Neuropsychology and Neuroscience, Kessler Foundation Research Center, West Orange, NJ, USA.
Neurology. 2013 Jun 11;80(24):2186-93. doi: 10.1212/WNL.0b013e318296e98b. Epub 2013 May 10.
We first tested the brain reserve (BR) hypothesis in multiple sclerosis (MS) by examining whether larger maximal lifetime brain volume (MLBV; determined by genetics) protects against disease-related cognitive impairment, and then investigated whether cognitive reserve (CR) gained through life experience (intellectually enriching leisure activities) protects against cognitive decline independently of MLBV (BR).
Sixty-two patients with MS (41 relapsing-remitting MS, 21 secondary progressive MS) received MRIs to estimate BR (MLBV, estimated with intracranial volume [ICV]) and disease burden (T2 lesion load; atrophy of gray matter, white matter, thalamus, and hippocampus). Early-life cognitive leisure was measured as a source of CR. We assessed cognitive status with tasks of cognitive efficiency and memory. Hierarchical regressions were used to investigate whether higher BR (ICV) protects against cognitive impairment, and whether higher CR (leisure) independently protects against cognitive impairment over and above BR.
Cognitive status was positively associated with ICV (R(2) = 0.066, p = 0.017). An ICV × disease burden interaction (R(2) = 0.050, p = 0.030) revealed that larger ICV attenuated the impact of disease burden on cognition. Controlling for BR, higher education (R(2) = 0.047, p = 0.030) and leisure (R(2) = 0.090, p = 0.001) predicted better cognition. A leisure × disease burden interaction (R(2) = 0.037, p = 0.030) showed that leisure independently attenuated the impact of disease burden on cognition. Follow-up analyses revealed that BR protected against cognitive inefficiency, not memory deficits, whereas CR was more protective against memory deficits than cognitive inefficiency.
We provide evidence of BR in MS, and show that CR independently protects against disease-related cognitive decline over and above BR. Lifestyle choices protect against cognitive impairment independently of genetic factors outside of one's control.
我们首先通过研究较大的最大终生脑容量(通过遗传学确定)是否可预防疾病相关认知障碍来检验多发性硬化症(MS)中的脑储备(BR)假说,然后调查通过生活经验获得的认知储备(CR)是否可以独立于 MLBV(BR)预防认知下降。
对 62 名 MS 患者(41 名复发缓解型 MS,21 名继发进展型 MS)进行 MRI 检查,以评估 BR(脑容量 [ICV] 估计的 MLBV)和疾病负担(T2 病变负荷;灰质、白质、丘脑和海马体萎缩)。通过早期认知休闲活动来衡量 CR 的来源。我们使用认知效率和记忆任务评估认知状态。使用层次回归来研究较高的 BR(ICV)是否可预防认知障碍,以及较高的 CR(休闲)是否可独立于 BR 预防认知障碍。
认知状态与 ICV 呈正相关(R²=0.066,p=0.017)。ICV×疾病负担交互作用(R²=0.050,p=0.030)表明,较大的 ICV 可减弱疾病负担对认知的影响。在控制 BR 后,较高的教育(R²=0.047,p=0.030)和休闲(R²=0.090,p=0.001)可预测更好的认知。休闲×疾病负担交互作用(R²=0.037,p=0.030)表明,休闲可独立减弱疾病负担对认知的影响。随访分析表明,BR 可预防认知效率低下,而不能预防记忆缺陷,而 CR 对记忆缺陷的保护作用大于认知效率低下。
我们提供了 MS 中 BR 的证据,并表明 CR 可以独立于自身无法控制的遗传因素之外,预防与疾病相关的认知下降。生活方式的选择可独立预防认知障碍,而不受遗传因素的影响。