Pavăl Denis, Nemeș Bogdan, Rusu Răzvan L, Dronca Eleonora
Department of Molecular Sciences, Faculty of Medicine, Iuliu Hațieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Third Psychiatry Clinic, Emergency County Hospital, Cluj-Napoca, Romania.
Clin Psychopharmacol Neurosci. 2018 Feb 28;16(1):32-38. doi: 10.9758/cpn.2018.16.1.32.
Recent studies suggest a possible involvement of low paraoxonase 1 (PON1) enzyme activities in the association between schizophrenia, treatment with atypical antipsychotics and increased cardiovascular (CVD) risk. In the present study, we aimed at investigating the PON1 status in a group of schizophrenic patients treated with either olanzapine or other antipsychotic, as compared to a group of healthy control participants.
We assessed the arylesterase (AREase) and paraoxonase (POase) activities of PON1, as well as three common polymorphisms of gene (Q192R, L55M, -108C>T).
We found significantly lower (-13.3%) AREase activity in schizophrenic patients, along with significantly lower (-18.2%) POase activity in olanzapine-treated patients with QQ genotype. Furthermore, we found a significant difference between groups in L55M polymorphism distribution, whereas Q192R and -108C>T polymorphisms distributions were similar.
We identified the olanzapine-treated patients with QQ genotype as having the lowest PON1 (POase) activity, providing a possible way of identifying schizophrenic patients exposed to the greatest risk of CVD.
近期研究表明,对氧磷酶1(PON1)酶活性降低可能与精神分裂症、非典型抗精神病药物治疗及心血管疾病(CVD)风险增加之间存在关联。在本研究中,我们旨在调查一组接受奥氮平或其他抗精神病药物治疗的精神分裂症患者与一组健康对照参与者相比的PON1状态。
我们评估了PON1的芳基酯酶(AREase)和对氧磷酶(POase)活性,以及该基因的三种常见多态性(Q192R、L55M、-108C>T)。
我们发现精神分裂症患者的AREase活性显著降低(-13.3%),在QQ基因型的奥氮平治疗患者中POase活性也显著降低(-18.2%)。此外,我们发现L55M多态性分布在各组之间存在显著差异,而Q192R和-108C>T多态性分布相似。
我们确定QQ基因型的奥氮平治疗患者的PON1(POase)活性最低,这为识别面临最大CVD风险的精神分裂症患者提供了一种可能的方法。