Department of gastroenterology, UHC Rijeka, Rijeka, Croatia; School of medicine, Rijeka, Croatia; Department of gastroenterology, UH Merkur, Zagreb, Croatia.
Department of Internal medicine, General hospital "Josip Benčević", Slavonski Brod, Croatia.
J Diabetes Complications. 2020 Mar;34(3):107512. doi: 10.1016/j.jdiacomp.2019.107512. Epub 2019 Dec 16.
To examine the temporal changes of both controlled attenuation parameter (CAP) and liver stiffness measurements (LSM), assessed by Fibroscan, in a large sample of patients with non-alcoholic fatty liver disease (NAFLD).
In this prospective, observational study, we consecutively enrolled 507 adult individuals with Fibroscan-defined NAFLD who were followed for a mean period of 21.2 ± 11.7 months.
During the follow-up period, 84 patients (16.5%) had a progression of CAP of at least 20% with a median time of 39.93 months, while 201 (39.6%) patients had a progression of LSM of at least 20% with median time of 30.46 months. There were significant differences in the proportion of LSM progression across body mass index (BMI) categories, with obese patients having the highest risk of progression over the follow-up (hazard ratio 1.66; 95%CI 1.23-2.25). Multivariable regression analysis showed that BMI and serum creatinine levels were the strongest predictors for CAP progression in the whole population, while HOMA-estimated insulin resistance was an independent predictor of LSM progression over time in the subgroup of obese patients.
This prospective study shows for the first time that the progression risk of both liver steatosis and fibrosis, detected non-invasively by Fibroscan, is relevant and shares essentially the same metabolic risk factors that are associated with NAFLD progression detected by other invasive methods.
在非酒精性脂肪性肝病(NAFLD)患者的大样本中,研究 Fibroscan 评估的受控衰减参数(CAP)和肝硬度测量(LSM)的时间变化。
在这项前瞻性、观察性研究中,我们连续纳入了 507 名 Fibroscan 定义的 NAFLD 成年患者,平均随访时间为 21.2±11.7 个月。
在随访期间,84 名患者(16.5%)的 CAP 至少增加了 20%,中位时间为 39.93 个月,而 201 名患者(39.6%)的 LSM 至少增加了 20%,中位时间为 30.46 个月。在 BMI 类别中,LSM 进展的比例存在显著差异,肥胖患者在随访期间进展的风险最高(危险比 1.66;95%CI 1.23-2.25)。多变量回归分析表明,BMI 和血清肌酐水平是整个人群 CAP 进展的最强预测因素,而在肥胖患者亚组中,HOMA 估计的胰岛素抵抗是 LSM 随时间进展的独立预测因素。
这项前瞻性研究首次表明,Fibroscan 无创检测到的肝脂肪变性和纤维化的进展风险是相关的,并且基本上与其他侵入性方法检测到的与 NAFLD 进展相关的相同代谢危险因素有关。