Key result
Angiotensin receptor blockers exhibit differences in treating hypertension in metabolic syndrome, such as losartan's uricosuric effect and telmisartan's partial PPAR-gamma agonism.
Why the study?
Do different angiotensin receptor blockers have distinct metabolic effects in the treatment of hypertension in metabolic syndrome?
Do different angiotensin receptor blockers have distinct metabolic effects in the treatment of hypertension in metabolic syndrome?
Different ARBs may offer unique metabolic benefits beyond blood pressure lowering in patients with metabolic syndrome, such as losartan's uricosuric effect and telmisartan's PPAR-gamma agonism.
Answers are grounded in this paper and cite their sources.
May support ARB selection by metabolic properties in metabolic syndrome; leaves open prospective validation.
The metabolic syndrome (MetS) is a strong predictor of cardiovascular morbidity and mortality, as well as new Type 2 diabetes. MetS consists of visceral obesity, elevated blood pressure, impaired glucose metabolism, atherogenic dyslipidaemia (elevated triglycerides and low levels of high-density lipoprotein cholesterol), as well as other metabolic abnormalities. The underlying pathophysiology seems to be largely, but not uniquely, attributable to insulin resistance. Existing antihypertensive drugs were designed to lower blood pressure rather than to modify the metabolic abnormalities associated with hypertension. This review considers the role of renin-angiotensin system inhibition and especially the use of angiotensin receptor blockers (ARBs) in the treatment of hypertension in MetS. There are differences among ARBs. Among them is the uricosuric effect of losartan. Furthermore, telmisartan may function as a partial agonist of the peroxisome proliferator-activated receptor-gamma (PPAR-gamma).
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Karagiannis et al. (2007) conducted a review in Hypertension in metabolic syndrome. Angiotensin receptor blockers (ARBs) was evaluated. Angiotensin receptor blockers exhibit differences in treating hypertension in metabolic syndrome, such as losartan's uricosuric effect and telmisartan's partial PPAR-gamma agonism.
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