Blood Pressure Control in Aging Predicts Cerebral Atrophy Related to Small-Vessel White Matter Lesions

被引:29
作者
Kern, Kyle C. [1 ]
Wright, Clinton B. [1 ]
Bergfield, Kaitlin L. [2 ,3 ,4 ,5 ]
Fitzhugh, Megan C. [4 ,5 ]
Chen, Kewei [6 ,7 ,8 ]
Moeller, James R. [9 ]
Nabizadehl, Nooshin [1 ]
Elkinds, Mitchell S. V. [10 ]
Sacco, Ralph L. [1 ]
Stern, Yaakov [9 ,10 ]
DeCarli, Charles S. [11 ,12 ]
Alexander, Gene E. [2 ,3 ,4 ,5 ,8 ,13 ,14 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Neurol, Evelyn F McKnight Brain Inst, Miami, FL 33136 USA
[2] Univ Arizona, Neurosci Grad Interdisciplinary Program, Tucson, AZ USA
[3] Univ Arizona, Physiol Sci Grad Interdisciplinary Programs, Tucson, AZ USA
[4] Univ Arizona, Dept Psychol, Tucson, AZ 85721 USA
[5] Univ Arizona, Evelyn F McKnight Brain Inst, Tucson, AZ 85721 USA
[6] Banner Alzheimer Inst, Computat Image Anal Program, Phoenix, AZ USA
[7] Arizona State Univ, Sch Math & Stat, Tempe, AZ USA
[8] Arizona Alzheimers Consortium, Phoenix, AZ USA
[9] Columbia Univ, Dept Psychiat, Coll Phys & Surg, New York, NY USA
[10] Columbia Univ, Dept Neurol, Coll Phys & Surg, New York, NY USA
[11] Univ Calif Davis, Dept Neurol, Davis, CA 95616 USA
[12] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[13] Univ Arizona, Dept Psychiat, Tucson, AZ USA
[14] Univ Arizona, Inst BIO5, Tucson, AZ USA
关键词
white matter hyperintensities; brain atrophy; hypertension; cerebrovascular disease; cognition; aging; scaled subprofile model; voxel-based morphometry; ALZHEIMERS-DISEASE; GRAY-MATTER; COGNITIVE FUNCTION; BRAIN ATROPHY; HYPERINTENSITY VOLUME; REGIONAL NETWORK; APOLIPOPROTEIN-E; HYPERTENSION; SPEED; DEMENTIA;
D O I
10.3389/fnagi.2017.00132
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Cerebral small-vessel damage manifests as white matter hyperintensities and cerebral atrophy on brain MRI and is associated with aging, cognitive decline and dementia. We sought to examine the interrelationship of these imaging biomarkers and the influence of hypertension in older individuals. We used a multivariate spatial covariance neuroimaging technique to localize the effects of white matter lesion load on regional gray matter volume and assessed the role of blood pressure control, age and education on this relationship. Using a case-control design matching for age, gender, and educational attainment we selected 64 participants with normal blood pressure, controlled hypertension or uncontrolled hypertension from the Northern Manhattan Study cohort. We applied gray matter voxel-based morphometry with the scaled subprofile model to (1) identify regional covariance patterns of gray matter volume differences associated with white matter lesion load, (2) compare this relationship across blood pressure groups, and (3) relate it to cognitive performance. In this group of participants aged 60-86 years, we identified a pattern of reduced gray matter volume associated with white matter lesion load in bilateral temporal-parietal regions with relative preservation of volume in the basal forebrain, thalami and cingulate cortex. This pattern was expressed most in the uncontrolled hypertension group and least in the normotensives, but was also more evident in older and more educated individuals. Expression of this pattern was associated with worse performance in executive function and memory. In summary, white matter lesions from small-vessel disease are associated with a regional pattern of gray matter atrophy that is mitigated by blood pressure control, exacerbated by aging, and associated with cognitive performance.
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页数:10
相关论文
共 54 条
[1]   Individual differences in PET activation of object perception and attention systems predict face matching accuracy [J].
Alexander, GE ;
Mentis, MJ ;
Van Horn, JD ;
Grady, CL ;
Berman, KF ;
Furey, ML ;
Pietrini, P ;
Rapoport, SI ;
Schapiro, MB ;
Moeller, JR .
NEUROREPORT, 1999, 10 (09) :1965-1971
[2]  
Alexander Gene E., 1994, Human Brain Mapping, V2, P79, DOI 10.1002/hbm.460020108
[3]   Age-related regional network of magnetic resonance iemaging gray matter in the rhesus macaque [J].
Alexander, Gene E. ;
Chen, Kewei ;
Aschenbrenner, Melaney ;
Merkley, Tricia L. ;
Santerre-Lemmon, Laura E. ;
Shamy, Jul Lea ;
Skaggs, William E. ;
Buonocore, Michael H. ;
Rapp, Peter R. ;
Barnes, Carol A. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (11) :2710-2718
[4]   Regional network of magnetic resonance imaging gray matter volume in healthy aging [J].
Alexander, Gene E. ;
Chen, Kewei ;
Merkley, Tricia L. ;
Reiman, Eric M. ;
Caselli, Richard J. ;
Aschenbrenner, Melaney ;
Santerre-Lemmon, Laura ;
Lewis, Diana J. ;
Pietrini, Pietro ;
Teipel, Stefan J. ;
Hampel, Harald ;
Rapoport, Stanley I. ;
Moeller, James R. .
NEUROREPORT, 2006, 17 (10) :951-956
[5]   Gray matter network associated with risk for Alzheimer's disease in young to middle-aged adults [J].
Alexander, Gene E. ;
Bergfield, Kaitlin L. ;
Chen, Kewei ;
Reiman, Eric M. ;
Hanson, Krista D. ;
Lin, Lan ;
Bandy, Daniel ;
Caselli, Richard J. ;
Moeller, James R. .
NEUROBIOLOGY OF AGING, 2012, 33 (12) :2723-2732
[6]  
[Anonymous], 2002, Model selection and multimodel inference: a practical informationtheoretic approach
[7]   White Matter Lesions and Brain Atrophy: More than Shared Risk Factors? A Systematic Review [J].
Appelman, Auke P. A. ;
Exalto, Lieza G. ;
van der Graaf, Yolanda ;
Biessels, Geert Jan ;
Mali, Willem P. T. M. ;
Geerlings, Mirjam I. .
CEREBROVASCULAR DISEASES, 2009, 28 (03) :227-242
[8]   Voxel-based morphometry - The methods [J].
Ashburner, J ;
Friston, KJ .
NEUROIMAGE, 2000, 11 (06) :805-821
[9]   White matter lesions on magnetic resonance imaging in dementia with Lewy bodies, Alzheimer's disease, vascular dementia, and normal aging [J].
Barber, R ;
Scheltens, F ;
Gholkar, A ;
Ballard, C ;
McKeith, I ;
Ince, P ;
Perry, R ;
O'Brien, J .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 67 (01) :66-72
[10]   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