Apolipoprotein M gene polymorphisms in childhood-onset type 1 diabetes in southern Brazil.
Autor: | de Souza SW; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Lopes MS; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Martins BR; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., da Costa MA; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Nesi-França S; Pediatric Endocrinology Unit, Department of Pediatrics, Federal University of Parana Curitiba, PR, Brazil., Manica GCM; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Winter Boldt AB; Postgraduate Program in Genetics, Department of Genetics, Federal University of Parana Curitiba, PR, Brazil., Couto Alves A; School of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey Guildford, Surrey, UK., Moure VR; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Valdameri G; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Picheth G; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil., Rego FGM; Department of Clinical Analysis, Post-Graduate Program in Pharmaceutical Sciences, Federal University of Parana Curitiba, PR, Brazil. |
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Jazyk: | angličtina |
Zdroj: | International journal of biochemistry and molecular biology [Int J Biochem Mol Biol] 2023 Aug 15; Vol. 14 (4), pp. 51-61. Date of Electronic Publication: 2023 Aug 15 (Print Publication: 2023). |
Abstrakt: | Type 1 diabetes mellitus (T1DM), associated with autoimmune destruction of pancreatic β cells, is observed in children and adolescents. Objective: We investigated the potential association of the apolipoprotein M ( APOM ) polymorphisms rs707921, rs805264, rs805296, rs805297, and rs9404941 in childhood-onset T1DM ( n = 144) and compared them to those in healthy (mostly Euro-Brazilian) children ( n = 168). Methods: This project was approved by the Ethics Committee of the Federal University of Parana (CAAE 24676613.6.0000.0102). Genotyping was performed using PCR-restriction fragment length polymorphisms (rs805296 and rs9404941) and TaqMan probes (rs707921, rs805264, and rs805297). Results: All polymorphisms were in Hardy-Weinberg equilibrium. In the codominant model, no significant differences ( P > 0.05) were observed in genotype and allele frequencies between healthy controls and children with T1DM. The minor allele frequencies (95% CI) for healthy subjects were rs707921 (A, 10.7%; 7-14%), rs805264 (A, 6.5%; 4-9%), rs805296 (C, 3.6%; 2-6%), rs805297 (A, 22.6%; 22-31%), and rs9404941 (C, 2.7%; 1-4%). The frequencies of the rs805297 A allele and rs805296 C allele were similar to those of other Caucasian populations; both the rs707921 and rs805264 A alleles were similar to American and Latin American populations, whereas that of the rs9404941 C allele was lower than that observed in the Caucasian and Asian populations. Conclusions: Haplotype analysis suggests that rs805297-C, rs9404941-T, rs805296-T, rs805264-G, and rs707921-C conferred risk (OR: 4.25; 95% CI: 1.81-10.1) to childhood-onset T1DM in the Euro-Brazilian population. Competing Interests: None. (IJBMB Copyright © 2023.) |
Databáze: | MEDLINE |
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