Relationships of Serum Ferritin, Transferrin Saturation, and HFE Mutations and Self-Reported Diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) Study

  1. Ronald T. Acton, PHD1,
  2. James C. Barton, MD2,
  3. Leah V. Passmore3,
  4. Paul C. Adams, MD4,
  5. Mark R. Speechley, PHD5,
  6. Fitzroy W. Dawkins, MD6,
  7. Phyliss Sholinsky, MSPH7,
  8. David M. Reboussin, PHD3,
  9. Gordon D. McLaren, MD89,
  10. Emily L. Harris, PHD, MPH10,
  11. Thomas C. Bent, MD8,
  12. Thomas M. Vogt, MD10 and
  13. Oswaldo Castro, MD6
  1. 1Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama
  2. 2Southern Iron Disorders Center, Birmingham, Alabama
  3. 3Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina
  4. 4Department of Medicine, London Health Sciences Centre, London, Ontario, Canada
  5. 5Department of Epidemiology and Biostatistics, University of Western Ontario, London, Ontario, Canada
  6. 6Department of Medicine, Howard University, Washington, DC
  7. 7Epidemiology and Biometry Program, National Heart, Lung, and Blood Institute, Bethesda, Maryland
  8. 8Department of Medicine, University of California, Irvine, California
  9. 9Veterans Affairs Long Beach Healthcare System, Long Beach, California
  10. 10Kaiser Permanente Center for Health Research, Portland, Oregon, and Honolulu, Hawaii
  1. Address correspondence and reprint requests to Ronald T. Acton, PhD, MCLM 265, 1530 3rd Ave. South, Birmingham, AL 35294-0005. E-mail: acton{at}uab.edu

Abstract

OBJECTIVE—We evaluated the associations of self-reported diabetes with serum ferritin concentration, transferrin saturation (TfSat), and HFE C282Y and H63D mutations in six racial/ethnic groups recruited at five field centers in the Hemochromatosis and Iron Overload Screening (HEIRS) study.

RESEARCH DESIGN AND METHODS—Analyses were conducted on 97,470 participants. Participants who reported a previous diagnosis of diabetes and/or hemochromatosis or iron overload were compared with participants who did not report a previous diagnosis.

RESULTS—The overall prevalence of diabetes was 13.8%; the highest prevalence was in Pacific Islanders (20.1%). Of all participants with diabetes, 2.0% reported that they also had hemochromatosis or iron overload. The mean serum ferritin concentration was significantly greater in women with diabetes in all racial/ethnic groups and in Native-American men with diabetes than in those without diabetes. The mean serum ferritin concentration was significantly lower in Asian men with diabetes than in those without diabetes. Mean TfSat was lower in participants with diabetes from all racial/ethnic groups except Native-American women than in those without diabetes. There was no significant association of diabetes with HFE genotype. The mean serum ferritin concentration was greater (P < 0.0001) in women with diabetes than in those without diabetes for HFE genotypes except C282Y/C282Y and C282Y/H63D. Log serum ferritin concentration was significantly associated with diabetes in a logistic regression analysis after adjusting for age, sex, racial/ethnic group, HFE genotype, and field center.

CONCLUSIONS—Serum ferritin concentration is associated with diabetes, even at levels below those typically associated with hemochromatosis or iron overload.

Footnotes

  • A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted May 29, 2006.
    • Received August 24, 2005.
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