Key result
Gut microbiota influences myocarditis pathogenesis via barrier dysfunction, metabolite shifts, and molecular mimicry.
Why the study?
Myocarditis lacks targeted therapies and carries substantial risks of heart failure or sudden death, while emerging evidence increasingly links it to gut microbiota dysbiosis.
This review highlights the emerging role of the gut-heart axis in myocarditis pathogenesis and outlines potential microbiota-targeted therapeutic strategies.
Supports investigation of microbiota-targeted therapies in myocarditis; leaves open validation in prospective trials before clinical use.
Myocarditis is a clinically challenging form of inflammatory heart disease with heterogeneous etiologies, limited diagnostic tools, no targeted therapies, and a substantial risk of progression to heart failure or sudden cardiac death, particularly in young adults. Emerging evidence has increasingly associated myocarditis with gut microbiota dysbiosis. This review explores the gut–myocarditis axis, highlighting key mechanisms and therapeutic strategies. Significant alterations in gut microbial composition are observed in myocarditis patients and animal models. Gut microbiota influences disease development through multiple pathways: compromised intestinal barrier integrity leading to bacterial translocation and systemic inflammation via MAMP/PRR signaling (e.g., TLRs, NLRs); production of metabolites—including pro-inflammatory trimethylamine N-oxide (TMAO), anti-inflammatory short-chain fatty acids (SCFAs), and immunomodulatory bile acids—that regulate host inflammatory responses, immune cell differentiation, oxidative stress, and fibrotic remodeling; and molecular mimicry, where microbial peptides (e.g., from Bacteroides thetaiotaomicron) trigger cross-reactive autoimmune responses against cardiac proteins. Regarding therapeutic strategies, this review discusses fecal microbiota transplantation (FMT), probiotics, prebiotics, dietary modulation, and emerging approaches including engineered bacteria and oral nanomedicines. Although these strategies hold promise, their efficacy and safety remain to be validated in large-scale clinical trials, and further investigation is warranted.
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Liu et al. (2026) conducted a review in Myocarditis. Gut microbiota dysbiosis was evaluated. Gut microbiota influences myocarditis development through compromised intestinal barrier integrity, production of metabolites like TMAO and SCFAs, and molecular mimicry.
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