A neuropeptide Y variant (rs16139) associated with major depressive disorder in replicate samples from Chinese Han population

PLoS One. 2013;8(2):e57042. doi: 10.1371/journal.pone.0057042. Epub 2013 Feb 27.

Abstract

Objective: This study aimed to investigate the single nucleotide polymorphisms (SNPs) of neuropeptide Y (NPY) and major depressive disorder (MDD) in Chinese Han population.

Design: Prospective and randomized studies were carried out.

Patients: A total of 700 patients (324 male and 376 female; mean age = 40±14.9 years) with depression who met the diagnostic criteria of Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) and 673 healthy controls (313 male and 360 female; mean age = 41.9±17.2 years) were used to investigate the relationship between SNPs of NPY and the pathogenesis of MDD. A total of 417 patients (195 male and 202 female; mean age = 36±14.2 years) diagnosed with MDD and 314 healthy controls (153 male and 161 female; mean age = 37.9±14.2 years) from Chinese Han population were used to verify the relationship between SNPs of NPY and the pathogenesis of MDD.

Intervention and outcome: Ligase detection reactions were performed to detect the SNP sites of NPY. A series of statistical methods was carried out to investigate the correlation between the NPY gene SNP and MDD.

Results: Statistical analysis showed a significant correlation between the SNP sites rs16139 in NPY and the morbidity of depression. Patients with MDD have a lower frequency of A-allele in rs16139 in replicate samples from Chinese Han population. However, the frequency varied between male and female patients.

Conclusion: The gene polymorphism loci rs16139 was closely related to MDD in Chinese Han population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Asian People / genetics*
  • Case-Control Studies
  • China
  • Depressive Disorder, Major / genetics*
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Neuropeptide Y / genetics*
  • Polymorphism, Single Nucleotide*

Substances

  • Neuropeptide Y

Grants and funding

This work was funded by the Beijing Municipal Natural Science Foundation of China (7091002), and the National Science and Technology Support Program of China (2007BAI17B05). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.