Frontiers in Genetics ( IF 2.8 ) Pub Date : 2020-07-09 , DOI: 10.3389/fgene.2020.00832 Dandan Wang 1 , Wei Tang 2 , Junxiong Zhao 3 , Weixing Fan 3 , Yi Zhang 1 , Chen Zhang 1
Depressive symptoms could be considered a mutual manifestation of major depressive disorder and schizophrenia. Rs3758391 is a functional locus of Sirtuin (SIRT1) involving depression etiology. In this study, we hypothesized that the SIRT1 SNP rs3758391 might be a hazard for schizophrenia pathogenesis, especially related to the appearance of depressive symptoms. We recruited 723 healthy controls and 715 schizophrenia patients, the occurrence of psychotic and depressive symptoms was evaluated by Calgary Depression Scale (CDSS) and PANSS. Meanwhile, qt-PCR was used to detect the mRNA levels of SIRT1 in peripheral blood of 197 olanzapine monotherapy schizophrenia patients. 45.6% of schizophrenia patients had depressive symptoms. In the patient group, mRNA levels of patients with depressive symptoms were significantly lower than those without depressive symptoms (
中文翻译:
SIRT1变异对精神分裂症和抑郁症状风险的影响的综合分析。
抑郁症状可以被认为是主要抑郁症和精神分裂症的共同表现。Rs3758391是Sirtuin(SIRT1)的一个功能位点,涉及抑郁症的病因。在这项研究中,我们假设SIRT1 SNP rs3758391可能是精神分裂症发病的危险因素,尤其与抑郁症状的出现有关。我们招募了723名健康对照者和715名精神分裂症患者,通过卡尔加里抑郁量表(CDSS)和PANSS评估了精神病和抑郁症状的发生。同时,采用qt-PCR检测197例奥氮平单药治疗精神分裂症患者外周血SIRT1的mRNA水平。45.6%的精神分裂症患者有抑郁症状。在患者组中,