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本文引用的文献

1
Head-to-head comparisons of metabolic side effects of second generation antipsychotics in the treatment of schizophrenia: a systematic review and meta-analysis.二代抗精神病药治疗精神分裂症时代谢副作用的头对头比较:系统评价和荟萃分析。
Schizophr Res. 2010 Nov;123(2-3):225-33. doi: 10.1016/j.schres.2010.07.012. Epub 2010 Aug 7.
2
Acute clozapine exposure in vivo induces lipid accumulation and marked sequential changes in the expression of SREBP, PPAR, and LXR target genes in rat liver.体内急性氯氮平暴露可诱导大鼠肝脏脂质蓄积,并使固醇调节元件结合蛋白(SREBP)、过氧化物酶体增殖物激活受体(PPAR)和肝X受体(LXR)靶基因的表达发生显著的顺序性变化。
Psychopharmacology (Berl). 2009 Mar;203(1):73-84. doi: 10.1007/s00213-008-1370-x. Epub 2008 Oct 30.
3
Dyslipidemia independent of body mass in antipsychotic-treated patients under real-life conditions.在现实生活条件下,接受抗精神病药物治疗的患者中,血脂异常与体重无关。
J Clin Psychopharmacol. 2008 Apr;28(2):132-7. doi: 10.1097/JCP.0b013e318166c4f7.
4
Atypical antipsychotic-induced metabolic side effects: insights from receptor-binding profiles.非典型抗精神病药物引起的代谢副作用:来自受体结合谱的见解。
Mol Psychiatry. 2008 Jan;13(1):27-35. doi: 10.1038/sj.mp.4002066. Epub 2007 Sep 11.
5
Changes in serum lipids, independent of weight, are associated with changes in symptoms during long-term clozapine treatment.在长期使用氯氮平治疗期间,血清脂质的变化(与体重无关)与症状变化相关。
J Psychiatry Neurosci. 2007 Sep;32(5):331-8.
6
Physical illness in people with mental disorders.精神障碍患者的躯体疾病
World Psychiatry. 2007 Feb;6(1):3-4.
7
Hyperlipidemia following treatment with antipsychotic medications.抗精神病药物治疗后出现的高脂血症。
Am J Psychiatry. 2006 Oct;163(10):1821-5. doi: 10.1176/ajp.2006.163.10.1821.
8
H1-histamine receptor affinity predicts short-term weight gain for typical and atypical antipsychotic drugs.H1组胺受体亲和力可预测典型和非典型抗精神病药物的短期体重增加。
Neuropsychopharmacology. 2003 Mar;28(3):519-26. doi: 10.1038/sj.npp.1300027.
9
Clozapine, diabetes mellitus, weight gain, and lipid abnormalities: A five-year naturalistic study.氯氮平、糖尿病、体重增加与脂质异常:一项为期五年的自然主义研究。
Am J Psychiatry. 2000 Jun;157(6):975-81. doi: 10.1176/appi.ajp.157.6.975.
10
Novel antipsychotics and new onset diabetes.新型抗精神病药物与新发糖尿病
Biol Psychiatry. 1998 Oct 15;44(8):778-83. doi: 10.1016/s0006-3223(98)00100-0.

氯氮平所致急性高甘油三酯血症

Clozapine-induced Acute Hypertriglyceridemia.

作者信息

Kumar Mitesh, Sidana Ajeet

机构信息

Department of Psychiatry, Government Medical College and Hospital, Chandigarh, India.

出版信息

Indian J Psychol Med. 2017 Sep-Oct;39(5):682-684. doi: 10.4103/0253-7176.217031.

DOI:10.4103/0253-7176.217031
PMID:29200570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5688901/
Abstract

The aim of this study is to highlight the association between the use of clozapine and the early development of hypertriglyceridemia, a condition that substantially increases the risk of cardiovascular events and other medical complications. A 34-year-old female with a background history of schizophrenia presented with acute elevation of serum triglycerides and cholesterol within 2 weeks of starting clozapine. Her metabolic parameters normalized following discontinuation of clozapine. Possible hypotheses for lipid dysregulation with atypical antipsychotics include weight gain, dietary changes, and development of glucose intolerance; however, some other factors may be responsible for this rapid escalation of lipid levels. Lipid and metabolic profiles should be closely monitored in patients receiving clozapine to facilitate early detection and intervention to prevent further health complications.

摘要

本研究的目的是强调使用氯氮平与高甘油三酯血症早期发展之间的关联,高甘油三酯血症会大幅增加心血管事件和其他医学并发症的风险。一名有精神分裂症病史的34岁女性在开始使用氯氮平后2周内出现血清甘油三酯和胆固醇急性升高。停用氯氮平后,她的代谢参数恢复正常。非典型抗精神病药物导致脂质失调的可能假说包括体重增加、饮食变化和葡萄糖不耐受的发展;然而,其他一些因素可能是脂质水平迅速升高的原因。接受氯氮平治疗的患者应密切监测脂质和代谢情况,以便早期发现并进行干预,预防进一步的健康并发症。