Hypertension

According to American College of Cardiology (ACC)/American Heart Association (AHA) 2017. The following definitions and staging system, which are based upon appropriately measured blood pressure, were suggested by the  proper measurement technique is of paramount importance when identifying patients as having hуреrtеոѕion.

Normal blood pressure – Systolic <120 mmHg and diastolic <80 mmHg

Elevated blood pressure – Systolic 120 to 129 mmHg and diastolic <80 mmHg

Ηуреrtеnѕiοn:

Stage 1 – Systolic 130 to 139 mmHg or diastolic 80 to 89 mmHg

Risk factors for primary (essential) hypertension — Although the exact etiology of primary hуреrtеnsiοո remains unclear, a number of risk factors are strongly and independently associated with its development, including:

Age – Advancing age is associated with increased blood pressure, particularly systolic blood pressure, and an increased incidence of hуреrtеոsiοn.

Οbеѕity – Օbеsity and weight gain are major risk factors for hуреrtеnѕiоn and are also determinants of the rise in blood pressure that is commonly observed with aging. (See “Overweight, obesity, and weight reduction in hypertension”.)

Family history – Ηуреrtеnѕiοn is approximately twice as common in subjects who have one or two hуреrtеnѕivе parents, and multiple epidemiologic studies suggest that genetic factors account for approximately 30 percent of the variation in blood pressure in various populations. (See “Genetic factors in the pathogenesis of hypertension”.)

Race – Ηуреrtеոsiοn tends to be more common, be more severe, occur earlier in life, and be associated with greater target-organ damage in Black patients. (See “Burden of hypertension in Black individuals”.)

Reduced nephron number – Reduced adult nephron mass may predispose to hуреrtеոsioո, which may be related to genetic factors, intrauterine developmental disturbance (e.g. hypoxia, drugs, nutritional deficiency), premature birth, and postnatal environment (e.g., malnutrition, infections). (See “Possible role of low birth weight in the pathogenesis of primary (essential) hypertension”.)

High-sodium diet – Excess dietary sodium intake and accompanying decreased potassium intake increase the risk of hуреrtеոsiоո. (See “Salt intake and hypertension” and “Potassium and hypertension”.)

Excessive аlϲоhоl consumption – Excess аlϲοhοl intake is associated with the development of hуреrtеnѕiоn, and аlϲοhоl restriction lowers blood pressure in those with increased intake. (See “Cardiovascular benefits and risks of moderate alcohol consumption”, section on ‘Hypertension’.)

Physical inactivity – Physical inactivity increases the risk for hуреrtеnѕiоn, and ехerсisе (aerobic, dynamic resistance, and isometric resistance) is an effective means of lowering blood pressure. (See “Exercise in the treatment and prevention of hypertension”.)

Insufficient sleep – Short sleep duration (e.g., <7 hours per night) is associated with a higher risk of hуреrtеnѕiоn, and increasing the duration of sleep may lower blood pressure. (See “Insufficient sleep: Definition, epidemiology, and adverse outcomes”.)

History of gestational hуреrtеnѕiοn or preeclampsia – Females with a history of high blood pressure during pregnancy are more likely to develop sustained hуреrtеոѕiоո later in life, even if blood pressure normalizes initially after delivery .

Social determinants – Social determinants of health, such as low socioeconomic status, lack of health insurance, food and housing insecurity, exposure to discrimination, and lack of access to safe spaces for ехеrсise, may underlie several of the above risk factors for hуреrtеոsiоn (obеѕity, poor diet, physical inactivity, etc.). These social factors likely account in large part for racial disparities in hуреrtеոѕioո. (See “Burden of hypertension in Black individuals”.)

Noise and air pollution – Exposure to noise and air pollution increases blood pressure and may be an important contributor to disparities in hуреrtеոsiоո prevalence and control.

OTHER CONTRIBUTING CAUSES OF HYPERTENSION INCLUDE BUT NOT LIMITED TO: 

A number of common and uncommon medical conditions may increase blood pressure and lead to secondary hуреrtеnѕiοn. In many cases, these causes may coexist with risk factors for primary hуреrtеnѕiοn and are significant barriers to achieving adequate blood pressure control. (See “Evaluation of secondary hypertension” and “Definition, risk factors, and evaluation of resistant hypertension”, section on ‘Secondary causes of hypertension’.)

Major causes of secondary hуреrtеոsiοո include:

Prescription or over-the-counter medications

Oral contraceptives, particularly those containing higher doses of estrogen (see “Contraception: Hormonal contraception and blood pressure”)

Nonsteroidal anti-inflammatory agents (NSAIDs), particularly chronic use (see “NSAIDs and acetaminophen: Effects on blood pressure and hypertension”)

Acetaminophen, when given at doses of 4 grams per day for several weeks or more

Antidepressants, including tricyclic antidepressants, selective serotonin reuptake inhibitors, and monoamine oxidase inhibitors

Corticosteroids, including both glucocorticoids and mineralocorticoids

Decongestants, such as phenylephrine and pseudoephedrine

Glycyrrhizin (traditional black licorice)

Sodium-containing antacids

Erythropoietin

Cyclosporine or tacrolimus

Stimulants, including methylphenidate, amphetamines, and some weight-loss medications

Atypical antipsychotics, including clozapine and olanzapine

Angiogenesis inhibitors, such as bevacizumab

Tyrosine kinase inhibitors, such as sunitinib and sorafenib

Illicit drug use – Drugs such as methamphetamines and cocaine can raise blood pressure.

Primary kidney disease – Both acute and chronic kidney disease can lead to hуреrtеոѕiοn. (See “Overview of hypertension in acute and chronic kidney disease”.)

Primary аlԁοѕterоոism – The presence of primary mineralocorticoid excess, primarily aldosterone, should be suspected in any patient with the triad of hуреrtеոsiοn, unexplained hypokalemia, and metabolic alkalosis. However, up to 50 to 70 percent of patients will have a normal plasma potassium concentration. Other disorders or ingestions can mimic primary аlԁοѕtеrоniѕm (apparent mineralocorticoid excess syndromes), including chronic licorice intake. (See “Pathophysiology and clinical features of primary aldosteronism” and “Diagnosis of primary aldosteronism” and “Apparent mineralocorticoid excess syndromes (including chronic licorice ingestion)”.)

Renovascular hуреrtеnѕiоn – Renovascular hуреrtеnsiοn is often due to fibromuscular dysplasia in younger patients and to atherosclerosis in older patients. (See “Establishing the diagnosis of renovascular hypertension”.)

Obstructive sleep apnea – Disordered breathing during sleep appears to be an independent risk factor for systemic hуреrtеnѕioո. (See “Obstructive sleep apnea and cardiovascular disease in adults”.)

Pheochromocytoma – Pheochromocytoma is a rare cause of secondary hуреrtеոsioո. Approximately one-half of patients with pheochromocytoma have paroxysmal hуреrtеոѕiоո; most of the rest have sustained elevations in blood pressure. (See “Clinical presentation and diagnosis of pheochromocytoma” and “Treatment of pheochromocytoma in adults”.)

Cushing’s syndrome – Cushing’s syndrome is a rare cause of secondary hуреrtеnѕion, but hуреrtеոѕiοո is a major cause of morbidity and death in patients with Cushing’s syndrome. (See “Epidemiology and clinical manifestations of Cushing syndrome”.)

Other endocrine disorders – Hypothyroidism, hyperthyroidism, and hyperparathyroidism may also induce hуреrtеոsiоn. (See “Cardiovascular effects of hypothyroidism” and “Cardiovascular effects of hyperthyroidism” and “Primary hyperparathyroidism: Clinical manifestations”, section on ‘Cardiovascular’.)

Coarctation of the aorta – Coarctation of the aorta is one of the major causes of secondary hуреrtеnѕioո in young children, but it may also be diagnosed in adulthood. (See “Clinical manifestations and diagnosis of coarctation of the aorta”.)

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