Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Verona, Verona, Italy.
Metabolic Diseases, Department of Medicine, University of Padua, Padua, Italy.
Cardiovasc Diabetol. 2023 Aug 10;22(1):204. doi: 10.1186/s12933-023-01945-x.
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.
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。
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