联合使用关法辛和 N-乙酰半胱氨酸治疗创伤性脑损伤后的认知缺陷。

IF 1.8 Q3 CLINICAL NEUROLOGY
Neurotrauma reports Pub Date : 2024-03-13 eCollection Date: 2024-01-01 DOI:10.1089/neur.2023.0124
Siddharth Khasnavis, Timothy Belliveau, Amy Arnsten, Arman Fesharaki-Zadeh
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引用次数: 0

摘要

创伤性脑损伤(TBI)是导致全球残疾的一个重要因素。创伤性脑损伤的严重程度各不相同,大多数病例被认定为轻度创伤性脑损伤(mTBI),仅涉及短暂的意识丧失,影像学检查未发现颅内损伤。尽管有这样的分类,但许多人在受伤后的数月至数年内仍报告有持续的认知变化,尤其是前额叶皮层的认知和执行功能受损。对于这些患者,目前还没有获得批准的药物,治疗方法仅限于症状管理和认知或行为疗法。目前的病例研究探讨了使用α-2A肾上腺素受体激动剂关法辛(guanfacine)结合抗氧化剂N-乙酰半胱氨酸(NAC)治疗创伤后认知症状,这是基于关法辛能够增强前额叶皮质功能,以及NAC在治疗创伤后认知症状中的开放标签使用。我们创伤性脑损伤诊所的两名患者接受了这种联合疗法的治疗,并在治疗前后进行了神经心理学测试。Guanfacine + NAC 可改善两人的注意力、处理速度、记忆力和执行功能,且副作用极小。这些结果鼓励我们在未来开展安慰剂对照试验,以更准确地确定关法辛和 NAC 对治疗创伤性脑损伤引起的认知功能障碍的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined Use of Guanfacine and N-Acetylcysteine for the Treatment of Cognitive Deficits After Traumatic Brain Injury.

Traumatic Brain Injury (TBI) is a significant contributor to disability across the world. TBIs vary in severity, and most cases are designated mild TBI (mTBI), involving only brief loss of consciousness and no intracranial findings on imaging. Despite this categorization, many persons continue to report persistent cognitive changes in the months to years after injury, with particular impairment in the cognitive and executive functions of the pre-frontal cortex. For these persons, there are no currently approved medications, and treatment is limited to symptom management and cognitive or behavioral therapy. The current case studies explored the use of the alpha-2A adrenoreceptor agonist, guanfacine, combined with the antioxidant, N-acetylcysteine (NAC), in the treatment of post-TBI cognitive symptoms, based on guanfacine's ability to strengthen pre-frontal cortical function, and the open-label use of NAC in treating TBI. Two persons from our TBI clinic were treated with this combined regimen, with neuropsychological testing performed pre- and post-treatment. Guanfacine + NAC improved attention, processing speed, memory, and executive functioning with minimal side effects in both persons. These results encourage future placebo-controlled trials to more firmly establish the efficacy of guanfacine and NAC for the treatment of cognitive deficits caused by TBI.

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