# Phenome-Wide Association Study of Latent Autoimmune Diabetes from a Southern Mexican Population Implicates rs7305229 with Plasmatic Anti-Glutamic Acid Decarboxylase Autoantibody (GADA) Levels

**Authors:** Germán Alberto Nolasco-Rosales, José Jaime Martínez-Magaña, Isela Esther Juárez-Rojop, Ester Rodríguez-Sánchez, David Ruiz-Ramos, Jorge Ameth Villatoro-Velázquez, Marycarmen Bustos-Gamiño, Maria Elena Medina-Mora, Carlos Alfonso Tovilla-Zárate, Juan Daniel Cruz-Castillo, Humberto Nicolini, Alma Delia Genis-Mendoza

PMC · DOI: 10.3390/ijms251810154 · International Journal of Molecular Sciences · 2024-09-21

## TL;DR

This study identifies a genetic variant linked to GADA levels in LADA patients from southern Mexico, highlighting a potential genetic risk factor.

## Contribution

The study reports a novel association between rs7305229 and GADA levels in LADA from a non-European population.

## Key findings

- rs7305229 is strongly associated with serum GADA levels in LADA patients (p = 1.84 × 10−8).
- Nine polymorphisms showed nominal association in the GWAS of LADA.
- rs7305229 is located downstream of the FAIM2 gene, previously linked to obesity and immune-related traits.

## Abstract

Latent autoimmune diabetes in adults (LADA) is characterized by the presence of glutamate decarboxylase autoantibodies (GADA). LADA has intermediate features between type 1 diabetes and type 2 diabetes. In addition, genetic risk factors for both types of diabetes are present in LADA. Nonetheless, evidence about the genetics of LADA in non-European populations is scarce. This study aims to perform a genome-wide association study with a phenome-wide association study of LADA in a southeastern Mexican population. We included 59 patients diagnosed with LADA from a previous study and 3121 individuals without diabetes from the MxGDAR/ENCODAT database. We utilized the GENESIS package in R to perform the genome-wide association study (GWAS) of LADA and PLINK for the phenome-wide association study (PheWAS) of LADA features. Nine polymorphisms reach the nominal association level (1 × 10−5) in the GWAS. The PheWAS showed that rs7305229 is genome-wide and associated with serum GADA levels in our sample (p = 1.84 × 10−8). rs7305229 is located downstream of the FAIM2 gene; previous reports associate FAIM2 variants with childhood obesity, body mass index, body adiposity measures, lymphocyte CD8+ activity, and anti-thyroid peroxidase antibodies. Our findings reveal that rs7305229 affects the GADA levels in patients with LADA from southeastern Mexico. More studies are needed to determine if this risk genotype exists in other populations with LADA.

## Linked entities

- **Genes:** FAIM2 (Fas apoptotic inhibitory molecule 2) [NCBI Gene 23017]
- **Diseases:** type 1 diabetes (MONDO:0005147), type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** FAIM2 (Fas apoptotic inhibitory molecule 2) [NCBI Gene 23017] {aka LFG, LFG2, NGP35, NMP35, TMBIM2}, GLUL (glutamate-ammonia ligase) [NCBI Gene 2752] {aka DEE116, GLNS, GS, PIG43, PIG59}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** Autoimmune Diabetes (MESH:D003922), diabetes (MESH:D003920), adiposity (MESH:D018205), type 2 diabetes (MESH:D003924), LADA (MESH:D000071698), obesity (MESH:D009765)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs7305229

## Full text

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC11432505/full.md

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Source: https://tomesphere.com/paper/PMC11432505