Investigation of

TSPO is a neuroinflammatory biomarker and emerging therapeutic target in psychiatric disorders. We evaluated whether polymorphisms contribute to interindividual variability in schizophrenia, antipsychotic efficacy and antipsychotic-induced weight gain. We analyzed polymorphisms in 670 schizophrenia...

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Veröffentlicht in:Pharmacogenomics 2015-01, Vol.16 (1), p.5-22
Hauptverfasser: Pouget, Jennie G, Gonçalves, Vanessa F, Nurmi, Erika L, P Laughlin, Christopher, Mallya, Karyn S, McCracken, James T, Aman, Michael G, McDougle, Christopher J, Scahill, Lawrence, Misener, Virginia L, Tiwari, Arun K, Zai, Clement C, Brandl, Eva J, Felsky, Daniel, Leung, Amy Q, Lieberman, Jeffrey A, Meltzer, Herbert Y, Potkin, Steven G, Niedling, Charlotte, Steimer, Werner, Leucht, Stefan, Knight, Jo, Müller, Daniel J, Kennedy, James L
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Sprache:eng
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Zusammenfassung:TSPO is a neuroinflammatory biomarker and emerging therapeutic target in psychiatric disorders. We evaluated whether polymorphisms contribute to interindividual variability in schizophrenia, antipsychotic efficacy and antipsychotic-induced weight gain. We analyzed polymorphisms in 670 schizophrenia cases and 775 healthy controls. Gene-gene interactions between and other mitochondrial membrane protein-encoding genes ( and ) were explored. Positive findings were evaluated in two independent samples (Munich, n = 300; RUPP, n = 119). rs6971 was independently associated with antipsychotic-induced weight gain in the discovery (p = 0.04) and RUPP samples (p = 3.00 × 10 ), and interacted with rs10024068 in the discovery (p = 1.15 × 10 ) and RUPP samples (p = 2.76 × 10 ). Our findings highlight as a candidate for future investigations of antipsychotic-induced weight gain, and support the involvement of mitochondrial membrane components in this serious treatment side effect. Original submitted 20 August 2014; Revision submitted 3 November 2014
ISSN:1462-2416
1744-8042
DOI:10.2217/pgs.14.158