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


Journal

Cardiovascular diabetology
ISSN: 1475-2840
Titre abrégé: Cardiovasc Diabetol
Pays: England
ID NLM: 101147637

Informations de publication

Date de publication:
10 08 2023
Historique:
received: 26 06 2023
accepted: 28 07 2023
medline: 14 8 2023
pubmed: 11 8 2023
entrez: 10 8 2023
Statut: epublish

Résumé

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). 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 37563618
doi: 10.1186/s12933-023-01945-x
pii: 10.1186/s12933-023-01945-x
pmc: PMC10416459
doi:

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

204

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Alessandro Mantovani (A)

Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Verona, Verona, Italy.

Mario Luca Morieri (ML)

Metabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.

Luisa Palmisano (L)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Maria Masulli (M)

Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.

Efisio Cossu (E)

Diabetology Unit, Policlinico Universitario of Cagliari, Cagliari, Italy.

Marco Giorgio Baroni (MG)

Department of Clinical Medicine, Life, Health and Environmental Sciences, University of Aquila, L'Aquila, Italy.
Neuroendocrinology and Metabolic Diseases, IRCCS Neuromed, Pozzilli, Italy.

Katia Bonomo (K)

Diabetes and Metabolic Diseases Unit, San Luigi Gonzaga University Hospital, Turin, Italy.

Flavia Agata Cimini (FA)

Department of Experimental Medicine, Sapienza University, Rome, Italy.

Gisella Cavallo (G)

Department of Experimental Medicine, Sapienza University, Rome, Italy.

Raffaella Buzzetti (R)

Department of Experimental Medicine, Sapienza University, Rome, Italy.

Carmen Mignogna (C)

Department of Experimental Medicine, Sapienza University, Rome, Italy.

Frida Leonetti (F)

Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University, Rome, Italy.

Simonetta Bacci (S)

Section of Endocrinology, Department of Medicine, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.

Roberto Trevisan (R)

Department of Medicine and Surgery, University of Milan Bicocca, Milan, Italy.

Riccardo Maria Pollis (RM)

Metabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.

Raffaella Aldigeri (R)

Division of Nutritional and Metabolic Sciences, Azienda Ospedaliero-Universitaria, Parma, Italy.

Alessandra Dei Cas (AD)

Division of Nutritional and Metabolic Sciences, Azienda Ospedaliero-Universitaria, Parma, Italy.
Department of Medicine and Surgery, University of Parma, Parma, Italy.

Saula Vigili de Kreutzenberg (SV)

Metabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.

Giovanni Targher (G)

Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Verona, Verona, Italy. giovanni.targher@univr.it.
IRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, VR, Italy. giovanni.targher@univr.it.
Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University and Azienda Ospedaliera Universitaria Integrata, Piazzale Stefani, 1, Verona, 37126, Italy. giovanni.targher@univr.it.

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