Cited by 129Liver Disease Diagnosis and TreatmentAlcohol Consumption and Health EffectsLiver Diseases and Immunity

Sexual Dimorphism of NAFLD in Adults. Focus on Clinical Aspects and Implications for Practice and Translational Research

Open access
Lonardo, Amedeo, Suzuki, Ayako·2020·Journal of Clinical Medicine

Abstract

Nonalcoholic fatty liver disease (NAFLD) embraces the clinico-pathological consequences of hepatic lipotoxicity and is a major public health problem globally. Sexual dimorphism is a definite feature of most human diseases but, under this aspect, NAFLD lags behind other medical fields. Here, we aim at summarizing and critically discussing the most prominent sex differences and gaps in NAFLD in humans, with emphasis on those aspects which are relevant for clinical practice and translational research. Sexual dimorphism of NAFLD is covered with references to the following areas: disease prevalence and risk factors, pathophysiology, comorbidities, natural course and complications. Finally, we also discuss selected gender differences and whether sex-specific lifestyle changes should be adopted to contrast NAFLD in men and women.

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Crossref · 10.3390/jcm9051278

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  • Assessment of MASH components may be flawed by inter-reader variability.

    “Of note, although also MASH resolution correlates with fibrosis regression, especially assessment of MASH components may be flawed by inter-reader variability [239].”

    From Obesity and MASLD: Is weight loss the (only) key to treat metabolic liver disease? (2024) · cites this paper as [239]

    Section 2.2 discusses histological diagnosis and staging in NAFLD, but does not address disagreement between readers assessing MASH components. Searches for inter-reader and interobserver variability, pathologist agreement, and reproducibility found no passage supporting the attributed point. (LLM, conf=0.75)

    Experimental — accuracy not yet measured
  • MASH resolution correlates with fibrosis regression.

    “Of note, although also MASH resolution correlates with fibrosis regression, especially assessment of MASH components may be flawed by inter-reader variability [239].”

    From Obesity and MASLD: Is weight loss the (only) key to treat metabolic liver disease? (2024) · cites this paper as [239]

    The Epidemiology section (2.2; page unavailable) discusses NASH and fibrosis severity, and the Insulin Resistance section (3.3; page unavailable) discusses fibrotic progression. Neither addresses whether MASH/NASH resolution correlates with fibrosis regression. Searches for both “NASH resolution fibrosis regression” and “resolution regression fibrosis histological improvement” found no passage making that point. (LLM, conf=0.74)

    Experimental — accuracy not yet measured

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References 182 · Cited by 129

Authors
Lonardo, A., & Suzuki, A.
Affiliations
  • Azienda Ospedaliero-Universitaria di Modena (IT)
  • Duke Medical Center (US)
Corresponding author
Lonardo, Amedeo
Venue
Journal of Clinical Medicine
Publisher
MDPI AG
Published
2020-04-28
Volume
9
Issue
5
Pages
1278
ISSN
2077-0383 (ISSN-L)
OpenAlex
W3023490585
Cited by
129
References
182
Citations by year
2026: 3 · 2025: 17 · 2024: 20 · 2023: 20 · 2022: 22 · 2021: 33 · 2020: 12 · 2019: 2
FWCI
3.17
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Medicine (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
  • Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
Keywords
non-alcoholic fatty liver disease, sexual dimorphism, sex differences, hepatic lipotoxicity, disease prevalence, risk factors, pathophysiology, comorbidities, disease complications, women's health

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