Predicting acute lung injury in infants with congenital heart disease after cardiopulmonary bypass by gut microbiota.

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2024-10-24 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1362040
Lan Jiang, Yueshuang Cun, Qiang Wang, Kede Wu, Menglong Hu, Zhen Wu, Tianyi Zhu, Zhaocong Yang, Nishant Patel, Xinyu Cai, Jirong Qi, Xuming Mo
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Abstract

Background: Acute lung injury (ALI) is a serious and common complication that occurs in children with congenital heart disease after cardiopulmonary bypass (CPB) surgery, leading to higher mortality rates and poorer prognosis. Currently, there is no reliable predictive strategy for CPB-associated lung injury (CPB-ALI) in infants. Certain characteristics of the gut microbiota could potentially serve as biomarkers for predicting the development of CPB-ALI.

Methods: We conducted 16S rRNA sequencing to analyze the characteristics of the intestinal microbiota in healthy controls and infants with CHD admitted to the hospital. The CHD infants were divided into CPB-ALI and non-ALI (CPB-NALI) groups based on postoperative outcomes. Bacterial functional pathway prediction analysis was performed using PIRCUSt2, and the gut microbiota composition associated with immune status was determined with heatmap. Random forest regression models and ROC curves were utilized to predict the occurrence of CPB-ALI.

Results: Our study revealed significantly different microbiota compositions among three groups (CON, CPB-ALI, and CPB-NALI). The microbiota diversity was low in the CPB-ALI group with high pathogen abundance and significant decrease in Bacteroides, while the opposite was observed in the CPB-NALI group. The microbiota dysbiosis index was high in the CPB-ALI group, with its dominant microbiota significantly associated with multiple metabolic pathways. Additionally, CPB-ALI patients showed high levels of inflammatory cytokines IL-8 and HMGB1 in their serum, with high expression of IL-8 being associated with Enterobacteriaceae. Further correlation analysis showed that the differences in gut bacterial taxonomy were related to the occurrence of ALI, length of stay in the cardiac care unit, and ventilation time. It is noteworthy that Escherichia Shigella performed best in distinguishing CPB-ALI patients from non-ALI patients.

Conclusions: Our study suggests that postoperative ALI patients have distinct gut microbiota upon admission compared to non-ALI patients after surgery. Dysbiosis of the gut microbiota may potentially impact the progression of ALI through metabolic pathways, quorum sensing, and the levels of inflammatory factors expressed in the serum. Escherichia Shigella represents a potential predictive factor for the occurrence of ALI in CHD infants after surgery. Acute lung injury, congenital heart disease, cardiopulmonary bypass surgery, gut microbiota, biomarker.

通过肠道微生物群预测先天性心脏病婴儿心肺搭桥术后的急性肺损伤。
背景:急性肺损伤(ALI)是先天性心脏病患儿在心肺旁路(CPB)手术后常见的严重并发症,可导致较高的死亡率和较差的预后。目前,尚无可靠的婴儿 CPB 相关肺损伤(CPB-ALI)预测策略。肠道微生物群的某些特征有可能成为预测 CPB-ALI 发生的生物标志物:我们进行了 16S rRNA 测序,以分析健康对照组和入院的患有先天性心脏病的婴儿的肠道微生物群特征。根据术后结果,CHD患儿被分为CPB-ALI组和非ALI(CPB-NALI)组。使用 PIRCUSt2 进行细菌功能通路预测分析,并使用热图确定与免疫状态相关的肠道微生物群组成。利用随机森林回归模型和 ROC 曲线预测 CPB-ALI 的发生:结果:我们的研究发现,三组(CON、CPB-ALI 和 CPB-NALI)的微生物群组成存在明显差异。CPB-ALI 组微生物群多样性较低,病原体丰度较高,Bacteroides 明显减少,而 CPB-NALI 组则相反。CPB-ALI 组的微生物群失调指数较高,其优势微生物群与多种代谢途径显著相关。此外,CPB-ALI 患者血清中的炎性细胞因子 IL-8 和 HMGB1 水平较高,其中 IL-8 的高表达与肠杆菌科细菌有关。进一步的相关分析表明,肠道细菌分类的差异与 ALI 的发生、心脏监护室的住院时间和通气时间有关。值得注意的是,志贺氏菌在区分 CPB ALI 患者和非 ALI 患者方面表现最佳:我们的研究表明,与非 ALI 患者相比,术后 ALI 患者入院时的肠道微生物群截然不同。肠道微生物群的菌群失调可能会通过代谢途径、定量感应和血清中表达的炎症因子水平影响 ALI 的进展。志贺氏菌是先天性心脏病婴儿术后发生 ALI 的潜在预测因素。急性肺损伤、先天性心脏病、心肺旁路手术、肠道微生物群、生物标志物。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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