Yang Q, Lin S L, Au Yeung S L, Kwok M K, Xu L, Leung G M, Schooling C M
School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
School of Public Health and Health Policy, City University of New York, New York, NY, USA.
Eur J Clin Nutr. 2017 Aug;71(8):1008-1012. doi: 10.1038/ejcn.2017.8. Epub 2017 Feb 22.
BACKGROUND/OBJECTIVES: Milk provides protein and micronutrients, and is recommended by some dietary guidelines, particularly for bone health. Meta-analysis of small randomized controlled trials suggests that milk may increase bone mineral density, but they are very heterogeneous. No randomized controlled trial has assessed the effects of milk on major chronic diseases. Previous Mendelian randomization studies of milk did not consider bone health, found no effects on ischemic heart disease (IHD) or type 2 diabetes (T2D) but higher body mass index. Using larger genetic studies, we estimated the effects of milk on osteoporosis, IHD, T2D, adiposity, lipids and glycemic traits.
SUBJECTS/METHODS: Instrumental variable analysis based on a genetic variant endowing lactase persistence (rs4988235 (MCM6)) was used to obtain estimates for osteoporosis (GEFOS), IHD (CARDIoGRAMplusC4D), T2D (DIAGRAM), adiposity (GIANT), lipids (GLGC) and glycaemic traits (MAGIC). Eye color was a negative control for IHD, as it mirrors the distribution of lactase persistence and IHD in Western Europe.
Genetically predicted adult milk consumption was not clearly associated with bone mineral density, IHD (odds ratio (OR): 1.03 per s.d., 95% confidence interval (CI): 0.95-1.12) and or T2D (OR: 0.92, 95% CI: 0.83-1.02) but was associated with higher log-transformed fasting insulin (0.05, 95% CI: 0.02-0.07) and body mass index (0.06, 95% CI: 0.03-0.09). Genetically predicted eye color was not associated with IHD.
The lack of association of genetically predicted milk consumption with bone health, IHD or T2D suggests few beneficial effects but is more consistent with milk promoting adiposity.
背景/目的:牛奶能提供蛋白质和微量营养素,一些饮食指南推荐饮用牛奶,特别是对骨骼健康有益。对小型随机对照试验的荟萃分析表明,牛奶可能会增加骨密度,但这些试验差异很大。尚无随机对照试验评估牛奶对主要慢性疾病的影响。先前关于牛奶的孟德尔随机化研究未考虑骨骼健康,未发现对缺血性心脏病(IHD)或2型糖尿病(T2D)有影响,但发现与较高的体重指数有关。我们利用规模更大的基因研究,评估了牛奶对骨质疏松症、IHD、T2D、肥胖、血脂和血糖特征的影响。
对象/方法:基于赋予乳糖酶持续性的基因变异(rs4988235(MCM6))进行工具变量分析,以获得骨质疏松症(GEFOS)、IHD(CARDIoGRAMplusC4D)、T2D(DIAGRAM)、肥胖(GIANT)、血脂(GLGC)和血糖特征(MAGIC)的估计值。眼睛颜色作为IHD的阴性对照,因为它反映了西欧乳糖酶持续性和IHD的分布情况。
基因预测的成年期牛奶摄入量与骨密度、IHD(优势比(OR):每标准差1.03,95%置信区间(CI):0.95 - 1.12)和T2D(OR:0.92,95%CI:0.83 - 1.02)无明显关联,但与经对数转换的空腹胰岛素水平升高(0.05,95%CI:0.02 - 0.07)和体重指数升高(0.06,95%CI:0.03 - 0.09)有关。基因预测的眼睛颜色与IHD无关。
基因预测的牛奶摄入量与骨骼健康、IHD或T2D缺乏关联,表明其益处不大,但更符合牛奶促进肥胖的观点。