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作 者:李禄全[1] 刘晓晨 LI Luquan;LIU Xiaochen(Department of Neonatology,Children’s Hospital of Chongqing Medical University,Key Laboratory of Pediatrics in Chongqing,National Clinical Research Center for Child Health and Disorders,China International Science and Technology Cooperation Base of Child Development and Critical Disorders,Ministry of Education Key Laboratory of Child Development and Disorders,Chongqing 400014,China)
机构地区:[1]重庆医科大学附属儿童医院新生儿科,儿科学重庆市重点实验室,国家儿童健康与疾病临床医学研究中心,儿童发育重大疾病国家国际科技合作基地,儿童发育疾病研究教育部重点实验室,重庆400014
出 处:《临床儿科杂志》2022年第9期654-660,共7页Journal of Clinical Pediatrics
基 金:重庆市科卫联合医学科研基金(No.2022MSXM039);重庆市自然科学基金(No.cstc2021jcyj-msxmX0063)。
摘 要:肠道菌群及其代谢产物早期预测坏死性小肠结肠炎(NEC)是近年来研究的热点。近年研究发现NEC患儿肠道菌群不仅生物多样性较低,且菌群构成比例与健康新生儿明显不同。NEC患儿氨基酸、脂代谢以及与此相关的代谢酶类也存在异常。肠道菌群及其代谢产物在预测NEC发病及病情进展等方面有一定价值,但目前只能作为科学研究探讨的依据,临床运用尚需要高质量、多中心、大样本量临床研究予以验证。The early prediction of necrotizing enterocolitis(NEC)by intestinal microbiota and its metabolites has been a hot research topic in recent years.Recent studies have found that infants with necrotizing enterocolitis(NEC)not only have low biodiversity of the intestinal microbiota,but also the composition proportion of microbiota is significantly different from that of healthy newborns.There are also abnormalities in amino acid,lipid metabolism and related metabolic enzymes in infants with NEC.Intestinal microbiota and its metabolites have certain value in predicting the onset and progression of NEC,but they can only be used as the basis for scientific research.High-quality,multi-center,and large-scale clinical studies are needed for clinical application in the future.
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