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本文引用的文献

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Healthy Adolescent Performance With Standardized Scoring Tables for the MATRICS Consensus Cognitive Battery: A Multisite Study.基于 MATRICS 共识认知电池标准化评分表的健康青少年表现:一项多中心研究。
Schizophr Bull. 2019 Jun 18;45(4):773-783. doi: 10.1093/schbul/sby131.
2
BDNF and TrkB Mediate the Improvement from Chronic Stress-induced Spatial Memory Deficits and CA3 Dendritic Retraction.脑源性神经营养因子和 TrkB 介导慢性应激引起的空间记忆缺陷和 CA3 树突回缩的改善。
Neuroscience. 2018 Sep 15;388:330-346. doi: 10.1016/j.neuroscience.2018.07.049. Epub 2018 Aug 2.
3
White matter changes in treatment refractory schizophrenia: Does cognitive control and myelination matter?治疗抵抗性精神分裂症的脑白质变化:认知控制和髓鞘形成是否重要?
Neuroimage Clin. 2018 Jan 28;18:186-191. doi: 10.1016/j.nicl.2018.01.010. eCollection 2018.
4
Chronic atypical antipsychotics, but not haloperidol, increase neurogenesis in the hippocampus of adult mouse.慢性非典型抗精神病药物,而非氟哌啶醇,可增加成年小鼠海马体中的神经发生。
Brain Res. 2017 Dec 1;1676:77-82. doi: 10.1016/j.brainres.2017.09.006. Epub 2017 Sep 9.
5
Volumetric and morphological characteristics of the hippocampus are associated with progression to schizophrenia in patients with first-episode psychosis.海马体的容积和形态特征与首发精神病患者向精神分裂症的进展有关。
Eur Psychiatry. 2017 Sep;45:1-5. doi: 10.1016/j.eurpsy.2017.06.006. Epub 2017 Jul 5.
6
Clinical correlates of hippocampus volume and shape in antipsychotic-naïve schizophrenia.抗精神病药初治精神分裂症患者海马体积和形态的临床相关性。
Psychiatry Res Neuroimaging. 2017 May 30;263:93-102. doi: 10.1016/j.pscychresns.2017.03.014. Epub 2017 Mar 29.
7
Hippocampal-prefrontal connectivity as a translational phenotype for schizophrenia.海马-前额叶连接作为精神分裂症的转化表型。
Eur Neuropsychopharmacol. 2017 Feb;27(2):93-106. doi: 10.1016/j.euroneuro.2016.12.007. Epub 2017 Jan 12.
8
Treatment-Resistant Schizophrenia: Treatment Response and Resistance in Psychosis (TRRIP) Working Group Consensus Guidelines on Diagnosis and Terminology.难治性精神分裂症:精神病治疗反应与抵抗(TRRIP)工作组关于诊断和术语的共识指南
Am J Psychiatry. 2017 Mar 1;174(3):216-229. doi: 10.1176/appi.ajp.2016.16050503. Epub 2016 Dec 6.
9
First and second generation antipsychotics differentially affect structural and functional properties of rat hippocampal neuron synapses.第一代和第二代抗精神病药物对大鼠海马神经元突触的结构和功能特性有不同影响。
Neuroscience. 2016 Nov 19;337:117-130. doi: 10.1016/j.neuroscience.2016.08.055. Epub 2016 Sep 8.
10
Brain-imaging studies of treatment-resistant schizophrenia: a systematic review.难治性精神分裂症的脑成像研究:一项系统综述
Lancet Psychiatry. 2016 May;3(5):451-63. doi: 10.1016/S2215-0366(15)00540-4. Epub 2016 Mar 4.

难治性精神分裂症患者的海马体与认知领域缺陷:与匹配的治疗反应性患者及健康对照的比较

Hippocampus and cognitive domain deficits in treatment-resistant schizophrenia: A comparison with matched treatment-responsive patients and healthy controls.

作者信息

Huang Junchao, Zhu Yu, Fan Fengmei, Chen Song, Hong Yuan, Cui Yimin, Luo Xingguang, Tan Shuping, Wang Zhiren, Shang Lan, Yuan Ying, Zhang Jianxin, Yang Fude, Li Chiang-Shan R, Rowland Laura M, Kochunov Peter, Zhang Fengyu, Hong L Elliot, Tan Yunlong

机构信息

Peking University HuiLongGuan Clinical Medical School, Beijing Huilongguan Hospital, Beijing, P. R. China.

Department of Epidemiology and Biostatistics, University of South Carolina Arnold School of Public Health, Columbia, SC, United States.

出版信息

Psychiatry Res Neuroimaging. 2020 Feb 4;297:111043. doi: 10.1016/j.pscychresns.2020.111043.

DOI:10.1016/j.pscychresns.2020.111043
PMID:32062167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7490244/
Abstract

Some patients with schizophrenia do not respond to pharmacotherapy. More severe cognitive dysfunctions have been associated with treatment-resistant schizophrenia (TRS). This study examines cognitive functions and hippocampal volumes in 43 patients with TRS and compared them to 43 treatment-responsive patients (NTRS), matched on age, sex and education, as well as 53 healthy controls (HC). The results showed that there were significant deficits in all domains of cognition and hippocampal volumes in TRS as compared to HC group. However, TRS specific deficits, as indicated by comparisons with matched NTRS, were limited to poorer performance in working memory (p = 0.003) and smaller total hippocampal volume (p = 0.01). Logistic regression analysis showed that working memory deficits [OR 0.94 (95% CI 0.89-0.98), p = 0.005] and smaller hippocampal volume [OR 0.89 (95% CI 0.81-0.97), p = 0.01], but not their interactions (p = 0.68), contributed to higher risk of treatment resistance. The findings suggest that treatment-resistance to currently available antipsychotic medications may not be due to global cognitive deficits in these patients, but be associated with specific deficits in working memory and hippocampus deficits in the subgroup of schizophrenia.

摘要

一些精神分裂症患者对药物治疗没有反应。更严重的认知功能障碍与难治性精神分裂症(TRS)有关。本研究调查了43例TRS患者的认知功能和海马体积,并将他们与43例年龄、性别和教育程度相匹配的治疗反应性患者(NTRS)以及53名健康对照者(HC)进行比较。结果显示,与HC组相比,TRS患者在所有认知领域和海马体积方面均存在显著缺陷。然而,与匹配的NTRS组相比,TRS特有的缺陷仅限于工作记忆表现较差(p = 0.003)和海马总体积较小(p = 0.01)。逻辑回归分析表明,工作记忆缺陷[比值比0.94(95%置信区间0.89 - 0.98),p = 0.005]和较小的海马体积[比值比0.89(95%置信区间0.81 - 0.97),p = 0.01],而非它们的相互作用(p = 0.68),导致了更高的治疗抵抗风险。研究结果表明,对目前可用抗精神病药物的治疗抵抗可能并非由于这些患者的整体认知缺陷,而是与精神分裂症亚组中工作记忆的特定缺陷和海马缺陷有关。