Brain reserve and cognitive reserve in multiple sclerosis What you've got and how you use it

被引:138
作者
Sumowski, James F. [1 ,2 ]
Rocca, Maria A. [4 ,5 ]
Leavitt, Victoria M. [1 ,2 ]
Riccitelli, Gianna [4 ]
Comi, Giancarlo [5 ]
DeLuca, John [1 ,2 ,3 ]
Filippi, Massimo [4 ,5 ]
机构
[1] Kessler Fdn Res Ctr, W Orange, NJ 07052 USA
[2] UMDNJ New Jersey Med Sch, Dept Phys Med & Rehabil, Newark, NJ USA
[3] UMDNJ New Jersey Med Sch, Dept Neurol & Neurosci, Newark, NJ USA
[4] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Neuroimaging Res Unit, Milan, Italy
[5] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Dept Neurol, Milan, Italy
关键词
HEAD CIRCUMFERENCE; ALZHEIMER-DISEASE; INTRACRANIAL VOLUME; NORMATIVE VALUES; SIZE; ATROPHY; INTELLIGENCE; IMPAIRMENT; EDUCATION; MEMORY;
D O I
10.1212/WNL.0b013e318296e98b
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: 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). Methods: 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. Results: Cognitive status was positively associated with ICV (R-2 = 0.066, p = 0.017). An ICV x 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 3 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. Conclusion: 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.
引用
收藏
页码:2186 / 2193
页数:8
相关论文
共 39 条
[1]   The Rao's Brief Repeatable Battery and Stroop test: normative values with age, education and gender corrections in an Italian population [J].
Amato, M. P. ;
Portaccio, E. ;
Goretti, B. ;
Zipoli, V. ;
Ricchiu, L. ;
De Caro, M. F. ;
Patti, F. ;
Vecchio, R. ;
Sorbi, S. ;
Trojano, M. .
MULTIPLE SCLEROSIS, 2006, 12 (06) :787-793
[2]   Genetic variability of human brain size and cortical gyral patterns [J].
Bartley, AJ ;
Jones, DW ;
Weinberger, DR .
BRAIN, 1997, 120 :257-269
[3]   Neuropathology of older persons without cognitive impairment from two community-based studies [J].
Bennett, D. A. ;
Schneider, J. A. ;
Arvanitakis, Z. ;
Kelly, J. F. ;
Aggarwal, N. T. ;
Shah, R. C. ;
Wilson, R. S. .
NEUROLOGY, 2006, 66 (12) :1837-1844
[4]   Education modifies the relation of AD pathology to level of cognitive function in older persons [J].
Bennett, DA ;
Wilson, RS ;
Schneider, JA ;
Evans, DA ;
de Leon, CFM ;
Arnold, SE ;
Barnes, LL ;
Bienias, JL .
NEUROLOGY, 2003, 60 (12) :1909-1915
[5]   Cognitive impairment in multiple sclerosis [J].
Chiaravalloti, Nancy D. ;
DeLuca, John .
LANCET NEUROLOGY, 2008, 7 (12) :1139-1151
[6]   Normal brain development and aging: Quantitative analysis at in vivo MR imaging in healthy volunteers [J].
Courchesne, E ;
Chisum, HJ ;
Townsend, J ;
Cowles, A ;
Covington, J ;
Egaas, B ;
Harwood, M ;
Hinds, S ;
Press, GA .
RADIOLOGY, 2000, 216 (03) :672-682
[7]   The neuroscience of human intelligence differences [J].
Deary, Ian J. ;
Penke, Lars ;
Johnson, Wendy .
NATURE REVIEWS NEUROSCIENCE, 2010, 11 (03) :201-211
[8]   Temporal and spatial dynamics of brain structure changes during extensive learning [J].
Draganski, Bogdan ;
Gaser, Christian ;
Kempermann, Gerd ;
Kuhn, H. Georg ;
Winkler, Juergen ;
Buechel, Christian ;
May, Arne .
JOURNAL OF NEUROSCIENCE, 2006, 26 (23) :6314-6317
[9]   Total intracranial volume: Normative values and lack of association with Alzheimer's disease [J].
Edland, SD ;
Xu, Y ;
Plevak, M ;
O'Brien, P ;
Tangalos, EG ;
Petersen, RC ;
Jack, CR .
NEUROLOGY, 2002, 59 (02) :272-274
[10]   Maximal brain size remains an important predictor of cognition in old age, independent of current brain pathology [J].
Farias, Sarah Tomaszewski ;
Mungas, Dan ;
Reed, Bruce ;
Carmichael, Owen ;
Beckett, Laurel ;
Harvey, Danielle ;
Olichney, John ;
Simmons, Amanda ;
DeCarli, Charles .
NEUROBIOLOGY OF AGING, 2012, 33 (08) :1758-1768