The Prevalence of Cortical Gray Matter Atrophy May Be Overestimated In the Healthy Aging Brain

被引:31
作者
Burgmans, Saartje [1 ]
van Boxtel, Martin P. J. [1 ]
Vuurman, Eric F. P. M. [1 ]
Smeets, Floortje [1 ]
Gronenschild, Ed H. B. M. [1 ]
Uylings, Harry B. M. [2 ]
Jolles, Jelle [1 ,3 ]
机构
[1] Maastricht Univ, Sch Mental Hlth & Neurosci, Dept Psychiat & Neuropsychol, European Grad Sch Neurosci EURON, NL-6200 MD Maastricht, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Anat & Neurosci, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, AZIRE Res Inst, Fac Psychol & Educ, Amsterdam, Netherlands
关键词
healthy aging; gray matter atrophy; cognitive decline; cerebral cortex; MRI; MILD COGNITIVE IMPAIRMENT; PARTICIPANTS AGED 24-81; NORMATIVE DATA; ALZHEIMERS-DISEASE; OLDER-ADULTS; MRI DATA; EDUCATION; SEX; RELIABILITY; DEMENTIA;
D O I
10.1037/a0016161
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Prevailing opinion holds that normal brain aging is characterized by substantial atrophy of cortical gray matter. However, this conclusion is based on earlier studies whose findings may be influenced by the inclusion of subjects with subclinical cognitive disorders like preclinical dementia. The present magnetic resonance imaging study tested this hypothesis. Cognitively healthy subjects (mean age 72 years, range 52-82) who remained cognitively stable over a 3-year period were compared to subjects with significant cognitive decline. Subjects who developed dementia within 6 years after the scan session were excluded. The gray matter volumes of seven cortical regions were delineated on T1-weighted magnetic resonance imaging scans. Participants without cognitive decline did not exhibit an age effect on the gray matter volume. Conversely, participants with cognitive decline exhibited a significant age effect in all the seven areas. These results suggest that cortical gray matter atrophy may have been overestimated in studies on healthy aging, since most studies were unable to exclude participants with a substantial atypical cognitive decline or preclinical dementia. Our results underscore the importance of establishing stringent inclusion criteria for future studies on normal aging.
引用
收藏
页码:541 / 550
页数:10
相关论文
共 36 条
[1]  
[Anonymous], 1994, Diagnostic and Statistical Manual of mental disorders, V4
[2]  
BURGMANS S, 2008, NEUROBIOLOGY AGING
[3]   G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences [J].
Faul, Franz ;
Erdfelder, Edgar ;
Lang, Albert-Georg ;
Buchner, Axel .
BEHAVIOR RESEARCH METHODS, 2007, 39 (02) :175-191
[4]  
Insausti R, 1998, AM J NEURORADIOL, V19, P659
[5]   Inter-rater reliability of manual segmentation of the superior, inferior and middle frontal gyri [J].
John, John P. ;
Wang, Lei ;
Moffitt, Amanda J. ;
Singh, Harmeeta K. ;
Gado, Mokhtar H. ;
Csernansky, John G. .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2006, 148 (2-3) :151-163
[6]  
Jolles J., 1995, The Maastricht Aging Study: Determinants of Cognitive Aging
[7]   Differential regional atrophy of the cingulate gyrus in Alzheimer disease: A volumetric MRI study [J].
Jones, Bethany F. ;
Barnes, Josephine ;
Uylings, Harry B. M. ;
Fox, Nick C. ;
Frost, Chris ;
Witter, Menno P. ;
Scheftens, Philip .
CEREBRAL CORTEX, 2006, 16 (12) :1701-1708
[8]   Longitudinal MRI and cognitive change in healthy elderly [J].
Kramer, Joel H. ;
Mungas, Dan ;
Reed, Bruce R. ;
Wetzel, Margaret E. ;
Burnett, Molly M. ;
Chui, Helena C. ;
Miller, Bruce L. ;
Weiner, Michael W. .
NEUROPSYCHOLOGY, 2007, 21 (04) :412-418
[9]   The birth of the International Classification of Primary Care (ICPC) - Serendipity at the border of Lac Leman [J].
Lamberts, H ;
Wood, M .
FAMILY PRACTICE, 2002, 19 (05) :433-435
[10]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939