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皮质[H]哌仑西平结合水平较低可定义为认知缺陷较轻的老年精神分裂症亚组人群。

Lower levels of cortical [H]pirenzepine binding to postmortem tissue defines a sub-group of older people with schizophrenia with less severe cognitive deficits.

机构信息

The Synaptic Biology and Cognition Laboratory, The Florey Institute for Neuroscience and Mental Health, Parkville, Victoria, Australia; Florey Department of Neuroscience and Mental Health, the University of Melbourne, Parkville, Victoria, Australia.

Departments of Psychiatry and Neuroscience, The Icahn School of Medicine at Mount Sinai, New York, NY, USA; The Mental Illness Research, Education and Clinical Centers, JJ Peters VA Medical Center, Bronx, NY, USA.

出版信息

Schizophr Res. 2023 May;255:274-282. doi: 10.1016/j.schres.2023.03.035. Epub 2023 Apr 19.

Abstract

Multiple lines of evidence argue for lower levels of cortical muscarinic M1 receptors (CHRM1) in people with schizophrenia which is possibly due to a sub-group within the disorder who have a marked loss of CHRM1 (muscarinic receptor deficit sub-group (MRDS)). In this study we sought to determine if the lower levels of CHRM1 was apparent in older people with schizophrenia and whether the loss of CHRM1 was associated with symptom severity by measuring levels of cortical [H]pirenzepine binding to CHRM1 from 56 people with schizophrenia and 43 controls. Compared to controls (173 ± 6.3 fmol / mg protein), there were lower levels of cortical [H]pirenzepine binding in the people with schizophrenia (mean ± SEM: 153 ± 6.0 fmol / mg protein; p = 0.02; Cohen's d = - 0.46). [H]pirenzepine binding in the people with schizophrenia, but not controls, was not normally distributed and best fitted a two-population solution. The nadir of binding separating the two groups of people with schizophrenia was 121 fmol / mg protein and levels of [H]pirenzepine binding below this value had a 90.7 % specificity for the disorder. Compared to controls, the score from the Clinical Dementia Rating Scale (CDR) did not differ significantly in MRDS but were significantly higher in the sub-group with normal radioligand binding. Positive and Negative Syndrome Scale scores did not differ between the two sub-groups with schizophrenia. Our current study replicates and earlier finding showing a MRDS within schizophrenia and, for the first time, suggest this sub-group have less severe cognitive deficits others with schizophrenia.

摘要

有多项证据表明,精神分裂症患者大脑皮层毒蕈碱 M1 受体 (CHRM1) 水平较低,这可能是由于该疾病的亚组人群中 CHRM1 明显缺失(毒蕈碱受体缺陷亚组 (MRDS))。在这项研究中,我们试图确定老年精神分裂症患者是否存在 CHRM1 水平降低的情况,以及 CHRM1 的缺失是否与症状严重程度有关,方法是从 56 名精神分裂症患者和 43 名对照者中测量大脑皮层 [H] 哌仑西平与 CHRM1 的结合水平。与对照组(173 ± 6.3 fmol / mg 蛋白)相比,精神分裂症患者大脑皮层 [H] 哌仑西平结合水平较低(平均值 ± SEM:153 ± 6.0 fmol / mg 蛋白;p = 0.02;Cohen's d = - 0.46)。精神分裂症患者而非对照组的 [H] 哌仑西平结合呈非正态分布,最佳拟合为两群体解决方案。将两组精神分裂症患者分开的结合最低点为 121 fmol / mg 蛋白,低于该值的 [H] 哌仑西平结合水平对该疾病具有 90.7%的特异性。与对照组相比,MRDS 组的临床痴呆评定量表 (CDR) 评分无显著差异,但在正常配体结合亚组中评分显著升高。阳性和阴性综合征量表评分在精神分裂症的两个亚组之间没有差异。我们目前的研究复制了早期研究结果,表明精神分裂症中存在 MRDS,并且首次表明该亚组的认知缺陷比其他精神分裂症患者的认知缺陷更为严重。

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