Arndt Michael B, Richardson Barbra A, Ahmed Tahmeed, Mahfuz Mustafa, Haque Rashidul, John-Stewart Grace C, Denno Donna M, Petri William A, Kosek Margaret, Walson Judd L
Department of Epidemiology, University of Washington, Seattle, Washington.
Department of Biostatistics, University of Washington, Seattle, Washington. Department of Global Health, University of Washington, Seattle, Washington.
Am J Trop Med Hyg. 2016 Sep 7;95(3):694-701. doi: 10.4269/ajtmh.16-0098. Epub 2016 Jun 27.
Environmental enteropathy (EE), a subclinical intestinal disorder characterized by mucosal inflammation, reduced barrier integrity, and malabsorption, appears to be associated with increased risk of stunting in children in low- and middle-income countries. Fecal biomarkers indicative of EE (neopterin [NEO], myeloperoxidase [MPO], and alpha-1-antitrypsin [AAT]) have been negatively associated with 6-month linear growth. Associations between fecal markers (NEO, MPO, and AAT) and short-term linear growth were examined in a birth cohort of 246 children in Bangladesh. Marker concentrations were categorized in stool samples based on their distribution (< first quartile, interquartile range, > third quartile), and a 10-point composite EE score was calculated. Piecewise linear mixed-effects models were used to examine the association between markers measured quarterly (in months 3-21, 3-9, and 12-21) and 3-month change in length-for-age z-score (ΔLAZ). Children with high MPO levels at quarterly time points lost significantly more LAZ per 3-month period during the second year of life than those with low MPO (ΔLAZ = -0.100; 95% confidence interval = -0.167 to -0.032). AAT and NEO were not associated with growth; however, composite EE score was negatively associated with subsequent 3-month growth. In this cohort of children from an urban setting in Bangladesh, elevated MPO levels, but not NEO or AAT levels, were associated with decreases in short-term linear growth during the second year of life, supporting previous data suggesting the relevance of MPO as a marker of EE.
环境肠病(EE)是一种以黏膜炎症、屏障完整性降低和吸收不良为特征的亚临床肠道疾病,在低收入和中等收入国家,它似乎与儿童发育迟缓风险增加有关。指示EE的粪便生物标志物(新蝶呤[NEO]、髓过氧化物酶[MPO]和α-1抗胰蛋白酶[AAT])与6个月时的线性生长呈负相关。在孟加拉国一个有246名儿童的出生队列中,研究了粪便标志物(NEO、MPO和AAT)与短期线性生长之间的关联。根据粪便样本中标志物浓度的分布(<第一四分位数、四分位间距、>第三四分位数)进行分类,并计算出一个10分的综合EE评分。采用分段线性混合效应模型来研究每季度(第3至21个月、第3至9个月和第12至21个月)测量的标志物与年龄别身长Z评分(ΔLAZ)的3个月变化之间的关联。在生命的第二年,每3个月期间,季度时间点MPO水平高的儿童比MPO水平低的儿童失去的LAZ明显更多(ΔLAZ = -0.100;95%置信区间 = -0.167至-0.032)。AAT和NEO与生长无关;然而,综合EE评分与随后的3个月生长呈负相关。在这个来自孟加拉国城市地区的儿童队列中,MPO水平升高而非NEO或AAT水平升高与生命第二年的短期线性生长下降有关,这支持了之前的数据,表明MPO作为EE标志物的相关性。