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Research Article| Volume 117, P4-11, July 2016

Shorter telomeres in adults with Type 1 diabetes correlate with diabetes duration, but only weakly with vascular function and risk factors

  • Author Footnotes
    1 Equal contribution.
    Andrzej S. Januszewski
    Footnotes
    1 Equal contribution.
    Affiliations
    NHMRC Clinical Trials Centre, The University of Sydney, Camperdown, Sydney, NSW, Australia

    University of Melbourne, Department of Medicine, St Vincent’s Hospital, Fitzroy, Melbourne, VIC, Australia
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  • Author Footnotes
    1 Equal contribution.
    Surya S. Sutanto
    Footnotes
    1 Equal contribution.
    Affiliations
    Greg Brown Diabetes and Endocrine Laboratory, Sydney Medical School, Charles Perkins Centre, The University of Sydney, Camperdown, Sydney, NSW, Australia
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  • Susan McLennan
    Affiliations
    Greg Brown Diabetes and Endocrine Laboratory, Sydney Medical School, Charles Perkins Centre, The University of Sydney, Camperdown, Sydney, NSW, Australia

    Department of Endocrinology, Royal Prince Alfred Hospital, Camperdown, Sydney, NSW, Australia
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  • David N. O’Neal
    Affiliations
    University of Melbourne, Department of Medicine, St Vincent’s Hospital, Fitzroy, Melbourne, VIC, Australia
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  • Anthony C. Keech
    Affiliations
    NHMRC Clinical Trials Centre, The University of Sydney, Camperdown, Sydney, NSW, Australia
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  • Author Footnotes
    2 Equal senior authors.
    Stephen M. Twigg
    Footnotes
    2 Equal senior authors.
    Affiliations
    Greg Brown Diabetes and Endocrine Laboratory, Sydney Medical School, Charles Perkins Centre, The University of Sydney, Camperdown, Sydney, NSW, Australia

    Department of Endocrinology, Royal Prince Alfred Hospital, Camperdown, Sydney, NSW, Australia
    Search for articles by this author
  • Author Footnotes
    2 Equal senior authors.
    Alicia J. Jenkins
    Correspondence
    Corresponding author at: NHMRC Clinical Trials Centre, The University of Sydney, 92-94 Parramatta Rd, Camperdown, 2050 Sydney, NSW, Australia. Tel.: +61 2 95625000; fax: +61 2 95651863.
    Footnotes
    2 Equal senior authors.
    Affiliations
    NHMRC Clinical Trials Centre, The University of Sydney, Camperdown, Sydney, NSW, Australia

    University of Melbourne, Department of Medicine, St Vincent’s Hospital, Fitzroy, Melbourne, VIC, Australia
    Search for articles by this author
  • Author Footnotes
    1 Equal contribution.
    2 Equal senior authors.

      Highlights

      • Cross-sectional study of telomeres in Type 1 diabetes and non-diabetic subjects.
      • Shorter telomeres in T1D vs. non-diabetic subjects.
      • Relative telomere length (RTL) do not correlate with HbA1c, oxidation or smoking.
      • RTL correlates inversely with age, T1D duration, inflammation and vascular function.

      Abstract

      Objective

      To determine if white blood cell (WBC) telomeres are shorter in Type 1 diabetes (T1D) than in subjects without diabetes (non-DB), and shorter in T1D subjects with vs. without vascular complications; and to determine associations with vascular biomarkers.

      Research design and methods

      WBC relative telomere length (RTL) was determined by quantitative PCR in a cross-sectional study of 140 non-DB and 199 T1D adults, including 128 subjects without vascular complications (T1DNoCx) and 71 subjects with vascular complications (T1DCx). Relationships of RTL with age, T1D duration, arterial elasticity, pulse pressure and vascular risk factors were determined.

      Results

      RTL did not differ by gender within T1D and non-DB groups. Age-adjusted RTL was shorter in T1D vs. non-DB subjects (1.48 ± 0.03 AU vs. 1.64 ± 0.04 AU, p = 0.002), but did not differ by T1D complication status (T1DNoCX 1.50 ± 0.04 vs. T1DCX 1.46 ± 0.05, p = 0.50), nor correlate with arterial elasticity. Univariate analysis in T1D showed RTL correlated (inversely) with age r = −0.27, p = 0.0001, T1D duration r = −0.16, p = 0.03, and pulse pressure (r = −0.15, p = 0.04), but not with HbA1c, BP, renal function (serum creatinine, ACR, eGFR), lipids, insulin sensitivity, inflammation (CRP, CAMs) or oxidative stress (OxLDL, OxLDL/LDL-C, MPO, PON-1). Multiple regression analysis showed independent determinants of RTL were age and T1D presence (r = 0.29, p < 0.0001).

      Conclusions

      In this cross-sectional study telomeres were shorter in T1D. RTL correlated inversely with T1D duration, but did not differ by complication status and weakly correlated with pulse pressure and vascular risk factors. Only age and T1D were independent determinants of RTL. Longitudinal studies are merited.

      Keywords

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