Exploring the Relationship of rs2802292 with Diabetes and NAFLD in a Southern Italian Cohort—Nutrihep Study

Author:

Forte Giovanna1,Donghia Rossella2ORCID,Lepore Signorile Martina1,Tatoli Rossella2ORCID,Bonfiglio Caterina2ORCID,Losito Francesco3,De Marco Katia1,Manghisi Andrea1,Guglielmi Filomena Anna1,Disciglio Vittoria1,Fasano Candida1,Sanese Paola1,Cariola Filomena1,Buonadonna Antonia Lucia1,Grossi Valentina1ORCID,Giannelli Gianluigi4ORCID,Simone Cristiano15

Affiliation:

1. Medical Genetics, National Institute of Gastroenterology, IRCCS “Saverio de Bellis” Research Hospital, 70013 Castellana Grotte, Italy

2. Data Science Unit, National Institute of Gastroenterology, IRCCS “Saverio de Bellis” Research Hospital, 70013 Castellana Grotte, Italy

3. Gastroenterology Unit, National Institute of Gastroenterology, IRCCS “Saverio de Bellis” Research Hospital, 70013 Castellana Grotte, Italy

4. Scientific Direction, National Institute of Gastroenterology, IRCCS “Saverio de Bellis” Research Hospital, 70013 Castellana Grotte, Italy

5. Medical Genetics, Department of Precision and Regenerative Medicine and Jonic Area (DiMePRe-J), University of Bari Aldo Moro, 70124 Bari, Italy

Abstract

Background: The minor G-allele of FOXO3 rs2802292 is associated with human longevity. The aim of this study was to test the protective effect of the variant against the association with type 2 Diabetes and NAFLD. Methods: rs2802292 was genotyped in a large population of middle-aged subjects (n = 650) from a small city in Southern Italy. All participants were interviewed to collect information about lifestyle and dietary habits; clinical characteristics were recorded, and blood samples were collected from all subjects. The association between rs2802292 and NAFLD or diabetes was tested using a logistic model and mediation analysis adjusted for covariates. Results: Overall, the results indicated a statistical association between diabetes and rs2802292, especially for the TT genotype (OR = 2.14, 1.01 to 4.53 95% C.I., p = 0.05) or in any case for those who possess the G-allele (OR = 0.45, 0.25 to 0.81 95% C.I., p = 0.008). Furthermore, we found a mediation effect of rs2802292 on diabetes (as mediator) and NAFLD. There is no direct relationship between rs2802292 and NAFLD, but the effect is direct (β = 0.10, −0.003 to 0.12 95% C.I., p = 0.04) on diabetes, but only in TT genotypes. Conclusions: The data on our cohort indicate that the longevity-associated FOXO3 variant may have protective effects against diabetes and NAFLD.

Funder

Italian Association for Cancer Research

Italian Ministry of Health “Starting Grant”

Publisher

MDPI AG

Reference49 articles.

1. (2024, June 19). Genetics of Healthy Aging and Longevity—PubMed, Available online: https://pubmed.ncbi.nlm.nih.gov/23925498/.

2. (2024, June 19). Genetic Factors Associated with Longevity: A Review of Recent Findings—PubMed, Available online: https://pubmed.ncbi.nlm.nih.gov/25446805/.

3. (2024, June 19). The Metabolic Syndrome: Is This Diagnosis Necessary?—PubMed, Available online: https://pubmed.ncbi.nlm.nih.gov/16762930/.

4. Comparison of the Mammalian Insulin Signalling Pathway to Invertebrates in the Context of FOXO-Mediated Ageing;Papatheodorou;Bioinformatics,2014

5. Forkhead Transcription Factor FKHR-L1 Modulates Cytokine-Dependent Transcriptional Regulation of P27(KIP1);Dijkers;Mol. Cell Biol.,2000

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