Significant liver fibrosis, as assessed by fibroscan, is independently associated with chronic vascular complications of type 2 diabetes: A multicenter study

医学 内科学 糖尿病 2型糖尿病 瞬态弹性成像 脂肪变性 视网膜病变 胃肠病学 慢性肝病 肾脏疾病 优势比 2型糖尿病 纤维化 肝硬化 内分泌学 肝纤维化
作者
Ivana Mikolašević,Dario Rahelić,T. Turk-Wensween,Alen Ruzic,V. Domislovic,Gerd Hauser,Tomislav Matić,Delfa Radić-Krišto,Željko Krznarić,M. Radic,Tajana Filipec Kanižaj,Marko Martinović,Helena Jerkić,M. Medjimurec,Giovanni Targher
出处
期刊:Diabetes Research and Clinical Practice [Elsevier BV]
卷期号:177: 108884-108884 被引量:8
标识
DOI:10.1016/j.diabres.2021.108884
摘要

Aims The aim of this study was to investigate whether controlled attenuation parameter (CAP) and liver stiffness measurement (LSM), as assessed by vibration-controlled transient elastography (VCTE), are associated with chronic vascular complications of diabetes mellitus type 2 (T2DM). Methods We studied 442 outpatients with established T2DM, and who underwent VCTE and extensive assessment of chronic vascular complications of diabetes. Results A quarter of analyzed patients had a previous history of myocardial infarction and/or ischemic stroke, and about half of them had at least one microvascular complication (chronic kidney disease (CKD), retinopathy or polyneuropathy). The prevalence of liver steatosis (i.e., CAP ≥ 238 dB/m) and significant liver fibrosis (i.e., LSM ≥ 7.0/6.2 kPa) was 84.2% and 46.6%, respectively. Significant liver fibrosis was associated with an increased likelihood of having myocardial infarction (adjusted-odds ratio 6.61, 95%CI 1.66–37.4), peripheral polyneuropathy (adjusted-OR 4.55, 95%CI 1.25–16.6), CKD (adjusted-OR 4.54, 95%CI 1.24–16.6) or retinopathy (adjusted-OR 1.81, 95%CI 1.62–1.97), independently of cardiometabolic risk factors, diabetes-related variables, and other potential confounders. Liver steatosis was not independently associated with any macro-/microvascular diabetic complications. Conclusions Significant liver fibrosis is strongly associated with the presence of macro-/microvascular complications in patients with T2DM. These results offer a new perspective on the follow-up of people with T2DM.
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