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可卡因成瘾及双重病理中的前脉冲抑制

Prepulse Inhibition in Cocaine Addiction and Dual Pathologies.

作者信息

Gil-Miravet Isis, Fuertes-Saiz Alejandro, Benito Ana, Almodóvar Isabel, Ochoa Enrique, Haro Gonzalo

机构信息

TXP Research Group, Universidad Cardenal Herrera-CEU, CEU Universities, 12006 Castellón, Spain.

Predepartamental Unit of Medicine, Universitat Jaume I, 12071 Castellón, Spain.

出版信息

Brain Sci. 2021 Feb 20;11(2):269. doi: 10.3390/brainsci11020269.

DOI:10.3390/brainsci11020269
PMID:33672693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7924364/
Abstract

Cocaine addiction is frequently associated with different psychiatric disorders, especially schizophrenia and antisocial personality disorder. A small number of studies have used prepulse inhibition (PPI) as a discriminating factor between these disorders. This work evaluated PPI and the phenotype of patients with cocaine-related disorder (CRD) who presented a dual diagnosis of schizophrenia or antisocial personality disorder. A total of 74 men aged 18-60 years were recruited for this research. The sample was divided into four groups: CRD ( = 14), CRD and schizophrenia ( = 21), CRD and antisocial personality disorder ( = 16), and a control group ( = 23). We evaluated the PPI and other possible vulnerability factors in these patients by using different assessment scales. PPI was higher in the CRD group at 30 ms (F(3, 64) = 2.972, = 0.038). Three discriminant functions were obtained which allowed us to use the overall Hare Psychopathy Checklist Revised score, reward sensitivity, and PPI at 30 ms to predict inclusion of these patients in the different groups with a success rate of 79.7% (42.9% for CRD, 76.2% for CRD and schizophrenia, 100% for CRD and antisocial personality disorder, and 91.3% in the control group). Despite the differences we observed in PPI, this factor is of little use for discriminating between the different diagnostic groups and it acts more as a non-specific endophenotype in certain mental disorders, such as in patients with a dual diagnosis.

摘要

可卡因成瘾常与不同的精神障碍相关,尤其是精神分裂症和反社会人格障碍。少数研究将前脉冲抑制(PPI)作为区分这些障碍的一个因素。这项研究评估了患有可卡因相关障碍(CRD)且同时诊断为精神分裂症或反社会人格障碍的患者的PPI及表型。本研究共招募了74名年龄在18至60岁之间的男性。样本分为四组:CRD组( = 14)、CRD合并精神分裂症组( = 21)、CRD合并反社会人格障碍组( = 16)以及对照组( = 23)。我们通过使用不同的评估量表来评估这些患者的PPI及其他可能的易患因素。CRD组在30毫秒时的PPI较高(F(3, 64) = 2.972, = 0.038)。获得了三个判别函数,这使我们能够使用修订版的哈瑞精神病态检查表总分、奖赏敏感性以及30毫秒时的PPI来预测这些患者被纳入不同组别的情况,成功率为79.7%(CRD组为42.9%,CRD合并精神分裂症组为76.2%,CRD合并反社会人格障碍组为100%,对照组为91.3%)。尽管我们观察到了PPI的差异,但该因素在区分不同诊断组方面作用不大,在某些精神障碍中,如双重诊断的患者中,它更像是一种非特异性的内表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/7924364/06a4e9ebcd42/brainsci-11-00269-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/7924364/334c31b0002a/brainsci-11-00269-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/7924364/06a4e9ebcd42/brainsci-11-00269-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/7924364/334c31b0002a/brainsci-11-00269-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/7924364/06a4e9ebcd42/brainsci-11-00269-g003.jpg

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Brain Sci. 2020 Sep 16;10(9):639. doi: 10.3390/brainsci10090639.
2
Prepulse Inhibition of the Startle Reflex as a Predictor of Vulnerability to Develop Locomotor Sensitization to Cocaine.惊吓反射的前脉冲抑制作为对可卡因产生运动敏化易感性的预测指标。
Front Behav Neurosci. 2020 Feb 3;13:296. doi: 10.3389/fnbeh.2019.00296. eCollection 2019.
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Increased cortisol levels are associated with low treatment retention in crack cocaine users.
皮质醇水平升高与快克可卡因使用者治疗依从性低有关。
Addict Behav. 2020 Apr;103:106260. doi: 10.1016/j.addbeh.2019.106260. Epub 2019 Dec 23.
4
Sensorimotor Gating in Cocaine-Related Disorder with Comorbid Schizophrenia or Antisocial Personality Disorder.感觉运动门控在可卡因相关障碍伴发精神分裂症或反社会人格障碍中的作用。
J Dual Diagn. 2019 Oct-Dec;15(4):243-253. doi: 10.1080/15504263.2019.1633489. Epub 2019 Jul 9.
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Endophenotypes in Schizophrenia: Digging Deeper to Identify Genetic Mechanisms.精神分裂症的内表型:深入挖掘以确定遗传机制。
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Strengths in patients with schizophrenia and healthy people - similarities and differences.精神分裂症患者与健康人的优势——异同
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