Analysis of schizophrenia‐associated genetic markers in the HLA region as risk factors for tardive dyskinesia

Author:

Wang Ruoyu1,Lu Justin Y.1,Herbert Deanna1,Lieberman Jeffrey A.2,Meltzer Herbert Y.3,Tiwari Arun K.14,Remington Gary145,Kennedy James L.145,Zai Clement C.14567ORCID

Affiliation:

1. Tanenbaum Centre for Pharmacogenetics Campbell Family Mental Health Research Institute Centre for Addiction and Mental Health Toronto Ontario Canada

2. Columbia University New York State Psychiatric Institute New York City New York USA

3. Psychiatry and Behavioral Sciences Pharmacology and Physiology Chemistry of Life Processes Institute Northwestern University Feinberg School of Medicine Chicago Illinois USA

4. Department of Psychiatry University of Toronto Toronto Ontario Canada

5. Institute of Medical Science Faculty of Medicine University of Toronto Toronto Ontario Canada

6. Laboratory Medicine and Pathobiology University of Toronto Toronto Ontario Canada

7. Stanley Center for Psychiatric Research Broad Institute of Harvard and MIT Cambridge Massachusetts USA

Abstract

AbstractObjectivesThe pathology of Tardive Dyskinesia (TD) has yet to be fully understood, but there have been proposed hypotheses for the cause of this condition. Our team previously reported a possible association of TD with the Complement Component C4 gene in the HLA region. In this study, we explored the HLA region further by examining two previously identified schizophrenia‐associated HLA‐region single‐nucleotide polymorphisms (SNPs), namely rs13194504 and rs210133.MethodsThe SNPs rs13194504 and rs210133 were tested for association with the occurrence and severity of TD in a sample of 172 schizophrenia patients who were recruited for four studies from three different clinical sites in Canada and USA.ResultsThe rs13194504 AA genotype was associated with decreased severity for TD as measured by Abnormal Involuntary Movement Scale (AIMS) scores (p = 0.047) but not for TD occurrence. SNP rs210133 was not significantly associated with either TD occurrence or AIMS scores.ConclusionOur findings suggest that the rs13194504 AA genotype may play a role in TD severity, while SNP rs210133 may not have a major role in the risk or severity of TD.

Funder

Brain and Behavior Research Foundation

Centre for Addiction and Mental Health Foundation

Publisher

Wiley

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