Extracellular vesicles isolated from muscle biopsies of FSHD patients showed distinct RNA cargo signatures that correlate with MRI markers of disease activity and muscle degeneration, with specific miRNAs differentially expressed in STIR-positive muscles.
Observational (n=32)
Yes
RNA profiling of muscle-derived extracellular vesicles identified specific miRNA and isomiR signatures associated with disease activity and muscle degeneration in FSHD, highlighting their potential as biomarkers.
Facioscapulohumeral muscular dystrophy (FSHD) is a progressive neuromuscular disorder characterized by high inter- and intra-individual variability in muscle involvement, disease severity, and rate of progression, even among affected relatives. Remarkably, asymptomatic relatives of FSHD patients, referred to as non-penetrant gene carriers, remain clinically unaffected throughout their lives, despite carrying the genetic background sufficient to cause FSHD. The clinical heterogeneity of FSHD, together with the increasing number of clinical trials involving FSHD patients, underscores the urgent need for reliable biomarkers enabling disease monitoring, stratification of patients and evaluation of treatment efficacy. Extracellular vesicles (EVs) have emerged as promising biomarkers since their cargo reflects physiological state of muscle tissue and remains stable into bloodstream. To explore their potential in FSHD, we isolated EVs from ex-vivo muscle explants obtained from a cross-sectional cohort of 22 FSHD patients, 4 non-penetrant gene carriers and 6 healthy controls. EV-RNA cargo was profiled using small RNA and total RNA sequencing. Our exploratory study identified distinct EV-RNA signatures, including microRNA, isomiRs and long transcripts, associated with disease activity, assessed by short-tau inversion recovery signal on magnetic resonance imaging (MRI). Our analyses also identified EV-RNA profiles linked to muscle degeneration, assessed by T1-weighted signal on (MRI). A preliminary investigation of the identified EV-RNA profiles also showed an association with the presence or absence of T1 progression at 2-year MRI follow-up. In this exploratory study, we present a comprehensive characterization of RNA cargo from muscle EVs in FSHD. The identification of EV-RNA signatures linked to disease activity and muscle degeneration supports their evaluation as potential non-invasive biomarkers for disease monitoring, with validation in systemic circulation and in larger cohorts needed to assess their potential contribution to clinical trial design. Moreover, these findings provide novel insights into FSHD disease mechanisms.
Ragozzino et al. (Wed,) conducted a observational in Facioscapulohumeral muscular dystrophy (n=32). Isolation and profiling of extracellular vesicles (EVs) from muscle biopsies vs. Healthy controls and non-penetrant gene carriers was evaluated on Identification of distinct EV-RNA signatures associated with disease activity assessed by short-tau inversion recovery (STIR) on MRI and muscle degeneration assessed by T1-weighted MRI; association of EV-RNA with 2-year MRI progression. Extracellular vesicles isolated from muscle biopsies of FSHD patients showed distinct RNA cargo signatures that correlate with MRI markers of disease activity and muscle degeneration, with specific miRNAs differentially expressed in STIR-positive muscles.