# The association between the GNB3 rs5443 C/C genotype and obesity phenotypes in Taiwanese individuals

**Authors:** Ling-Yi Xiao, Zi-Lun Lai, Yang-Di Su, Szu-Yun Wang, Nia-Jia Zheng, Po-Ren Hsueh

PMC · DOI: 10.37796/2211-8039.1697 · BioMedicine · 2026-03-01

## TL;DR

This study investigates how a specific genetic variant in the GNB3 gene is linked to obesity in Taiwanese individuals, especially in females.

## Contribution

The study identifies a potential association between the GNB3 rs5443 C/C genotype and increased obesity risk in Taiwanese females.

## Key findings

- The C/C genotype of GNB3 rs5443 was more common in individuals with higher BMI.
- Females with C/C genotype had higher obesity risk when body fat was below 30%.
- The study suggests combining GNB3 polymorphisms with other genes for obesity risk screening.

## Abstract

The prevalence of obesity has increased significantly over the years, and its health concerns cannot be underestimated. Obesity not only causes potential mobility limitations in daily life but also increases the risk of developing cardiovascular diseases, diabetes, cancer and other health conditions. While an imbalanced diet and lack of exercise are well-known causes of obesity, genetic patterns also influence its development. Although the GNB3 gene is known to be involved in lipid metabolism and fat cell differentiation, studies have shown inconsistent associations between a common single nucleotide polymorphism of GNB3 (c.825C > T, rs5443) and obesity across different populations. Therefore, this study aims to analyze the association between the GNB3 c.825C > T polymorphism and obesity in the Taiwanese population using various grouping criteria.

The study recruited 372 eligible subjects for GNB3 SNP rs5443 (c.825C > T) testing at China Medical University Hospital in Taichung, Taiwan. Clinical parameters, including age, sex, weight, BMI and body fat percentage were assessed for all participants. The GNB3 rs5443 C/T genotypes were determined using two differentially labeled allele-specific probes and a specific paired PCR primer set.

Our results demonstrated that the distribution of GNB3 rs5443 genotypes (C/C, C/T, T/T) was not significantly correlated with sex and age ( p > 0.05). However, the distribution of GNB3 genotypes (C/C, T/T) showed a statistical significance between subjects with BMI < 24 and BMI ≥ 27. Furthermore, our results revealed that the C/T and T/T genotypes had higher frequency distributions compared to the C/C genotype in females with body fat percentages below 30 % ( p = 0.022 and p = 0.004, respectively).

Taiwanese individuals carrying the C/C homozygous genotype of the GNB3 gene may have a higher susceptibility to obesity, particularly among females. This finding could potentially be combined with polymorphisms of other obesity-related genes to develop a clinical screening tool for assessing obesity risk.

## Linked entities

- **Genes:** GNB3 (G protein subunit beta 3) [NCBI Gene 2784]
- **Diseases:** obesity (MONDO:0011122), diabetes (MONDO:0005015), cancer (MONDO:0004992)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, ADRB2 (adrenoceptor beta 2) [NCBI Gene 154] {aka ADRB2R, ADRBR, ARB2, B2AR, BAR, BETA2AR}, SDC3 (syndecan 3) [NCBI Gene 9672] {aka SDCN, SYND3}, FTO (FTO alpha-ketoglutarate dependent dioxygenase) [NCBI Gene 79068] {aka ALKBH9, BMIQ14, GDFD, IFEX9}, PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, GNB3 (G protein subunit beta 3) [NCBI Gene 2784] {aka CSNB1H, HG2D}
- **Diseases:** NCDs (MESH:D000073296), Overweight (MESH:D050177), stroke (MESH:D020521), Obesity (MESH:D009765), underweight (MESH:D013851), type 2 diabetes (MESH:D003924), cancer (MESH:D009369), diabetes (MESH:D003920), gastrointestinal disorders (MESH:D005767), cardiovascular disease (MESH:D002318), atherosclerosis (MESH:D050197), chronic respiratory disease (MESH:D012140), hypertension (MESH:D006973), hyperlipidemia (MESH:D006949)
- **Chemicals:** cholesterol (MESH:D002784), glucose (MESH:D005947), lipid (MESH:D008055), triglyceride (MESH:D014280), VIC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C/T, T/T, 825-C/T, C/T, Pro12Ala, rs2282440

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12962761/full.md

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Source: https://tomesphere.com/paper/PMC12962761