首页|期刊导航|福建中医药|慢性萎缩性胃炎气虚证患者病位证素分布特点与肠道微生态特征

慢性萎缩性胃炎气虚证患者病位证素分布特点与肠道微生态特征OA

Distribution Characteristics of Disease Location Syndrome Elements and Gut Microbiota Features in Patients with Chronic Atrophic Gastritis of Qi Deficiency Syndrome

中文摘要英文摘要

目的 探讨慢性萎缩性胃炎(CAG)气虚证患者的病位证素分布特点,并探讨其肠道菌群结构与功能特征.方法 选取2022年3月—2023年1月于福建中医药大学附属晋江中医院脾胃病科就诊的68例CAG患者作为研究对象,根据中医证素辨证方法,将患者分为气虚证组和非气虚证组进行对比分析,每组34例.采用福建中医药大学研发的中医健康状态智能分析平台分析2组患者的病位证素分布情况,同时纳入福建中医药大学附属晋江中医院体检中心26名健康体检者作为健康组.通过16S rRNA测序技术对3组的肠道菌群进行分析:计算Alpha多样性指数,包括群落丰富度指标(ACE、Chao1)和多样性指标(Shannon、Simpson);采用主坐标分析(PCoA)和非度量多维尺度分析(NMDS)进行Beta多样性分析,以评估组间群落结构差异;在门和属分类水平上选取相对丰度排名前10的优势物种绘制柱状图分析物种组成情况;利用线性判别分析(LEfSe)鉴定组间显著差异菌群;提取核心产短链脂肪酸(SCFAs)菌属的相对丰度数据进行组间比较;最后,通过PICRUSt2功能预测算法对3组肠道菌群进行KEGG通路富集分析以及差异代谢通路平均丰度统计分析.结果 ① 病位证素分布:气虚证组以胃(79.41%)、脾(52.94%)为核心病位,肝(26.47%)次之,且脾证素在气虚证组的出现频率显著高于非气虚证组(P<0.05).② 菌群多样性:气虚证组ACE、Chao1及Shannon指数均显著低于健康组(P<0.05),非气虚证组ACE和Chao1同样低于健康组(P<0.05),PCoA分析和NMDS分析结果均显示3组菌群结构差异具有统计学意义(P<0.05).③ 门、属水平物种组成分析与差异菌群分析结果显示:3组样本的核心菌群结构整体相似,但关键菌属的相对丰度存在显著组间差异.与健康组比较,气虚证组产SCFAs的菌属(罗氏菌属、巨单胞菌属)相对丰度显著降低(P<0.05),而埃希氏菌-志贺氏菌属相对丰度显著升高(P<0.05).与气虚证组比较,非气虚证组罗氏菌属相对丰度显著升高(P<0.05),而埃希氏菌-志贺氏菌属相对丰度降低(P<0.05).LEfSe分析进一步显示,肠杆菌科、埃希氏菌-志贺氏菌属等在气虚证组中显著富集(P<0.05),罗氏菌属等在非气虚证组中富集(P<0.05).④ KEGG通路分析以及差异代谢通路平均丰度统计结果显示:"其他类型O-聚糖生物合成"通路丰度在气虚证组显著上调,其在气虚证组的平均丰度均显著高于非气虚证组和健康组(P<0.05).此外,"氯代烷烃和氯代烯烃降解"通路在气虚证组、非气虚证组中均存在,而健康组完全缺失,且组间差异具有统计学意义(P<0.05).结论 CAG气虚证病位以胃、脾为主,肠道微生态特征表现为菌群多样性降低,产SCFAs菌减少及致病菌增多.罗氏菌属等菌属或可作为辅助辨证的生物标志物,为中医微观辨证及菌群干预提供依据.

Objective:To investigate distribution characteristics of disease location syndrome elements in patients with chronic atrophic gastritis(CAG)of Qi deficiency syndrome and to explore the structural and functional features of their gut microbiota.Meth-ods:A total of 68 CAG patients treated in the Department of Spleen and Stomach Diseases,Jinjiang Hospital of Traditional Chinese Medicine(TCM)Affiliated to Fujian University of TCM from March 2022 to January 2023 were selected as the study subjects.Ac-cording to the TCM syndrome element differentiation method,patients were divided into Qi deficiency syndrome group and a non-Qi deficiency syndrome group for comparative analysis,with 34 cases in each group.The intelligent analysis platform for TCM health status developed by Fujian University of TCM was used to analyze the distribution of disease location syndrome elements in the two groups.Meanwhile,26 healthy subjects from the Physical Examination Center of Jinjiang Hospital of TCM Affiliated to Fujian Uni-versity of TCM were included as a healthy control group.The gut microbiota of the three groups were analyzed using 16S rRNA se-quencing technology:Alpha diversity indices,including community richness indices(ACE,Chao1)and diversity indices(Shannon,Simpson),were calculated;principal coordinate analysis(PCoA)and non-metric multidimensional scaling(NMDS)were used for Be-ta diversity analysis to assess differences in community structure between groups;at the phylum and genus taxonomic levels,the top 10 dominant species by relative abundance were selected to draw bar charts for analyzing species composition;linear discriminant analysis effect size(LEfSe)was used to identify significantly different microbiota between groups;the relative abundance data of core short-chain fatty acids(SCFAs)-producing genera were extracted for inter-group comparison;finally,the PICRUSt2 functional predic-tion algorithm was used to perform KEGG pathway enrichment analysis and statistical analysis of the average abundance of differen-tial metabolic pathways among the three groups.Results:1)Distribution of disease location syndrome elements:in the Qi deficiency syndrome group,the stomach(79.41%)and spleen(52.94%)were the core disease locations,followed by the liver(26.47%),and the frequency of the spleen syndrome element in the Qi deficiency syndrome group was significantly higher than that in the non-Qi defi-ciency syndrome group(P<0.05).2)Microbiota diversity:the ACE,Chao1,and Shannon indices in the Qi deficiency syndrome group were significantly lower than those in the healthy group(P<0.05);the ACE and Chao1 indices in the non-Qi deficiency syndrome group were also lower than those in the healthy group(P<0.05).PCoA and NMDS analyses both showed statistically significant differ-ences in microbiota structure among the three groups(P<0.05).3)Results of species composition analysis at phylum and genus levels and differential microbiota analysis showed that the core microbiota structure of the three groups was generally similar,but the rela-tive abundance of key genera had statistically significant differences between groups(P<0.05).Compared with the healthy group,the relative abundance of SCFAs-producing genera(Roseburia,Blautia)in the Qi deficiency syndrome group significantly reduced(P<0.05),while the relative abundance of Escherichia-Shigella significantly increased(P<0.05).Compared with the Qi deficiency syn-drome group,the relative abundance of Roseburia in the non-Qi deficiency syndrome group significantly increased(P<0.05),while the relative abundance of Escherichia-Shigella decreased(P<0.05).LEfSe analysis further showed that Enterobacteriaceae and Esche-richia-Shigella were significantly enriched in the Qi deficiency syndrome group(P<0.05),while Roseburia was enriched in the non-Qi deficiency syndrome group(P<0.05).4)KEGG pathway analysis and statistical results of the average abundance of differential metabolic pathways showed that the abundance of the''other types of O-glycan biosynthesis''pathway was significantly up-regulated in the Qi deficiency syndrome group,and its average abundance in the Qi deficiency syndrome group was significantly higher than that in the non-Qi deficiency syndrome group and the healthy group(P<0.05).In addition,the"Chloroalkane and chloroalkene degra-dation"pathway was present in both the Qi deficiency syndrome group and the non-Qi deficiency syndrome group,but completely ab-sent in the healthy group,and the difference between groups was statistically significant(P<0.05).Conclusion:The disease location of CAG with Qi deficiency syndrome is primarily in the stomach and spleen.Its gut microbiota characteristics are manifested by re-duced microbial diversity,decreased SCFAs-producing bacteria,and increased pathogenic bacteria.Genera such as Roseburia may serve as biomarkers to assist syndrome differentiation,providing a basis for TCM micro-differentiation and microbiota intervention.

粟克军;付肖岩;林雪娟;侯小芬;卓祖顺;张梦婷;赵玲玲;魏汝佳;谢嵛嵛;黄伟荣;邵岩峰

福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学附属第二人民医院,福建 福州 350003福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学中医学院,福建 福州 350122福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学中医学院,福建 福州 350122||福建中医药大学中医证研究基地,福建 福州 350122福建中医药大学附属晋江中医院,福建 晋江 362200福建中医药大学附属第三人民医院,福建 福州 350108

慢性萎缩性胃炎气虚证肠道菌群SCFAs16S rRNA证素

chronic atrophic gastritisQi deficiency syndromegut microbiotaSCFAs16S rRNAsyndrome elements

《福建中医药》 2026 (1)

34-41,8

国家自然科学基金项目(82474391)

10.13260/j.cnki.jfjtcm.2026.01008

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