Evidence for Independent Heritability of the Glycation Gap (Glycosylation Gap) Fraction of HbA1c in Nondiabetic Twins

  1. Robert M. Cohen, MD1,
  2. Harold Snieder, PHD23,
  3. Christopher J. Lindsell, PHD1,
  4. Huriya Beyan, PHD5,
  5. Mohammed I. Hawa, BSC5,
  6. Stuart Blinko, PHD4,
  7. Raymond Edwards, PHD6,
  8. Timothy D. Spector, MD, MSC, FRCP3 and
  9. R. David G. Leslie, MD5
  1. 1Division of Endocrinology, Medicine, General Clinical Research Center, Emergency Medicine, University of Cincinnati, Medical Service, Cincinnati Veterans Affairs Medical Center, Cincinnati, Ohio
  2. 2Department of Pediatrics, Georgia Prevention Institute, Medical College of Georgia, Augusta, Georgia
  3. 3Twin Research & Genetic Epidemiology Unit, St. Thomas’ Hospital, London, U.K.
  4. 4Abbott Murex Biotech, Dartford, U.K.
  5. 5Centre for Diabetes and Metabolic Medicine, Institute of Cell and Molecular Science, St. Bartholomew’s Hospital, London, U.K.
  6. 6The Royal London Medical School and NETRIA, St. Bartholomew’s Hospital, London, U.K.
  1. Address correspondence and reprint requests to Prof. David Leslie, Diabetes and Metabolic Medicine, Institute of Cell and Molecular Science, London E1 2AT, U.K. E-mail: r.d.g.leslie{at}qmul.ac.uk

Abstract

OBJECTIVE—HbA1c (A1C) is substantially determined by genetic factors not shared in common with glucose. Fractions of the variance in A1C, the glycation gap (GG; previously called the glycosylation gap) and the hemoglobin glycosylation index, correlate with diabetes complications. We therefore tested whether GG (measured A1C − A1C predicted from glycated serum proteins [GSPs]) was genetically determined and whether it accounted for the heritability of A1C.

RESEARCH DESIGN AND METHODS—We conducted a classic twin study on A1C and GSP collected in 40 and 46 pairs of monozygotic and dizygotic healthy female twins, respectively. The predicted A1C was based on the regression line between A1C and GSP in a separate population spanning the pathophysiologic range.

RESULTS—GG was more strongly correlated between monozygotic (r = 0.65) than dizygotic (r = 0.48) twins, adjusted for age and BMI. The best-fitting quantitative genetic model adjusted for age and BMI showed that 69% of population variance in GG is heritable, while the remaining 31% is due to unique environmental influences. In contrast, GSP was similarly correlated between monozygotic (r = 0.55) and dizygotic (r = 0.49) twins, hence not genetically determined. GG was strongly correlated to A1C (r = 0.48), attributable mostly to genetic factors. About one-third of the heritability of A1C is shared with GG; the remainder is specific to A1C.

CONCLUSIONS—Heritability of the GG accounts for about one-third of the heritability of A1C. By implication, there are gene(s) that preferentially affect erythrocyte lifespan or glucose and/or nonenzymatic glycation or deglycation in the intracellular, rather than extracellular, compartment.

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 8, 2006.
    • Received February 3, 2006.
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  1. doi: 10.2337/dc06-0286 Diabetes Care August 2006 vol. 29 no. 8 1739-1743
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