MASLD in people with HIV exhibits higher fibrosis stage despite lower disease activity than in matched controls

Author:

Allende Daniela S.1,Cummings Oscar2,Sternberg Alice L.3,Behling Cynthia A.4,Carpenter Danielle5,Gill Ryan M.6,Guy Cynthia D.7,Yeh Matthew M.8,Gawrieh Samer9ORCID,Sterling Richard K.10,Naggie Susanna11,Loomba Rohit12,Price Jennifer C.6ORCID,McLaughlin Mary13,Hadigan Colleen13,Crandall Holly2,Belt Patricia3,Wilson Laura3,Chalasani Naga P.9ORCID,Kleiner David E.14,

Affiliation:

1. Cleveland Clinic Cleveland Ohio USA

2. Department of Pathology Indiana University School of Medicine Indianapolis Indiana USA

3. Johns Hopkins Bloomberg School of Public Health Baltimore Maryland USA

4. Pacific Rim Pathology San Diego California USA

5. Saint Louis University St. Louis Missouri USA

6. University of California San Francisco San Francisco California USA

7. Duke University Durham North Carolina USA

8. University of Washington Seattle Washington USA

9. Department of Medicine Indiana University School of Medicine Indianapolis Indiana USA

10. Virginia Commonwealth University Health System Richmond Virginia USA

11. Duke Clinical Research Institute Durham North Carolina USA

12. University of California San Diego San Diego California USA

13. National Institute of Allergy and Infectious Disease (NIAID) Bethesda Maryland USA

14. Laboratory of Pathology National Cancer Institute Bethesda Maryland USA

Abstract

SummaryBackgroundMetabolic dysfunction‐associated steatotic liver disease (MASLD) is common in people with HIV (PWH). The morphological spectrum of MASLD compared to matched controls and of the correlation between the NAFLD activity score (NAS) and fibrosis stage in PWH remains unknown.MethodsOverall, 107 liver biopsies from PWH with MASLD (MASLD‐PWH) were matched to 107 biopsies from individuals with MASLD and without HIV (MASLD controls) on age at biopsy, race/ethnicity, sex, type 2 diabetes, body mass index (BMI) and alanine aminotransferase (ALT) level. Biopsies were scored using NAS.ResultsCompared to MASLD‐controls, MASLD‐PWH had lower steatosis grade (OR: 0.65, 95% CI: (0.47–0.90), p = 0.01), lower lobular inflammation grade (OR: 0.55, 95% CI: (0.34–0.89), p = 0.02), less portal inflammation (OR: 0.42, 95% CI: (0.25–0.72), p = 0.002) and less ballooned hepatocytes (OR: 0.60, 95% CI: (0.41–0.88), p = 0.01). Thus, NAS was lower in MASLD‐PWH (OR: 0.69, 95% CI: (0.56–0.85), p < 0.001) than in MASLD controls. There was a trend towards lower prevalence of steatohepatitis in MASLD‐PWH (OR: 0.84, 95% CI: (0.68–1.03), p = 0.09). A multivariate analysis demonstrated that MASLD‐PWH cases had significantly less steatosis (OR: 0.66, p = 0.03), portal inflammation (OR: 0.34, p = 0.001) and ballooned hepatocytes (OR: 0.55, p = 0.01), yet higher stage fibrosis (OR: 1.42, p = 0.03) compared to MASLD controls.ConclusionThe NAS and histological drivers of fibrosis (e.g. inflammation and hepatocyte ballooning) are less pronounced in MASLD‐PWH, and yet fibrosis stage was generally higher when compared to matched controls with MASLD without HIV. This suggests HIV‐specific factors beyond hepatic necroinflammation may contribute to fibrosis progression in MASLD‐PWH.

Funder

National Center for Advancing Translational Sciences

National Institute of Diabetes and Digestive and Kidney Diseases

National Cancer Institute

Publisher

Wiley

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