Association between gene polymorphism and depression in Parkinson's disease: A case-control study

J Neurol Sci. 2017 Apr 15:375:231-234. doi: 10.1016/j.jns.2017.02.001. Epub 2017 Feb 3.

Abstract

Objective: To investigate possible associations of Parkinson's disease (PD) with polymorphism in depression-related genes and in the alpha-synuclein (SNCA) gene.

Methods: A consecutive series of patients with PD were divided into those with depression and those without it. Patients (330) were genotyped at four single-nucleotide polymorphisms (SNPs) in four genes previously associated with depression, as well as four SNPs in the PD-associated SNCA gene.

Results: Of 330 patients, 125 (37.9%) had depression and 205 (62.1%) did not. Univariate analysis revealed significant differences between the two groups in minor allele frequency at the SNP rs1545843 in the SLC6A15 gene (p<0.05), as well as in frequencies of genotypes and minor alleles at rs78162420 in the TPH2 gene (all p<0.05). Logistic regression identified the following risk factors for depression among patients with PD: Hoehn and Yahr stage>2 (OR 1.759, 95%CI 1.035-2.989, p=0.037), AA genotype at rs1545843 (OR 1.866, 95%CI 1.017-3.426, p=0.044), and AC genotype at rs78162420 (OR 5.036, 95%CI 1.451-17.484, p=0.011).

Conclusions: Among patients with PD, depression is associated with polymorphism at rs78162420 and rs1545843, both previously linked with depression. Our results may help clarify the pathogenesis of depression in PD.

Keywords: Association studies in genetics; Depression; Parkinson's disease; rs1545843; rs78162420.

MeSH terms

  • Aged
  • Amino Acid Transport Systems, Neutral / genetics*
  • Asian People
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Case-Control Studies
  • Depression / etiology
  • Depression / genetics*
  • Female
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Humans
  • Logistic Models
  • Male
  • Middle Aged
  • Nerve Tissue Proteins / genetics*
  • Parkinson Disease / complications
  • Parkinson Disease / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • Tryptophan Hydroxylase / genetics*
  • alpha-Synuclein / genetics

Substances

  • Amino Acid Transport Systems, Neutral
  • Basic-Leucine Zipper Transcription Factors
  • Nerve Tissue Proteins
  • SLC6A15 protein, human
  • TEF protein, human
  • alpha-Synuclein
  • TPH2 protein, human
  • Tryptophan Hydroxylase