Division of Neonatology, Rady Children's Hospital, University of California, San Diego, San Diego, CA, USA.
Division of Neonatology, Department of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Sci Rep. 2022 Apr 19;12(1):6437. doi: 10.1038/s41598-022-10276-y.
Preterm infants are at a greater risk for the development of asthma and atopic disease, which can lead to lifelong negative health consequences. This may be due, in part, to alterations that occur in the gut microbiome and metabolome during their stay in the Neonatal Intensive Care Unit (NICU). To explore the differential roles of family history (i.e., predisposition due to maternal asthma diagnosis) and hospital-related environmental and clinical factors that alter microbial exposures early in life, we considered a unique cohort of preterm infants born ≤ 34 weeks gestational age from two local level III NICUs, as part of the MAP (Microbiome, Atopic disease, and Prematurity) Study. From MAP participants, we chose a sub-cohort of infants whose mothers had a history of asthma and matched gestational age and sex to infants of mothers without a history of asthma diagnosis (control). We performed a prospective, paired metagenomic and metabolomic analysis of stool and milk feed samples collected at birth, 2 weeks, and 6 weeks postnatal age. Although there were clinical factors associated with shifts in the diversity and composition of stool-associated bacterial communities, maternal asthma diagnosis did not play an observable role in shaping the infant gut microbiome during the study period. There were significant differences, however, in the metabolite profile between the maternal asthma and control groups at 6 weeks postnatal age. The most notable changes occurred in the linoleic acid spectral network, which plays a role in inflammatory and immune pathways, suggesting early metabolomic changes in the gut of preterm infants born to mothers with a history of asthma. Our pilot study suggests that a history of maternal asthma alters a preterm infants' metabolomic pathways in the gut, as early as the first 6 weeks of life.
早产儿患哮喘和特应性疾病的风险更高,这可能导致终生的负面健康后果。这可能部分是由于他们在新生儿重症监护病房(NICU)停留期间肠道微生物组和代谢组发生了改变。为了探索家族史(即母亲哮喘诊断导致的易感性)和改变生命早期微生物暴露的与医院相关的环境和临床因素的差异作用,我们考虑了来自两个当地三级 NICU 的≤34 周胎龄早产儿的独特队列,作为 MAP(微生物组、特应性疾病和早产)研究的一部分。从 MAP 参与者中,我们选择了一组母亲有哮喘病史的婴儿亚组,并与母亲无哮喘诊断史的婴儿匹配胎龄和性别(对照)。我们对出生时、2 周和 6 周龄时采集的粪便和牛奶喂养样本进行了前瞻性、配对的宏基因组和代谢组分析。尽管有与粪便相关细菌群落多样性和组成变化相关的临床因素,但在研究期间,母亲哮喘诊断并没有在塑造婴儿肠道微生物组方面发挥可观察到的作用。然而,在 6 周龄时,母亲哮喘组和对照组之间的代谢物谱存在显著差异。最显著的变化发生在亚油酸谱网络中,该网络在炎症和免疫途径中发挥作用,这表明母亲有哮喘病史的早产儿肠道中存在早期代谢变化。我们的初步研究表明,母亲哮喘史会改变早产儿肠道中的代谢途径,早在生命的前 6 周就会发生。