Racial and ethnic disparities in alcohol-associated liver disease in the United States: A systematic review and meta-analysis

Author:

Anouti Ahmad1,Seif El Dahan Karim1ORCID,Rich Nicole E.1ORCID,Louissaint Jeremy1ORCID,Lee William M.1,Lieber Sarah R.1ORCID,Arab Juan Pablo23ORCID,Zhang Bill Y.4,Patel Mausam J.5,Thimphittaya Chanattha5,Díaz Luis Antonio3ORCID,Gregory Dyanna L.1,Kozlitina Julia6,VanWagner Lisa B.1ORCID,King Andrea C.7,Mitchell Mack C.1,Singal Amit G.1ORCID,Cotter Thomas G.1ORCID

Affiliation:

1. Department of Internal Medicine, Division of Digestive and Liver Diseases, UT Southwestern Medical Center, Dallas, Texas, USA

2. Department of Medicine, Division of Gastroenterology, Schulich School of Medicine, Western University & London Health Sciences Centre, London, Ontario, Canada

3. Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile

4. University of Texas Southwestern Medical School, Dallas, Texas, USA

5. Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA

6. Department of Internal Medicine, The Eugene McDermott Center for Human Growth and Development, University of Texas Southwestern, Dallas, Texas, USA

7. Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Comprehensive Cancer Center, Chicago, Illinois, USA

Abstract

Background: Alcohol-associated liver disease (ALD), encompassing alcohol-associated hepatitis and alcohol-associated cirrhosis, is rising in the United States. Racial and ethnic disparities are evident within ALD; however, the precise nature of these disparities is poorly defined. Methods: We conducted a search of the PubMed/MEDLINE and EMBASE databases to identify studies published from inception through September 2023 that reported ALD incidence, prevalence, and mortality within the United States, stratified by race and ethnicity. We calculated pooled prevalence and incidence by race and ethnicity, including risk ratios and ORs for ALD pooled prevalence and alcohol-associated hepatitis/alcohol-associated cirrhosis pooled proportions, and OR for ALD mortality using the DerSimonian and Laird method for random-effect models. Results: We identified 25 relevant studies (16 for quantitative meta-analysis), comprising 76,867,544 patients. ALD prevalence was highest in Hispanic (4.5%), followed by White (3.1%) and Black (1.4%) individuals. Pooled risk ratios of ALD prevalence were 1.64 (95% CI: 1.12–2.39) for Hispanic and 0.59 (95% CI: 0.35–0.87) for Black compared to White individuals. Mortality among those with ALD did not significantly differ between White and Hispanic (OR: 1.54, 95% CI: 0.9–2.5; I 2=0%), Black (OR: 1.2, 95% CI: 0.8–1.6; I 2=0%), or Native American (OR: 2.41, 95% CI: 0.9–2.9) individuals, while there was a significant difference between White and Asian (OR: 0.1; 95% CI: 0.03–0.5) individuals. Most data were cross-sectional and assessed to be of poor or fair quality. Conclusions: Differences were observed in ALD epidemiology, including higher prevalence among Hispanic and lower prevalence among Black individuals, although there were smaller differences in ALD mortality. Differences in ALD prevalence and prognosis remain poorly defined based on existing data, highlighting a need for higher-quality epidemiological studies in this area.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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