1 Lee's Endocrinology Clinic, Pingtung, Taiwan.
2 LiTzung Biotechnology, Inc., Kaohsiung, Taiwan.
Ann Clin Biochem. 2019 Jan;56(1):141-147. doi: 10.1177/0004563218796259. Epub 2018 Aug 27.
Serum cytokeratin-18 is believed to be a marker of hepatic cell damage. However, few studies have discussed about the serum cytokeratin-18 concentration in type 2 diabetes mellitus patients and investigated its association with non-alcoholic fatty liver disease as well as metabolic biomarkers.
Healthy participants and type 2 diabetes mellitus patients were enrolled. Physical and metabolic factors were recorded, and non-alcoholic fatty liver disease was screened by abdominal ultrasound and the fatty liver index. The cytokeratin-18 concentration was detected using two commercially available immunoassay kits (M30 and M65 ELISA kit, Previa AB, Sweden).
Overall, 22.8% (29/127) and 35.9% (42/117) of the participants were diagnosed with non-alcoholic fatty liver disease in the non-diabetes mellitus group and type 2 diabetes mellitus group, respectively. In the non-diabetes mellitus group and type 2 diabetes mellitus group, our result showed that participants with non-alcoholic fatty liver disease had a higher serum cytokeratin-18 M30 and cytokeratin-18 M65 concentration as compared with participants without non-alcoholic fatty liver disease. Interestingly, as compared with healthy participants without non-alcoholic fatty liver disease, our result also demonstrated that type 2 diabetes mellitus patients without non-alcoholic fatty liver disease had a higher serum cytokeratin-18 M30 (108.4 ± 66.2 vs. 87.1 ± 34.6 U/L; P = 0.038) and cytokeratin-18 M65 concentration (285.4 ± 115.3 vs. 248.5 ± 111.3 U/L; P = 0.031). The independent relationship between type 2 diabetes mellitus and cytokeratin-18 was further strengthened by the significant positive association between fasting plasma glucose and serum cytokeratin-18 concentration via multivariate regression analyses (cytokeratin-18 M30: β = 0.034, P = 0.029; cytokeratin-18 M65: β = 0.044, P = 0.002).
Independent of non-alcoholic fatty liver disease, our results suggested that the cytokeratin-18 concentration is closely associated with the hyperglycaemic milieu. The association between serum cytokeratin-18 and type 2 diabetes mellitus may be worthy of further investigation.
血清细胞角蛋白 18 被认为是肝损伤的标志物。然而,很少有研究探讨 2 型糖尿病患者的血清细胞角蛋白 18 浓度,并研究其与非酒精性脂肪性肝病以及代谢生物标志物的关系。
纳入健康参与者和 2 型糖尿病患者。记录身体和代谢因素,并通过腹部超声和脂肪肝指数筛查非酒精性脂肪性肝病。使用两种商业上可获得的免疫测定试剂盒(M30 和 M65 ELISA 试剂盒,Previa AB,瑞典)检测细胞角蛋白 18 浓度。
总体而言,在非糖尿病组和 2 型糖尿病组中,分别有 22.8%(29/127)和 35.9%(42/117)的参与者被诊断为非酒精性脂肪性肝病。在非糖尿病组和 2 型糖尿病组中,我们的结果表明,与无非酒精性脂肪性肝病的参与者相比,患有非酒精性脂肪性肝病的参与者的血清细胞角蛋白 18 M30 和细胞角蛋白 18 M65 浓度更高。有趣的是,与无非酒精性脂肪性肝病的健康参与者相比,我们的结果还表明,无非酒精性脂肪性肝病的 2 型糖尿病患者的血清细胞角蛋白 18 M30 更高(108.4 ± 66.2 vs. 87.1 ± 34.6 U/L;P = 0.038)和细胞角蛋白 18 M65 浓度更高(285.4 ± 115.3 vs. 248.5 ± 111.3 U/L;P = 0.031)。通过多元回归分析进一步加强了 2 型糖尿病与细胞角蛋白 18 之间的独立关系,空腹血糖与血清细胞角蛋白 18 浓度之间存在显著正相关(细胞角蛋白 18 M30:β=0.034,P=0.029;细胞角蛋白 18 M65:β=0.044,P=0.002)。
独立于非酒精性脂肪性肝病,我们的结果表明细胞角蛋白 18 浓度与高血糖环境密切相关。血清细胞角蛋白 18 与 2 型糖尿病之间的关系值得进一步研究。