» Articles » PMID: 30410834

Fok-I, Bsm-I, and Taq-I Variants of Vitamin D Receptor Polymorphism in the Development of Autism Spectrum Disorder: A Literature Review

Overview
Journal Cureus
Date 2018 Nov 10
PMID 30410834
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

The role of vitamin D in the development of autism spectrum disorder (ASD) is of intensified interest in medical science in recent years. Vitamin D has a significant role in neurogenesis, neuroprotection, and neurodevelopment. Due to the close association of vitamin D with the brain, it has been found that in the pathophysiology of several neuropsychiatric disorders vitamin D receptor (VDR) polymorphism plays a significant role. In this review article, we looked for a relation between VDR polymorphism and ASD. We systemically reviewed all the potential articles on the relation between VDR polymorphism and ASD. We found that several VDR variants FokI, BsmI, and TaqI polymorphisms are related to ASD. Even paternal VDR polymorphism can be a causative factor for ASD in the offspring. The relation between FokI (ff) genotype polymorphism and increased level of serum 1,25(OH)D3 in ASD patients is a very significant finding. Variation of ASD-related genotypes in different ethnic population raises a big question on whether the environmental factors also can do changes in human genotypes leading to ASD.

Citing Articles

Re-emerging concepts of immune dysregulation in autism spectrum disorders.

Erbescu A, Papuc S, Budisteanu M, Arghir A, Neagu M Front Psychiatry. 2022; 13:1006612.

PMID: 36339838 PMC: 9626859. DOI: 10.3389/fpsyt.2022.1006612.


Vitamin D Receptor Gene Polymorphism and Vitamin D Status in Population of Patients with Cardiovascular Disease-A Preliminary Study.

Abouzid M, Kruszyna M, Burchardt P, Kruszyna L, Glowka F, Karazniewicz-Lada M Nutrients. 2021; 13(9).

PMID: 34578994 PMC: 8465937. DOI: 10.3390/nu13093117.


Vitamin D receptor, vitamin D binding protein and CYP27B1 single nucleotide polymorphisms and susceptibility to viral infections in infants.

Zacharioudaki M, Messaritakis I, Galanakis E Sci Rep. 2021; 11(1):13835.

PMID: 34226633 PMC: 8257681. DOI: 10.1038/s41598-021-93243-3.


Vitamin D status and vitamin D deficiency risk factors among pregnancy of Shanghai in China.

Yang C, Jing W, Ge S, Sun W BMC Pregnancy Childbirth. 2021; 21(1):431.

PMID: 34144704 PMC: 8214247. DOI: 10.1186/s12884-021-03889-0.


Expression analysis of selected genes involved in tryptophan metabolic pathways in Egyptian children with Autism Spectrum Disorder and learning disabilities.

Higazi A, Kamel H, Abdel-Naeem E, Abdullah N, Mahrous D, Osman A Sci Rep. 2021; 11(1):6931.

PMID: 33767242 PMC: 7994393. DOI: 10.1038/s41598-021-86162-w.


References
1.
Hawes J, Tesic D, Whitehouse A, Zosky G, Smith J, Wyrwoll C . Maternal vitamin D deficiency alters fetal brain development in the BALB/c mouse. Behav Brain Res. 2015; 286:192-200. DOI: 10.1016/j.bbr.2015.03.008. View

2.
Ashwood P, Krakowiak P, Hertz-Picciotto I, Hansen R, Pessah I, Van de Water J . Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome. Brain Behav Immun. 2010; 25(1):40-5. PMC: 2991432. DOI: 10.1016/j.bbi.2010.08.003. View

3.
Harrison P, Weinberger D . Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence. Mol Psychiatry. 2004; 10(1):40-68. DOI: 10.1038/sj.mp.4001558. View

4.
Schmidt R, Hansen R, Hartiala J, Allayee H, Sconberg J, Schmidt L . Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE Study. Early Hum Dev. 2015; 91(8):483-9. PMC: 4871694. DOI: 10.1016/j.earlhumdev.2015.05.008. View

5.
Lai C, Fisher S, Hurst J, Vargha-Khadem F, Monaco A . A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001; 413(6855):519-23. DOI: 10.1038/35097076. View