Metabolic dysfunction‐associated steatohepatitis exhibits sex differences in people with HIV
- Authors: Kablawi, Dana; Milic, Jovana; Thomas, Tyler; Fotsing Tadjo, Thierry; Cinque, Felice; Elgretli, Wesal; Gioè, Claudia; Lebouché, Bertrand; Tsochatzis, Emmanuel; Finkel, Jemima; Bhagani, Sanjay; Cascio, Antonio; Guaraldi, Giovanni; Mazzola, Giovanni; Saeed, Sahar; Sebastiani, Giada
- Publication year: 2024
- Type: Articolo in rivista
- OA Link: http://hdl.handle.net/10447/665593
Abstract
Objectives: People with HIV are at increased risk for metabolic dysfunction-associated steatohepatitis (MASH). Although sex differences are documented in the general population, their role in the context of HIV is less understood. Methods: This was a multicentre cohort study including people with HIV without viral hepatitis coinfection. A FibroScan-AST (FAST) score >0.35 was used to diagnose MASH with significant liver fibrosis (stage F2–F4). We investigated sex-based differences in MASH trends as a function of age using a segmented linear mixed-effects model. Random effects accounted for clustering by the four sites. Adjusted models included ethnicity, diabetes, hypertension, and detectable HIV viral load. Results: We included 1472 people with HIV (25% women). At baseline, the prevalence of MASH with fibrosis by FAST score was lower in women than in men (4.8% vs. 9.2%, p = 0.008). Based on the adjusted model, male sex (+0.034; p = 0.04), age per year (+0.003; p = 0.05), detectable HIV viral load (+0.034; p = 0.02), and hypertension (+0.03; p = 0.01) were positively associated with MASH with fibrosis. Although men exhibited generally higher FAST scores, FAST scores increased in women during the critical biological age of presumed perimenopause to menopause (between 40 and 50 years), reaching levels similar to those in men by the age of 55 years. Conclusion: Despite women with HIV having a lower prevalence of MASH with fibrosis than men, they exhibit an acceleration in FAST score increase around the perimenopausal age. Future studies should target adequate consideration of sex differences in clinical investigation of metabolic dysfunction-associated steatotic liver disease to fill current gaps and implement precision medicine for people with HIV.