# Association of erythropoietin gene polymorphism (rs1617640 C>T/G) with diabetic retinopathy in Type 2 diabetes mellitus patients of Punjabi population in Pakistan

**Authors:** Cyrollah Disoma, Aqsa Malik, Ayesha Nisar, Inam Ullah, Sikandar Hayat, Abdul Qadeer, Sardar Azhar Mehmood, Sawar Khan, Zanxian Xia

PMC · DOI: 10.1371/journal.pone.0336014 · PLOS One · 2025-11-06

## TL;DR

This study found that a specific genetic variant in the erythropoietin gene is linked to a lower risk of diabetic retinopathy in Punjabi people with type 2 diabetes.

## Contribution

The study identifies a novel association between the EPO gene polymorphism rs1617640 and diabetic retinopathy in the Punjabi population.

## Key findings

- The CC genotype of rs1617640 was significantly more common in controls and associated with reduced DR risk.
- The GG and TT genotypes were absent in controls but present in DR patients, indicating increased susceptibility.
- The C allele was predominant in controls, while G and T alleles were enriched in DR cases.

## Abstract

Diabetic retinopathy (DR) is a leading cause of vision loss in individuals with type 2 diabetes mellitus (T2DM) and is influenced by genetic factors. We investigated the association between the erythropoietin (EPO) gene polymorphism (rs1617640 C > T/G) and DR risk in a Punjabi Pakistani cohort of adults with T2DM. In a case–control design, 573 T2DM patients (294 with DR, 279 controls without retinopathy, CDR) were genotyped by ARMS-PCR. The protective CC genotype was significantly more frequent in controls (96.77%) than in cases (30.61%) and was associated with markedly reduced DR risk (OR = 68; 95% CI 33.468–138.162; p < 0.001). Conversely, the GG and TT genotypes were absent in controls but present in DR patients (27.55% and 21.43%, respectively) and were strongly associated with increased DR risk (p < 0.001). Allele-level analysis mirrored genotype findings: the C allele predominated in controls (98.39%) but was significantly less frequent in cases (39%), while G and T alleles were enriched among DR patients (p < 0.001). Together, genotype- and allele-based results indicate that the rs1617640 C variant is protective against DR in this Punjabi T2DM population, whereas G and T variants increase DR susceptibility.

## Linked entities

- **Genes:** EPO (erythropoietin) [NCBI Gene 2056]
- **Diseases:** diabetic retinopathy (MONDO:0005266), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}
- **Diseases:** DR (MESH:D003930), vision loss (MESH:D014786), T2DM (MESH:D003924), retinopathy (MESH:D058437)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C > T/G, rs1617640

## Full text

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## Figures

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## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12591492/full.md

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Source: https://tomesphere.com/paper/PMC12591492