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. 2024 Dec 28;14(1):31452.
doi: 10.1038/s41598-024-83099-8.

XbaI polymorphism in the APOB gene and its association with increased cholesterol in children and adolescents: Ouro Preto study

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XbaI polymorphism in the APOB gene and its association with increased cholesterol in children and adolescents: Ouro Preto study

Thomás Viana de Souza et al. Sci Rep. .

Abstract

Atherosclerotic vascular changes can begin during childhood, providing risk for cardiovascular disease (CVD) in adulthood. Identifiable risk factors such as dyslipidemia accelerate this process for some children. The apolipoprotein B (APOB) gene could help explain the inter-individual variability in lipid levels among young individuals and identify groups that require greater attention to prevent CVD. A cross-sectional study was conducted with school-aged children and adolescents in Ouro Preto, Minas Gerais. The study evaluated cardiovascular risk factors' variables and XbaI polymorphism in the APOB gene for associations with increased total cholesterol (TC). The prevalence of increased TC was notably high, reaching 68.9% in the study population. Carriers of the variant T allele were 1.45 times more likely to develop increased TC in a dominant model (1.09-1.94, p = 0.011). After adjustments, excess weight and a family history of dyslipidemia interacted significantly with XbaI polymorphism in increased TC, resulting in Odds Ratio of 1.74 (1.11-2.71, p = 0.015) and 2.04 (1.14-3.67, p = 0.016), respectively. The results suggest that XbaI polymorphism in the APOB gene may affect the lipid profile of Brazilian children and adolescents and could contribute to the CVD in adulthood.

Keywords: Adolescent Health; Apolipoproteins B; Cardiovascular Risk Factor; Child Health; Hyperlipidemia; Single Nucleotide Polymorphism.

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Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests. Ethics approval: This study was performed in line with the principles of the Declaration of Helsinki. Approval was granted by the Ethics Committee of Federal University of Ouro Preto (CAAE 28680020.0.0000.5150). Consent for publication: Informed consent was obtained from all individual participants included in the study and written informed consent was obtained from the parents.

Figures

Fig. 1
Fig. 1
Directed acyclic graph (DAG) about XbaI polymorphism (exposure), increased total cholesterol (outcome), and covariates.
Fig. 2
Fig. 2
Risk modification between XbaI polymorphism genotypes and clinical variables with total cholesterol in children and adolescents.

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