4.7 Article

ADAMTS13 activity as a novel risk factor for incident type 2 diabetes mellitus: a population-based cohort study

Journal

DIABETOLOGIA
Volume 60, Issue 2, Pages 280-286

Publisher

SPRINGER
DOI: 10.1007/s00125-016-4139-5

Keywords

ADAMTS13; Diabetes; Epidemiology; Incidence; Prediabetes; Risk factor; VonWillebrand factor

Funding

  1. Erasmus Medical Center
  2. Erasmus University, Rotterdam
  3. Netherlands Organisation for the Health Research and Development
  4. Research Institute for Diseases in the Elderly [RIDE2 014-93-015]
  5. Ministry of Education, Culture and Science
  6. Ministry for Health, Welfare and Sports
  7. European Commission (Directorate-General XII)
  8. Municipality of Rotterdam
  9. Netherlands Organisation of Scientific Research (NWO) [175.010.2005.011, 911-03-012]
  10. Netherlands Genomics Initiative [NWO 050-060-810]
  11. Baxalta Innovations GmbH, Vienna, Austria
  12. NWO [veni 916.12.154]
  13. Erasmus University Rotterdam Fellowship

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Aims/hypothesis ADAMTS13 is a protease that breaks down von Willebrand factor (VWF) multimers into smaller, less active particles. VWF has been associated with an increased risk of incident type 2 diabetes mellitus. Here, we determine whether ADAMTS13 activity and VWF antigen are associated with incident diabetes. Methods This study included 5176 participants from the Rotterdam Study, a prospective population-based cohort study. Participants were free of diabetes at baseline and followed up for more than 20 years. Cox proportional hazards models were used to examine the association of ADAMTS13 activity and VWF antigen with incident diabetes. Results ADAMTS13 activity was associated with an increased risk of incident diabetes (HR 1.17 [95% CI 1.08, 1.27]) after adjustment for known risk factors and VWF antigen levels. Although ADAMTS13 activity was positively associated with fasting glucose and insulin, the association with incident diabetes did not change when we adjusted for these covariates. ADAMTS13 activity was also associated with incident prediabetes (defined on the basis of both fasting and non-fasting blood glucose) after adjustment for known risk factors (HR 1.11 [95% CI 1.03, 1.19]), while the VWF antigen level was not. VWF antigen was associated with incident diabetes, but this association was attenuated after adjustment for known risk factors. Conclusions/interpretation ADAMTS13 activity appears to be an independent risk factor for incident prediabetes and type 2 diabetes. As the association between ADAMTS13 and diabetes did not appear to be explained by its cleavage of VWF, ADAMTS13 may have an independent role in the development of diabetes.

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