4.7 Article

Nutritional Factors and Preservation of C-Peptide in Youth With Recently Diagnosed Type 1 Diabetes SEARCH Nutrition Ancillary Study

Journal

DIABETES CARE
Volume 36, Issue 7, Pages 1842-1850

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc12-2084

Keywords

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Funding

  1. National Institutes of Health (NIH)/National Institute of Diabetes and Digestive and Kidney Diseases [R01 DK077949]
  2. Centers for Disease Control and Prevention [00097, DP-05-069, DP-10-001]
  3. National Institute of Diabetes and Digestive and Kidney Diseases
  4. NIH/National Center for Research Resources [UL1RR029882]
  5. Children's Hospital and Regional Medical Center [M01RR00037]
  6. Colorado Pediatric General Clinical Research Center [M01 RR00069]
  7. Barbara Davis Center at the University of Colorado at Denver [DERC NIH P30 DK57516]
  8. Institutional Clinical and Translational Science Award (CTSA) from the NIH/National Center for Research Resources at the University of Cincinnati [1UL1RR026314-01]

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OBJECTIVE-To test the novel hypothesis that nutritional factors previously associated with type 1 diabetes etiology or with insulin secretion are prospectively associated with fasting C-peptide (FCP) concentration among youth recently diagnosed with type 1 diabetes. RESEARCH DESIGN AND METHODS-Included were 1,316 youth with autoantibody-positive type 1 diabetes who participated in the SEARCH for Diabetes in Youth study (baseline disease duration, 9.9 months; SD, 6.3). Nutritional exposures included breastfeeding and age at introduction of complementary foods, baseline plasma long-chain omega-3 fatty acids including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DNA), vitamin D, vitamin E, and, from a baseline food frequency questionnaire, estimated intake of the branched-chain amino acid leucine and total carbohydrate. Multiple linear regression models were conducted to relate each nutritional factor to baseline FCP adjusted for demographics, disease-related factors, and other confounders. Prospective analyses included the subset of participants with preserved beta-cell function at baseline (baseline FCP >= 0.23 ng/mL) with additional adjustment for baseline FCP and time (mean follow-up, 24.3 months; SD, 8.2; n = 656). FCP concentration was analyzed as log(FCP). RESULTS-In adjusted prospective analyses, baseline EPA (P = 0.02), EPA plus DNA (P = 0.03), and leucine (P = 0.03) were each associated positively and significantly with FCP at followup. Vitamin D was unexpectedly inversely associated with FCP (P = 0.002). CONCLUSIONS-Increased intake of branched-chain amino acids and long-chain omega-3 fatty acids may support preservation of beta-cell function. This represents a new direction for research to improve prognosis for type 1 diabetes.

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