Serum level of the autophagy biomarker Beclin-1 in patients with diabetic kidney disease

被引:34
|
作者
Naguib, Mervat [1 ]
Rashed, Laila A. [2 ]
机构
[1] Cairo Univ, Sch Med, Dept Internal Med, Cairo, Egypt
[2] Cairo Univ, Sch Med, Dept Med Biochem, Cairo, Egypt
关键词
Diabetes; Kidney; Autophagy; Beclin-1; EXACERBATES PROTEINURIA; NEPHROPATHY;
D O I
10.1016/j.diabres.2018.06.022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autophagy is a major cellular clearance mechanism that maintains cellular survival and homeostasis. Autophagy has a crucial role in the progression of diabetes and kidney diseases. Aims: To investigate serum concentrations of Beclin-1, a key regulator of autophagy, in patients with diabetic kidney disease (DKD). Methods: The study included 70 patients with type 2 diabetes and DKD (group 1; 35 patients with estimated glomerular filtration rate (eGFR) >= 30 ml/min/1.73 m(2) and group 2; 35 patients with eGFR < 30 ml/min/1.73 m(2)) and 20 age-and sex-matched healthy subjects (group 3). Laboratory work up included; glycated hemoglobin (HbA1c), serum creatinine, eGFR using modification of diet in renal disease (MDRD) formula, urine albumin to creatinine ratio (ACR), and serum Beclin-1 measurement. Results: Patients with DKD had significantly lower Beclin-1 levels (2.38 +/- 1.46 ng/mL) compared to control group (6.03 +/- 1.94 ng/mL; P < 0.001). Moreover, serum Beclin-1 significantly decreased in group 2 (1.43 +/- 0.83 ng/mL) compared to group 1 (3.36 +/- 1.30 ng/mL; P < 0.001). In univariate analysis, the concentration of Beclin-1 correlated well with eGFR (r = 0.64, P < 0.001), ACR (r = -0.63, P < 0.001), and duration of diabetes (r = -0.43, P < 0.001) but didn't correlate with HbA1c (r = -0.17, P = 0.15). However, ACR was the only significant predictor of Beclin-1 level on performing multiple regression analysis (beta = -0.40, P = 0.01). Conclusion: Serum level of Beclin-1 is reduced in patients with DKD. Furthermore, its level is related to the stage of DKD and correlates with the degree of albuminuria. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:56 / 61
页数:6
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