Lower vitamin D levels and the rare rs1338135647 variant may independently co-occur with ASD in Indonesian children; however, these hypothesis-generating findings require replication and functional validation in larger independent cohorts.
Abstract
Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental condition arising from interactions between genetic susceptibility and environmental factors, including vitamin D status. This study investigated the associations of serum vitamin D levels and vitamin D receptor (VDR) gene variants with ASD in Indonesian children. This exploratory case-control study included 80 children aged 24-59 months from Surabaya, Indonesia, comprising 40 children with ASD and 40 typically developing controls. Serum 25-hydroxyvitamin D3 (25[OH]D3) concentrations were measured using an enzyme-linked immunosorbent assay, while the VDR region containing rs731236 was amplified by polymerase chain reaction and analyzed using bidirectional Sanger sequencing. Sequencing additionally identified rs11574113, rs7975232, and the rare missense variant rs1338135647 (p.Gly375Asp). Children with ASD had lower serum 25(OH)D3 concentrations than controls (median, 46.13 vs 69.27 ng/mL; p = 0.027), and the difference remained significant after adjustment for age and sex (adjusted median difference, -24.86 ng/mL; 95% confidence interval [CI], -42.42 to -7.30; p = 0.007). The rs1338135647 AG genotype was more frequent in children with ASD than in controls (22.5% vs 2.5%) and remained associated with ASD after adjustment for age and sex using Firth penalized logistic regression (odds ratio, 6.44; 95% CI, 1.21-67.64; p = 0.028). No significant associations were observed for the other VDR variants. Lower vitamin D levels and the rare rs1338135647 variant may independently co-occur with ASD in Indonesian children; however, these hypothesis-generating findings require replication and functional validation in larger independent cohorts.
The findings suggest no significant association between the HTR2A rs6313 and ASD susceptibility in the Jordanian population, and emphasize the need for larger, multi-marker studies to account for regional genetic diversity.
Wiam Khalil, Elaf Adel Al-Dalabeeh, M. Zihlif· Drug Metabolism and Personal...· 0 citations
Although no statistically significant genetic associations were identified in the present cohort, the bioinformatics findings suggest that these loci remain biologically relevant within Wnt-related pathways.
Semra Uğur, E. Akbaş· Molecular Biology Reports· 0 citations
This study contributes additional cases to the expanding phenotypic and mutational spectrum of ZNF292-related neurodevelopmental disorder and indicates growth retardation was observed in all eight individuals, but given the limitations of a single-center referral cohort, this observation should be interpreted with caution and requires validation in larger studies.
Yaping Shen, R. Pan, Chen Liu et al.· Genes· 0 citations
Vitamin D has significant effects on neurofibroma development in patients with neurofibromatosis type 1 (NF1). Additionally,
vitamin D receptor
(
VDR
) gene polymorphisms are associated with various cancers.
This study aimed to determine the correlation between NF1 and the serum vitamin D level, along with the
VDR
single nucleotide polymorphisms (SNPs)
Fok1, Bsm1, Taq1, Apa1
, and
Cd × 2
.
This observational study included 64 patients with NF-1 and 64 age- and gender-matched controls. The serum 25(OH) D3 level was measured, and 5
VDR
SNPs were analysed.
The median serum 25(OH) D3 level was lower in the NF1 patients than in the controls (
P
< 0.001). Heterozygous and mutant type
FokI
and
TaqI
polymorphisms decrease the risk of NF1, whereas mutant and heterozygous
ApaI
polymorphisms increase the risk of NF1. The primary limitation of this study is its small population. Extrapolation of the present findings to the general Turkish population may not be valid. Causality was not assessed due to case-control design of the study.
The findings indicate that some alleles of
FokI, ApaI
, and
TaqI
nucleotides are strongly associated with NF1. Additionally, there is a possible role for vitamin D and
VDR
gene SNP pathways in the pathogenesis of NF1.
Neslihan Akdoğan, T. Çandar, E. Karabulut et al.· Indian Journal of Dermatolog...· 0 citations
Background: Psoriasis is an inflammatory skin disease caused by genetic and environmental factors. Although data on Iraqi patients are poor, there may be a relation between the vitamin D receptor (VDR) gene and susceptibility to psoriasis. Objective: This study aims to analyze the association between the VDR ApaI (rs7975232) gene polymorphism and the tendency toward psoriasis in Iraqi patients and to evaluate serum levels of vitamin D3, ferritin, and zinc. Method: A case-control study was conducted on 45 patients with psoriasis and 35 age- and sex-matched control group. Genotyping of the Vitamin D receptor rs7975232 polymorphism was done by high-resolution melting (HRM) analysis. Automated analyzers tested serum vitamin D3, ferritin, and zinc levels. Statistical analyses were performed using GraphPad Prism software. Results: The allele frequency was considerably higher in patients (40.0%) than in the control group (24.3%), which conferred an elevated risk of psoriasis (OR = 2.07, 95% CI: 1.01–4.24, p = 0.046). AA carriers showed the lowest mean vitamin D3 level (15.0 ± 3.7 ng/mL, p = 0.0043) and highest mean ferritin level (223.6 ± 67.2 ng/mL, p = 0.0136). Levels of vitamin D3 and zinc were considerably lower in patients than in the control group (p<0.001 for both), and the highest mean ferritin level (p<0.001). Conclusions: The A allele of the VDR rs7975232 polymorphism was associated with increased susceptibility to psoriasis in Iraqi patients. AA carriers showed the lowest mean vitamin D3 and zinc levels and the highest mean ferritin level; however, genotype-related differences in these biochemical parameters were not statistically significant within the patient group.
Safana S. Dardouh, M. Mohammed, Mohammad M. F. Al-Halbosiy· Adolescência e Saúde· 0 citations
The research identified highly significant associations across multiple inheritance models, validating the technical robustness of the findings, and establish DRD2 intronic polymorphisms as critical determinants of schizophrenia risk.
Ishrat Yaseen, Saleem Ahmad, Muhammad Ghalib et al.· Journal of Molecular Neurosc...· 0 citations
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