Ghosh Abhishek, Mahintamani Tathagata, Rana Devender K, Basu Debasish, Mattoo Surendra K
Department of Psychiatry, Drug De-addiction and Treatment Centre, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Community Mental Health Clinic, Cumbria Northumberland Tyne and Wear Foundation NHS Trust, Molineux NHS Centre, Molineux Street, Byker, Newcastle Upon Tyne NE 6 1SG, United Kingdom.
Indian J Psychiatry. 2022 Mar-Apr;64(2):199-208. doi: 10.4103/indianjpsychiatry.indianjpsychiatry_792_21. Epub 2022 Mar 24.
The number of longitudinal studies on cognitive functions in patients on buprenorphine-based agonist treatment is limited. Our objective was to assess the change in neurocognitive functions over the first 6 months of buprenorphine-naloxone (BNX) treatment for opioid dependence (OD) and compare cognitive functions on BNX and controls.
We selected 60 patients with OD aged 18 to 55 years and 20 sex-matched controls; and excluded patients with other substance dependence, human immunodeficiency virus (HIV), head injury, epilepsy, and severe mental illness. We assessed patients thrice: at baseline, 3, and 6 months and Controls once. Cognitive tests included Wisconsin card sorting test (WCST), Iowa gambling task (IGT), trail making tests A and B (TMT-A and B), verbal and visual N-back test (NBT), and standard progressive matrices (SPM). We measured with-in group effect size with Cohen's D (d).
A total of 24 participants completed at least one follow-up; 17 completed both follow-up assessments. All participants were men. At baseline, the patients performed worse than healthy controls in IGT, TMT-A, and B, and visual and verbal NBT. At 3 months, the performance of visual NBT improved significantly (d = 1.2 for NBT1; 1.3 for NBT2). At 6 months, additional performance improvements were seen in WCST ("perseverative error" d = 1.2), IGT ("net total score" d = 1.2), TMT-A (d = 1.1), and verbal NBT ("omission error" d = 1.7). Except for visual-NBT, results did not differ between patients and controls at both follow-ups.
Cognitive flexibility, decision making, attention, working memory, and psychomotor speed showed improvements over 6 months of a stable dose of BNX.
关于接受丁丙诺啡激动剂治疗的患者认知功能的纵向研究数量有限。我们的目标是评估丁丙诺啡 - 纳洛酮(BNX)治疗阿片类药物依赖(OD)的前6个月神经认知功能的变化,并比较接受BNX治疗的患者与对照组的认知功能。
我们选取了60名年龄在18至55岁的OD患者和20名性别匹配的对照组;并排除了有其他物质依赖、人类免疫缺陷病毒(HIV)、头部损伤、癫痫和严重精神疾病的患者。我们对患者进行了三次评估:在基线、3个月和6个月时,对对照组进行了一次评估。认知测试包括威斯康星卡片分类测试(WCST)、爱荷华赌博任务(IGT)、连线测验A和B(TMT - A和B)、言语和视觉n - 回溯测试(NBT)以及标准渐进矩阵(SPM)。我们用科恩d值(d)测量组内效应量。
共有24名参与者完成了至少一次随访;17名完成了两次随访评估。所有参与者均为男性。在基线时,患者在IGT、TMT - A和B以及视觉和言语NBT方面的表现比健康对照组差。在3个月时,视觉NBT的表现显著改善(NBT1的d = 1.2;NBT2的d = 1.3)。在6个月时,WCST(“持续性错误”d = 1.2)、IGT(“净总分”d = 1.2)、TMT - A(d = 1.1)和言语NBT(“遗漏错误”d = 1.7)的表现进一步改善。除视觉NBT外,在两次随访中患者与对照组的结果无差异。
在稳定剂量的BNX治疗6个月期间,认知灵活性、决策能力、注意力、工作记忆和心理运动速度均有所改善。