Key result
Unexplained syncope is linked to distinct gut microbiota profiles compared to cardiac syncope.
Why the study?
The pathogenesis of many syncopal episodes remains unexplained, and intestinal dysbiosis via the microbiota-gut-brain axis could be involved in the pathophysiological mechanisms of syncope.
Do cardiometabolic risk factors and gut microbiota differ in patients with unexplained syncope compared to other types of syncope?
Cross-Sectional (n=86)
No
Do cardiometabolic risk factors and gut microbiota differ in patients with unexplained syncope compared to other types of syncope?
Unexplained syncope exhibits a distinct gut microbiota profile and cardiometabolic risk factor pattern compared to cardiac syncope, suggesting they may have different pathophysiological origins.
Answers are grounded in this paper and cite their sources.
No immediate change to syncope evaluation; leaves open whether microbiota differences mark distinct etiologies versus confounders.
BACKGROUND: The pathogenesis of many syncopal episodes remains unexplained. Intestinal dysbiosis could be involved in the pathophysiological mechanisms of syncope due to its connection with the central nervous system via the microbiota-gut-brain axis. This pilot study aimed to explore the specific cardiometabolic risk factors and gut microbiota in unexplained syncope (US), compared to other types of syncope, to assess their similarity or verify their different origins. METHODS: = 27). We evaluated the anthropometric, clinical, and metabolic characteristics of the four groups; the α- and β-diversity; and the differences in the abundance of the microbial taxa. RESULTS: The US group had a lower incidence of systolic hypertension at the first visit and a lower frequency of patients with nocturnal hypertension than the CS group. Compared to the OH and NMS groups, the US group had a higher incidence of carotid plaques and greater carotid intima-media thickness, respectively. The microbiota differed significantly between the US and CS groups, but not between the US group and the OH or NMS group. CONCLUSIONS: We observed significant differences in the gut microbiota between CS and US. Future studies are necessary to evaluate the involvement of the gut microbiota in the complex pathogenesis of syncope and whether its analysis could support the interpretation of the pathophysiological mechasnisms underlying some episodes classifiable as US.
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Longo et al. (2024) conducted a cross-sectional in Syncope (n=86). Unexplained syncope vs. Cardiac, orthostatic, and neuromediated syncope was evaluated on Differences in gut microbiota composition and cardiometabolic risk factors. Unexplained syncope exhibited a significantly different gut microbiota profile compared to cardiac syncope, but not compared to orthostatic or neuromediated syncope.
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