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Arteriosclerosis, Thrombosis, and Vascular Biology. 1996;16:727-733

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(Arteriosclerosis, Thrombosis, and Vascular Biology. 1996;16:727-733.)
© 1996 American Heart Association, Inc.


Articles

Low Whole-Blood S-Adenosylmethionine and Correlation Between 5-Methyltetrahydrofolate and Homocysteine in Coronary Artery Disease

Franziska M.T. Loehrer; Christian P. Angst; Walter E. Haefeli; Paul P. Jordan; Rudolf Ritz; Brian Fowler

From the Metabolic Unit, University Children's Hospital (F.M.T.L., C.P.A., B.F.); University Computer Center (P.P.J.); and the Divisions of Clinical Pharmacology (W.E.H.) and Intensive Care (R.R.), University Hospital, Basel, Switzerland.

Abstract Mild elevation of plasma homocysteine is an independent risk factor for vascular disease. We studied the role of 5-methyltetrahydrofolate (5-MTHF), the folate form directly involved in homocysteine metabolism, in contrast to previous studies, which used total folate measurements, in 70 coronary artery disease (CAD) patients and control subjects. We also measured S-adenosylmethionine (SAM), which controls the activity of critical enzymes of homocysteine metabolism. Fasting plasma total homocysteine was elevated (>12.4 µmol/L for women, >13.3 µmol/L for men) in 17% of patients, in accordance with earlier studies. These patients showed lower 5-MTHF (12.4±1.0 nmol/L, mean±SD) than control subjects (24.2±15.0, P<.001), and there was a clear correlation (multiple linear regression analysis: P=.002) of this relevant form of folate with homocysteine. However, 37% of the normohomocysteinemic patients also revealed similarly low 5-MTHF levels, suggesting that a decrease of 5-MTHF does not necessarily cause hyperhomocysteinemia. SAM was significantly decreased in patients (1.4±0.4 µmol/L) compared with control subjects (1.8±0.3, P<.001) but was not correlated to homocysteine or 5-MTHF. The correlation between homocysteine and 5-MTHF that was found in CAD patients but not in control subjects confirms the direct relationship between these compounds in vivo. The new finding of low SAM in patients demands further studies, since it might indicate that low levels pose risk and that SAM might be a protective factor against the development of CAD.


Key Words: 5-methyltetrahydrofolate • coronary artery disease • homocysteine • methylenetetrahydrofolate reductase • S-adenosylmethionine




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