Investigation of TSPO variants in schizophrenia and antipsychotic treatment outcomes

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

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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 TSPO polymorphisms contribute to interindividual variability in schizophrenia, antipsychotic efficacy and antipsychotic-induced weight gain. We analyzed TSPO polymorphisms in 670 schizophrenia cases and 775 healthy controls. Gene-gene interactions between TSPO and other mitochondrial membrane protein-encoding genes (VDAC1 and ANT1) were explored. Positive findings were evaluated in two independent samples (Munich, n = 300; RUPP, n = 119). TSPO rs6971 was independently associated with antipsychotic-induced weight gain in the discovery (puncor = 0.04) and RUPP samples (p = 3.00 × 10(-3)), and interacted with ANT1 rs10024068 in the discovery (p = 1.15 × 10(-3)) and RUPP samples (p = 2.76 × 10(-4)). Our findings highlight TSPO 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.
ISSN:1462-2416
1744-8042
DOI:10.2217/PGS.14.158