Stokholm Jakob, Thorsen Jonathan, Schoos Ann-Marie Malby, Rasmussen Morten Arendt, Brandt Sarah, Sørensen Søren Johannes, Vahman Nilo, Chawes Bo, Bønnelykke Klaus
Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Copenhagen, Denmark.
Department of Food Science, University of Copenhagen, Frederiksberg, Denmark.
Allergy. 2024 Dec;79(12):3360-3372. doi: 10.1111/all.16274. Epub 2024 Aug 19.
Infantile colic is a common condition with limited knowledge about later clinical manifestations. We evaluated the role of the early life gut microbiome in infantile colic and later development of atopic and gastrointestinal disorders.
Copenhagen Prospective Studies on Asthma in Childhood cohort was followed with 6 years of extensive clinical phenotyping. The 1-month gut microbiome was analyzed by 16S rRNA sequencing. Infantile colic was evaluated at age 3 months by interviews. Clinical endpoints included constipation to age 3 years and prospectively diagnosed asthma and atopic dermatitis in the first 6 years of life, and allergic sensitization from skin prick tests, specific Immunoglobulin E, and component analyses.
Of 695 children, 55 children (7.9%) had infantile colic. Several factors were associated with colic including race, breastfeeding, and pets. The 1-month gut microbiome composition and taxa abundances were not associated with colic, however a sparse Partial Least Squares model including combined abundances of nine species was moderately predictive of colic: median, cross-validated AUC = 0.627, p = .003. Children with infantile colic had an increased risk of developing constipation (aOR, 2.88 [1.51-5.35], p = .001) later in life, but also asthma (aHR, 1.69 [1.02-2.79], p = .040), atopic dermatitis (aHR, 1.84 [1.20-2.81], p = .005) and had a higher number of positive allergic components (adjusted difference, 116% [14%-280%], p = .012) in the first 6 years. These associations were not mediated by gut microbiome differences.
We link infantile colic with risk of developing constipation and atopic disorders in the first 6 years of life, which was not mediated through an altered gut microbiome at age 1-month. These results suggest infantile colic to involve gastrointestinal and/or atopic mechanisms.
婴儿腹绞痛是一种常见病症,人们对其后期临床表现了解有限。我们评估了早期肠道微生物群在婴儿腹绞痛以及后期特应性疾病和胃肠道疾病发展中的作用。
对哥本哈根儿童哮喘前瞻性研究队列进行了为期6年的广泛临床表型分析。通过16S rRNA测序分析1月龄时的肠道微生物群。在3月龄时通过访谈评估婴儿腹绞痛。临床终点包括3岁前的便秘以及生命最初6年中前瞻性诊断的哮喘和特应性皮炎,以及皮肤点刺试验、特异性免疫球蛋白E和成分分析得出的过敏致敏情况。
在695名儿童中,55名儿童(7.9%)患有婴儿腹绞痛。几个因素与腹绞痛相关,包括种族、母乳喂养和宠物。1月龄时的肠道微生物群组成和分类群丰度与腹绞痛无关,然而,一个包含9个物种组合丰度的稀疏偏最小二乘模型对腹绞痛有中度预测性:中位数,交叉验证AUC = 0.627,p = 0.003。患有婴儿腹绞痛的儿童在生命后期发生便秘的风险增加(调整优势比,2.88 [1.51 - 5.35],p = 0.001),同时哮喘(调整风险比,1.69 [1.02 - 2.79],p = 0.040)、特应性皮炎(调整风险比,1.84 [1.20 - 2.81],p = 0.005)的风险也增加,并且在最初6年中有更多的阳性过敏成分(调整差异,116% [14% - 280%],p = 0.012)。这些关联并非由肠道微生物群差异介导。
我们将婴儿腹绞痛与生命最初6年中发生便秘和特应性疾病的风险联系起来,这并非通过1月龄时肠道微生物群的改变介导。这些结果表明婴儿腹绞痛涉及胃肠道和/或特应性机制。