Your browser doesn't support javascript.
loading
Manifestation and Progression of Metabolic Dysfunction-Associated Steatotic Liver Disease in a Predominately African American Population at a Multi-Specialty Healthcare Organization.
Saini, Astha; Rutledge, Brian; Damughatla, Anirudh R; Rasheed, Mina; Naylor, Paul; Mutchnick, Milton.
Affiliation
  • Saini A; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
  • Rutledge B; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
  • Damughatla AR; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
  • Rasheed M; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
  • Naylor P; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
  • Mutchnick M; Department of Internal Medicine, School of Medicine, Wayne State University, Detroit, MI 48201, USA.
Healthcare (Basel) ; 12(15)2024 Jul 25.
Article in En | MEDLINE | ID: mdl-39120181
ABSTRACT
African Americans (AA) have a high incidence of risk factors associated with MASLD (metabolic dysfunction-associated steatotic liver disease); the AA population has a lower incidence of MASLD and MASH (metabolic-associated steatotic hepatitis) than Caucasian and Hispanic Americans (non-AA). We investigated if underlying risk factor variation between AA and non-AA individuals could provide a rationale for the racial diversity seen in MASLD/MASH. Using ICD-10 codes, patients from 2017 to 2020 with MASLD/MASH were identified and confirmed to have either MASLD or MASH. Despite the large (>80%) AA population in our clinics, only 54% of the MASLD/MASH patients were African American. When the non-invasive NAFLD Fibrosis Scores (NFS) evaluated at early diagnosis were compared to the most recent values, the only increase in fibrosis score by NFS over time was in non-AA MASH patients. The increase in fibrosis only in non-AA MASLD patients is consistent with racial disparity in the disease progression in non-AA as compared to AA patients. Even with the large proportion of AA patients in our study, there was no significant racial disparity in the earliest assessment of either risk factors, laboratory values, or fibrosis scores that would account for racial disparity in the development and progression of MASLD.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Healthcare (Basel) Year: 2024 Document type: Article Affiliation country: United States Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Healthcare (Basel) Year: 2024 Document type: Article Affiliation country: United States Country of publication: Switzerland