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Pregled bibliografske jedinice broj: 945494

Haplotypic and genotypic association of catechol-O- methyltransferase rs4680 and rs4818 polymorphisms and treatment resistance in schizophrenia


Šagud, Marina; Tudor, Lucija; Nikolac Perković, Matea; Uzun, Suzana; Živković, Maja; Konjevod, Marcela; Kozumplik, Oliver; Vuksan Ćusa, Bjanka; Švob Štrac, Dubravka; Mihaljević-Peleš, Alma et al.
Haplotypic and genotypic association of catechol-O- methyltransferase rs4680 and rs4818 polymorphisms and treatment resistance in schizophrenia // Frontiers in Pharmacology, 9 (2018), 705, 14 doi:10.3389/fphar.2018.00705 (međunarodna recenzija, članak, znanstveni)


Naslov
Haplotypic and genotypic association of catechol-O- methyltransferase rs4680 and rs4818 polymorphisms and treatment resistance in schizophrenia

Autori
Šagud, Marina ; Tudor, Lucija ; Nikolac Perković, Matea ; Uzun, Suzana ; Živković, Maja ; Konjevod, Marcela ; Kozumplik, Oliver ; Vuksan Ćusa, Bjanka ; Švob Štrac, Dubravka ; Mihaljević-Peleš, Alma ; Radoš, Iva ; Mimica, Ninoslav ; Nedić Erjavec, Gordana ; Pivac, Nela

Izvornik
Frontiers in Pharmacology (1663-9812) 9 (2018); 705, 14

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Treatment-resistant schizophrenia ; COMT rs4680 polymorphism ; COMT rs4818 polymorphism ; COMT rs4680 and rs4818 haplotype ; sex-specific association

Sažetak
Treatment-resistant schizophrenia (TRS) continues to be a challenge. It was related to different factors, including alterations in the activity of brain dopaminergic system, which could be influenced by the dopamine-degrading enzyme, catechol-O-methyl-transferase (COMT). Variants of the COMT gene have been extensively studied as risk factors for schizophrenia ; however, their association with TRS has been poorly investigated. The aim of the present study was to determine the haplotypic and genotypic association of COMT rs4680 and rs4818 polymorphisms with the presence of TRS. Overall, 931 Caucasian patients diagnosed with schizophrenia (386 females and 585 males) were included, while 270 participants met the criteria for TRS. In males, no significant haplotypic and genotypic associations between COMT rs4680 and rs4818 polymorphisms and TRS were detected. However, genotypic analyses demonstrated higher frequency of COMT rs4680 AA genotype carriers compared to G- allele carriers (p=0.033) and higher frequency of COMT rs4818 CC genotype carriers than G-allele carriers (p=0.014) in females with TRS. Haplotype analyses confirmed that the presence of the G allele in females was associated with lower risk of TRS. In women with TRS, the high activity G-G/G-G haplotype was rare, while carriers of other haplotypes were overrepresented (p=0.009). Such associations of COMT rs4680 and rs4818 high-activity (G variants), as well as G- G/G-G haplotype, with the lower risk of TRS in females, but not in males, suggest significant, but sex-specific influence of COMT variants on the development of treatment-resistance in patients with schizophrenia. However, due to relatively low number of females, those findings require replication in a larger sample.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb,
Klinika za psihijatriju Vrapče,
Klinički bolnički centar Zagreb,
Medicinski fakultet, Osijek,
Sveučilište u Zagrebu,
Sveučilište J. J. Strossmayera u Osijeku

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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