Skip to main content

Advertisement

Log in

Associations Between Two Single-Nucleotide Polymorphisms in NINJ2 Gene and Risk of Psychiatric Disorders

  • Published:
Journal of Molecular Neuroscience Aims and scope Submit manuscript

Abstract

NINJ2 encodes a transmembrane protein that contributes in neurodevelopment and regeneration of neurons. Single-nucleotide polymorphisms (SNPs) within this gene have been associated with Alzheimer’s disease, ischemic stroke, and multiple sclerosis. The rs11833579 and rs3809263 SNPs have been associated with risk of ischemic stroke in Iranian population. While the NINJ2 rs12425791 has been with risk of ischemic stroke in East Asian population, the rs11833579 has not been associated with this condition either in East Asian population or Chinese Han population. In the current project, we genotyped rs11833579 and rs3809263 in a large cohort of neuropsychiatric patients including major depressive disorder, bipolar disorder, schizophrenia, and methamphetamine addiction. No significant difference was detected in frequencies of alleles, genotypes, or haplotypes between patients and controls. Thus, the current investigation failed to show association between rs11833579 and rs3809263 and the mentioned neuropsychiatric disorders. Future studies are needed to verify our results.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Araki T, Milbrandt J (2000) Ninjurin2, a novel homophilic adhesion molecule, is expressed in mature sensory and enteric neurons and promotes neurite outgrowth. J Neurosci 20:187–195

    Article  CAS  Google Scholar 

  • Corvin A, Donohoe G, Hargreaves A, Gallagher L, Gill M (2012) The cognitive genetics of neuropsychiatric disorders. Curr Top Behav Neurosci 12:579–613

    Article  CAS  Google Scholar 

  • Jensen KP (2016) A review of genome-wide association studies of stimulant and opioid use disorders. Mol Neuropsychiatry 2:37–45

    Article  CAS  Google Scholar 

  • Li BH, Zhang LL, Yin YW, Pi Y, Guo L, Yang QW, Gao CY, Fang CQ, Wang JZ, Li JC (2012) Association between 12p13 SNPs rs11833579/rs12425791 near NINJ2 gene and ischemic stroke in East Asian population: evidence from a meta-analysis. J Neurol Sci 316:116–121

    Article  CAS  Google Scholar 

  • Lian G, Yan Y, Jianxiong L, Juanjuan X, Qing C, Guangliang W, Li, S. (2012) The rs11833579 and rs12425791 polymorphisms and risk of ischemic stroke in an Asian population: a meta-analysis. Thromb Res 130:e95–e102

    Article  CAS  Google Scholar 

  • Lin KP, Chen SY, Lai LC, Huang YL, Chen JH, Chen TF, Sun Y, Wen LL, Yip PK, Chu YM, Chen WJ, Chen YC (2011) Genetic polymorphisms of a novel vascular susceptibility gene, Ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer’s disease. PLoS One 6:e20573

    Article  CAS  Google Scholar 

  • Malekzadeh V, Azari I, Noroozi R, Shams R, Farzaneh M, Taheri M, Ghafouri-Fard S (2019) Genetic variants within Ninjurin 2 gene are associated with risk of ischemic stroke in Iranian population. Neurol Sci

  • Noroozi R, Azari I, Taheri M, Omrani MD, Ghafouri-Fard S (2019) A single nucleotide polymorphism within Ninjurin 2 is associated with risk of multiple sclerosis. Metab Brain Dis

  • Seilheimer B, Schachner M (1988) Studies of adhesion molecules mediating interactions between cells of peripheral nervous system indicate a major role for L1 in mediating sensory neuron growth on Schwann cells in culture. J Cell Biol 107:341–351

    Article  CAS  Google Scholar 

  • Smeland OB, Bahrami S, Frei O, Shadrin A, O'connell K, Savage J, Watanabe K, Krull F, Bettella F, Steen NE, Ueland T, Posthuma D, Djurovic S, Dale AM, Andreassen OA (2019) Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence. Mol Psychiatry

  • Treutlein J, Rietschel M (2011) Genome-wide association studies of alcohol dependence and substance use disorders. Curr Psychiatry Rep 13:147–155

    Article  Google Scholar 

  • Ward LD, Kellis M (2012) HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res 40:D930–D934

    Article  CAS  Google Scholar 

  • Whiteford HA, Degenhardt L, Rehm J, Baxter AJ, Ferrari AJ, Erskine HE, Charlson FJ, Norman RE, Flaxman AD, Johns N, Burstein R, Murray CJ, Vos T (2013) Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. Lancet 382:1575–1586

    Article  Google Scholar 

  • Zhang Z, Ni G, Xu G, Xu J, Liu X (2016) A novel functional polymorphism in the NINJ2 promoter predicts risk of large artery atherosclerotic stroke. Mol Neurobiol 53:7178–7183

    Article  CAS  Google Scholar 

Download references

Funding

The current study was supported by a grant from Shahid Beheshti University of Medical Sciences.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Mir Davood Omrani or Mohammad Taheri.

Ethics declarations

The study protocol was approved by the ethics committees of Shahid Beheshti Universities of Medical Sciences.

Conflict of Interest

The authors declare they have no conflict of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sayad, A., Ghafouri-Fard, S., Omrani, M.D. et al. Associations Between Two Single-Nucleotide Polymorphisms in NINJ2 Gene and Risk of Psychiatric Disorders. J Mol Neurosci 70, 236–245 (2020). https://doi.org/10.1007/s12031-019-01462-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12031-019-01462-1

Keywords

Navigation