Lewis blood group phenotype as an independent risk factor for coronary heart disease (the NHLBI Family Heart Study)

R. Curtis Ellison, Yuqing Zhang, Richard H. Myers, Jane L. Swanson, Millicent Higgins, John H Eckfeldt

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35 Scopus citations

Abstract

In the Copenhagen Male Study, men with Lewis blood group phenotype Le(a- b-) were found to have increased risk for coronary heart disease (CHD); such a relation has not been confirmed in men, and has not been evaluated in women. In the NHLBI Family Heart Study, we determined the Lewis blood type of 1,620 white subjects (790 male and 830 female subjects). The Lewis(a-b-) phenotype was found in 142 subjects (8.8%), 6.3% of subjects from randomly chosen families and 9.7% of subjects from families found to be at high risk for CHD. A history of CHD was present in 39.1% of men with Le(a-b-) versus 27.2% of men with other Lewis types; for women, the corresponding numbers were 12.3% versus 9.4%, respectively. In multivariate analysis, adjusting for age, sex, and risk group, the odds ratio for CHD was 2.0 (95% confidence interval = 1.2 to 3.1) for Le(a-b-) versus other Lewis groups. Mean values for body mass index, blood pressure, total cholesterol, low-density lipoprotein and high-density lipoprotein cholesterol, glucose, insulin, homocysteine, and fibrinogen were not significantly different between Le(a- b-) subjects and others, but triglycerides (p = 0.002) were higher in the Le(a-b-) subjects. However, inclusion of all risk factors in multivariate analysis did not diminish the increased risk for CHD associated with the Le(a-b-) phenotype. We conclude that the Le(a-b-) phenotype is associated with an increased risk for CHD; its effect does not appear to act predominantly through conventional cardiovascular risk factors. At present, mechanisms of effect are unknown.

Original languageEnglish (US)
Pages (from-to)345-348
Number of pages4
JournalAmerican Journal of Cardiology
Volume83
Issue number3
DOIs
StatePublished - Feb 1 1999

Bibliographical note

Funding Information:
This study was supported by contracts NO1-HC-25104, NO1-HC-25105, NO1-HC-25106, NO1-HC-25107, NO1-HC-25108, and NO1-HC-25109, from the National Heart, Lung, & Blood Institute, Bethesda, Maryland.

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