NORMENT, K.G. Jebsen Center for Psychosis Research, Department of Clinical Science, University of Bergen, 5021 Bergen, Norway; Dr. Einar Martens Research Group for Biological Psychiatry, Center for Medical Genetics and Molecular Medicine, Haukeland University Hospital, 5021 Bergen, Norway.
NORMENT, K.G. Jebsen Centre for Psychosis Research, Oslo University Hospital, 0424 Oslo, Norway.
Schizophr Res. 2018 Jul;197:253-260. doi: 10.1016/j.schres.2017.10.042. Epub 2017 Nov 10.
A potential link between increase in total cholesterol and triglycerides and clinical improvement has been observed during antipsychotic drug treatment in chronic schizophrenia patients, possibly due to drug related effects on lipid biosynthesis. We examined whether changes in serum lipids are associated with alleviation of psychosis symptoms after one year of antipsychotic drug treatment in a cohort of first-episode psychosis (FEP) patients.
A total of 132 non-affective antipsychotic-treated FEP patients were included through the Norwegian Thematically Organized Psychosis (TOP) project. Data on antipsychotic usage, serum lipids (total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol and triglycerides (TG)), body mass index (BMI) and clinical state were obtained at baseline and after 12months. The Positive and Negative Syndrome Scale (PANSS) was used to assess psychotic symptoms. Mixed-effects models were employed to examine the relationship between serum lipids and psychotic symptoms while controlling for potential confounders including BMI.
An increase in HDL during one year of antipsychotic treatment was associated with reduction in PANSS negative subscores (B=-0.48, p=0.03). This relationship was not affected by concurrent change in BMI (adjusted HDL: B=-0.54, p=0.02). No significant associations were found between serum lipids, BMI and PANSS positive subscores.
We found that an increase in HDL level during antipsychotic treatment is associated with improvement in negative symptoms in FEP. These findings warrant further investigation to clarify the interaction between lipid pathways and psychosis.
在慢性精神分裂症患者接受抗精神病药物治疗期间,总胆固醇和甘油三酯的增加与临床改善之间存在潜在联系,这可能是由于药物对脂质生物合成的影响。我们研究了在首发精神病(FEP)患者队列中,经过一年的抗精神病药物治疗后,血清脂质的变化是否与精神病症状的缓解有关。
共有 132 名非情感性抗精神病药物治疗的 FEP 患者通过挪威主题组织精神病(TOP)项目被纳入研究。在基线和 12 个月时收集了关于抗精神病药物使用、血清脂质(总胆固醇、高密度脂蛋白(HDL)胆固醇、低密度脂蛋白(LDL)胆固醇和甘油三酯(TG))、体重指数(BMI)和临床状态的数据。阳性和阴性症状量表(PANSS)用于评估精神病症状。采用混合效应模型,在控制 BMI 等潜在混杂因素的情况下,考察了血清脂质与精神病症状之间的关系。
在抗精神病药物治疗的一年中,HDL 的增加与 PANSS 阴性症状评分的降低相关(B=-0.48,p=0.03)。这一关系不受同时 BMI 变化的影响(调整后的 HDL:B=-0.54,p=0.02)。未发现血清脂质、BMI 和 PANSS 阳性症状评分之间存在显著相关性。
我们发现,在抗精神病药物治疗过程中,HDL 水平的升高与 FEP 阴性症状的改善有关。这些发现值得进一步研究,以阐明脂质途径与精神病之间的相互作用。