Article

Mechanisms of hypertension in the cardiometabolic syndrome.

University of Valencia, CIBER 06/03 Fisiopatología de la Obesidad y Nutrición, Institute of Health Carlos III, Madrid, Spain.
Journal of hypertension (impact factor: 4.02). 04/2009; 27(3):441-51. DOI:10.1097/HJH.0b013e32831e13e5 pp.441-51
Source: PubMed

ABSTRACT Arterial hypertension is often part of a constellation of anthropometric and metabolic abnormalities that occur simultaneously to a higher degree than would be expected by chance alone, supporting the existence of a discrete disorder, the so-called metabolic syndrome. It is the result of interactions among a large number of interconnected mechanisms, which eventually lead to both an increase in cardiovascular and renal risk, and the development of diabetes. Mechanisms involved in the metabolic syndrome are obesity, insulin resistance, and a constellation of independent factors, which include molecules of hepatic, vascular, and immunologic origin with pro-inflammatory properties. At each of these key points are interactions of demographics, lifestyle, genetic factors, and environmental fetal programming. Superimposing upon these are infections or chronic exposure or both to certain drugs that can also make their contribution. Skeletal muscle and the liver, not adipose tissue, are the two key insulin-response tissues involved in maintaining glucose balance, although abnormal insulin action in the adipocytes also plays a role in development of the syndrome. Factors commonly associated with and partly dependent on obesity, insulin resistance, such as overactivity of the sympathetic, stimulation of the renin-angiotensin-aldosterone systems, abnormal renal sodium handling, endothelial dysfunction, and large vessels' alterations, may play a key role in the blood pressure elevation of the syndrome.

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Keywords

abnormal insulin action
 
abnormal renal sodium handling
 
Arterial hypertension
 
blood pressure elevation
 
chronic exposure
 
discrete disorder
 
endothelial dysfunction
 
environmental fetal programming
 
genetic factors
 
immunologic origin
 
include molecules
 
independent factors
 
insulin resistance
 
interactions
 
key points
 
large vessels' alterations
 
pro-inflammatory properties
 
renal risk
 
Skeletal muscle
 
two key insulin-response tissues