4.7 Article

Type 2 diabetes and HbA1c are independently associated with wider retinal arterioles: the Maastricht study

期刊

DIABETOLOGIA
卷 63, 期 7, 页码 1408-1417

出版社

SPRINGER
DOI: 10.1007/s00125-020-05146-z

关键词

Clinical diabetes; Epidemiology; Human; Microvascular disease; Pathogenic mechanism; Pathophysiology; metabolism

资金

  1. European Regional Development Fund via OP-Zuid
  2. Province of Limburg
  3. Dutch Ministry of Economic Affairs [31O.041]
  4. Stichting De Weijerhorst (Maastricht, the Netherlands)
  5. Pearl String Initiative Diabetes (Amsterdam, the Netherlands)
  6. CARIM, School for Cardiovascular Diseases (Maastricht, the Netherlands)
  7. School CAPHRI, Care and Public Health Research Institute (Maastricht, the Netherlands)
  8. NUTRIM, School of Nutrition and Translational Research in Metabolism (Maastricht, the Netherlands)
  9. Stichting Annadal (Maastricht, the Netherlands)
  10. Health Foundation Limburg (Maastricht, the Netherlands)
  11. Janssen-Cilag B.V. (Tilburg, the Netherlands)
  12. Novo Nordisk Farma B.V. (Alphen aan den Rijn, the Netherlands)
  13. Sanofi-Aventis Netherlands B.V. (Gouda, the Netherlands)
  14. Chinese Scholarship Council [201606260039]

向作者/读者索取更多资源

Aims/hypothesis Retinal microvascular diameters are biomarkers of cardio-metabolic risk. However, the association of (pre)diabetes with retinal microvascular diameters remains unclear. We aimed to investigate the association of prediabetes (impaired fasting glucose or impaired glucose tolerance) and type 2 diabetes with retinal microvascular diameters in a predominantly white population. Methods In a population-based cohort study with oversampling of type 2 diabetes (N = 2876; n = 1630 normal glucose metabolism [NGM], n = 433 prediabetes and n = 813 type 2 diabetes, 51.2% men, aged 59.8 +/- 8.2 years; 98.6% white), we determined retinal microvascular diameters (measurement unit as measured by retinal health information and notification system [RHINO] software) and glucose metabolism status (using OGTT). Associations were assessed with multivariable regression analyses adjusted for age, sex, waist circumference, smoking, systolic blood pressure, lipid profile and the use of lipid-modifying and/or antihypertensive medication. Results Multivariable regression analyses showed a significant association for type 2 diabetes but not for prediabetes with arteriolar width (vs NGM; prediabetes: beta = 0.62 [95%CI -1.58, 2.83]; type 2 diabetes: 2.89 [0.69, 5.08]; measurement unit); however, there was a linear trend for the arteriolar width across glucose metabolism status (p for trend = 0.013). The association with wider venules was not statistically significant (prediabetes: 2.40 [-1.03, 5.84]; type 2 diabetes: 2.87 [-0.55, 6.29], p for trend = 0.083; measurement unit). Higher HbA(1c) levels were associated with wider retinal arterioles (standardised beta = 0.043 [95% CI 0.00002, 0.085]; p = 0.050) but the association with wider venules did not reach statistical significance (0.037 [-0.006, 0.080]; p = 0.092) after adjustment for potential confounders. Conclusions/interpretation Type 2 diabetes, higher levels of HbA(1c) and, possibly, prediabetes, are independently associated with wider retinal arterioles in a predominantly white population. These findings indicate that microvascular dysfunction is an early phenomenon in impaired glucose metabolism.

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