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HLA typing using genome wide data reveals susceptibility types for infections in a psychiatric disease enriched sample.
Parks, Samuel; Avramopoulos, Dimitrios; Mulle, Jennifer; McGrath, John; Wang, Ruihua; Goes, Fernando S; Conneely, Karen; Ruczinski, Ingo; Yolken, Robert; Pulver, Ann E; Pearce, Brad D.
Afiliação
  • Parks S; Dept. of Epidemiology, Rollins School of Public Health, USA.
  • Avramopoulos D; Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Mulle J; Department of Human Genetics, Emory University, Atlanta, GA, USA.
  • McGrath J; Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Wang R; McKusick Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Goes FS; Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Conneely K; Department of Human Genetics, Emory University, Atlanta, GA, USA.
  • Ruczinski I; Bloomberg School of Public Heath, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Yolken R; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Pulver AE; Bloomberg School of Public Heath, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Pearce BD; Dept. of Epidemiology, Rollins School of Public Health, USA. Electronic address: bpearce@emory.edu.
Brain Behav Immun ; 70: 203-213, 2018 05.
Article em En | MEDLINE | ID: mdl-29574260
ABSTRACT

BACKGROUND:

The infections Toxoplasma gondii (T. gondii), cytomegalovirus, and Herpes Simplex Virus Type 1 (HSV1) are common persistent infections that have been associated with schizophrenia and bipolar disorder. The major histocompatibility complex (MHC, termed HLA in humans) region has been implicated in these infections and these mental illnesses. The interplay of MHC genetics, mental illness, and infection has not been systematically examined in previous research.

METHODS:

In a cohort of 1636 individuals, we used genome-wide association data to impute 7 HLA types (A, B, C, DRB1, DQA1, DQB1, DPB1), and combined this data with serology data for these infections. We used regression analysis to assess the association between HLA alleles, infections (individually and collectively), and mental disorder status (schizophrenia, bipolar disorder, controls).

RESULTS:

After Bonferroni correction for multiple comparisons, HLA C∗0701 was associated with increased HSV1 infection among mentally healthy controls (OR 3.4, p = 0.0007) but not in the schizophrenia or bipolar groups (P > 0.05). For the multiple infection outcome, HLA B∗ 3801 and HLA C∗1203 were protective in the healthy controls (OR ≈ 0.4) but did not have a statistically-significant effect in the schizophrenia or bipolar groups. T. gondii had several nominally-significant positive associations, including the haplotypes HLA DRB∗0301 ∼ HLA DQA∗0501 ∼ HLA DQB∗0201 and HLA B∗0801 ∼ HLA C∗0701.

CONCLUSIONS:

We identified HLA types that showed strong and significant associations with neurotropic infections. Since some of these associations depended on mental illness status, the engagement of HLA-related pathways may be altered in schizophrenia due to immunogenetic differences or exposure history.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Transtorno Bipolar / Antígenos HLA Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Transtorno Bipolar / Antígenos HLA Idioma: En Ano de publicação: 2018 Tipo de documento: Article