Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA.
Nutrition Branch, Division of Nutrition, Physical Activity, and Obesity, Centers for Disease Control & Prevention, Atlanta, GA 30341, USA.
Nutrients. 2018 Sep 5;10(9):1240. doi: 10.3390/nu10091240.
Globally, vitamin A deficiency (VAD) affects nearly 200 million children with negative health consequences. VAD can be measured by a retinol-binding protein (RBP) and serum retinol concentrations. Their concentrations are not always present in a 1:1 molar ratio and are affected by inflammation. This study sought to quantify VAD and its impact on infant mortality and infectious morbidity during the first 18 months of life in a cohort of mother-infant dyads in El Alto, Bolivia, while accounting for the previously mentioned measurement issues. Healthy mother-infant dyads ( = 461) were enrolled from two hospitals and followed for 12 to 18 months. Three serum samples were collected (at one to two, six to eight, and 12 to 18 months of infant age) and analyzed for RBP, and a random 10% subsample was analyzed for retinol. Linear regression of RBP on retinol was used to generate RBP cut-offs equivalent to retinol <0.7 µmol/L. All measures of RBP and retinol were adjusted for inflammation, which was measured by a C-reactive protein and alpha (1)-acid glycoprotein serum concentrations using linear regression. Infant mortality and morbidity rates were calculated and compared by early VAD status at two months of age. Retinol and RBP were weakly affected by inflammation. This association varied with infant age. Estimated VAD (RBP < 0.7 µmol/L) decreased from 71.0% to 14.8% to 7.7% at two, six to eight, and 12 to 18 months of age. VAD was almost nonexistent in mothers. Early VAD was not significantly associated with infant mortality or morbidity rates. This study confirmed a relationship between inflammation and vitamin A biomarkers for some subsets of the population and suggested that the vitamin A status in early infancy improves with age and may not have significantly affected morbidity in this population of healthy infants.
全球范围内,约有 2 亿儿童患有维生素 A 缺乏症(VAD),对其健康造成负面影响。维生素 A 缺乏症可通过视黄醇结合蛋白(RBP)和血清视黄醇浓度来衡量。但是,它们的浓度并不总是呈 1:1 的摩尔比,而且会受到炎症的影响。本研究旨在量化维生素 A 缺乏症及其对玻利维亚埃尔阿尔托母婴队列在生命的前 18 个月内婴儿死亡率和传染性发病率的影响,同时考虑到之前提到的测量问题。从两家医院招募了健康的母婴对(n=461),并对其进行了 12 至 18 个月的随访。收集了三份血清样本(婴儿 1 至 2 个月、6 至 8 个月和 12 至 18 个月龄时),并分析了 RBP,同时对 10%的随机样本进行了视黄醇分析。使用线性回归分析 RBP 与视黄醇之间的关系,生成 RBP 切点,切点相当于视黄醇<0.7 μmol/L。所有 RBP 和视黄醇的测量值都经过了炎症的调整,炎症通过 C 反应蛋白和α(1)-酸性糖蛋白血清浓度的线性回归来测量。根据两个月时的早期 VAD 状态计算和比较婴儿死亡率和发病率。视黄醇和 RBP 受到炎症的轻微影响。这种关联因婴儿年龄而异。估计的 VAD(RBP<0.7 μmol/L)在两个月、六至八个月和十二至十八个月时从 71.0%降至 14.8%至 7.7%。母亲中几乎不存在 VAD。早期 VAD 与婴儿死亡率或发病率之间没有显著相关性。本研究证实了某些人群的炎症和维生素 A 生物标志物之间存在关系,并表明在这个健康婴儿群体中,婴儿早期的维生素 A 状况会随着年龄的增长而改善,并且可能没有对发病率产生显著影响。