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伴有显著纤维化的肝脂肪变性与 1 型糖尿病成人中心血管疾病 10 年估计风险增加相关。

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

机构信息

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

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

出版信息

Cardiovasc Diabetol. 2023 Aug 10;22(1):204. doi: 10.1186/s12933-023-01945-x.


DOI:10.1186/s12933-023-01945-x
PMID:37563618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10416459/
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.

摘要

背景:我们评估了伴有或不伴有显著纤维化的肝脂肪变性(通过验证的非侵入性生物标志物确定)是否与 1 型糖尿病(T1DM)患者 10 年心血管疾病(CVD)风险增加相关。

方法:我们进行了一项回顾性、多中心、横断面研究,纳入了 1254 名无预先存在的 CVD 的确诊 T1DM 成人患者。我们使用肝脂肪变性指数(HSI)和纤维化(FIB)-4 指数对肝脂肪变性(定义为 HSI>36)进行非侵入性检测,同时检测是否存在伴发的显著纤维化(定义为 FIB-4 指数≥1.3 或<1.3)。我们计算了 Steno1 风险引擎和动脉粥样硬化性 CVD(ASCVD)风险评分,以估计发生首次致命或非致命 CVD 事件的 10 年风险。

结果:使用 Steno1 风险引擎,与仅存在肝脂肪变性(n=509)或不存在肝脂肪变性(n=654)的患者相比,伴有显著纤维化的肝脂肪变性患者(n=91)具有更高的高 10 年 CVD 风险的比例显著更高(75.8%比 23.2%比 24.9%,p<0.001)。在校正性别、BMI、糖尿病病程、糖化血红蛋白、慢性肾脏病和降脂药物使用后,伴有显著纤维化的肝脂肪变性患者发生首次致命或非致命 CVD 事件的 10 年估计风险增加(校正优势比 11.4,95%置信区间 3.54-36.9),高于无肝脂肪变性的患者。我们使用 ASCVD 风险计算器观察到几乎相同的结果。

结论:与仅存在肝脂肪变性或无肝脂肪变性的 T1DM 成人患者相比,伴有肝脂肪变性和显著纤维化的 T1DM 成人患者的 10 年 CVD 风险显著增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/10416459/38876b4e6ac0/12933_2023_1945_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/10416459/96cc063ac895/12933_2023_1945_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/10416459/38876b4e6ac0/12933_2023_1945_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/10416459/96cc063ac895/12933_2023_1945_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ace/10416459/38876b4e6ac0/12933_2023_1945_Fig2_HTML.jpg

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[2]
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Cardiovasc Diabetol. 2025-5-29

[3]
The association between non-high-density lipoprotein cholesterol to high-density lipoprotein cholesterol ratio and hepatic steatosis and liver fibrosis among US adults based on NHANES.

Sci Rep. 2025-2-23

[4]
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Cardiovasc Diabetol. 2024-8-22

[5]
The correlation between liver fibrosis and the 10-year estimated risk of cardiovascular disease in adults with metabolic-associated fatty liver disease: A cross-sectional study in Vietnam.

Health Sci Rep. 2024-5-8

[6]
Type 1 diabetes mellitus and non-alcoholic fatty liver disease: a two-sample Mendelian randomization study.

Front Endocrinol (Lausanne). 2024

[7]
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Front Med (Lausanne). 2024-3-28

[8]
Machine Learning Identifies Metabolic Dysfunction-Associated Steatotic Liver Disease in Patients With Diabetes Mellitus.

J Clin Endocrinol Metab. 2024-7-12

本文引用的文献

[1]
Sex Differences in Cardiovascular Disease and Cardiovascular Risk Estimation in Patients With Type 1 Diabetes.

J Clin Endocrinol Metab. 2023-8-18

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Hepatology. 2023-5-1

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The associations of hepatic steatosis and fibrosis using fatty liver index and BARD score with cardiovascular outcomes and mortality in patients with new-onset type 2 diabetes: a nationwide cohort study.

Cardiovasc Diabetol. 2022-4-16

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Nutr Metab Cardiovasc Dis. 2022-1

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