4.7 Article

HFE H63D Polymorphism as a Modifier of the Effect of Cumulative Lead Exposure on Pulse Pressure: The Normative Aging Study

Journal

ENVIRONMENTAL HEALTH PERSPECTIVES
Volume 118, Issue 9, Pages 1261-1266

Publisher

US DEPT HEALTH HUMAN SCIENCES PUBLIC HEALTH SCIENCE
DOI: 10.1289/ehp.1002251

Keywords

gene-environment interaction; hemochromatosis gene; H63D mutation; lead exposure; pulse pressure

Funding

  1. U.S. Department of Veterans Affairs, Massachusetts Veterans Epidemiology Research and Information Center, Boston, Massachusetts
  2. National Institute of Environmental Health Sciences (NIEHS) [R01-ES05257, R01-ES07821, P42-ES05947, P30-ES00002, K01-ES016587-01A1]
  3. National Center for Research Resources General Clinical Research Centers [M01RR02635]
  4. Small Business Innovation Research [2R44 ES03918]
  5. National Institutes of Health [T32 ES07062]

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BACKGROUND: Cumulative lead exposure is associated with a widened pulse pressure (PP; the difference between systolic and diastolic blood pressure), a marker of arterial stiffness and a predictor of cardiovascular disease. Polymorphisms in the hemochromatosis gene (HFE) have been shown to modify the impact of cumulative lead exposure on measures of adult cognition and cardiac function. OBJECTIVES: We examined whether the HFE mutations modify the impact of lead on PP in community-dwelling older men. METHODS: We examined 619 participants with a total of 1,148 observations of PP from a substudy of bone lead levels (a measure of cumulative exposure, measured by in vivo K-shell X-ray fluorescence) and health in the Normative Aging Study between 1991 and 2001. Linear mixed-effects regression models with random intercepts were constructed. RESULTS: Of the 619 subjects, 138 and 72 carried the HFE H63D and C282Y variants, respectively. After adjusting for age; education; alcohol intake; smoking; daily intakes of calcium, sodium, and potassium; total calories; family history of hypertension; diabetes; height; heart rate; high-density lipoprotein (HDL); total cholesterol:HDL ratio; and waist circumference, baseline bone lead levels were associated with steeper increases in PP in men with at least one H63D allele (p-interaction = 0.03 for tibia and 0.02 for patella) compared with men with only the wild types or C282Y variant. CONCLUSIONS: The HFE H63D polymorphism, but not the C282Y mutation, appears to enhance susceptibility to the deleterious impact of cumulative lead on PP, possibly via prooxidative or proinflammatory mechanisms.

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