# Association of long noncoding RNA MEG3 genetic variants with the risk of diabetic neuropathy

**Authors:** Ying-Chi Fan, Po-Jen Yang, Yu-Fan Liu, Lun-Ching Chang, Shih-Chi Su, Shun-Fa Yang

PMC · DOI: 10.7150/ijms.112883 · International Journal of Medical Sciences · 2025-07-10

## TL;DR

This study finds that a genetic variant in the MEG3 gene is linked to increased risk of diabetic neuropathy in women but not in men.

## Contribution

The study identifies a gender-specific association between MEG3 gene polymorphism rs7158663 and diabetic neuropathy risk.

## Key findings

- The MEG3 SNP rs7158663 is associated with increased DN risk in diabetic women but not in men.
- Carrying the GG allele of rs7158663 is linked to higher LDL cholesterol in female DN patients.
- The genetic effect of rs7158663 appears to modulate lipoprotein levels in a gender-specific manner.

## Abstract

Diabetic neuropathy (DN), known to result from an interplay of acquired and genetic factors, is a common comorbidity of diabetes characterized by various forms of nerve damage. Maternally expressed gene 3 (MEG3) is an imprinted, non-coding RNA gene originally identified as a tumor suppressor. Recently, dysregulation of MEG3 levels was also observed in various neurodegenerative diseases. In this study, we aimed to investigate the potential association of MEG3 gene polymorphisms with the risk for DN through genotyping five single-nucleotide polymorphisms (SNPs) of MEG3 gene (rs4081134, rs10144253, rs7158663, rs3087918, and rs11160608) between 712 DN patients and 820 controls (diabetic individuals without neuropathic conditions). Our survey revealed a gender-specific association of rs7158663 with DN. We found that rs7158663 of MEG3 gene was associated with an increased risk for DN in diabetic women (GA vs GG, AOR=1.604, p=0.005; GA+AA vs GG, AOR=1.547, p=0.007). Nevertheless, such genetic association was particularly seen in women but not detected in diabetic males. Moreover, a higher level of LDL-cholesterol was noted in female DN patients who carry homozygous major allele of rs7158663 (GG) than in those bearing at least one minor allele (GA+AA) (p=0.016), suggesting an effect of rs7158663 on modulating lipoprotein levels. Taken together, our results demonstrate a link of MEG3 gene variants with dyslipidemia and neuropathic conditions in diabetic patients in a gender-specific manner.

## Linked entities

- **Genes:** MEG3 (maternally expressed 3) [NCBI Gene 55384]
- **Diseases:** diabetic neuropathy (MONDO:0006626)

## Full-text entities

- **Genes:** MEG3 (maternally expressed 3) [NCBI Gene 55384] {aka FP504, GTL2, LINC00023, Lnc-DLK1-35, NCRNA00023, PRO0518}
- **Diseases:** DN (MESH:D003929), tumor (MESH:D009369), neuropathic conditions (MESH:D009437), nerve damage (MESH:D000080902), diabetes (MESH:D003920), neurodegenerative diseases (MESH:D019636), dyslipidemia (MESH:D050171)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs10144253, rs3087918, rs4081134, rs7158663, rs11160608

## Full text

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## Figures

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## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12320800/full.md

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Source: https://tomesphere.com/paper/PMC12320800