Diagnostic Uptake of Targeted Sequencing in Adults With Steatotic Liver Disease and a Suspected Genetic Contribution
Year: 2025
Type: article
Study design: Observational Study
Abstract: BACKGROUND AND AIMS: In patients with steatotic liver diseases (SLD), genetic factors may account for severe liver involvement despite mild or absence of triggering factors or a strong family history. Aim of this study was to examine the diagnostic uptake of targeted sequencing (TS), covering both coding and non-coding regions, of a broad panel of 82 liver and lipid metabolism genes in patients with unexplained SLD. METHODS: We enrolled 49 adult patients with SLD and a suspected genetic contribution. Genetic variants were detected through a customised TS panel, whereas the contribution of common genetic variation to the individual susceptibility to SLD was captured by a polygenic risk score (SLD-PRS). RESULTS: A diagnosis of rare Mendelian disorder was established in 11 patients (22%), independently of age or family history. Rare variants possibly contributing to clinical phenotype were detected in additional 29 patients (59%). Increased SLD-PRS values were detected in 17 patients (35%), enabling an increase in diagnostic uptake of 24%, especially in those without a strong family history (p = 0.03). Genetic diagnosis allowed refinement of clinical management in 23 (47%) patients. CONCLUSIONS: The diagnostic uptake of TS was 22% for Mendelian disorder and 59% for possible contribution to clinical phenotype in selected adult patients with SLD. Evaluation of common variants, as captured by SLD-PRS, yields complementary information increasing the overall utility of the genetic examination.
Source: Liver International
DOI: 10.1111/liv.70010
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,780
Awards: G1143825280, G1345875553, G1535130713, Liver Investigation: Testing Marker Utility in Steatohepatitis, G2076520454, Neuronal microscopy for cell behavioural examination and manipulation, G2220771028, G2332353369, G298858806, G303857671, Understanding Gene ENvironment Interaction in ALcohol-related hepatocellular carcinoma, G3562261265, G434337789, G4828916014, G488200810, G4937468798, G5015164659, G520487022, G5456500157, G5911110335, G5990168095, G686558340, G969404240, G972786147
OpenAlex ID: W4407541533
