Identification of Novel Genetic Variants and Food Intake Factors Associated with Type 2 Diabetes in South Korean Adults, Using an Illness–Death Model

Type 2 diabetes (T2D) is a prevalent chronic disease in the Korean population, influenced by lifestyle, dietary habits, and genetics. This study aimed to identify the effects of food intake and genetic factors on T2D progression in Korean adults using a multi-state illness-death model. We analyzed three transition models: normal glucose tolerance (NGT) to prediabetes (PD), NGT to T2D, and PD to T2D. We first identified dietary patterns significantly associated with each transition, using multivariate Cox proportional hazards models. Then, we assessed the impact of single-nucleotide polymorphisms (SNPs) on each transition, incorporating these dietary patterns as covariates. Our analysis revealed significant associations between the identified dietary patterns and the risk of PD and T2D incidence among individuals with NGT. We also identified novel genetic variants associated with disease progression: two SNPs (<i>rs4607517</i> in Glucokinase [<i>GCK</i>] and <i>rs758982</i> in Calcium/Calmodulin-Dependent Protein Kinase II Beta [<i>CAMK2B</i>]) in the NGT to PD model, and eight SNPs in the NGT to T2D model, including variants in the Zinc Finger Protein 106 (<i>ZNF106</i>), PTOV1 Extended AT-Hook Containing Adaptor Protein (<i>PTOV1</i>), Proprotein Convertase Subtilisin/Kexin Type 2 (<i>PCSK2</i>), Forkhead Box D2 (<i>FOXD2</i>), Solute Carrier Family 38 Member 7 (<i>SLC38A7</i>), and Neuronal Growth Regulator 1 (<i>NEGR1</i>) genes. Functional annotation analysis using ANNOVAR revealed that <i>rs4607517</i> (<i>GCK</i>) and <i>rs59595912</i> (<i>PTOV1</i>) exhibited high Combined Annotation-Dependent Depletion (CADD) and Deleterious Annotation of Genetic Variants using Neural Networks (DANN) scores, suggesting potential pathogenicity and providing a functional basis for their association with T2D progression. Integrating dietary and genetic factors with a multi-state model, this comprehensive approach offers valuable insights into T2D development and highlights potential targets for prevention and personalized interventions.

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Journal
International Journal of Molecular Sciences
Published
2025-03-13
DOI
https://doi.org/10.3390/ijms26062597
Citations
3
Primary Topic
Metabolism, Diabetes, and Cancer
Type
article
Field-Weighted Citation Impact
2.42

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article

Identification of Novel Genetic Variants and Food Intake Factors Associated with Type 2 Diabetes in South Korean Adults, Using an Illness–Death Model

Je-Heon Oh, Sungkyoung Choi, Jun-Ho Cha
3 citations
International Journal of Molecular Sciences
Metabolism, Diabetes, and Cancer
2.42
article

Identification of Novel Genetic Variants and Food Intake Factors Associated with Type 2 Diabetes in South Korean Adults, Using an Illness–Death Model

Je-Heon Oh, Sungkyoung Choi, Jun-Ho Cha
article en
3 citations

Abstract

Type 2 diabetes (T2D) is a prevalent chronic disease in the Korean population, influenced by lifestyle, dietary habits, and genetics. This study aimed to identify the effects of food intake and genetic factors on T2D progression in Korean adults using a multi-state illness-death model. We analyzed three transition models: normal glucose tolerance (NGT) to prediabetes (PD), NGT to T2D, and PD to T2D. We first identified dietary patterns significantly associated with each transition, using multivariate Cox proportional hazards models. Then, we assessed the impact of single-nucleotide polymorphisms (SNPs) on each transition, incorporating these dietary patterns as covariates. Our analysis revealed significant associations between the identified dietary patterns and the risk of PD and T2D incidence among individuals with NGT. We also identified novel genetic variants associated with disease progression: two SNPs (<i>rs4607517</i> in Glucokinase [<i>GCK</i>] and <i>rs758982</i> in Calcium/Calmodulin-Dependent Protein Kinase II Beta [<i>CAMK2B</i>]) in the NGT to PD model, and eight SNPs in the NGT to T2D model, including variants in the Zinc Finger Protein 106 (<i>ZNF106</i>), PTOV1 Extended AT-Hook Containing Adaptor Protein (<i>PTOV1</i>), Proprotein Convertase Subtilisin/Kexin Type 2 (<i>PCSK2</i>), Forkhead Box D2 (<i>FOXD2</i>), Solute Carrier Family 38 Member 7 (<i>SLC38A7</i>), and Neuronal Growth Regulator 1 (<i>NEGR1</i>) genes. Functional annotation analysis using ANNOVAR revealed that <i>rs4607517</i> (<i>GCK</i>) and <i>rs59595912</i> (<i>PTOV1</i>) exhibited high Combined Annotation-Dependent Depletion (CADD) and Deleterious Annotation of Genetic Variants using Neural Networks (DANN) scores, suggesting potential pathogenicity and providing a functional basis for their association with T2D progression. Integrating dietary and genetic factors with a multi-state model, this comprehensive approach offers valuable insights into T2D development and highlights potential targets for prevention and personalized interventions.

International Journal of Molecular SciencesVol. 26(6)
Hanyang University (KR)
National Research Foundation of Korea
Good health and well-being
Openalex Percentile: Top 13%
Metabolism, Diabetes, and Cancer
2.42
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