Evidence map›Paper›PMID 37563618›Full record

ArticleCardiovascular diabetology2023

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

Alessandro Mantovani, Mario Luca Morieri, Luisa Palmisano, Maria Masulli, Efisio Cossu, Marco Giorgio Baroni, Katia Bonomo, Flavia Agata Cimini, Gisella Cavallo, Raffaella Buzzetti and 9 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cardiovascular diabetology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 24 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 10 institutions in 1 country.

Alessandro MantovaniSection of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Verona, Verona, Italy.
Mario Luca MorieriMetabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.
Luisa PalmisanoDepartment of Clinical Medicine and Surgery, Federico II University, Naples, Italy.
Maria MasulliDepartment of Clinical Medicine and Surgery, Federico II University, Naples, Italy.
Efisio CossuDiabetology Unit, Policlinico Universitario of Cagliari, Cagliari, Italy.
Marco Giorgio BaroniDepartment of Clinical Medicine, Life, Health and Environmental Sciences, University of Aquila, L'Aquila, Italy.
Katia BonomoDiabetes and Metabolic Diseases Unit, San Luigi Gonzaga University Hospital, Turin, Italy.
Flavia Agata CiminiDepartment of Experimental Medicine, Sapienza University, Rome, Italy.
Gisella CavalloDepartment of Experimental Medicine, Sapienza University, Rome, Italy.
Raffaella BuzzettiDepartment of Experimental Medicine, Sapienza University, Rome, Italy.
Carmen MignognaDepartment of Experimental Medicine, Sapienza University, Rome, Italy.
Frida LeonettiDepartment of Medical-Surgical Sciences and Biotechnologies, Sapienza University, Rome, Italy.
Simonetta BacciSection of Endocrinology, Department of Medicine, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
Roberto TrevisanDepartment of Medicine and Surgery, University of Milan Bicocca, Milan, Italy.
Riccardo Maria PollisMetabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.
Raffaella AldigeriDivision of Nutritional and Metabolic Sciences, Azienda Ospedaliero-Universitaria, Parma, Italy.
Alessandra Dei CasDivision of Nutritional and Metabolic Sciences, Azienda Ospedaliero-Universitaria, Parma, Italy.
Saula Vigili de Kreutzenberg *Metabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.
Giovanni Targher *Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Verona, Verona, Italy. giovanni.targher@univr.it.
Sapienza University of Rome · ITUniversity of Padua · ITFederico II University Hospital · ITAzienda Ospedaliera Universitaria Integrata Verona · ITCasa Sollievo della Sofferenza · ITOspedale San Luigi Gonzaga · ITUniversity of L'Aquila · ITUniversity of Milano-Bicocca · ITUniversity of Parma · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe 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).

methodsWe 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.

resultsUsing 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.

conclusionsThe 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.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 1Non-alcoholic Fatty Liver DiseaseAdultCross-Sectional StudiesHumansLiver CirrhosisRetrospective StudiesCardiovascular diseaseCVDNAFLDNon-alcoholic fatty liver diseaseT1DMType 1 diabetes

Identifiers

PMID37563618
PMCPMC10416459
OpenAlexW4385737888

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.