Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia; Centre for Liver Disease Research, Translational Research Institute, Faculty of Medicine and Biomedical Science, The University of Queensland, Brisbane, Australia.
Inala Primary Care, Brisbane, Australia.
J Diabetes Complications. 2018 Aug;32(8):799-804. doi: 10.1016/j.jdiacomp.2018.05.008. Epub 2018 May 12.
To examine the relationship between steatosis quantified by controlled attenuation parameter (CAP) values and glycaemic/metabolic control.
230 patients, recruited from an Endocrine clinic or primary care underwent routine Hepatology assessment, with liver stiffness measurements and simultaneous CAP. Multivariable logistic regression was performed to identify potential predictors of Metabolic Syndrome (MetS), HbA1c ≥ 7%, use of insulin, hypertriglyceridaemia and CAP ≥ 300 dB/m.
Patients were 56.7 ± 12.3 years of age with a high prevalence of MetS (83.5%), T2DM (81.3%), and BMI ≥ 40 kg/m (18%). Median CAP score was 344 dB/m, ranging from 128 to 400 dB/m. BMI (aOR 1.140 95% CI 1.068-1.216), requirement for insulin (aOR 2.599 95% CI 1.212-5.575), and serum ALT (aOR 1.018 95% CI 1.004-1.033) were independently associated with CAP ≥ 300 dB/m. Patients with CAP interquartile range < 40 (68%) had a higher median serum ALT level (p = 0.029), greater prevalence of BMI ≥ 40 kg/m (p = 0.020) and higher median CAP score (p < 0.001). Patients with higher CAP scores were more likely to have MetS (aOR 1.011 95% CI 1.003-1.019), HBA1c ≥ 7 (aOR 1.010 95% CI 1.003-1.016), requirement for insulin (aOR 1.007 95% CI 1.002-1.013) and hypertriglyceridemia (aOR 1.007 95% CI 1.002-1.013).
Our data demonstrate that an elevated CAP reflects suboptimal metabolic control. In diabetic patients with NAFLD, CAP may be a useful point-of-care test to identify patients at risk of poorly controlled metabolic comorbidities or advanced diabetes.
研究受控衰减参数(CAP)值定量评估的脂肪变与血糖/代谢控制之间的关系。
本研究纳入了 230 例来自内分泌科或初级保健诊所的患者,进行常规肝脏评估,包括肝硬度测量和同时进行 CAP 检测。采用多变量逻辑回归分析来识别代谢综合征(MetS)、糖化血红蛋白(HbA1c)≥7%、使用胰岛素、高甘油三酯血症和 CAP≥300dB/m 的潜在预测因素。
患者的平均年龄为 56.7±12.3 岁,代谢综合征(MetS)、2 型糖尿病(T2DM)和 BMI≥40kg/m²的患病率较高(分别为 83.5%、81.3%和 18%)。CAP 评分中位数为 344dB/m,范围为 128-400dB/m。BMI(优势比[OR]1.140,95%置信区间[CI]1.068-1.216)、需要使用胰岛素(OR 2.599,95%CI 1.212-5.575)和血清丙氨酸转氨酶(ALT)(OR 1.018,95%CI 1.004-1.033)与 CAP≥300dB/m 独立相关。CAP 四分位距<40(68%)的患者的中位血清 ALT 水平更高(p=0.029)、BMI≥40kg/m²的患病率更高(p=0.020)、CAP 评分中位数更高(p<0.001)。CAP 评分较高的患者更可能患有 MetS(OR 1.011,95%CI 1.003-1.019)、糖化血红蛋白(HbA1c)≥7%(OR 1.010,95%CI 1.003-1.016)、需要使用胰岛素(OR 1.007,95%CI 1.002-1.013)和高甘油三酯血症(OR 1.007,95%CI 1.002-1.013)。
我们的数据表明,CAP 升高反映了代谢控制不佳。在患有非酒精性脂肪性肝病的糖尿病患者中,CAP 可能是一种有用的即时检测方法,可以识别代谢合并症控制不佳或糖尿病进展风险较高的患者。