Wang Hong-Mao, Zhang Ming-Ming, Lin Yao, Liu Yang, Xue Guan-Hua, Shi Lin, Yuan Jing, Li Xiao-Hui
Department of Cardiovascular Disease, Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing 100020, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2024 Oct 15;26(10):1101-1107. doi: 10.7499/j.issn.1008-8830.2405111.
To study the composition, abundance, and functional profiles of the intestinal microbiota in infants and young children with Kawasaki disease (KD) during the acute phase, and to explore the potential role of intestinal microbiota in the pathogenesis of KD.
Six children aged 0-3 years with acute KD admitted to the Department of Cardiology, Children's Hospital Affiliated to Capital Institute of Pediatrics from July to October 2021 were prospectively included as the KD group. Six age- and sex-matched healthy children who underwent physical examinations at the hospital during the same period were selected as the healthy control group. Metagenomics sequencing was used to detect and compare the differences in the microflora structure and functional profiles of fecal samples between the two groups.
There were significant differences in the structural composition and diversity of intestinal microbiota between the two groups (<0.05). Compared with the healthy control group, the abundance of _ (family and genus ), _, _, and _ was significantly higher in the intestinal microbiota in the KD group (LDA>2.0, <0.05). The steroid degradation and apoptosis pathways were significantly upregulated in the KD group compared with the healthy control group, while the Bacterial_secretion_system, Sulfur_metabolism, Butanoate_metabolism, Benzoate_degradation, β-alanine metabolism, and α-linolenic acid pathways were significantly downregulated (|LDA|>2, <0.05).
There are significant differences in the structure and diversity of intestinal microbiota between children aged 0-3 years with acute KD and healthy children, suggesting that disturbances in intestinal microbiota occur during the acute phase of KD. In particular, _, _, and _ may be involved in the pathogenesis of KD through steroid degradation and apoptosis pathways.
研究川崎病(KD)婴幼儿急性期肠道微生物群的组成、丰度和功能概况,探讨肠道微生物群在KD发病机制中的潜在作用。
前瞻性纳入2021年7月至10月首都儿科研究所附属儿童医院心内科收治的6例0 - 3岁急性KD患儿作为KD组。选取同期在该院进行体检的6例年龄和性别匹配的健康儿童作为健康对照组。采用宏基因组测序检测并比较两组粪便样本中微生物群落结构和功能概况的差异。
两组肠道微生物群的结构组成和多样性存在显著差异(<0.05)。与健康对照组相比,KD组肠道微生物群中_(科和属)、_、_和_的丰度显著更高(LDA>2.0,<0.05)。与健康对照组相比,KD组类固醇降解和凋亡途径显著上调,而细菌分泌系统、硫代谢、丁酸代谢、苯甲酸降解、β-丙氨酸代谢和α-亚麻酸途径显著下调(|LDA|>2,<0.05)。
0 - 3岁急性KD患儿与健康儿童的肠道微生物群结构和多样性存在显著差异,提示KD急性期存在肠道微生物群紊乱。特别是,_、_和_可能通过类固醇降解和凋亡途径参与KD的发病机制。