Pregled bibliografske jedinice broj: 666200
Acute extrapyramidal side effects in haloperidol-treated patients with schizophrenia: no association with serotonergic 5-HT2A and 5-HT2C receptor gene polymorphisms
Acute extrapyramidal side effects in haloperidol-treated patients with schizophrenia: no association with serotonergic 5-HT2A and 5-HT2C receptor gene polymorphisms // Pharmacogenomics and Personalised Medicine in Psychiatry
Jeruzalem, Izrael, 2013. (poster, međunarodna recenzija, sažetak, ostalo)
CROSBI ID: 666200 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Acute extrapyramidal side effects in haloperidol-treated patients with schizophrenia: no association with serotonergic 5-HT2A and 5-HT2C receptor gene polymorphisms
Autori
Muck-Šeler, Dorotea ; Mustapić, Maja ; Živković, Maja ; Mihaljević Peleš, Alma ; Švob Štrac, Dubravka ; Šagud, Marina ; Pivac, Nela
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Skup
Pharmacogenomics and Personalised Medicine in Psychiatry
Mjesto i datum
Jeruzalem, Izrael, 21.04.2013. - 23.04.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Serotonergic receptors; gene; extrapyramidal side effects; haloperidol
Sažetak
Literature data suggest that both dopaminergic and serotonergic system and their receptors are involved in the development of extrapyramidal side effects (EPS) in schizophrenic patients treated with first generation antipsychotic drug like haloperidol. There are limited data that gene variants of serotonergic 5-HT2A and 5-HT2C receptor could be the risk factors for the incidence of EPS. The aim of the study was to determine 5-HT2A and 5-HT2C receptor gene polymorphisms and the occurrence of EPS in schizophrenic patients (DSM-IV criteria) after 2 weeks monotherapy with haloperidol (15 mg/day). The hypothesis was that there is a genetic predisposition for the development of EPS after acute treatment with haloperidol. The severity of EPS was evaluated using Simpson Angus Rating Scale for Extrapyramidal Side Effects, Barnes Akathisia Rating Scale and Extrapyramidal Symptom Rating Scale. Genomic DNA was extracted from whole blood and genotyping of 5-HT2A (102T/C ; rs6313) and 5-HT2C (-759C/T ; rs3813929) receptors was performed using TaqMan based commercial kits. After treatment with haloperidol, 60% of patients developed EPS. Akathisia, acute dystonia and dyskinesia were observed in 29%, 21% and 44% of patients, respectively. There was no significant difference in genotype and allele frequencies of 5-HT2A or 5-HT2C polymorphisms between patients with or without EPS and their particular symptoms. The results did not confirm the hypothesis that 5-HT2A and 5-HT2C variants might be the risk factors for haloperidol-induced EPS in schizophrenic patients. Additional genetic studies and haplotype analysis are necessary to determine the role of serotonergic system and its genes in development of EPS.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
098-0000000-2448 - Stres, GABA-A receptori i mehanizmi djelovanja neuropsihofarmaka (Švob Štrac, Dubravka, MZOS ) ( CroRIS)
098-0982522-2455 - Molekularna podloga i liječenje psihijatrijskih i stresom izazvanih poremećaja (Pivac, Nela, MZOS ) ( CroRIS)
098-0982522-2457 - Farmakogenomika i proteomika serotoninskog i kateholaminskog sustava (Muck-Šeler, Dorotea, MZOS ) ( CroRIS)
108-1083509-3513 - Farmakogenetska varijabilnost u psihijatrijskih bolesnika (Mihaljević-Peleš, Alma, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb
Profili:
Alma Mihaljević-Peleš
(autor)
Marina Šagud
(autor)
Dubravka Švob Štrac
(autor)
Dorotea Muck-Šeler
(autor)
Nela Pivac
(autor)
Maja Mustapić
(autor)