학술논문

Non-alcoholic fatty liver disease and compromised endothelial function in people with type 2 diabetes.
Document Type
Article
Source
BMC Endocrine Disorders. 9/25/2023, Vol. 23 Issue 1, p1-6. 6p.
Subject
*ATHEROSCLEROSIS risk factors
*ENDOTHELIUM physiology
*ENDOTHELIAL cells
*HYPERTENSION
*BRACHIAL artery
*CONFIDENCE intervals
*CROSS-sectional method
*MULTIVARIATE analysis
*NON-alcoholic fatty liver disease
*REGRESSION analysis
*TYPE 2 diabetes
*VASODILATION
*SEX distribution
*BLOOD circulation
*DESCRIPTIVE statistics
*RESEARCH funding
*ODDS ratio
*CARDIOVASCULAR disease diagnosis
*DISEASE complications
Language
ISSN
1472-6823
Abstract
Introduction: Nonalcoholic fatty liver disease (NAFLD) frequently coexists with type 2 diabetes mellitus (T2DM) and synergistically contributes to the development of atherosclerosis. Flow-mediated dilation (FMD) is a commonly used noninvasive test for assessing endothelial function. The main objective of this study was to explore FMD in patients with T2DM with and without NAFLD. Methods: In this cross-sectional study, conducted on people with T2DM, NAFLD was defined as controlled attenuation parameter (CAP) score > 302 dB/m. Endothelial dysfunction was detected when arterial FMD of brachial artery was equal or less than 0.7%. Regression analyses were applied to assess factors associated with impaired FMD. Result: A total of 147 patients (72 with NAFLD and 75 without NAFLD) were included in the final analysis. Patients with NAFLD were more likely to develop FMD ≤ 7% (77.8% vs. 58.7%, P = 0.01). In multivariate analysis, NAFLD (OR = 2.581, 95% CI (1.18–5.62), P = 0.017) and hypertension (HTN) (OR = 3.114, 95% CI (1.31–7.35), P = 0.010) were associated with an increased risk of impaired FMD. However, female sex was associated with a decreased risk of impaired FMD (OR = 0.371, 95% CI (0.15–0.87), P = 0.024). Conclusion: NAFLD is associated with endothelial dysfunction in people with T2DM. This risk is comparable with the risk imposed by HTN, highlighting the importance of screening and management of NAFLD in these patients. [ABSTRACT FROM AUTHOR]