Meta-analyses of clozapine, norclozapine levels and their ratio across three genome wide association studies

dc.contributor.authorRask, Susanna Maria
dc.contributor.authorSolismaa, Anssi
dc.contributor.authorAhola-Olli, Ari
dc.contributor.authorMolden, Espen
dc.contributor.authorO’Connell, Kevin Sean
dc.contributor.authorLyytikäinen, Leo-Pekka
dc.contributor.authorMononen, Nina
dc.contributor.authorLehtimäki, Terho
dc.contributor.authorKampman, Olli
dc.contributor.organizationfi=psykiatria|en=Psychiatry|
dc.contributor.organization-code1.2.246.10.2458963.20.16217176722
dc.converis.publication-id504988799
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/504988799
dc.date.accessioned2026-01-21T14:48:41Z
dc.date.available2026-01-21T14:48:41Z
dc.description.abstract<p>Recent genome wide association studies (GWAS) found associations between clozapine serum levels and single nucleotide polymorphisms (SNP) in intragenic region between cytochrome P450 1A1 (<em>CYP1A1</em>) and <em>CYP1A2</em> and nuclear factor 1B (<em>NFIB</em>). The aim of this study was to perform another GWAS of polymorphisms associated with the serum levels of clozapine and norclozapine, their ratios, and to perform meta-analyses with two previous GWAS. Finnish clozapine patients (n = 170) with known smoking habits were genotyped. GWAS was performed with clozapine concentration/dose ratio (C/D), norclozapine C/D and clozapine/norclozapine-ratio as phenotypes, adjusting for age, sex and first four genetic principal components, and additionally for smoking and valproate use. The two other patient populations were from the British CLOZUK2 study (n = 2989) and Norwegian Diakonhjemmet Hospital study (n = 484). In the three population (n = 3643) meta-analyses the top SNP associated with the clozapine C/D ratio was rs2472297, located between the <em>CYP1A1</em> and <em>CYP1A2</em> genes. For the norclozapine C/D ratio, an association signal was found near uridine-5´-diphospho-glucunorosyltransferase (<em>UGT</em>) <em>UGT2B10</em> gene. Additionally, rs3732218, an intron variant in the <em>UGT1A</em> family gene complex, was associated with norclozapine C/D. Lead SNP associated with the clozapine/norclozapine ratio was rs6827692, an intron variant near <em>UGT2B7</em> gene. In the two population meta-analyses (n = 654) adjusting for smoking and valproate use, the <em>UGT2B10</em> intron variant rs835309 was associated with the clozapine/norclozapine ratio. We suggest a <em>UGT2B10</em> missense SNP rs61750900, in perfect linkage disequilibrium with <em>UGT2B10</em> rs835309, as the probable causal variant. Our study confirms and extends the number of genetic variants affecting clozapine and norclozapine metabolism.<br></p>
dc.identifier.eissn2158-3188
dc.identifier.olddbid213731
dc.identifier.oldhandle10024/196749
dc.identifier.urihttps://www.utupub.fi/handle/11111/55810
dc.identifier.urlhttps://doi.org/10.1038/s41398-025-03649-0
dc.identifier.urnURN:NBN:fi-fe202601216973
dc.language.isoen
dc.okm.affiliatedauthorKampman, Olli
dc.okm.discipline3124 Neurology and psychiatryen_GB
dc.okm.discipline3124 Neurologia ja psykiatriafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSpringer Nature
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumber431
dc.relation.doi10.1038/s41398-025-03649-0
dc.relation.ispartofjournalTranslational Psychiatry
dc.relation.volume15
dc.source.identifierhttps://www.utupub.fi/handle/10024/196749
dc.titleMeta-analyses of clozapine, norclozapine levels and their ratio across three genome wide association studies
dc.year.issued2025

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