Clinical spectrum of non-alcoholic fatty liver disease in patients with diabetes mellitus

被引:30
|
作者
Chen, Kaina [1 ,2 ]
Sng, Wei Kwan [3 ]
Quah, Joanne Hui-Min [2 ,3 ]
Liu, Jin [2 ]
Chong, Bee Yen [3 ]
Lee, Hwee Khim [3 ]
Wang, Xue Fei [3 ]
Tan, Ngiap Chuan [2 ,3 ]
Chang, Pik-Eu [1 ,2 ]
Tan, Hong Chang [4 ]
Bee, Yong Mong [4 ]
Goh, George Boon Bee [1 ,2 ]
机构
[1] Singapore Gen Hosp, Dept Gastroenterol & Hepatol, Singapore, Singapore
[2] Duke NUS Med Sch, Singapore, Singapore
[3] SingHlth Polyclin, Singapore, Singapore
[4] Singapore Gen Hosp, Dept Endocrinol, Singapore, Singapore
来源
PLOS ONE | 2020年 / 15卷 / 08期
关键词
FIBROSIS; VARIABILITY; ASSOCIATION; POPULATION; CHINESE;
D O I
10.1371/journal.pone.0236977
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Non-alcoholic fatty liver disease (NAFLD) is increasingly widespread with an overall global estimated prevalence of 25%. Type 2 diabetes Mellitus (T2DM) is a key contributor to NAFLD progression and predicts moderate-severe liver fibrosis and mortality. However, there is currently no uniform consensus on routine NAFLD screening among T2DM patients, and the risk factors of NAFLD and advanced fibrosis among T2DM patients remain to be clarified fully. Aim We explored the prevalence, clinical spectrum, and risk factors of NAFLD and liver fibrosis among T2DM patients. Methods This is a cross-sectional study that enrolled subjects from a primary care clinic and a diabetes centre in Singapore. Subjects aged 21 to 70 years of all ethnic groups with an established T2DM diagnosis were included. Subjects with chronic liver diseases of other aetiologies were excluded. All subjects underwent transient elastography for hepatic steatosis and fibrosis assessment. Their demographics, anthropometric measurements and clinical parameters were collected. Statistical analysis was performed using STATA/SE16.0 software. Results Among 449 enrolled T2DM subjects, 436 with complete data and valid transient elastography results were analysed. Overall, 78.72% (344/436) of the T2DM subjects had NAFLD, of which 13.08% (45/344) had increased liver stiffness. Higher ALT level (OR = 1.08; 95% CI: 1.03-1.14; p = 0.004), obesity (BMI >= 27.5 kg/m2, OR = 2.64; 95% CI: 1.28-5.44; p = 0.008) and metabolic syndrome (OR = 4.36; 95% CI 1.40-13.58; p = 0.011) were independent factors associated with increased CAP (NAFLD). Higher AST level (OR = 1.06; 95% CI: 1.02-1.11; p = 0.008), CAP value (OR = 1.02; 95% CI: 1.00-1.03; p = 0.003), lower platelet count (OR = 0.99; 95% CI: 0.98-1.00; p = 0.009) and concomitant hypertension (OR = 4.56; 95% CI: 1.18-17.62; p = 0.028) were independent factors associated with increased liver stiffness. Conclusions Our study demonstrated a considerably high prevalence of NAFLD among T2DM patients, with the proportion of advanced liver fibrosis among T2DM NAFLD patients much higher than the general population. Given that NAFLD is largely asymptomatic, increased awareness and vigilance for identifying NAFLD and increased liver stiffness among T2DM patients should be advocated.
引用
收藏
页数:13
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