Evidence map›Paper›PMID 40200020›Full record

ArticleScientific reports2025

Genetic association between glucocorticoid receptor gene Bcl1 rs41423247 and rs6198 polymorphisms and risk of obesity in Egyptian children : By.

Nanees A Salem, Angi A Alwakeel, Mayada Abdel-Latif, Shaimaa R Hendawy, Mai S Korkor

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Nanees A SalemPediatric Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.ORCID http://orcid.org/0000-0001-6783-9095
Angi A AlwakeelPediatric Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mayada Abdel-LatifPediatric Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Shaimaa R HendawyClinical Pathology department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mai S KorkorPediatric Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt. mai.korkor618@yahoo.com.ORCID http://orcid.org/0000-0001-8406-6733

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity represents a major global public-health problem during childhood and adolescence. The genetic contribution to obesity and its consequences is well-established. Variation in glucocorticoid (GC)-sensitivity can be partly explained by polymorphisms in GC receptor (GR) gene where NR3C1; Bcl1 rs41423247 and NR3C1 rs6198 single nucleotide polymorphisms (SNPs) have been linked to higher and lower GC sensitivity, respectively. We aimed to explore the potential association between the GR gene SNPs and risk of obesity in a cohort of Egyptian children. We included 100 pre-pubertal children; 60 obese children and 40 age-and sex-matched normal-weight controls. Bcl1 rs41423247 SNP was genotyped using PCR-restriction fragment length polymorphism technique and NR3C1 rs6198 SNP was genotyped using Real-time-PCR.In Bcl1 rs41423247, obese children had more frequent CG, GG genotypes and G allele compared to healthy controls (P = 0.039, 0.019 and 0.007 respectively). Moreover, insulin resistance was significantly higher in combined CG + GG group compared to CC group. On the contrary, no significant differences were found in genotypes, alleles frequencies or insulin resistance between obese and non-obese children in NR3C1 rs6198. GR Bcl1 rs41423247 gene polymorphism may play a role in genetic susceptibility to obesity that can be a future targeted therapy for obesity.

Indexed as

Genetic Predisposition to DiseaseObesityPediatric ObesityPolymorphism, Single NucleotideReceptors, GlucocorticoidAllelesCase-Control StudiesChildEgyptFemaleGene FrequencyGenetic Association StudiesGenotypeHumansInsulin ResistanceMaleNR3C1 protein, humanReceptors, GlucocorticoidBcl1 gene polymorphismChildrenGlucocorticoidObesity

Identifiers

PMID40200020
PMCPMC11978808

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.