Laboratory of Cellular and Molecular Immunology, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czechia.
Laboratory of Fungal Genetics and Metabolism, Institute of Microbiology of the Czech Academy of Sciences, Prague, Czechia.
Front Endocrinol (Lausanne). 2022 Sep 5;13:970825. doi: 10.3389/fendo.2022.970825. eCollection 2022.
Gestation is linked to changes in gut microbiota composition and function. Since gestational (GDM) can develop at any time of the pregnancy, we stratified the women into four groups according to the time and test used for the diagnosis. We focused on the gut microbiota pattern in early pregnancy to detect changes which could be linked to later GDM development.
We collected stool samples from 104 pregnant women including obese individuals (first trimester body mass index median was 26.73). We divided the women into four groups according to routine screening of fasting plasma glucose (FPG) levels and oral glucose tolerance test (oGTT) in the first and third trimesters, respectively. We processed the stool samples for bacterial 16S rRNA and fungal ITS1 genes sequencing by Illumina MiSeq approach and correlated the gut microbiota composition with plasma short-chain fatty acid levels (SCFA).
We found that gut bacterial microbiota in the first trimester significantly differs among groups with different GDM onset based on unweighted UniFrac distances (p=0.003). Normoglycemic women had gut microbiota associated with higher abundance of family Prevotellaceae, and order Fusobacteriales, and genus . Women diagnosed later during pregnancy either by FGP levels or by oGTT had higher abundances of genera , or , respectively. We observed significant enrichment of fungal genus in healthy pregnant women whereas was more abundant in the group of pregnant women with impaired oGTT. Using correlation analysis, we found that negatively correlated with and abundances and that / abundance positively correlated and negatively correlated with plasma lipid levels. , , , and positively correlated with acetate, valerate, 2-hydroxybutyrate and 2-methylbutyrate levels, respectively, in women with GDM.
We conclude that there are significant differences in the gut microbiota composition between pregnant women with and without GDM already at the early stage of pregnancy in our cohort that included also overweight and obese individuals. Specific microbial pattern associated with GDM development during early pregnancy and its correlation to plasma lipid or SCFA levels could help to identify women in higher risk of GDM development.
妊娠与肠道微生物群落组成和功能的变化有关。由于妊娠期糖尿病(GDM)可在妊娠的任何时间发生,因此我们根据诊断时的时间和检测方法将女性分为四组。我们专注于早期妊娠的肠道微生物群模式,以检测可能与以后 GDM 发展相关的变化。
我们收集了 104 名孕妇的粪便样本,其中包括肥胖个体(孕早期的体重指数中位数为 26.73)。我们根据空腹血糖(FPG)水平和口服葡萄糖耐量试验(oGTT)在第一和第三孕期的常规筛查,将女性分为四组。我们通过 Illumina MiSeq 方法对粪便样本进行细菌 16S rRNA 和真菌 ITS1 基因测序,并将肠道微生物群落组成与血浆短链脂肪酸(SCFA)水平相关联。
我们发现,根据非加权 UniFrac 距离,基于不同 GDM 发病时间的分组,早期妊娠时肠道细菌微生物群存在显著差异(p=0.003)。血糖正常的女性具有与丰度较高的家族 Prevotellaceae、目 Fusobacteriales 和属 相关的肠道微生物群。在妊娠后期通过 FGP 水平或 oGTT 诊断的女性,分别具有较高丰度的属 或 。我们观察到健康孕妇中真菌属 的丰度显著增加,而 oGTT 受损的孕妇组中 丰度较高。通过相关分析,我们发现 与 和 的丰度呈负相关,而 / 的丰度与血浆脂质水平呈正相关,与呈负相关。在 GDM 女性中, 、 、 、 和 分别与醋酸盐、戊酸盐、2-羟丁酸和 2-甲基丁酸水平呈正相关。
我们的结论是,在我们的队列中,包括超重和肥胖个体在内,已经在妊娠早期,患有和不患有 GDM 的孕妇之间的肠道微生物群落组成存在显著差异。与 GDM 发展相关的特定微生物模式及其与血浆脂质或 SCFA 水平的相关性,有助于识别具有更高 GDM 发展风险的女性。