Abstract
Background: Nonalcoholic fatty liver disease has attracted considerable attention with continuously increasing morbidity.
Objective: To evaluate the aortic distensibility in patients with non-diabetic and hypertension-type Nonalcoholic Fatty Liver Disease (NAFLD) through Dual-Source Computed Tomography (DSCT).
Methods: 120 patients with NAFLD (experimental group) and 30 healthy subjects (control group) were consecutively enrolled in the study. In the two groups, aortic distensibility was calculated as D = ΔA/(A0 ×Δp). Record fasting insulin, fasting blood glucose, fasting lipid status, age, heart rate, waist circumference, systolic blood pressure, and diastolic blood pressure. Calculate homeostasis model assessment of insulin resistance (HOMA-IR) and Body Mass Index (BMI). A comparative analysis between the two groups was carried out, followed by a correlation analysis between D value and risk factors.
Results: D value and liver attenuation of the patients in the NAFLD group were significantly reduced relative to those in the control group (2.24±0.63×10-3 mmHg-1 vs. 3.19±0.86×10-3 mmHg-1, P<0.001 and 41±6HU vs. 53±5HU, P<0.001, respectively) and their fasting blood glucose, fasting insulin, triglyceride, low-density lipoprotein, aspartate aminotransferase, alanine transaminase, HOMA- IR, and BMI were higher than those in the control group. Liver attenuation, HOMA-IR, age, and BMI were significantly correlated with D value in the NAFLD group. The stepwise multiple linear regression analysis indicates that liver attenuation and HOMA-IR were the significant risk factors for D value (β coefficient =0.43, P =0.001, and β coefficient =-0.33, P =0.02, respectively).
Conclusion: Patients with NAFLD suffer from a reduction in aortic distensibility, and insulin resistance may play a significant role in the early atherosclerosis stage.
Keywords: Coronary computed tomography angiography, nonalcoholic fatty liver, aorta, liver disease, distensibility, cardiovascular disease.
Graphical Abstract
[http://dx.doi.org/10.1002/hep.29367] [PMID: 28714183]
[http://dx.doi.org/10.2337/diacare.24.4.683] [PMID: 11315831]
[http://dx.doi.org/10.2337/dc12-0393] [PMID: 23474588]
[http://dx.doi.org/10.1007/s00330-011-2077-7] [PMID: 21327586]
[http://dx.doi.org/10.1016/j.clinimag.2014.06.003] [PMID: 25034400]
[http://dx.doi.org/10.1148/radiol.10101233] [PMID: 21212369]
[http://dx.doi.org/10.1016/s0895-7061(01)02319-6] [PMID: 12022246]
[http://dx.doi.org/10.1007/BF00280883] [PMID: 3899825]
[http://dx.doi.org/10.1002/hep.20466] [PMID: 15565570]
[http://dx.doi.org/10.3748/wjg.v23.i36.6571] [PMID: 29085206]
[http://dx.doi.org/10.1093/oxfordjournals.aje.a117315] [PMID: 7942769]
[http://dx.doi.org/10.1161/01.HYP.33.5.1111] [PMID: 10334796]
[http://dx.doi.org/10.1172/JCI134165] [PMID: 31805015]
[http://dx.doi.org/10.1038/sj.bjp.0701496] [PMID: 9401792]
[http://dx.doi.org/10.4291/wjgp.v8.i2.51] [PMID: 28573067]
[http://dx.doi.org/10.1097/MED.0b013e3283444b09] [PMID: 21297467]
[http://dx.doi.org/10.1177/147323001204000224] [PMID: 22613423]