrome, such as dyslipidemia, as amplifiers of prehypertension risk. Specific mechanisms include salt sensitivity, observed in about 50% of hypertension cases especially among older adults and those with obesity, leading to exaggerated blood pressure responses to sodium. Insulin resistance serves as a key bridge to hypertension, promoting endothelial dysfunction and vascular remodeling in susceptible individuals.
Risk Factor CategoryExamplesKey Impact
ModifiableObesity (BMI >30 kg/m²), high-sodium diet (>2,300 mg/day), physical inactivity (<150 min/week), excessive alcohol (>1-2 drinks/day), smokingDoubles or substantially increases incidence; lifestyle changes can reduce systolic by 4-13 mm Hg
Non-ModifiableAge (>45 years), family history ( 30-50%), ethnicity (e.g., higher in )2-3x higher prevalence with age; genetic and demographic factors drive baseline susceptibility
EmergingPoor (<7 hours/night), , low potassium intake, (e.g., )Elevates risk via hormonal and inflammatory pathways; salt sensitivity in ~50% of cases

Pathophysiology

Underlying Mechanisms

Prehypertension involves several interconnected biological processes that contribute to elevated in the range of 120-139/80-89 mm Hg. A primary mechanism is , characterized by reduced (NO) bioavailability, which impairs endothelium-dependent and promotes . This dysfunction arises from an altered L-arginine-NO pathway, where exogenous L-arginine can restore in early stages, indicating a reversible defect without significant involvement of endothelium-derived contracting factors. overactivity further exacerbates this by increasing and vascular tone, as evidenced by enhanced modulation and impaired parasympathetic activity in prehypertensive individuals. Additionally, activation of the renin-angiotensin-aldosterone system (RAAS) leads to increased angiotensin II levels, which stimulate and sodium retention, contributing to the progression from prehypertension to frank . Vascular changes in prehypertension include early arterial remodeling and hypertrophy, driven by mechanical stress and neurohormonal factors, resulting in increased vascular stiffness and reduced compliance. This remodeling is associated with low-grade inflammation, where cytokines such as tumor necrosis factor-α (TNF-α) play a key role in promoting vascular smooth muscle proliferation and extracellular matrix deposition. These inflammatory processes, part of a broader immuno-metabolic syndrome, link prehypertension to premature vascular aging. Renal factors contribute through impaired sodium excretion and blunted pressure natriuresis, where elevated renal pressure fails to adequately increase sodium output, leading to fluid retention and higher . This impairment shifts the pressure-natriuresis curve rightward, a feature observed in early models and linked to genetic and sympathetic influences on renal function. Recent insights from the 2025 advisory highlight the role of the gut in salt handling, noting that high sodium intake disrupts microbial balance—depleting beneficial taxa like —and reduces prohypotensive metabolites such as , thereby exacerbating renal sodium retention and elevation. Hemodynamically, prehypertension in younger individuals often features elevated , driven by increased and , which transitions over time to predominant increases in peripheral as stiffness develops. Studies in adolescents and young adults show prehypertensives have higher (approximately 5624 mL/min) and total peripheral resistance index (2805 dynes·s·cm⁻⁵·m²) compared to normotensives, underscoring this shift as a core pathogenic feature.

Contributing Physiological Factors

Insulin resistance, a hallmark of , contributes to prehypertension by enhancing renal sodium retention through activation of the sodium-hydrogen exchanger in the , thereby increasing and pressure. This mechanism is exacerbated in individuals with , where elevated insulin levels promote activation and vascular smooth muscle proliferation. Additionally, elevates levels, which can activate the renin-angiotensin-aldosterone system (RAAS), leading to and further sodium retention that sustains elevated . Metabolic disturbances such as , characterized by high (LDL) , impair endothelial function by promoting and , which reduces bioavailability and contributes to in prehypertension. similarly damages the through advanced end-product formation, fostering a pro-thrombotic state that elevates over time. Visceral releases adipokines like , which heighten tone and increase renal sympathetic outflow, thereby amplifying and in prehypertensive states. Autonomic imbalances, including baroreceptor dysfunction, disrupt the normal feedback regulation of blood pressure, resulting in heightened variability and sustained elevations due to impaired vagal tone and excessive sympathetic activity. Obstructive sleep apnea induces intermittent hypoxia, which activates chemoreceptors and the sympathetic nervous system, leading to nocturnal surges in blood pressure that persist into daytime prehypertension. Genetic and environmental factors interplay in prehypertension through polymorphisms in the (ACE) gene, such as the I/D variant, which influences ACE activity and RAAS-mediated , increasing susceptibility in certain populations. Recent 2025 research highlights epigenetic modifications, including alterations induced by diet and lifestyle, that modulate related to vascular function and , thereby exacerbating prehypertensive risk without altering the underlying DNA sequence.

Signs and Symptoms

Typical Presentations

Prehypertension is characteristically and is typically detected only through routine screenings. This silent progression underscores the importance of regular monitoring, as emphasized in the 2025 AHA/ACC guidelines, which highlight early detection in high-risk groups such as youth to prevent advancement to . Prehypertension itself does not cause symptoms. In some cases, individuals may have co-occurring conditions, such as or , that present with signs like or daytime fatigue, but these are not due to the elevated . The "white coat" effect, where anxiety elevates readings in clinical settings, may occur but does not produce symptoms attributable to prehypertension.

Asymptomatic Nature

Prehypertension is characterized by its lack of noticeable symptoms in affected individuals, earning it recognition as a precursor to the "silent killer" often associated with hypertension. The gradual elevation in blood pressure that defines this condition—typically ranging from 120-139 mm Hg systolic or 80-89 mm Hg diastolic—does not provoke acute physiological alerts, and at this stage, there is generally no significant end-organ damage to the heart, kidneys, or blood vessels that could manifest as overt signs, allowing the condition to progress undetected for years. This asymptomatic profile contributes substantially to underdiagnosis, as individuals often remain unaware of their elevated without routine medical evaluation. The U.S. Preventive Services Task Force (USPSTF) emphasizes the importance of screening, recommending in office settings for all adults aged 18 years and older to identify such cases early (B recommendation). Data indicate significant underdiagnosis of elevated blood pressure, contributing to increased (CVD) risk, with studies showing approximately a 30-40% higher risk of outcomes like and compared to those with normal levels. By contrasting with , where symptoms may emerge from organ strain in later stages, prehypertension underscores the need for proactive detection to mitigate long-term vascular harm.

Diagnosis

Blood Pressure Measurement Methods

Accurate measurement of () is essential for identifying prehypertension, defined as systolic of 120-129 mm Hg and diastolic less than 80 mm Hg, to facilitate early intervention and prevent progression to . The 2025 American Heart Association () guidelines recommend using validated devices across office, ambulatory, and home settings to ensure reliability, with a strong emphasis on out-of-office methods to account for variability and phenomena like white-coat or masked . Office-based BP measurement serves as the initial screening tool and involves the use of validated oscillometric devices, preferred over manual auscultatory methods for consistency (Class of Recommendation [COR] 2a, Level of C-EO). The protocol requires averaging at least two readings, taken 1-2 minutes apart after a 5-minute rest in a seated position, with the arm supported at heart level and an appropriately sized based on arm circumference (typically 80% width and 40% length of the upper arm). These measurements should be repeated on at least two separate occasions to confirm prehypertension, as single readings can be influenced by factors such as recent intake or stress. Proper staff training and periodic competency checks (every 6-12 months) are advised to minimize errors. Ambulatory BP monitoring (ABPM) provides a comprehensive 24-hour profile and is considered the gold standard for confirming prehypertension, particularly to detect masked effects where office readings underestimate true (COR 1, Level of Evidence A). Patients wear a validated oscillometric device that records readings every 15-30 minutes during hours and every 30-60 minutes at night, yielding averages for , nighttime, and overall periods. This method identifies nocturnal hypertension or non-dipping patterns, which are predictive of cardiovascular risk, and corresponds prehypertension thresholds to averages of 120-129/<80 mm Hg. ABPM is especially useful for initial diagnosis in adults with borderline readings. Home BP monitoring (HBPM) empowers patients for ongoing assessment and is recommended for confirming and tracking prehypertension using devices from the validated list at validatebp.org, ensuring accuracy against reference standards. The standard protocol involves duplicate morning and evening measurements (1-2 minutes apart), performed in a seated position with the arm at heart level, for seven consecutive days; the first day's readings are often discarded to account for acclimation, with subsequent averages used for evaluation. Home thresholds align with office values for diagnosis (≥130/80 mm Hg), targeting less than 130/80 mm Hg overall for control, though prehypertension-specific monitoring focuses on maintaining levels below hypertension thresholds through lifestyle tracking. on technique and with healthcare teams enhances adherence and reliability.
MethodKey ProtocolValidated DevicesAdvantages for Prehypertension Detection
Office MeasurementAverage ≥2 readings on ≥2 occasions; 5-min rest, seatedOscillometric via validatebp.orgInitial screening; standardized clinical setting
ABPM24-hour automated; 15-30 min daytime intervalsOscillometric monitorsDetects variability, masked/white-coat effects
HBPMTwice daily for 7 days (discard day 1); seated duplicatesUpper-arm cuff devices from validatebp.orgLongitudinal tracking; patient involvement
The 2025 AHA guidelines underscore out-of-office methods like ABPM and HBPM for precise prehypertension identification, recommending a universal BP control target of less than 130/80 mm Hg to mitigate cardiovascular risks, with encouragement for systolic BP below 120 mm Hg where tolerated.

Screening and Diagnostic Criteria

Screening for prehypertension, now reclassified as elevated blood pressure under contemporary guidelines, is recommended for all adults aged 18 years and older. For adults 18 to 39 years of age who are not at increased risk for hypertension, screening every 3 to 5 years is appropriate; annual screening is advised for adults 40 years and older or those with elevated risk factors such as obesity, diabetes, or family history of hypertension. For individuals identified with elevated blood pressure or stage 1 hypertension and low cardiovascular disease (CVD) risk, repeat measurements are suggested every 3 to 6 months to monitor progression. The historical diagnostic criteria for prehypertension, established by the Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High (JNC 7) in 2003, defined it as systolic blood pressure (SBP) of 120 to 139 mm Hg or diastolic blood pressure (DBP) of 80 to 89 mm Hg. Current guidelines from the 2025 (AHA)/ (ACC) Joint Committee refine this into elevated blood pressure (SBP 120-129 mm Hg and DBP <80 mm Hg) or stage 1 hypertension (SBP 130-139 mm Hg or DBP 80-89 mm Hg), emphasizing that these categories indicate increased CVD risk warranting lifestyle interventions. requires confirmation through the average of at least two blood pressure readings obtained on two separate occasions using standardized office measurement protocols. To exclude secondary causes of elevated blood pressure, initial evaluation includes laboratory assessments such as serum electrolytes, , fasting glucose, and a , particularly in cases with suggestive features like resistant readings or young onset. Escalation to pharmacologic therapy for stage 1 is recommended if the estimated 10-year CVD risk, calculated using the PREVENT equations, is 7.5% or greater. The 2025 AHA/ACC guideline updates incorporate home blood pressure monitoring (HBPM) and ambulatory blood pressure monitoring (ABPM) as preferred methods for confirming office-based findings, with HBPM thresholds aligned to office readings for diagnosis (≥130/80 mm Hg) to detect white-coat or masked hypertension. integration facilitates broader access to screening and diagnostic confirmation, especially in underserved populations, by enabling remote HBPM data review and virtual consultations.
Blood Pressure CategorySystolic BP (mm Hg)Diastolic BP (mm Hg)
Normal<120<80
Elevated120–129<80
Stage 1 Hypertension130–13980–89
This classification, per the 2025 AHA/ACC guideline, guides screening and diagnostic decisions while prioritizing out-of-office monitoring for precision.

Management

Lifestyle Modifications

Lifestyle modifications represent the cornerstone of management for prehypertension, also known as elevated (120-129 mm Hg systolic and <80 mm Hg diastolic), aiming to prevent progression to and reduce cardiovascular risk through non-pharmacologic means. These interventions, supported by randomized controlled trials and meta-analyses, can lower systolic blood pressure by 2-7 mm Hg collectively, depending on adherence and baseline factors. Dietary changes are particularly effective, with the Dietary Approaches to Stop Hypertension (DASH) eating plan—emphasizing fruits, vegetables, whole grains, lean proteins, and low-fat dairy while limiting saturated fats and sweets—reducing systolic by 3-7 mm Hg in individuals with elevated . Reducing sodium intake to less than 2,300 mg per day, ideally 1,500 mg, further lowers systolic by 1-4 mm Hg, with greater effects in salt-sensitive populations. Increasing dietary to 3,500-5,000 mg per day from food sources complements these efforts, yielding an additional reduction; the guideline also recommends considering potassium-based salt substitutes to further support sodium reduction efforts. Regular physical activity is another key strategy, with at least 150 minutes per week of moderate-intensity aerobic exercise (such as brisk walking) combined with muscle-strengthening activities on two or more days per week lowering systolic blood pressure by 2-7 mm Hg. Resistance training alone provides a modest 2-4 mm Hg decrease. For overweight or obese individuals, achieving a 5-10% body weight reduction correlates with systolic blood pressure drops of 3-5 mm Hg. Additional modifications include limiting alcohol to no more than one per day for women or two for men, which can reduce systolic by approximately 3 mm Hg, and to mitigate vascular damage and overall cardiovascular risk, though direct effects are not quantified. techniques, such as or (20 minutes twice daily), lower systolic by 4-5 mm Hg, while ensuring 7-9 hours of per night and treating disorders like (e.g., via ) yield 2-5 mm Hg reductions. When implemented together, these strategies can achieve cumulative systolic reductions of 4-8 mm Hg, as evidenced by demonstrating slowed progression to ; for instance, in the PREVER-Prevention , initial counseling in the group resulted in stable or slightly decreased (systolic from 126.6 to 125.6 mm Hg over 18 months) and prevented in over 80% of participants. The 2025 AHA/ACC guideline emphasizes team-based implementation to enhance adherence and long-term benefits.

Pharmacologic Interventions

Pharmacologic interventions for prehypertension, encompassing elevated (120-129 mm Hg systolic and less than 80 mm Hg diastolic) and stage 1 (130-139 mm Hg systolic or 80-89 mm Hg diastolic), are reserved for individuals who do not achieve control through modifications alone, particularly those with elevated (CVD) risk. According to the 2025 AHA/ACC guideline, medication is recommended for adults with stage 1 and a 10-year CVD risk of 7.5% or greater (as assessed by the PREVENT tool), or in the presence of clinical CVD, , , or (CKD); for lower-risk individuals, a trial of 3-6 months of interventions is advised first, with pharmacologic initiated if remains at or above 130/80 mm Hg. In cases of isolated elevated without high CVD risk, pharmacologic treatment is generally avoided to minimize unnecessary exposure to medications. First-line agents include thiazide-type diuretics (e.g., ), angiotensin-converting enzyme () inhibitors, angiotensin receptor blockers (ARBs), and (CCBs), selected based on comorbidities such as CKD (where inhibitors or ARBs are preferred) or . Single-pill combinations, such as a renin-angiotensin system blocker with a or CCB, are encouraged to improve adherence, particularly for stage 1 hypertension in high-risk patients or stage 2 hypertension. Therapy should begin with low doses, titrated upward based on response and tolerability, following product labeling for approved indications. The target is less than 130/80 mm Hg for most adults, with consideration of intensive control to less than 120 mm Hg systolic in select high-risk individuals without . Evidence supporting these interventions derives from trials like the Systolic Intervention (SPRINT), which demonstrated that intensive blood pressure lowering to less than 120 mm Hg systolic in high-risk adults (baseline systolic blood pressure 130 mm Hg or higher) reduced CVD events by 25% compared to standard control targeting less than 140 mm Hg systolic. Subset analyses from SPRINT and related studies, such as PREVER-Prevention, indicate similar benefits for stage 1 hypertension equivalents, with combination therapy (e.g., 12.5 mg plus amiloride 2.5 mg daily) achieving targets below 130/80 mm Hg and reducing CVD risk without excessive adverse events in lower-risk groups. Monitoring is essential to ensure safety and efficacy, including assessment for before initiation and regular evaluation of serum electrolytes, , and using home or ambulatory monitoring. Common side effects to watch for include with diuretics, or with ACE inhibitors or ARBs, and across agents; laboratory checks are recommended 2-4 weeks after starting or dose changes, then annually if stable. These measures help balance the 20-25% relative reduction in CVD risk against potential harms in prehypertensive patients.

Monitoring and Follow-up

Home and Ambulatory Monitoring

Home blood pressure monitoring (HBPM) involves the use of validated automatic, upper-arm cuff-style devices to track blood pressure outside clinical settings, which is particularly useful for managing prehypertension. Devices should be selected from validated lists such as those available at validatebp.org. The American Heart Association (AHA) recommends these devices over wrist or finger monitors due to their superior accuracy and reliability. A standard protocol entails taking two readings at least one minute apart, both in the morning before eating or taking medications and in the evening before dinner, ideally over 3 to 7 consecutive days to compute a weekly average. According to the 2025 AHA/ACC guidelines, HBPM is preferred for confirming prehypertension diagnoses, with average thresholds below 130/80 mm Hg considered equivalent to normal office blood pressure readings (<120/<80 mm Hg), while 130-139/80-89 mm Hg confirms stage 1 hypertension, aligning with office measurements; many modern devices integrate with smartphone apps and telehealth platforms to facilitate data sharing and remote clinician review. Ambulatory blood pressure monitoring (ABPM) employs a portable, wearable device that automatically records every 15 to 30 minutes over a 24-hour period, providing a comprehensive profile of daily fluctuations. This method is valuable in prehypertension for identifying patterns such as nocturnal dipping, where normally decreases by more than 10% (typically 10-20%) during compared to daytime levels. The 2025 AHA/ACC guidelines endorse ABPM alongside HBPM for out-of-office confirmation, especially when or masked effects are suspected. Both HBPM and ABPM offer benefits in prehypertension management by enhancing patient adherence to lifestyle interventions and minimizing the effect, where office readings are artificially elevated due to anxiety. Evidence from the PAMELA study demonstrates that ambulatory and home measurements provide superior prognostic value over office readings, with lower average ambulatory pressures correlating to reduced cardiovascular risk in individuals with elevated baseline .

Regular Assessment Protocols

Regular assessment protocols for prehypertension, encompassing elevated (systolic 120-129 mm Hg and diastolic <80 mm Hg) and stage 1 (systolic 130-139 mm Hg or diastolic 80-89 mm Hg), emphasize periodic clinical evaluations to monitor progression and guide interventions. For individuals with elevated and low (CVD) risk, assessments are recommended every 3 to 6 months, while those with stage 1 require follow-up every 3 to 6 months, particularly after initiating lifestyle modifications. If risk factors change or trends upward, evaluations should occur more frequently, such as monthly during treatment intensification. Assessments during these visits include repeat blood pressure measurements to track changes, laboratory tests such as lipid profiles, fasting glucose or HbA1c, electrolytes, , and urine albumin-to-creatinine ratio to detect comorbidities, and recalibration of 10-year CVD risk using the PREVENT equations. These evaluations help identify progression, with remaining at or above 130/80 mm Hg after 3 to 6 months of efforts prompting consideration of pharmacologic therapy in low-risk patients. The 2025 AHA/ACC guidelines advocate for multidisciplinary reviews involving physicians, pharmacists, nurses, and dietitians to address barriers to control and tailor management, with adjustments based on progression—such as escalating to stage 2 protocols if targets are unmet. Protocols also incorporate on treatment adherence and lifestyle adherence, reinforced through shared decision-making to enhance long-term engagement. Telehealth options are integrated into these protocols, particularly for patients in remote areas, enabling virtual follow-ups and integration with home or monitoring tools to facilitate timely data review and adjustments without in-person visits.

Prognosis

Progression Risks

Individuals with prehypertension face a substantial of progressing to stage 1 or 2 , with studies indicating that 30% to 38% of cases advance within 4 years in the absence of intervention. This progression rate varies by population and baseline characteristics, but untreated prehypertension consistently shows a higher incidence compared to normal levels. The presence of concomitant risk factors, such as , elevates the progression rate significantly, with some cohorts, particularly those with obesity-related increases in body weight and fat mass, experiencing up to 50% advancement to over 10 years. Key predictors include older age, elevated baseline within the prehypertensive range (e.g., closer to 139/89 mm Hg), and , often indicated by family history of . According to the 2025 AHA/ACC guideline, elevated (120-129/<80 mm Hg) is linked to a markedly higher progression risk than normal , with incremental increases approximately doubling associated cardiovascular hazards that drive hypertensive development. Lifestyle interventions, such as , dietary sodium reduction, and increased , can mitigate this risk by 30% to 50%, as demonstrated in longitudinal analyses from the . These modifications not only slow progression but also address modifiable predictors like , emphasizing their role in primary prevention.

Long-term Cardiovascular Outcomes

Prehypertension is associated with a 1.5- to 2-fold increased risk of (CVD) events, including and , compared to normal levels. A of prospective cohort studies reported a (RR) of 1.55 (95% CI, 1.41-1.71) for overall CVD, 1.50 (95% CI, 1.30-1.74) for coronary heart disease, and 1.71 (95% CI, 1.55-1.89) for among individuals with prehypertension. Similarly, in the Women's Health Initiative cohort of postmenopausal women, prehypertension conferred adjusted hazard ratios (HR) of 1.76 (95% CI, 1.40-2.22) for and 1.93 (95% CI, 1.49-2.50) for over a mean follow-up of 7.7 years. These risks persist even in the lower range of prehypertension (systolic 120-129 mm Hg or diastolic 80-84 mm Hg), with an RR of 1.46 (95% CI, 1.32-1.62) for CVD. Prehypertension also elevates the risk of CVD mortality by approximately 50-60% and contributes to end-organ damage, such as (LVH). In the , the adjusted HR for CVD death was 1.58 (95% CI, 1.12-2.21). Although associations with all-cause mortality are less consistent across studies, prehypertension accounts for about one-third of excess CVD events attributable to elevated levels overall. The 2025 American Heart Association/ guideline highlights prehypertension (defined as systolic 120-129 mm Hg and diastolic <80 mm Hg) as a precursor to overt , with meta-analyses showing dose-dependent increases in CVD, (HF; 2-fold risk), and (CKD) risks; it recommends using PREVENT equations to estimate 10- and 30-year CVD risk for individuals with elevated , aiding in . Evidence from trials like SPRINT demonstrates that achieving systolic below 120 mm Hg reduces HF incidence by 38% (HR 0.62, 95% CI 0.45-0.84) and overall CVD events by 25% in high-risk adults, while meta-analyses of -lowering interventions indicate 12-19% reductions in related outcomes like and cognitive decline. Long-term outcomes improve with early modification, as untreated prehypertension links to higher CKD progression and HF hospitalization rates. Cohort studies with extended follow-up underscore these risks. In the Coronary Artery Risk Development in Young Adults (CARDIA) study, young adults (aged 18-30 years) with elevated in the prehypertension range had a 67% higher adjusted HR (1.67, 95% CI 1.01-2.77) for CVD events over nearly 19 years, with cumulative incidence rates of 2.74 per 1,000 person-years versus 1.37 for normal . Over 30 years of CARDIA follow-up, persistent prehypertension in early adulthood correlated with subclinical and doubled CVD risk in midlife. Cumulative exposure, measured in blood pressure-years (area under the curve of systolic or diastolic readings over time), provides a stronger predictor of CVD events than single measurements, particularly in prehypertensive ranges. In the CARDIA and Multi-Ethnic Study of Atherosclerosis cohorts, higher cumulative exposure during young adulthood—even if later controlled below 120/80 mm Hg—was associated with increased left ventricular mass, coronary calcification, and twofold higher CVD risk compared to lifelong optimal levels. This metric captures the lifelong burden, enhancing risk stratification beyond baseline readings. Ethnic disparities exacerbate outcomes in prehypertension, with individuals facing higher prevalence (approximately 40-60% in some studies) and elevated CVD risks compared to individuals, persisting after adjusting for socioeconomic factors and highlighting the need for targeted .

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