Social cognition in young adults who endorse a cannabis use disorder.

IF 3.3 3区 医学 Q2 NEUROSCIENCES
Gabrielle Abbott, Lisa-Marie Greenwood, Jessica G Bartschi, Suraya Dunsford, Isabella Goodwin, Anastasia Paloubis, Marianna Quinones-Valera, Eugene McTavish, Antonio Verdejo-Garcia, Janna Cousijn, Gary C K Chan, Nadia Solowij, Valentina Lorenzetti
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引用次数: 0

Abstract

Rationale: Cannabis use disorder (CUD) affects over 50 million people globally. Emerging evidence shows that some people with CUD may experience altered social cognition (e.g., emotion recognition or differentiation). These impairments can affect their ability to understand others' emotional states and navigate social interactions, potentially contributing to chronic cannabis use, even when it leads to interpersonal problems. However, the literature on social cognition in cannabis users is inconsistent, based on a paucity of studies, and characterised by methodological issues including conflation of remitted and current CUD (i.e., does not consider abstinence effects on cognition), limited assessment of cannabis metrics (e.g., dosage) and confounds entrenched with CUD (e.g., nicotine/alcohol use, anxiety).

Objectives/methods: We aimed to examine social cognition (i.e., emotion recognition and differentiation, immediate/delayed face memory) in relation to endorsement of CUD (n = 83) vs. controls (n = 32), and measures of level of problematic cannabis use (i.e., Cannabis Use Disorder Identification Test - Revised; CUDIT-R) and dosage (i.e., cannabis grams/past month), accounting for hours since last cannabis use, nicotine/alcohol use, and trait anxiety.

Results: There were no significant effects of CUD (d = 0-0.314) or dosage and level of problematic cannabis use on social cognition.

Conclusions: Altered social cognition may not be a key feature of CUD, or the relationship between CUD and cognition may be moderated by factors such as age, treatment seeking, education, and IQ. In this study, younger age and higher education or IQ may have served as protective factors against social alterations. Replication studies are required to validate this notion.

支持大麻使用障碍的年轻人的社会认知。
理由:大麻使用障碍(CUD)影响全球5000多万人。新出现的证据表明,一些患有CUD的人可能会经历社会认知的改变(例如,情绪识别或分化)。这些缺陷会影响他们理解他人情绪状态和驾驭社交互动的能力,可能会导致长期使用大麻,即使它会导致人际关系问题。然而,关于大麻使用者社会认知的文献是不一致的,这是基于研究的缺乏,其特点是方法学问题,包括将已缓解的和当前的CUD混为一谈(即不考虑戒断对认知的影响),对大麻指标(如剂量)的评估有限,以及与CUD根深蒂固的混淆(如尼古丁/酒精使用、焦虑)。目的/方法:我们旨在检查与CUD (n = 83)与对照组(n = 32)相关的社会认知(即情感识别和分化,即时/延迟面部记忆),以及问题大麻使用水平(即大麻使用障碍识别测试-修订;CUDIT-R)和剂量(即大麻克数/过去一个月)的测量,包括自上次使用大麻以来的小时数,尼古丁/酒精使用和特质焦虑。结果:CUD (d = 0-0.314)、问题大麻使用剂量和水平对社会认知无显著影响(d = 0-0.314)。结论:社会认知改变可能不是CUD的关键特征,或者CUD与认知之间的关系可能受到年龄、寻求治疗、教育和智商等因素的调节。在这项研究中,更年轻的年龄和更高的教育或智商可能是抵御社会变化的保护因素。需要进行重复性研究来验证这一观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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