Serum microRNA-126 expression as a biomarker of diabetic retinopathy

被引:0
|
作者
Surasmiati, Ni Made Ayu [1 ,2 ]
Suryathi, Ni Made Ari [1 ]
Andayani, Ari [1 ]
机构
[1] Udayana Univ, Fac Med, Ophthalmol Dept, Bali, Indonesia
[2] Gedung Cempaka lantai IV, Jalan Diponegoro Denpasar, Bali 80113, Indonesia
关键词
microRNA-126; diabetes mellitus; diabetic retinopathy; biomarker; MIR-126; BLOOD;
D O I
10.18051/UnivMed.2023.v42:121-127
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Diabetic retinopathy (DR) is a microvascular complication of diabetes mellitus (DM). Diabetic retinopathy causes permanent blindness in the productive age group and has a multifactorial pathogenesis. MicroRNA-126 (miRNA-126) regulates the expression of the vascular endothelial growth factor (VEGF) gene at the post-transcriptional level, VEGF being an important angiogenic protein regulating inflammation in DR development. This study aimed to determine serum miRNA-126 expression as a biomarker in DM patients with DR. METHODS This was a cross-sectional study involving 4 healthy persons and 21 type 2 DM patients. Subjects consisted of 4 groups: i) healthy controls, ii) DM patients without diabetic retinopathy (NDR), iii) DM patients with non-proliferative DR (NPDR) and iv) DM patients with proliferative DR (PDR). Venous blood was collected from subjects for miRNA-126 examination by real-time polymerase chain reaction (PCR). MiRNA-126 in each group was analyzed using the One-Way Anova test and p<0.05 was considered to be statistically significant. RESULTS Mean miRNA-126 expression was significantly decreased in PDR (1.86 +/- 1.03) and NPDR (1.01 +/- 0.43) groups when compared to healthy control (2.44 +/- 1.29) and NDR groups (2.15 +/- 0.48) (p=0.027). MiRNA-126 values of less than 1.81 can differentiate NDR from the control group (sensitivity 83%, specificity 75%) and miRNA-126 of less than 1.56 can be used to predict NPDR when compared to the control group (sensitivity 86%, specificity 75%). CONCLUSION Serum miRNA-126 is a potential biomarker for screening of NPDR and NDR in type 2 DM patients, and could be considered a non-invasive diagnostic parameter.
引用
收藏
页码:121 / 127
页数:7
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