Suppr超能文献

精神分裂症共病强迫症状:药理学和遗传学因素的贡献。

Comorbid obsessive-compulsive symptoms in schizophrenia: contributions of pharmacological and genetic factors.

机构信息

Central Institute of Mental Health, Department of Psychiatry and Psychotherapy, Faculty Medicine Mannheim, Heidelberg University Mannheim, Germany.

出版信息

Front Pharmacol. 2013 Aug 9;4:99. doi: 10.3389/fphar.2013.00099. eCollection 2013.

Abstract

A large subgroup of around 25% of schizophrenia patients suffers from obsessive-compulsive symptoms (OCS) and about 12% fulfill the diagnostic criteria of an obsessive-compulsive disorder (OCD). The additional occurrence of OCS is associated with high subjective burden of disease, additional neurocognitive impairment, poorer social and vocational functioning, greater service utilization and high levels of anxiety and depression. Comorbid patients can be assigned to heterogeneous subgroups. One hypothesis assumes that second generation antipsychotics (SGAs), most importantly clozapine, might aggravate or even induce second-onset OCS. Several arguments support this assumption, most importantly the observed chronological order of first psychotic manifestation, start of treatment with clozapine and onset of OCS. In addition, correlations between OCS-severity and dose and serum levels and duration of clozapine treatment hint toward a dose-dependent side effect. It has been hypothesized that genetic risk-factors dispose patients with schizophrenia to develop OCS. One study in a South Korean sample reported associations with polymorphisms in the gene SLC1A1 (solute carrier family 1A1) and SGA-induced OCS. However, this finding could not be replicated in European patients. Preliminary results also suggest an involvement of polymorphisms in the BDNF gene (brain-derived neurotrophic factor) and an interaction between markers of SLC1A1 and the gene DLGAP3 (disc large associated protein 3) as well as GRIN2B (N-methyl-D-aspartate receptor subunit 2B). Further research of well-defined samples, in particular studies investigating possible interactions of genetic risk-constellations and pharmacodynamic properties, are needed to clarify the assumed development of SGA-induced OCS. Results might improve pathogenic concepts and facilitate the definition of at risk populations, early detection and monitoring of OCS as well as multimodal therapeutic interventions.

摘要

大约 25%的精神分裂症患者存在强迫症状(OCS),约 12%符合强迫症(OCD)的诊断标准。OCS 的额外发生与疾病的主观负担增加、认知功能进一步受损、社会和职业功能更差、更多的服务利用以及更高的焦虑和抑郁水平有关。合并症患者可分为异质亚组。一种假设认为,第二代抗精神病药物(SGAs),尤其是氯氮平,可能会加重甚至诱发继发 OCS。有几个论据支持这一假设,最重要的是首次精神病发作的时间顺序、氯氮平治疗的开始和 OCS 的发作。此外,OCS 严重程度与氯氮平剂量和血清水平以及治疗持续时间之间的相关性表明存在剂量依赖性的副作用。有人假设,遗传风险因素使精神分裂症患者易发生 OCS。一项在韩国样本中的研究报告了 SLC1A1(溶质载体家族 1A1)基因和 SGA 诱导的 OCS 多态性的相关性。然而,这一发现在欧洲患者中未能得到复制。初步结果还表明,BDNF 基因(脑源性神经营养因子)多态性的参与以及 SLC1A1 标志物与基因 DLGAP3(Disc Large Associated Protein 3)和 GRIN2B(N-甲基-D-天冬氨酸受体亚单位 2B)之间的相互作用也可能参与其中。需要对定义明确的样本进行进一步研究,特别是研究遗传风险因素与药效学特性之间可能存在的相互作用,以阐明假设的 SGA 诱导 OCS 的发展。结果可能会改善发病机制概念,并有助于定义高危人群、早期发现和监测 OCS 以及多模式治疗干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9939/3738863/dec9c31e5e70/fphar-04-00099-g0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验