The inflammasome NLRP12 is associated with both depression and coronary artery disease in Vietnam veterans

Psychiatry Res. 2018 Dec:270:775-779. doi: 10.1016/j.psychres.2018.10.051. Epub 2018 Oct 27.

Abstract

Several studies have established that Major depressive disorder is associated with excess inflammation with an elevation of both pro and anti-inflammatory cytokines in major depressive disorder. In addition, individuals with major depressive disorder are at higher risk of developing coronary artery disease. The role of innate immunity and NFκB-mediated inflammation in depression and its increased association with coronary artery disease is yet to be fully elucidated. Polymorphisms in the Nucleotide-Binding Oligomerization Domain, Leucine Rich Repeat and Pyrin Domain Containing 12 (NLRP12), are associated with depression and coronary artery disease in trauma exposed individuals. In a cohort of Vietnam War veterans (n = 299) NLRP12 polymorphisms were analysed for association with depression and coronary calcium scores. The NLRP12 polymorphism, rs34436714 was associated with a higher DASS21 Score for depression (p = 0.037). NLRP12 polymorphisms rs34971363 and rs6509825 (p = 0.022 and p = 0.020) were associated with raised coronary calcium score. To our knowledge, this is the first time rs34436714 has been investigated in Vietnam veterans identifying AC as a risk genotype for depression in Caucasian cohorts. It is also the first time the rs34971363 (CG) and rs6509825 (CT) genotype have been associated with raised coronary calcium score.

Keywords: Coronary artery disease; Depression; NLRP12; rs34436714; rs34971363; rs6509825.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cohort Studies
  • Combat Disorders / genetics*
  • Combat Disorders / immunology
  • Coronary Artery Disease / genetics*
  • Coronary Artery Disease / immunology
  • Depressive Disorder, Major / genetics*
  • Depressive Disorder, Major / immunology
  • Genotype*
  • Humans
  • Immunity, Innate / genetics
  • Immunity, Innate / immunology
  • Inflammasomes / genetics*
  • Inflammasomes / immunology
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Male
  • NF-kappa B / genetics
  • Polymorphism, Genetic
  • Risk Factors
  • Veterans*

Substances

  • Inflammasomes
  • Intracellular Signaling Peptides and Proteins
  • NF-kappa B
  • NLRP12 protein, human