de Jonge E A L, Kiefte-de Jong J C, Campos-Obando N, Booij L, Franco O H, Hofman A, Uitterlinden A G, Rivadeneira F, Zillikens M C
Erasmus MC, Department of Internal Medicine, Rotterdam, The Netherlands.
Erasmus MC, Department of Epidemiology, Rotterdam, The Netherlands.
Eur J Clin Nutr. 2015 Dec;69(12):1360-8. doi: 10.1038/ejcn.2015.154. Epub 2015 Sep 16.
BACKGROUND/OBJECTIVES: High vitamin A intake may be associated with a decreased bone mineral density (BMD) and increased risk of fractures. Our objectives were to study whether dietary intake of vitamin A (total, retinol or beta-carotene) is associated with BMD and fracture risk and if associations are modified by body mass index (BMI) and vitamin D.
SUBJECTS/METHODS: Participants were aged 55 years and older (n=5288) from the Rotterdam Study, a population-based prospective cohort. Baseline vitamin A and D intake was measured by a food frequency questionnaire. BMD was measured by dual-energy X-ray absorptiometry at four visits between baseline (1989-1993) and 2004. Serum vitamin D was assessed in a subgroup (n=3161). Fracture incidence data were derived from medical records with a mean follow-up time of 13.9 years.
Median intake of vitamin A ranged from 684 retinol equivalents (REs)/day (quintile 1) to 2000 REs/day (quintile 5). After adjustment for confounders related to lifestyle and socioeconomic status, BMD was significantly higher in subjects in the highest quintile of total vitamin A (mean difference in BMD (95% confidence interval (CI))=11.53 (0.37-22.7) mg/cm(2)) and retinol intake (mean difference in BMD (95% CI)=12.57 (1.10-24.05) mg/cm(2)) than in the middle quintile. Additional adjustment for BMI diluted these associations. Fracture risk was reduced in these subjects. Significant interaction was present between intake of retinol and overweight (BMI >25 kg/m(2)) in relation to fractures (P for interaction =0.05), but not BMD. Stratified analysis showed that these favourable associations with fracture risk were only present in overweight subjects (BMI >25 kg/m(2)). No effect modification by vitamin D intake or serum levels was observed.
Our results suggest a plausible favourable relation between high vitamin A intake from the diet and fracture risk in overweight subjects, whereas the association between vitamin A and BMD is mainly explained by BMI.
背景/目的:高维生素A摄入量可能与骨矿物质密度(BMD)降低及骨折风险增加有关。我们的目的是研究膳食中维生素A(总维生素A、视黄醇或β-胡萝卜素)的摄入量是否与BMD及骨折风险相关,以及这些关联是否会因体重指数(BMI)和维生素D而改变。
受试者/方法:参与者来自鹿特丹研究,这是一项基于人群的前瞻性队列研究,年龄在55岁及以上(n = 5288)。通过食物频率问卷测量基线时维生素A和D的摄入量。在基线(1989 - 1993年)至2004年期间的四次访视中,采用双能X线吸收法测量BMD。在一个亚组(n = 3161)中评估血清维生素D。骨折发生率数据来自医疗记录,平均随访时间为13.9年。
维生素A的摄入量中位数范围为每天684视黄醇当量(REs)(第一五分位数)至2000 REs/天(第五五分位数)。在对与生活方式和社会经济地位相关的混杂因素进行调整后,总维生素A摄入量最高五分位数的受试者(BMD的平均差异(95%置信区间(CI))= 11.53(0.37 - 22.7)mg/cm²)和视黄醇摄入量最高五分位数的受试者(BMD的平均差异(95% CI)= 12.57(1.10 - 24.05)mg/cm²)的BMD显著高于中间五分位数的受试者。对BMI进行额外调整后,这些关联减弱。这些受试者的骨折风险降低。视黄醇摄入量与超重(BMI>25 kg/m²)之间在骨折方面存在显著交互作用(交互作用P值 = 0.05),但在BMD方面不存在。分层分析表明,这些与骨折风险的有利关联仅在超重受试者(BMI>25 kg/m²)中存在。未观察到维生素D摄入量或血清水平的效应修饰作用。
我们的结果表明,超重受试者从饮食中摄入高维生素A与骨折风险之间可能存在有利关系,而维生素A与BMD之间的关联主要由BMI解释。