Genetic Association Between NRXN3 Variants (rs12879016 & rs2270964) and Risk of Schizophrenia (SCZ)

Authors

  • Abdulmajeed Saleh Alzahrani, Wael Salah Alhazmi, Mohammad Talal Dandini, Maher Mohammed Alsubhi, Mohammed Ali Mohammed Alghamdi
  • Rayid Shabib Mofareh Alotaibi, Marzouq Mohsen Alnefaie, Faris Khader Hasan Alhassani, Fahad Mansour Alhulayfi, Mutlaq Dakhel Fawaz Almalki

DOI:

https://doi.org/10.63278/jicrcr.vi.963

Abstract

There hasn't been much study on the link between schizophrenia (SCZ) and neurexin 3 (NRXN3) genetic variations. The first association study of the NRXN3 rs12879016 G>C,T and rs2270964 C>A,T single-nucleotide polymorphisms (SNP)in a Saudi population is shown here.
We used real-time PCR to assess the genotypes for the polymorphisms in one hundred seventeen patients with SCZ and Seventy-eight healthy controls. We used endonuclease digestion of amplified genomic DNA to establish the genotypes for the polymorphisms in 117 patients with DSM-IV and PANSS (Positive and Negative Syndrome Scale) evaluations of schizophrenia and 78 healthy controls.
We aim to find out if there is a relation between NRXN3 variations (rs12879016 and rs2270964) and susceptibility of developing SCZ in a Saudi population.
We hypothesis that SCZ can be related to patients with NRXN3 variations (rs12879016 / rs2270964) among Saudi population.
According to our result both rs12879016 and rs2270964 polymorphisms were shown to be unrelated to the risk of schizophrenia.

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Published

2024-09-15

How to Cite

Abdulmajeed Saleh Alzahrani, Wael Salah Alhazmi, Mohammad Talal Dandini, Maher Mohammed Alsubhi, Mohammed Ali Mohammed Alghamdi, & Rayid Shabib Mofareh Alotaibi, Marzouq Mohsen Alnefaie, Faris Khader Hasan Alhassani, Fahad Mansour Alhulayfi, Mutlaq Dakhel Fawaz Almalki. (2024). Genetic Association Between NRXN3 Variants (rs12879016 & rs2270964) and Risk of Schizophrenia (SCZ). Journal of International Crisis and Risk Communication Research , 2109–2138. https://doi.org/10.63278/jicrcr.vi.963

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