Department of Epidemiology, Tulane School of Public Health and Tropical Medicine, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Department of Endocrinology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
J Diabetes. 2018 Jun;10(6):449-457. doi: 10.1111/1753-0407.12543. Epub 2017 Apr 6.
There may be sex-specific cardiometabolic mechanisms early in life that affect the development of type 2 diabetes mellitus (T2DM) through mid-adulthood. However, few studies have examined whether early life course interactions between cardiometabolic risk factors and sex are associated with incident T2DM.
This study followed 7725 children (3834 [49.6%] females, 3891 [50.4%] males) from the Bogalusa Heart Study through mid-adulthood to examine whether low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), body mass index (BMI), or systolic blood pressure (SBP) differentially affect the risk of T2DM for females versus males. Potential sex interactions were tested after adjusting for age, race, triglycerides, smoking, follow-up time, puberty stage, use of birth control, and enrollment year.
Mean (± SD) age at baseline was 9.4 ± 3.5 years. There were 176 cases of T2DM (cumulative incidence = 2.3%) during a median follow-up of 9.1 years. In females versus males, LDL-C and SBP were differentially associated with T2DM (P ≤ 0.001 and P = 0.017, respectively). The relationships of BMI and HDL-C with T2DM were non-differential between females and males (P = 0.79 and P = 0.27, respectively).
This study is the first to show evidence of sex-specific differential effects of LDL-C and SBP on the risk of T2DM from childhood to adulthood. Greater LDL-C places girls at disproportionally higher risk of T2DM as women, whereas greater SBP differentially exposes boys to a greater risk of T2DM as men. Additional studies within existing child cohorts are needed to confirm and investigate the mechanisms underlying these differential effects.
生命早期可能存在性别特异性的心脏代谢机制,这些机制会影响成年中期 2 型糖尿病(T2DM)的发展。然而,很少有研究探讨心脏代谢危险因素与性别的早期生命历程相互作用是否与 T2DM 的发生有关。
本研究通过中期随访,对博加卢萨心脏研究中的 7725 名儿童(女性 3834 名[49.6%],男性 3891 名[50.4%])进行了研究,以检验低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、体重指数(BMI)或收缩压(SBP)是否会对女性和男性的 T2DM 风险产生不同影响。在调整年龄、种族、甘油三酯、吸烟、随访时间、青春期阶段、避孕药使用和入组年份后,对潜在的性别交互作用进行了检验。
基线时的平均(±SD)年龄为 9.4±3.5 岁。中位随访 9.1 年后,共发生 176 例 T2DM(累积发病率为 2.3%)。与男性相比,女性的 LDL-C 和 SBP 与 T2DM 呈不同相关(P≤0.001 和 P=0.017)。BMI 和 HDL-C 与 T2DM 的关系在女性和男性之间无差异(P=0.79 和 P=0.27)。
本研究首次证明 LDL-C 和 SBP 对女性和男性 T2DM 风险的影响存在性别特异性差异。较高的 LDL-C 使女孩在成年女性中罹患 T2DM 的风险不成比例地升高,而较高的 SBP 则使男孩在成年男性中罹患 T2DM 的风险升高。需要在现有儿童队列中进行更多研究以证实和探讨这些差异作用的机制。