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Review
. 2019 Aug;21(8):1135-1143.
doi: 10.1111/jch.13622. Epub 2019 Jul 12.

Hypertension and patients with acute coronary syndrome: Putting blood pressure levels into perspective

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Review

Hypertension and patients with acute coronary syndrome: Putting blood pressure levels into perspective

Konstantinos Konstantinou et al. J Clin Hypertens (Greenwich). 2019 Aug.

Abstract

Arterial hypertension is a well-established cardiovascular risk factor, and blood pressure (BP) control has largely improved the prognosis of hypertensive patients. A number of studies have assessed the role of BP levels in the prognosis of patients with acute coronary syndromes. Pathophysiologic links of hypertension to acute myocardial infarction (MI) include endothelial dysfunction, autonomic nervous system dysregulation, impaired vasoreactivity, and a genetic substrate. A history of hypertension is highly prevalent among patients presenting with MI, and some, but not all, studies have associated it with a worse prognosis. Some data support that low levels of admission and in-hospital BP may indicate an increased risk for subsequent events. Risk scores used in patients with MI have, therefore, included BP levels and a history of hypertension in their variables. Of note, good long-term BP control, ideally initiated prior to discharge, should be pursued in order to improve secondary prevention.

Keywords: blood pressure; hospitalization; myocardial infarction.

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Conflict of interest statement

None.

Figures

Figure 1
Figure 1
Pathophysiological factors that link hypertension with acute coronary syndromes. A complex interplay of genetic predisposition, abnormal vasoreactivity, and vessel wall shear stress coupled with neurohormonal activation triggers endothelial dysfunction, vessel wall remodeling, and development of atherosclerotic lesions. Coronary plaque rupture in the setting of a hypercoagulant state eventually leads to an ACS. ACE, angiotensin‐converting enzyme; ACS, acute coronary syndrome; Ang II, angiotensin II; BKB2, bradykinin B2; KCNMA1, Ca++‐dependent potassium channel alpha1 subunit; LVH, left ventricular hypertrophy; NO, nitric oxide

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