Diabetes Care. 2018 Aug;41(8):1590-1599. doi: 10.2337/dc18-0240. Epub 2018 Jun 25.
To describe baseline characteristics of the Vitamin D and Type 2 Diabetes (D2d) study, the first large U.S. diabetes prevention clinical trial to apply current American Diabetes Association (ADA) criteria for prediabetes.
This is a multicenter ( = 22 sites), randomized, double-blind, placebo-controlled, primary prevention clinical trial testing effects of oral daily 4,000 IU cholecalciferol (D) compared with placebo on incident diabetes in U.S. adults at risk for diabetes. Eligible participants were at risk for diabetes, defined as not meeting criteria for diabetes but meeting at least two 2010 ADA glycemic criteria for prediabetes: fasting plasma glucose (FPG) 100-125 mg/dL, 2-h postload glucose (2hPG) after a 75-g oral glucose load 140-199 mg/dL, and/or a hemoglobin A (HbA) 5.7-6.4% (39-46 mmol/mol).
A total of 2,423 participants (45% of whom were women and 33% nonwhite) were randomized to cholecalciferol or placebo. Mean (SD) age was 59 (9.9) years and BMI 32 (4.5) kg/m. Thirty-five percent met all three prediabetes criteria, 49% met the FPG/HbA criteria only, 9.5% met the 2hPG/FPG criteria only, and 6.3% met the 2hPG/HbA criteria only. Black participants had the highest mean HbA and lowest FPG concentration compared with white, Asian, and other races ( < 0.01); 2hPG concentration did not differ among racial groups. When compared with previous prediabetes cohorts, the D2d cohort had lower mean 2hPG concentration but similar HbA and FPG concentrations.
D2d will establish whether vitamin D supplementation lowers risk of diabetes and will inform about the natural history of prediabetes per contemporary ADA criteria.
描述维生素 D 与 2 型糖尿病(D2d)研究的基线特征,这是首个在美国应用当前美国糖尿病协会(ADA)糖尿病前期标准的大型糖尿病预防临床试验。
这是一项多中心(=22 个地点)、随机、双盲、安慰剂对照、初级预防临床试验,旨在测试口服每日 4000IU 胆钙化醇(D)与安慰剂相比对美国糖尿病高危成年人新发糖尿病的影响。符合条件的参与者存在患糖尿病的风险,定义为不符合糖尿病标准但符合至少 2010 ADA 血糖标准的糖尿病前期:空腹血糖(FPG)100-125mg/dL,口服 75g 葡萄糖负荷后 2 小时血糖(2hPG)140-199mg/dL,和/或血红蛋白 A(HbA)5.7-6.4%(39-46mmol/mol)。
共有 2423 名参与者(45%为女性,33%为非白人)被随机分配至胆钙化醇或安慰剂组。平均(SD)年龄为 59(9.9)岁,BMI 为 32(4.5)kg/m。35%符合所有三种糖尿病前期标准,49%仅符合 FPG/HbA 标准,9.5%仅符合 2hPG/FPG 标准,6.3%仅符合 2hPG/HbA 标准。与白种人、亚洲人和其他种族相比,黑人参与者的平均 HbA 最高,FPG 浓度最低(<0.01);不同种族组之间的 2hPG 浓度无差异。与以前的糖尿病前期队列相比,D2d 队列的平均 2hPG 浓度较低,但 HbA 和 FPG 浓度相似。
D2d 将确定维生素 D 补充是否降低糖尿病风险,并提供关于当代 ADA 标准下糖尿病前期自然史的信息。