Pulmonary Arterial Hypertension Patients Have a Proinflammatory Gut Microbiome and Altered Circulating Microbial Metabolites

• Published in: American journal of respiratory and critical care medicine Vol. 207; no. 6; pp. 740 - 756
• Main Authors: Moutsoglou, Daphne M., Tatah, Jasmine, Prisco, Sasha Z., Prins, Kurt W., Staley, Christopher, Lopez, Sharon, Blake, Madelyn, Teigen, Levi, Kazmirczak, Felipe, Weir, E. Kenneth, Kabage, Amanda J., Guan, Weihua, Khoruts, Alexander, Thenappan, Thenappan
• Format: Journal Article
• Language: English
• Published: United States American Thoracic Society 15.03.2023
• Subjects: Bile Acids and Salts; Digestive system; Dysbiosis; Familial Primary Pulmonary Hypertension; Gastrointestinal Microbiome - genetics; Gut microbiota; Humans; Inflammation; Metabolites; Microbiology; Microbiota; Original; Phylogeny; Pulmonary Arterial Hypertension; Pulmonary arteries; Pulmonary hypertension; Vascular Diseases; metabolites; microbiome; pulmonary arterial hypertension; dysbiosis
• ISSN: 1073-449X; 1535-4970; 1535-4970
• DOI: 10.1164/rccm.202203-0490OC

Inflammation drives pulmonary arterial hypertension (PAH). Gut dysbiosis causes immune dysregulation and systemic inflammation by altering circulating microbial metabolites; however, little is known about gut dysbiosis and microbial metabolites in PAH. To characterize the gut microbiome and microbial metabolites in patients with PAH. We performed 16S ribosomal RNA gene and shotgun metagenomics sequencing on stool from patients with PAH, family control subjects, and healthy control subjects. We measured markers of inflammation, gut permeability, and microbial metabolites in plasma from patients with PAH, family control subjects, and healthy control subjects. The gut microbiome was less diverse in patients with PAH. Shannon diversity index correlated with measures of pulmonary vascular disease but not with right ventricular function. Patients with PAH had a distinct gut microbial signature at the phylogenetic level, with fewer copies of gut microbial genes that produce antiinflammatory short-chain fatty acids (SCFAs) and secondary bile acids and lower relative abundances of species encoding these genes. Consistent with the gut microbial changes, patients with PAH had relatively lower plasma concentrations of SCFAs and secondary bile acids. Patients with PAH also had enrichment of species with the microbial genes that encoded the proinflammatory microbial metabolite trimethylamine. The changes in the gut microbiome and circulating microbial metabolites between patients with PAH and family control subjects were not as substantial as the differences between patients with PAH and healthy control subjects. Patients with PAH have proinflammatory gut dysbiosis, in which lower circulating SCFAs and secondary bile acids may facilitate pulmonary vascular disease. These findings support investigating modulation of the gut microbiome as a potential treatment for PAH.