Zhang Yumeng, Zhao Jin, Qin Yunlong, Wang Yuwei, Yu Zixian, Ning Xiaoxuan, Sun Shiren
Department of Postgraduate Student, Xi'an Medical University, Xi'an, China.
Department of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Front Physiol. 2022 Nov 1;13:909491. doi: 10.3389/fphys.2022.909491. eCollection 2022.
The pathogenesis of idiopathic membranous nephropathy (IMN) has not yet been thoroughly clarified, and gut dysbiosis may be a contributor to IMN. However, the characterization of gut microbiota in patients with IMN remains uncertain. Cochrane Library, PubMed, China National Knowledge Internet, Web of Science, and Embase were used to search for studies through 18 May 2022. A meta-analysis based on the standardized mean difference (SMD) with 95% confidence interval (CI) was conducted on the alpha diversity index. The between-group comparison of the relative abundance of gut microbiota taxa and the beta diversity were extracted and qualitatively analyzed. Five studies were included involving 290 patients with IMN, 100 healthy controls (HCs), and 129 patients with diabetic kidney disease (DKD). The quantitative combination of alpha diversity indices indicated that although bacterial richness was impaired [ACE, SMD = 0.12, (-0.28, 0.52), = 0.55, = 0%; Chao1, SMD = -0.34, (-0.62, -0.06), < 0.05, = 36%], overall diversity was preserved [Shannon, SMD = -0.16, (-0.64, 0.31), = 0.50, = 53%; Simpson, SMD = 0.27, (-0.08, 0.61), = 0.13, = 0%]. The beta diversity was significantly varied compared to HCs or DKD patients. Compared to HCs, the abundance of increased, while that of decreased at the phylum level. Furthermore, the abundance of were depleted, while those of were enriched at the genus level. and were also increased compared to DKD patients. The expansion of and depletion of may be critical features of the altered gut microbiota in patients with IMN. This condition may play an important role in the pathogenesis of IMN and could provide bacterial targets for diagnosis and therapy.
特发性膜性肾病(IMN)的发病机制尚未完全阐明,肠道菌群失调可能是IMN的一个促成因素。然而,IMN患者肠道微生物群的特征仍不明确。通过检索考克兰图书馆、PubMed、中国知网、科学网和Embase,查找截至2022年5月18日的研究。基于标准化均值差(SMD)和95%置信区间(CI)对α多样性指数进行荟萃分析。提取肠道微生物分类群相对丰度的组间比较和β多样性并进行定性分析。纳入了五项研究,涉及290例IMN患者、100例健康对照(HC)和129例糖尿病肾病(DKD)患者。α多样性指数的定量合并表明,虽然细菌丰富度受损[ACE,SMD = 0.12,(-0.28,0.52),P = 0.55,I² = 0%;Chao1,SMD = -0.34,(-0.62,-0.06),P < 0.05,I² = 36%],但总体多样性得以保留[香农指数,SMD = -0.16,(-0.64,0.31),P = 0.50,I² = 53%;辛普森指数,SMD = 0.27,(-0.08,0.61),P = 0.13,I² = 0%]。与HC或DKD患者相比,β多样性有显著差异。与HC相比,门水平上[具体菌属1]的丰度增加,而[具体菌属2]的丰度降低。此外,属水平上[具体菌属3]的丰度减少,而[具体菌属4]的丰度增加。与DKD患者相比,[具体菌属5]和[具体菌属6]也增加。[具体菌属7]的扩张和[具体菌属8]的减少可能是IMN患者肠道微生物群改变的关键特征。这种情况可能在IMN的发病机制中起重要作用,并可为诊断和治疗提供细菌靶点。