Lemas Dominick J, Young Bridget E, Baker Peter R, Tomczik Angela C, Soderborg Taylor K, Hernandez Teri L, de la Houssaye Becky A, Robertson Charles E, Rudolph Michael C, Ir Diana, Patinkin Zachary W, Krebs Nancy F, Santorico Stephanie A, Weir Tiffany, Barbour Linda A, Frank Daniel N, Friedman Jacob E
Sections of Neonatology.
Nutrition, and.
Am J Clin Nutr. 2016 May;103(5):1291-300. doi: 10.3945/ajcn.115.126375.
Increased maternal body mass index (BMI) is a robust risk factor for later pediatric obesity. Accumulating evidence suggests that human milk (HM) may attenuate the transfer of obesity from mother to offspring, potentially through its effects on early development of the infant microbiome.
Our objective was to identify early differences in intestinal microbiota in a cohort of breastfeeding infants born to obese compared with normal-weight (NW) mothers. We also investigated relations between HM hormones (leptin and insulin) and both the taxonomic and functional potentials of the infant microbiome.
Clinical data and infant stool and fasting HM samples were collected from 18 NW [prepregnancy BMI (in kg/m(2)) <24.0] and 12 obese (prepregnancy BMI >30.0) mothers and their exclusively breastfed infants at 2 wk postpartum. Infant body composition at 2 wk was determined by air-displacement plethysmography. Infant gastrointestinal microbes were estimated by using 16S amplicon and whole-genome sequencing. HM insulin and leptin were determined by ELISA; short-chain fatty acids (SCFAs) were measured in stool samples by using gas chromatography. Power was set at 80%.
Infants born to obese mothers were exposed to 2-fold higher HM insulin and leptin concentrations (P < 0.01) and showed a significant reduction in the early pioneering bacteria Gammaproteobacteria (P = 0.03) and exhibited a trend for elevated total SCFA content (P < 0.06). Independent of maternal prepregnancy BMI, HM insulin was positively associated with both microbial taxonomic diversity (P = 0.03) and Gammaproteobacteria (e.g., Enterobacteriaceae; P = 0.04) and was negatively associated with Lactobacillales (e.g., Streptococcaceae; P = 0.05). Metagenomic analysis showed that HM leptin and insulin were associated with decreased bacterial proteases, which are implicated in intestinal permeability, and reduced concentrations of pyruvate kinase, a biomarker of pediatric gastrointestinal inflammation.
Our results indicate that, although maternal obesity may adversely affect the early infant intestinal microbiome, HM insulin and leptin are independently associated with beneficial microbial metabolic pathways predicted to increase intestinal barrier function and reduce intestinal inflammation. This trial was registered at clinicaltrials.gov as NCT01693406.
孕妇体重指数(BMI)升高是儿童后期肥胖的一个有力风险因素。越来越多的证据表明,母乳(HM)可能会减弱肥胖从母亲向后代的传递,这可能是通过其对婴儿微生物群早期发育的影响实现的。
我们的目的是确定一组由肥胖母亲与正常体重(NW)母亲所生的母乳喂养婴儿肠道微生物群的早期差异。我们还研究了母乳中的激素(瘦素和胰岛素)与婴儿微生物群的分类学和功能潜力之间的关系。
收集了18名NW[孕前BMI(kg/m²)<24.0]和12名肥胖(孕前BMI>30.0)母亲及其产后2周纯母乳喂养婴儿的临床数据、婴儿粪便和空腹母乳样本。通过空气置换体积描记法测定2周时婴儿的身体成分。使用16S扩增子和全基因组测序估计婴儿胃肠道微生物。通过ELISA法测定母乳中的胰岛素和瘦素;使用气相色谱法测量粪便样本中的短链脂肪酸(SCFA)。检验效能设定为80%。
肥胖母亲所生的婴儿接触到的母乳胰岛素和瘦素浓度高出2倍(P<0.01),并且早期先锋菌γ-变形菌显著减少(P=0.03),总SCFA含量有升高趋势(P<0.06)。独立于母亲孕前BMI,母乳胰岛素与微生物分类学多样性(P=0.03)和γ-变形菌(如肠杆菌科;P=0.04)均呈正相关,与乳杆菌目(如链球菌科;P=0.05)呈负相关。宏基因组分析表明,母乳中的瘦素和胰岛素与细菌蛋白酶减少有关,细菌蛋白酶与肠道通透性有关,并且与丙酮酸激酶浓度降低有关,丙酮酸激酶是儿童胃肠道炎症的一个生物标志物。
我们的结果表明,虽然母亲肥胖可能会对婴儿早期肠道微生物群产生不利影响,但母乳胰岛素和瘦素分别与预测可增强肠道屏障功能和减轻肠道炎症的有益微生物代谢途径相关。该试验已在clinicaltrials.gov注册,注册号为NCT01693406。