Abstract

We conducted a meta-analysis to evaluate the relationship between erythropoietin (EPO) polymorphisms and diabetic microvascular complications. We searched the PubMed, Embase, Cochrane library, Web of Science, Wanfang, and Chinese National Knowledge Infrastructure databases for appropriate studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to evaluate the associations. Ultimately, eight studies consisting of 2,861 cases and 2,136 controls were identified and included in our meta-analysis. Results with our genotype model indicated an association between rs1617640 polymorphisms and diabetic microvascular complications (TT vs. GG: OR = 1.544, 95% CI = 1.089–2.189, P = 0.015). No clear associations between the rs1617640 and rs507392 polymorphisms and diabetic retinopathy were observed. By contrast, rs551238 polymorphisms were associated with increased diabetic retinopathy risk (allele model: OR = 0.774, 95% CI = 0.658–0.911, P = 0.002; genotype model: AC vs. CC: OR = 0.598, 95% CI = 0.402–0.890, P = 0.011; dominant model: OR = 0.561, 95% CI = 0.385–0.817, P = 0.003; recessive model: OR = 0.791, 95% CI = 0.643–0.973, P = 0.026). These results indicate that EPO polymorphisms are a risk factor for diabetic microvascular complications.

Highlights

  • Several studies have examined associations betweenEPO polymorphisms and diabetic complications; the results have been inconsistent

  • Results with our genotype model indicated an association between rs1617640 polymorphisms and diabetic microvascular complications (TT vs. GG: Odds ratios (ORs) = 1.544, 95% confidence intervals (CIs) = 1.089–2.189, P = 0.015)

  • Rs551238 polymorphisms were associated with increased diabetic retinopathy risk

Read more

Summary

INTRODUCTION

EPO polymorphisms and diabetic complications; the results have been inconsistent. Et al suggested that erythropoietin polymorphisms increased diabetic retinopathy risk [14]. Our study investigated relationships between single-nucleotide polymorphisms (SNPs) in the EPO gene and diabetic complications. Diabetes can damage blood vessels, eyes, and kidneys, resulting in microvascular complications [1,2,3], and is a contributing factor in 2.6% of global blindness cases [1, 4]. Erythropoietin (EPO) is a kidney-derived peptide hormone that plays a major role in the stimulation of bone marrow stem cells and erythropoiesis [5,6,7]. EPO can promote retinal angiogenesis independently of VEGF in proliferative diabetic retinopathy [8, 9]. EPO can improve cardiac function by suppressing endoplasmic reticulum stress and inducing SERCA2a expression [13]

RESULTS
DISCUSSION
MATERIALS AND METHODS
CONFLICTS OF INTEREST
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call