Hyperhomocysteinemia as a component of syndrome X

Mor Oron-Herman, Talma Rosenthal, Ben Ami Sela

Research output: Contribution to journalArticlepeer-review

Abstract

Syndrome X, a cluster of several metabolic disorders that includes hyperinsulinemia, hypertriglyceridemia, and hypertension, is associated with severe vascular morbidity. Hyperhomocysteinemia is another risk factor for cardiovascular and cerebrovascular diseases, often exhibited by insulin-resistant patients. In the current study, we investigated the relationship between syndrome X and hyperhomocysteinemia in a rat model. Two groups of rats were fed either fructose-enriched diet or standard rat chow for 5 weeks. Systolic blood pressure (SBP), as well as fasting plasma insulin, triglycerides, total cholesterol, and total homocysteine levels, were determined at the beginning and at the end of the study. A complete metabolic syndrome was induced by the fructose-enriched diet, including hyperinsulinemia, hypertriglyceridemia, and hypertension. Homocysteine concentration was 72% higher after 5 weeks on the fructose diet (8.49 ± 1.6 v 4.92 ± 0.9 μmol/l, P < .01). Insulin, triglycerides, SBP, and homocysteine levels were insignificantly changed during 5 weeks on standard rat chow. Homocysteine was positively and significantly correlated with any original component of syndrome X (r = 0.565, P = .014 with insulin, r = 0.662, P = .001 with triglycerides, and r = 0.774, P < .001 with SBP). The results of the present study indicate that hyperhomocysteinemia is an integral component of this rat model of syndrome X. It is thus highly likely that hyperhomocysteinemia is an integral component of the human syndrome X as well, and thereby contributes to the overall high vascular risk associated with this condition.

Original languageEnglish
Pages (from-to)1491-1495
Number of pages5
JournalMetabolism: Clinical and Experimental
Volume52
Issue number11
DOIs
StatePublished - Nov 2003

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