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Hepatic steatosis with significant fibrosis is associated with an increased 10-year estimated risk of cardiovascular disease in adults with type 1 diabetes mellitus

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  • Additional Information
    • Contributors:
      Mantovani, Alessandro; Luca Morieri, Mario; Palmisano, Luisa; Masulli, Maria; Cossu, Efisio; Baroni, Marco Giorgio; Bonomo, Katia; Cimini, FLAVIA AGATA; Cavallo, Gisella; Buzzetti, Raffaella; Mignogna, Carmen; Leonetti, Frida; Bacci, Simonetta; Trevisan, Roberto; Maria Pollis, Riccardo; Aldigeri, Raffaella; Dei Cas, Alessandra; Vigili de Kreutzenberg, Saula; Targher, Giovanni
    • Publication Information:
      BMC
      London
    • Publication Date:
      2023
    • Collection:
      Sapienza Università di Roma: CINECA IRIS
    • Abstract:
      Background: We assessed whether hepatic steatosis with or without significant fibrosis (determined by validated non-invasive biomarkers) is associated with an increased 10-year estimated risk for cardiovascular disease (CVD) in people with type 1 diabetes mellitus (T1DM). Methods: We conducted a retrospective, multicenter, cross-sectional study involving 1,254 adults with established T1DM without pre-existing CVD. We used the hepatic steatosis index (HSI) and fibrosis (FIB)-4 index for non-invasively detecting hepatic steatosis (defined as HSI > 36), with or without coexisting significant fibrosis (defined as FIB-4 index ≥ 1.3 or < 1.3). We calculated the Steno type 1 risk engine and the atherosclerotic CVD (ASCVD) risk score to estimate the 10-year risk of developing a first fatal or nonfatal CVD event. Results: Using the Steno type 1 risk engine, a significantly greater proportion of patients with hepatic steatosis and significant fibrosis (n = 91) had a high 10-year estimated CVD risk compared to those with hepatic steatosis alone (n = 509) or without steatosis (n = 654) (75.8% vs. 23.2% vs. 24.9%, p < 0.001). After adjustment for sex, BMI, diabetes duration, hemoglobin A1c, chronic kidney disease, and lipid-lowering medication use, patients with hepatic steatosis and significant fibrosis had an increased 10-year estimated risk of developing a first fatal or nonfatal CVD event (adjusted-odds ratio 11.4, 95% confidence interval 3.54-36.9) than those without steatosis. We observed almost identical results using the ASCVD risk calculator. Conclusions: The 10-year estimated CVD risk is remarkably greater in T1DM adults with hepatic steatosis and significant fibrosis than in their counterparts with hepatic steatosis alone or without steatosis.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/37563618; info:eu-repo/semantics/altIdentifier/wos/WOS:001048626100001; volume:22; issue:1; numberofpages:12; journal:CARDIOVASCULAR DIABETOLOGY; https://hdl.handle.net/11573/1700467; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85167678840
    • Accession Number:
      10.1186/s12933-023-01945-x
    • Online Access:
      https://hdl.handle.net/11573/1700467
      https://doi.org/10.1186/s12933-023-01945-x
    • Rights:
      info:eu-repo/semantics/openAccess
    • Accession Number:
      edsbas.10BE6961