Ageing with Traumatic Brain Injury: Long-Term Cognition and Wellbeing.

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Amber Ayton, Gershon Spitz, Amelia J Hicks, Jennie Ponsford
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引用次数: 0

Abstract

Whether and how traumatic brain injury (TBI) impacts ageing in the decades post-injury remains a matter of debate, partly due to a lack of controlled studies. This study examined the long-term impact of TBI on cognition and wellbeing in middle-aged and older adults and explored the relationship between age, cognition, and wellbeing, compared with a non-TBI control group. Cross-sectional data from 143 participants aged ≥40 with moderate-severe TBI (6-33 years post-injury; mean age 59.64) were compared with 71 non-TBI controls (mean age 62.10) group matched on age, gender, and premorbid IQ. Individuals with significant confounding comorbidities were excluded. A battery of neuropsychological tests and wellbeing measures (emotional distress, sleep, health-related quality of life [HRQoL]) was administered. Older age and TBI were each independently associated with poorer cognition across multiple domains (p < 0.05). The relationship between verbal learning and memory impairment post-TBI differed between age groups: individuals with TBI in their 40s-60s performed significantly worse than same-aged controls on verbal story acquisition (B = 0.09, p = 0.040, 95% confidence interval [CI] [0.004, 0.17]) and recall (B = 0.12, p = 0.009, 95% CI [0.03, 0.21]), and verbal wordlist recall (B = 0.11, p = 0.007, 95% CI [0.03, 0.19]). In comparison, no significant group differences in verbal memory emerged for ages 70-90. The TBI group reported greater emotional distress (B = 3.55, p < 0.001, 95% CI [1.73, 5.37]), poorer sleep quality (B = 1.07, p = 0.016, 95% CI [0.20, 1.94]), and poorer physical HRQoL (B = -4.26, p = 0.003, 95% CI [-7.08, -1.43]) than controls at all ages. Poorer physical HRQoL was related to poorer cognition post-TBI (p < 0.05). Our results challenge the notion that TBI exacerbates ageing. Moderate-severe TBI resulted in significant long-term impairments in cognition and wellbeing, with verbal learning and memory more impaired during middle-adulthood but not older adulthood compared to controls. TBI was not associated with changes to wellbeing with ageing. Intervention for verbal memory deficits in middle-aged adults with TBI is important, along with wider long-term supports for cognition, wellbeing, and activity participation in all individuals with TBI.

老化与创伤性脑损伤:长期认知和健康。
创伤性脑损伤(TBI)是否以及如何影响损伤后几十年的衰老仍然是一个有争议的问题,部分原因是缺乏对照研究。本研究考察了创伤性脑损伤对中老年人认知和幸福感的长期影响,并与非创伤性脑损伤对照组进行了比较,探讨了年龄、认知和幸福感之间的关系。143名年龄≥40岁的中重度TBI患者的横断面数据(伤后6-33年;平均年龄59.64岁)与年龄、性别、病前智商相匹配的71例非tbi对照组(平均年龄62.10岁)进行比较。排除有显著混杂合并症的个体。进行了一系列神经心理测试和健康测量(情绪困扰、睡眠、健康相关生活质量[HRQoL])。年龄和脑外伤分别与多领域认知能力下降独立相关(p < 0.05)。言语学习与脑外伤后记忆障碍的关系在不同年龄组之间存在差异:40 -60岁脑外伤患者在言语故事习得(B = 0.09, p = 0.040, 95%可信区间[CI][0.004, 0.17])、回忆(B = 0.12, p = 0.009, 95% CI[0.03, 0.21])和言语词表回忆(B = 0.11, p = 0.007, 95% CI[0.03, 0.19])方面的表现明显差于同龄对照组。相比之下,70-90岁年龄段的人在言语记忆方面没有明显的组间差异。在所有年龄段,脑外伤组的情绪困扰(B = 3.55, p < 0.001, 95% CI[1.73, 5.37])、睡眠质量(B = 1.07, p = 0.016, 95% CI[0.20, 1.94])和身体HRQoL (B = -4.26, p = 0.003, 95% CI[-7.08, -1.43])均高于对照组。较差的HRQoL与tbi后较差的认知相关(p < 0.05)。我们的研究结果挑战了脑外伤会加剧衰老的观点。与对照组相比,中重度脑外伤导致认知和健康方面的长期损伤,言语学习和记忆在中年期受损更严重,而在老年期则没有。脑外伤与幸福感随年龄增长的变化无关。对中年TBI患者的言语记忆缺陷进行干预是很重要的,同时对所有TBI患者的认知、健康和活动参与提供更广泛的长期支持。
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
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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