Novo Nordisk Foundation Center for Basic Metabolic Research, Section for Metabolic Genetics, University of Copenhagen, Copenhagen, Denmark.
Department of Obstetrics and Gynaecology, Hvidovre University Hospital, Hvidovre, Denmark.
Front Cell Infect Microbiol. 2020 Oct 23;10:536282. doi: 10.3389/fcimb.2020.536282. eCollection 2020.
Offspring of mothers with gestational diabetes mellitus (GDM) have increased risk of developing metabolic disorders as they grow up. Microbial colonization of the newborn gut and environmental exposures affecting the configuration of the gut microbiota during infancy have been linked to increased risk of developing disease during childhood and adulthood. In a convenience sample, we examined whether the intestinal tract of children born to mothers with GDM is differentially colonized in early life compared to offspring of mothers with normal gestational glucose regulation. Secondly, we examined whether any such difference persists during infancy, thus potentially conferring increased risk of developing metabolic disease later in life. Fecal samples were collected from children of mothers with ( = 43) and without GDM ( = 82) during the first week of life and again at an average age of 9 months. The gut microbiota was characterized by 16S rRNA gene amplicon sequencing (V1-V2). Differences in diversity and composition according to maternal GDM status were assessed, addressing potential confounding by mode of delivery, perinatal antibiotics treatment, feeding and infant sex. Children of mothers with GDM were featured by a differential composition of the gut microbiota, both during the first week of life and at 9 months, at higher taxonomic and OTU levels. Sixteen and 15 OTUs were differentially abundant after correction for multiple testing during the first week of life and at 9 months, respectively. Two OTUs remained differentially abundant after adjustment for potential confounders both during the first week of life and at 9 months. Richness (OTU) was decreased in neonates born to mothers with GDM; however, at 9 months no difference in richness was observed. There was no difference in Shannon's diversity or Pielou's evenness at any timepoint. Longitudinally, we detected differential changes in the gut microbiota composition from birth to infancy according to GDM status. Differences in glycaemic regulation in late pregnancy is linked with relatively modest variation in the gut microbiota composition of the offspring during the first week of life and 9 months after birth.
患有妊娠糖尿病(GDM)的母亲所生的后代在成长过程中患代谢紊乱的风险增加。新生儿肠道的微生物定植以及婴儿期影响肠道微生物组结构的环境暴露,与儿童和成年期患疾病的风险增加有关。在一个方便的样本中,我们研究了与正常妊娠血糖调节的母亲所生的后代相比,患有 GDM 的母亲所生的儿童在生命早期的肠道是否存在不同程度的定植。其次,我们研究了这种差异是否在婴儿期持续存在,从而可能增加生命后期患代谢疾病的风险。
在生命的第一周和平均 9 个月大时,从患有 GDM 的母亲(n = 43)和没有 GDM 的母亲(n = 82)的孩子中收集粪便样本。通过 16S rRNA 基因扩增子测序(V1-V2)来描述肠道微生物群。根据母亲 GDM 状态评估多样性和组成的差异,同时考虑了分娩方式、围产期抗生素治疗、喂养方式和婴儿性别等潜在混杂因素。
患有 GDM 的母亲所生的孩子的肠道微生物群组成存在差异,无论是在生命的第一周还是 9 个月大时,在更高的分类和 OTU 水平上都是如此。在生命的第一周和 9 个月时,校正多重检验后,分别有 16 个和 15 个 OTU 存在差异丰度。在生命的第一周和 9 个月时,在调整了潜在混杂因素后,仍有两个 OTU 存在差异丰度。GDM 母亲所生的新生儿在生命的第一周时 OTU 丰富度降低;然而,在 9 个月时,OTU 丰富度没有差异。在任何时间点,Shannon 多样性或 Pielou 均匀度都没有差异。纵向研究发现,根据 GDM 状态,从出生到婴儿期,肠道微生物群组成存在差异变化。
妊娠晚期血糖调节的差异与后代在生命的第一周和出生后 9 个月时肠道微生物群组成的相对适度变化有关。