4.7 Article

Circulating Vitamin D Metabolites and Kidney Disease in Type 1 Diabetes

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 97, 期 12, 页码 4780-4788

出版社

ENDOCRINE SOC
DOI: 10.1210/jc.2012-2852

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资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [RC4DK090766, R01DK088762, R01HL096875, P30DK035816, P01DK02456]
  2. National Heart, Lung, and Blood Institute
  3. Division of Diabetes, Endocrinology and Metabolic Diseases of the National Institute of Diabetes and Digestive and Kidney Diseases
  4. National Eye Institute
  5. National Institute of Neurological Disorders and Stroke
  6. General Clinical Research Centers Program
  7. Clinical and Translational Science Awards Program, National Center for Research Resources
  8. Genentech through National Institute of Diabetes and Digestive and Kidney Diseases
  9. Abbott Laboratories
  10. Reata Pharmaceuticals
  11. Eli Lilly
  12. Novartis Pharmaceuticals
  13. Novo Nordisk
  14. Sanofi-Aventis
  15. Pharma Diagnostic

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Context: Impaired vitamin D metabolism may contribute to the development and progression of diabetic kidney disease. Objective: The aim of the study was to test associations of circulating vitamin D metabolites with risks of incident microalbuminuria, impaired glomerular filtration rate (GFR), and hypertension in type 1 diabetes. Design: We performed a cohort study of 1193 participants in the Diabetes Control and Complications Trial (DCCT), a randomized clinical trial of intensive diabetes therapy, and its observational follow-up, the Epidemiology of Diabetes Interventions and Complications (EDIC) Study. We measured plasma concentrations of 25-hydroxyvitamin D [25(OH)D], 1,25-dihydroxyvitamin D, and 24,25-dihydroxyvitamin D by mass spectrometry at the end of the DCCT and tested associations with incident microalbuminuria, impaired GFR, and hypertension over up to 16 yr of EDIC follow-up. Results: At the time metabolites were measured, mean age was 32.4 yr; mean duration of diabetes, 7.5 yr; mean iothalamate GFR, 132.9 ml/min/1.73 m(2); and geometric mean albumin excretion rate, 11.8 mg/24 h. Over follow-up, 166 cases of microalbuminuria, 54 cases of impaired GFR, and 541 cases of hypertension were observed. Compared with 25(OH)D of at least 30 ng/ml, 25(OH)D below 20 ng/ml was associated with a 65% higher risk of microalbuminuria (95% confidence interval, 7 to 154%) in adjusted analyses. Low concentrations of 24,25-dihydroxyvitamin D, but not 1,25-dihydroxyvitamin D, were also associated with increased risk of microalbuminuria. No circulating vitamin D metabolite was associated with risk of impaired GFR or hypertension. Conclusions: Low plasma concentrations of 25(OH)D and 24,25-dihydroxyvitamin D are associated with increased risk of microalbuminuria in type 1 diabetes. In contrast, we did not find evidence linking impaired vitamin D metabolism to early GFR loss or the development of hypertension. (J Clin Endocrinol Metab 97: 4780-4788, 2012)

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