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Pathophysiology/Complications

Monocyte Telomere Shortening and Oxidative DNA Damage in Type 2 Diabetes

  1. Mike J. Sampson, MD1,
  2. Mark S. Winterbone, BSC2,
  3. Jackie C. Hughes, BSC2,
  4. Nicoletta Dozio, PHD1 and
  5. David A. Hughes, PHD2
  1. 1Bertram Diabetes Research Unit, Norfolk and Norwich University Hospital National Health Service Trust, Norwich, U.K.
  2. 2Institute of Food Research, Norwich Research Park, Norwich, U.K.
  1. Address correspondence and reprint requests to Dr. Mike Sampson, Elsie Bertram Diabetes Centre, NorfolkNorwich University Hospital National Health Service Trust, Norwich NR4 7UA, U.K. E-mail: mike.sampson{at}nnuh.nhs.uk
Diabetes Care 2006 Feb; 29(2): 283-289. https://doi.org/10.2337/diacare.29.02.06.dc05-1715
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Abstract

OBJECTIVE—Telomeres are DNA sequences necessary for DNA replication, which shorten at cell division at a rate related to levels of oxidative stress. Once shortened to a critical length, cells are triggered into replicative senescence. Type 2 diabetes is associated with oxidative DNA damage, and we hypothesized that telomere shortening would characterize type 2 diabetes.

RESEARCH DESIGN AND METHODS—We studied 21 male type 2 diabetic subjects (mean age 61.2 years, mean HbA1c 7.9%) selected to limit confounding effects on telomere length and 29 matched control subjects. Telomere length was measured in peripheral venous monocyte and T-cells (naïve and memory) by fluorescent in situ hybridization and oxidative DNA damage by flow cytometry of oxidized DNA bases. Peripheral insulin resistance (homeostasis model assessment) and high-sensitivity C-reactive protein (hsCRP) were measured.

RESULTS—Mean monocyte telomere length in the diabetic group was highly significantly lower than in control subjects (4.0 [1.1] vs. 5.5 [1.1]; P < 0.0001), without significant differences in lymphocyte telomere length. There was a trend toward increased oxidative DNA damage in all diabetes cell types examined and a significant inverse relationship between oxidative DNA damage and telomere length (r = −0.55; P = 0.018) in the diabetic group. Telomere length was unrelated to plasma CRP concentration or insulin resistance.

CONCLUSIONS—Monocyte telomere shortening in type 2 diabetes could be due to increased oxidative DNA damage to monocyte precursors during cell division. This data suggests that monocytes adhering to vascular endothelium and entering the vessel wall in type 2 diabetes are from a population with shorter telomeres and at increased risk of replicative senescence within vascular plaque.

  • FITC, fluorescein isothiocyanate
  • HOMA, homeostasis model assessment
  • hsCRP, high- sensitivity C-reactive protein
  • MESF, mean monocyte telomere length
  • PBMC, peripheral blood mononuclear cell

Footnotes

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

    • Accepted October 15, 2005.
    • Received September 13, 2005.
  • DIABETES CARE
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Diabetes Care: 29 (2)

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February 2006, 29(2)
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Monocyte Telomere Shortening and Oxidative DNA Damage in Type 2 Diabetes
Mike J. Sampson, Mark S. Winterbone, Jackie C. Hughes, Nicoletta Dozio, David A. Hughes
Diabetes Care Feb 2006, 29 (2) 283-289; DOI: 10.2337/diacare.29.02.06.dc05-1715

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Monocyte Telomere Shortening and Oxidative DNA Damage in Type 2 Diabetes
Mike J. Sampson, Mark S. Winterbone, Jackie C. Hughes, Nicoletta Dozio, David A. Hughes
Diabetes Care Feb 2006, 29 (2) 283-289; DOI: 10.2337/diacare.29.02.06.dc05-1715
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