Evaluation of kidney injury molecule-1 as a disease progression biomarker in diabetic nephropathy

被引:28
|
作者
Khan, Fatima Abid [1 ]
Fatima, Syeda Sadia [2 ]
Khan, Ghulam Mustafa [3 ]
Shahid, Sana [4 ]
机构
[1] Jinnah Sindh Med Univ, Dept Physiol, Karachi, Pakistan
[2] Aga Khan Univ, Dept Biol & Biomed Sci, Stadium Rd, Karachi 74800, Pakistan
[3] Jinnah Post Grad Med Ctr, Dept Physiol, Basic Med Sci Inst, Karachi, Pakistan
[4] Sir Syed Coll Med Girls, Dept Physiol, Karachi, Pakistan
关键词
Diabetes Mellitus; Diabetic Nephropathy; KIM-1; PREVENTION; DIAGNOSIS; KIM-1; NGAL;
D O I
10.12669/pjms.35.4.154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background & Objective: Kidney Injury Molecule-1 (KIM-1) is a peptide whose release into circulation is specific to tubular injury. This study aimed to estimate levels of kidney injury molecule-1 in diabetic patients with and without kidney disease. And evaluate the role of KIM-1 as an early screening marker of progressive kidney injury. Methods: This follow-up study included n=85 subjects from the diabetic clinic of Jinnah Post Graduate Medical Center (JPMC) in collaboration with Aga Khan University from November 2016 till September 2017 They were divided as: i) Group A1 (n=30) participants with diabetes for <5 years without microalbuminuria ii) Group A2 (n= 30) subjects with diabetes for 6-10 years with microalbuminuria; iii) Group B (n=25) subjects as healthy control group. All study participants were followed for 6 months and their blood glucose, urea, creatinine, electrolytes, albuminuria and serum KIM-1 were assayed. Results: High KIM-1 at baseline was present in group A2 patients as compared to controls and group A1 (p<0.001). Higher levels were seen after six months in group A1 along with the presence of micro albuminuria (p<0.001) suggesting kidney damage. Moderate positive association were seen for KIM1 with creatinine levels (r=0.530; p<0.001), and HbA1 c (r=0.576; p<0.001) in all patients. While a strong positive association was seen for blood urea nitrogen as a marker for kidney function both at baseline (r= 0.728; p=0.000) and follow up (r=0.747; p=0.001). Multiple logistic regression controlling for age showed that KIM1 was independently associated with BUN (r=0.727; p<0.001), creatinine (r=0.510; p<0.001) and HbA1 c (r=0.401; p=0.008) in all groups. Conclusion: Rising KIM-1 levels with progressive kidney damage with or without derangement of kidney function is reported in this study. This finding may pave a way towards identifying KIM1 as a prognostic marker for kidney injury.
引用
收藏
页码:992 / 996
页数:5
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