Institute for Translational Medicine, Medical School, University of Pecs, Pecs, Hungary.
Department of Pediatrics, University of Pecs Medical School, Pecs, Hungary.
J Neurotrauma. 2021 Jun 1;38(11):1467-1483. doi: 10.1089/neu.2020.7265. Epub 2021 Apr 23.
One of the most devastating chronic consequences of traumatic brain injury (TBI) is cognitive impairment. One of the possible underlying causes is growth hormone deficiency (GHD) caused by TBI-induced hypopituitarism. Currently, TBI patients are not routinely screened for pituitary function, and there are no standard therapies when GHD is diagnosed. Further, the possible positive effects of GH replacement on cognitive function and quality of life after TBI are not well established. We aimed to assess the current knowledge regarding the effect of GH therapy on cognitive function and quality of life after TBI. We performed a literature search in PubMed, Embase, and Central databases from inception to October 2019. We extracted data on each term of severity (mild-moderate-severe) of TBI with and without GHD, time since injury, parameters of growth hormone treatment (dosing, length), and cognitive outcomes in terms of verbal and non-verbal memory, and executive, emotional, and motor functions, and performed a meta-analysis on the results of a digit span test assessing working memory. We identified 12 studies (containing two randomized controlled trials) with 264 mild-to-moderate-to-severe TBI patients (Glasgow Coma Score [GCS] varied between 6 and 15) with ( = 255) or without ( = 9) GHD who received GH therapy. GH was administered subcutaneously in gradually increasing doses, monitoring serum insulin-like growth factor-I (IGF-I) level. After TBI, regardless of GCS, 6-12 months of GH therapy, started in the chronic phase post-TBI, induced a moderate improvement in processing speed and memory capacities, decreased the severity of depression, and led to a marked improvement in quality of life. Limitations include the relatively low number of patients involved and the divergent neuropsychological tests used. These results indicate the need for further multi-centric controlled studies to substantiate the use of GH replacement therapy as a potential tool to alleviate TBI-related cognitive impairment and improve quality of life.
创伤性脑损伤 (TBI) 最具破坏性的慢性后果之一是认知障碍。其潜在原因之一可能是 TBI 引起的垂体功能减退导致生长激素缺乏 (GHD)。目前,TBI 患者并未常规筛查垂体功能,当诊断出 GHD 时也没有标准治疗方法。此外,GH 替代治疗对 TBI 后认知功能和生活质量的可能积极影响尚未得到充分证实。我们旨在评估目前关于 GH 治疗对 TBI 后认知功能和生活质量影响的知识。我们在 PubMed、Embase 和中央数据库中进行了文献检索,检索时间从建库至 2019 年 10 月。我们提取了关于 TBI 严重程度(轻度-中度-重度)和有无 GHD、受伤后时间、生长激素治疗参数(剂量、时长)以及认知结果(言语和非言语记忆、执行、情绪和运动功能)的每项研究的数据,并对评估工作记忆的数字跨度测试结果进行了荟萃分析。我们确定了 12 项研究(包含两项随机对照试验),共纳入 264 例轻度至中度至重度 TBI 患者(Glasgow 昏迷评分 [GCS] 为 6 至 15),其中 255 例有 GHD,9 例无 GHD,他们接受了 GH 治疗。GH 皮下逐渐递增剂量给药,监测血清胰岛素样生长因子-I (IGF-I) 水平。TBI 后,无论 GCS 如何,在 TBI 慢性期开始的 6-12 个月 GH 治疗可使处理速度和记忆能力得到中度改善,降低抑郁严重程度,并显著提高生活质量。局限性包括纳入的患者数量相对较少和使用的神经心理学测试存在差异。这些结果表明需要进一步开展多中心对照研究,以证实 GH 替代治疗作为缓解 TBI 相关认知障碍和提高生活质量的潜在工具的使用。