User:Madhero88/Complications of hypertension

Complications of hypertension are clinical outcomes that result from persistent elevation of blood pressure.[1] Hypertension is a risk factor for all clinical manifestations of atherosclerosis since it is a risk factor for atherosclerosis it self.[2][3][4][5][6] It is an independent predisposing factor for heart failure,[7][8] coronary artery disease,[9][10][11] stroke[1], renal disease,[12][13][14] and peripheral arterial disease.[15][16] it is the most important risk factor for cardiovascular morbidity and mortality, in industrialized countries.[17]

Complications affecting the Heart

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Hypertensive heart disease is the result of structural and functional adaptations[18] leading to left ventricular hypertrophy,[19][20][21] diastolic dysfunction,[20][18] CHF, abnormalities of blood flow due to atherosclerotic coronary artery disease[18] and microvascular disease,[19][9][10] and cardiac arrhythmias.[19] Individuals with left ventricular hypertrophy are at increased risk for, stroke,[22] CHF,[22] and sudden death[22]. Aggressive control of hypertension can regress or reverse left ventricular hypertrophy and reduce the risk of cardiovascular disease.[23] [24][25][26] left ventricular hypertrophy are seen in 25% of the hypertensive patients and can easily be diagnosed by using echocardiography.[27] Underlying mechanisms of hypertensive left ventricular hypertrophy are of 2 types: mechanical, mainly leading to myocyte hypertrophy; neuro-hormonal, mainly resulting in a fibroblastic proliferation.[27]

Abnormalities of diastolic function, ranging from asymptomatic heart disease[28][29][30] to overt heart failure,[31][32] are common in hypertensive patients. Patients with diastolic heart failure have a preserved ejection fraction, which is a measure of systolic function.[33][34] Diastolic dysfunction is an early consequence of hypertension-related heart disease and is exacerbated by left ventricular hypertrophy[34][20] and ischemia.

Complications affecting the Brain

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Hypertension is an important risk factor for brain infarction and hemorrhage.[35][36][37][1][10][38][39][40] Approximately 85% of strokes are due to infarction and the remainder are due to hemorrhage, either intracerebral hemorrhage or subarachnoid hemorrhage.[41] The incidence of stroke rises progressively with increasing blood pressure levels, particularly systolic blood pressure in individuals >65 years. Treatment of hypertension convincingly decreases the incidence of both ischemic and hemorrhagic strokes.[41]

Hypertension is also associated with impaired cognition in an aging population,[42][43][43][44][45] Hypertension-related cognitive impairment and dementia may be a consequence of a single infarct due to occlusion of a "strategic" larger vessel[46] or multiple lacunar infarcts due to occlusive small vessel disease resulting in subcortical white matter ischemia.[47][47][45][47][43] Several clinical trials suggest that antihypertensive therapy has a beneficial effect on cognitive function, although this remains an active area of investigation.[48][49][50]

Cerebral blood flow remains unchanged over a wide range of arterial pressures (mean arterial pressure of 50–150 mmHg) through a process termed autoregulation of blood flow.[51] Signs and symptoms of hypertensive encephalopathy may include severe headache, nausea and vomiting (often of a projectile nature), focal neurologic signs, and alterations in mental status. Untreated, hypertensive encephalopathy may progress to stupor, coma, seizures, and death within hours.[52][53][54][55] It is important to distinguish hypertensive encephalopathy from other neurologic syndromes that may be associated with hypertension, e.g., cerebral ischemia, hemorrhagic or thrombotic stroke, seizure disorder, mass lesions, pseudotumor cerebri, delirium tremens, meningitis, acute intermittent porphyria, traumatic or chemical injury to the brain, and uremic encephalopathy.[41]

Complications affecting the Eye

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Hypertensive retinopathy is a condition characterized by a spectrum of retinal vascular signs in people with elevated blood pressure.[56] It was first described by Liebreich in 1859.[57] The retinal circulation undergoes a series of pathophysiological changes in response to elevated blood pressure.[58] In the initial, vasoconstrictive stage, there is vasospasm and an increase in retinal arteriolar tone owing to local autoregulatory mechanisms. This stage is seen clinically as a generalized narrowing of the retinal arterioles. Persistently elevated blood pressure leads to intimal thickening, hyperplasia of the media wall, and hyaline degeneration in the subsequent, sclerotic, stage. This stage corresponds to more severe generalized and focal areas of arteriolar narrowing, changes in the arteriolar and venular junctions, and alterations in the arteriolar light reflex (i.e., widening and accentuation of the central light reflex, or "copper wiring").[59]

This is followed by an exudative stage, in which there is disruption of the blood–retina barrier, necrosis of the smooth muscles and endothelial cells, exudation of blood and lipids, and retinal ischemia. These changes are manifested in the retina as microaneurysms, hemorrhages, hard exudates, and cotton-wool spots. Swelling of the optic disk may occur at this time and usually indicates severely elevated blood pressure (i.e., malignant hypertension). Because better methods for the control of blood pressure are now available in the general population, malignant hypertension is rarely seen. In contrast, other retinal vascular complications of hypertension, such as macroaneurysms and branch-vein occlusions, are not uncommon in patients with chronically elevated blood pressure. These stages of hypertensive retinopathy however, may not be sequential.[60][58] For example, signs of retinopathy that reflect the exudative stage, such as retinal hemorrhage or microaneurysm, may be seen in eyes that do not have features of the sclerotic stage,[58] The exudative signs are nonspecific, since they are seen in diabetes and other conditions.

Complications affecting the Kidneys

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Hypertension is a risk factor for renal injury and ESRD.[61][62][63][64] [65][66][67] Renal risk appears to be more closely related to systolic than to diastolic blood pressure,[68][69] and black men are at greater risk than white men for developing ESRD at every level of blood pressure.[70][71][72][73][74]

The atherosclerotic, hypertension-related vascular lesions in the kidney primarily affect the preglomerular arterioles,[75][76][68] resulting in ischemic changes in the glomeruli and postglomerular structures.[41] Glomerular injury may also be a consequence of direct damage to the glomerular capillaries due to glomerular hyperperfusion. Glomerular pathology progresses to glomerulosclerosis,[77][78] and eventually the renal tubules may also become ischemic and gradually atrophic. The renal lesion associated with malignant hypertension consists of fibrinoid necrosis of the afferent arterioles,[79][80][81][82][83][84][85] sometimes extending into the glomerulus, and may result in focal necrosis of the glomerular tuft.[86][87][81]

Clinically, macroalbuminuria (a random urine albumin/creatinine ratio > 300 mg/g) or microalbuminuria (a random urine albumin/creatinine ratio 30–300 mg/g) are early markers of renal injury. These are also risk factors for renal disease progression and for cardiovascular disease.[41]

Complications affecting the Arteries

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In addition to contributing to the pathogenesis of hypertension, blood vessels may be a target organ for atherosclerotic disease secondary to long-standing elevated blood pressure. Hypertensive patients with arterial disease of the lower extremities are at increased risk for future cardiovascular disease. Although patients with stenotic lesions of the lower extremities may be asymptomatic, intermittent claudication is the classic symptom of PAD. This is characterized by aching pain in the calves or buttocks while walking that is relieved by rest. The ankle-brachial index is a useful approach for evaluating PAD and is defined as the ratio of noninvasively assessed ankle to brachial (arm) systolic blood pressure. An ankle-brachial index < 0.90 is considered diagnostic of PAD and is associated with >50% stenosis in at least one major lower limb vessel. Several studies suggest that an ankle-brachial index < 0.80 is associated with elevated blood pressure, particularly systolic blood pressure.

References

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