Department of Surgery, University of British Columbia, Vancouver, British Columbia, Canada.
Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
J Pediatr Gastroenterol Nutr. 2024 Sep;79(3):705-715. doi: 10.1002/jpn3.12327. Epub 2024 Jul 24.
Infants with small bowel stomas (SBstoma) frequently struggle with absorption and rely on parenteral nutrition (PN). Intestinal absorption is difficult to predict based solely on intestinal anatomy. The purpose of this study was to characterize the microbiota and metabolic by-products within stoma effluent and correlate with clinical features and intestinal absorption.
Prospective cohort study collecting stoma samples from neonates with SBstoma (N = 23) or colostomy control (N = 6) at initial enteral feed (first sample) and before stoma closure (last sample). Gut bacteriome (16S ribosomal RNA [rRNA] sequencing), short-chain fatty acids (SCFAs) and bile acids (BAs) were characterized along with volume and energy content of a 48 h collection via bomb calorimetry (last sample). Hierarchical clustering and linear regression were used to compare the bacteriome and BAs/SCFAs, to bowel length, PN, and growth.
Infants with ≤50% small bowel lost more fluid on average than those with >50% and controls (22, 18, 16 mL/kg/day, p = 0.013), but had similar energy losses (7, 10, 9 kcal/kg/day, p = 0.147). Infants growing poorly had enrichment of Proteobacteria compared to infants growing well (90% vs. 15%, p = 0.004). An increase in the ratio of secondary BAs within the small bowel over time, correlated with poor prognostic factors (≤50% small bowel, >50% of calories from PN, and poor growth).
Infants with SBstoma and poor growth have a unique bacteriome community and those with poor enteral tolerance have metabolic differences compared to infants with improved absorption.
患有小肠造口术(SBstoma)的婴儿经常在吸收方面存在困难,需要依赖肠外营养(PN)。仅根据肠道解剖结构很难预测肠道吸收情况。本研究旨在描述造口分泌物中的微生物群和代谢副产物,并与临床特征和肠道吸收相关联。
本前瞻性队列研究收集了 23 例 SBstoma 新生儿和 6 例结肠造口术对照组新生儿在开始肠内喂养时(第一份样本)和造口关闭前(最后一份样本)的造口样本。通过量热计对 48 小时收集的样本体积和能量含量(最后一份样本)进行分析,同时还对肠道细菌组(16S 核糖体 RNA [rRNA] 测序)、短链脂肪酸(SCFAs)和胆汁酸(BAs)进行了特征分析。使用层次聚类和线性回归来比较细菌组和 BAs/SCFAs 与肠长度、PN 和生长的关系。
SBstoma 婴儿中,≤50%小肠的婴儿平均丢失的液体多于>50%和对照组(22、18、16 mL/kg/天,p=0.013),但丢失的能量相似(7、10、9 kcal/kg/天,p=0.147)。生长不良的婴儿与生长良好的婴儿相比,变形菌门的丰度增加(90%比 15%,p=0.004)。随着时间的推移,小肠内次级 BAs 的比例增加与不良预后因素(≤50%小肠、>50%的热量来自 PN 和生长不良)相关。
患有 SBstoma 和生长不良的婴儿具有独特的细菌群落,与吸收改善的婴儿相比,肠内耐受性差的婴儿具有代谢差异。