Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
J Infect Dis. 2021 Dec 20;224(12 Suppl 2):S848-S855. doi: 10.1093/infdis/jiab434.
The association between childhood diarrheal disease and linear growth faltering in developing countries is well described. However, the impact attributed to specific pathogens has not been elucidated, nor has the impact of recommended antibiotic treatment.
The Global Enteric Multicenter Study enrolled children with moderate to severe diarrhea (MSD) seeking healthcare at 7 sites in sub-Saharan Africa and South Asia. At enrollment, we collected stool samples to identify enteropathogens. Length/height was measured at enrollment and follow-up, approximately 60 days later, to calculate change in height-for-age z scores (ΔHAZ). The association of pathogens with ΔHAZ was tested using linear mixed effects regression models.
Among 8077 MSD cases analyzed, the proportion with stunting (HAZ below -1) increased from 59% at enrollment to 65% at follow-up (P < .0001). Pathogens significantly associated with linear growth decline included Cryptosporidium (P < .001), typical enteropathogenic Escherichia coli (P = .01), and untreated Shigella (P = .009) among infants (aged 0-11 months) and enterotoxigenic E. coli encoding heat-stable toxin (P < .001) and Cryptosporidium (P = .03) among toddlers (aged 12-23 months). Shigella-infected toddlers given antibiotics had improved linear growth (P = .02).
Linear growth faltering among children aged 0-23 months with MSD is associated with specific pathogens and can be mitigated with targeted treatment strategies, as demonstrated for Shigella.
发展中国家儿童腹泻病与线性生长迟缓之间的关联已有详细描述。然而,特定病原体的影响以及推荐的抗生素治疗的影响尚未阐明。
全球肠道多中心研究在撒哈拉以南非洲和南亚的 7 个地点招募了患有中度至重度腹泻(MSD)并寻求医疗保健的儿童。在入组时,我们收集了粪便样本以鉴定肠道病原体。在入组和大约 60 天后的随访时测量了长度/身高,以计算身高年龄 z 分数的变化(ΔHAZ)。使用线性混合效应回归模型测试病原体与 ΔHAZ 的关联。
在分析的 8077 例 MSD 病例中,出现发育迟缓(HAZ 低于-1)的比例从入组时的 59%增加到随访时的 65%(P<0.0001)。与线性生长下降显著相关的病原体包括隐孢子虫(P<0.001)、典型肠致病性大肠杆菌(P=0.01)和未经治疗的志贺菌(P=0.009),这些病原体在婴儿(0-11 个月)中,以及肠毒素性大肠杆菌编码耐热毒素(P<0.001)和隐孢子虫(P=0.03)在幼儿(12-23 个月)中。接受抗生素治疗的志贺菌感染幼儿的线性生长得到改善(P=0.02)。
患有 MSD 的 0-23 个月儿童的线性生长迟缓与特定病原体有关,通过针对特定病原体的治疗策略可以减轻这种影响,如志贺菌感染的情况所示。