Metabolic dysfunction‐associated steatohepatitis exhibits sex differences in people with HIV

Author:

Kablawi Dana12,Milic Jovana3,Thomas Tyler4,Fotsing Tadjo Thierry2,Cinque Felice12,Elgretli Wesal5,Gioè Claudia6,Lebouché Bertrand178,Tsochatzis Emmanuel9,Finkel Jemima9,Bhagani Sanjay9,Cascio Antonio610,Guaraldi Giovanni3ORCID,Mazzola Giovanni11,Saeed Sahar4,Sebastiani Giada1258ORCID

Affiliation:

1. Chronic Viral Illness Service, Division of Infectious Disease, Department of Medicine McGill University Health Centre Montreal Quebec Canada

2. Division of Gastroenterology and Hepatology McGill University Health Centre Montreal Quebec Canada

3. Modena HIV Metabolic Clinic University of Modena and Reggio Emilia Modena Italy

4. Public Health Sciences Queen's University Kingston Ontario Canada

5. Division of Experimental Medicine McGill University Montreal Quebec Canada

6. Infectious and Tropical Diseases Unit, Sicilian Regional Reference Center for the Fight against AIDS AOU Policlinico “P. Giaccone” Palermo Italy

7. Department of Family Medicine, Faculty of Medicine and Health Sciences McGill University Health Centre Montreal Quebec Canada

8. Center for Outcomes Research and Evaluation, Research Institute McGill University Health Centre Montreal Quebec Canada

9. Royal Free London NHS Foundation Trust London UK

10. Department of Health Promotion, Mother and Child Care Internal Medicine and Medical Specialties “G. D'Alessandro” Palermo Italy

11. Department of Infectious Diseases Sant'Elia Hospital Caltanissetta Italy

Abstract

AbstractObjectivesPeople 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.MethodsThis 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.ResultsWe 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.ConclusionDespite 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.

Publisher

Wiley

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