Genetic risk of neurodegenerative diseases is associated with mild cognitive impairment and conversion to dementia

被引:70
作者
Adams, Hieab H. H. [1 ,2 ]
de Bruijn, Renee F. A. G. [1 ,3 ]
Hofman, Albert [1 ]
Uitterlinden, Andre G. [4 ]
van Duijn, Cornelia M. [1 ]
Vernooij, Meike W. [1 ,2 ]
Koudstaal, Peter J. [3 ]
Ikram, M. Arfan [1 ,2 ,3 ]
机构
[1] Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands
[2] Erasmus MC, Dept Radiol, Rotterdam, Netherlands
[3] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[4] Erasmus MC, Dept Internal Med, Rotterdam, Netherlands
关键词
Mild cognitive impairment; Genetics; Dementia; Alzheimer's disease; Parkinson's disease; Frontotemporal lobar degeneration; Amyotrophic lateral sclerosis; AMYOTROPHIC-LATERAL-SCLEROSIS; GENOME-WIDE ASSOCIATION; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; MENTAL STATE; METAANALYSIS; DIAGNOSIS; VARIANTS; IDENTIFICATION; DEGENERATION;
D O I
10.1016/j.jalz.2014.12.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Neurodegenerative diseases are a major cause of cognitive impairment and can ultimately lead to dementia. Genome-wide association studies have uncovered many genetic variants conferring risk of neurodegenerative diseases, but their role in cognitive impairment remains unexplored. Methods: In the prospective, population-based Rotterdam Study, 3605 nondemented persons aged >= 55 years were genotyped, screened for mild cognitive impairment (MCI) in 2002 to 2005 and underwent continuous follow-up for dementia until 2012. Weighted polygenic risk scores of genetic variants for Alzheimer's disease (AD), Parkinson's disease (PD), and the frontotemporal lobar degeneration/amyotrophic lateral sclerosis disease spectrum (FTLD/ALS) were constructed and investigated for association with MCI and the subsequent conversion to dementia. Results: In total, 360 (10.0%) persons had MCI, of whom 147 (4.1%) were amnestic and 213 (5.9%) nonamnestic. The AD risk score was associated with both MCI subtypes (odds ratio for all MCI 1.15 [95% CI, 1.03-1.28]), whereas PD and FTLD/ALS risk scores were associated only with nonamnestic MCI (odds ratios 1.15 [1.00-1.32] and 1.19 [1.03-1.37], respectively). The AD risk score, but not PD and FTLD/ALS risk scores, was associated with an increased risk of dementia (hazard ratio 1.55 [1.37-1.77]). Discussion: Genetic evidence supports the view that multiple neurodegenerative pathways lead to MCI and that the subsequent conversion to dementia, primarily of the AD subtype, is mainly due to the AD pathway(s). (C) 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1277 / 1285
页数:9
相关论文
共 34 条
[1]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[2]  
Bos Daniel, 2012, Alzheimers Dement, V8, pS104, DOI 10.1016/j.jalz.2012.01.008
[3]   Prediction of Age-related Macular Degeneration in the General Population The Three Continent AMD Consortium [J].
Buitendijk, Gabrielle H. S. ;
Rochtchina, Elena ;
Myers, Chelsea ;
van Duijn, Cornelia M. ;
Lee, Kristine E. ;
Klein, Barbara E. K. ;
Meuer, Stacy M. ;
de Jong, Paulus T. V. M. ;
Holliday, Elizabeth G. ;
Tan, Ava G. ;
Uitterlinden, Andre G. ;
Sivakumaran, Theru S. ;
Attia, John ;
Hofman, Albert ;
Mitchell, Paul ;
Vingerling, Johannes R. ;
Iyengar, Sudha K. ;
Janssens, A. Cecile J. W. ;
Wang, Jie Jin ;
Klein, Ronald ;
Klaver, Caroline C. W. .
OPHTHALMOLOGY, 2013, 120 (12) :2644-2655
[4]   Neuroimaging and APOE genotype:: A systematic qualitative review [J].
Cherbuin, Nicolas ;
Leach, Liana S. ;
Christensen, Helen ;
Anstey, Kaarin J. .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2007, 24 (05) :348-362
[5]   SEMI-STRUCTURED CLINICAL INTERVIEW FOR ASSESSMENT OF DIAGNOSIS AND MENTAL STATE IN ELDERLY - GERIATRIC MENTAL STATE SCHEDULE .1. DEVELOPMENT AND RELIABILITY [J].
COPELAND, JRM ;
KELLEHER, MJ ;
KELLETT, JM ;
GOURLAY, AJ ;
GURLAND, BJ ;
FLEISS, JL ;
SHARPE, L .
PSYCHOLOGICAL MEDICINE, 1976, 6 (03) :439-449
[6]   Determinants, MRI Correlates, and Prognosis of Mild Cognitive Impairment: The Rotterdam Study [J].
de Bruijn, Renee F. A. G. ;
Akoudad, Saloua ;
Cremers, Lotte G. M. ;
Hofman, Albert ;
Niessen, Wiro J. ;
van der Lugt, Aad ;
Koudstaal, Peter J. ;
Vernooij, Meike W. ;
Ikram, M. Arfan .
JOURNAL OF ALZHEIMERS DISEASE, 2014, 42 :S239-S249
[7]  
Dean DC, 2012, NEUROBIOL AGING, V33
[8]   Brain Differences in Infants at Differential Genetic Risk for Late-Onset Alzheimer Disease A Cross-sectional Imaging Study [J].
Dean, Douglas C., III ;
Jerskey, Beth A. ;
Chen, Kewei ;
Protas, Hillary ;
Thiyyagura, Pradeep ;
Roontiva, Auttawat ;
O'Muircheartaigh, Jonathan ;
Dirks, Holly ;
Waskiewicz, Nicole ;
Lehman, Katie ;
Siniard, Ashley L. ;
Turk, Mari N. ;
Hua, Xue ;
Madsen, Sarah K. ;
Thompson, Paul M. ;
Fleisher, Adam S. ;
Huentelman, Matthew J. ;
Deoni, Sean C. L. ;
Reiman, Eric M. .
JAMA NEUROLOGY, 2014, 71 (01) :11-22
[9]   Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease [J].
Do, Chuong B. ;
Tung, Joyce Y. ;
Dorfman, Elizabeth ;
Kiefer, Amy K. ;
Drabant, Emily M. ;
Francke, Uta ;
Mountain, Joanna L. ;
Goldman, Samuel M. ;
Tanner, Caroline M. ;
Langston, J. William ;
Wojcicki, Anne ;
Eriksson, Nicholas .
PLOS GENETICS, 2011, 7 (06)
[10]   A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis [J].
Fogh, Isabella ;
Ratti, Antonia ;
Gellera, Cinzia ;
Lin, Kuang ;
Tiloca, Cinzia ;
Moskvina, Valentina ;
Corrado, Lucia ;
Soraru, Gianni ;
Cereda, Cristina ;
Corti, Stefania ;
Gentilini, Davide ;
Calini, Daniela ;
Castellotti, Barbara ;
Mazzini, Letizia ;
Querin, Giorgia ;
Gagliardi, Stella ;
Del Bo, Roberto ;
Conforti, Francesca L. ;
Siciliano, Gabriele ;
Inghilleri, Maurizio ;
Sacca, Francesco ;
Bongioanni, Paolo ;
Penco, Silvana ;
Corbo, Massimo ;
Sorbi, Sandro ;
Filosto, Massimiliano ;
Ferlini, Alessandra ;
Di Blasio, Anna M. ;
Signorini, Stefano ;
Shatunov, Aleksey ;
Jones, Ashley ;
Shaw, Pamela J. ;
Morrison, Karen E. ;
Farmer, Anne E. ;
Van Damme, Philip ;
Robberecht, Wim ;
Chi, Adriano ;
Traynor, Bryan J. ;
Sendtner, Michael ;
Melki, Judith ;
Meininger, Vincent ;
Hardiman, Orla ;
Andersen, Peter M. ;
Leigh, Nigel P. ;
Glass, Jonathan D. ;
Overste, Daniel ;
Diekstra, Frank P. ;
Veldink, Jan H. ;
van Es, Michael A. ;
Shaw, Christopher E. .
HUMAN MOLECULAR GENETICS, 2014, 23 (08) :2220-2231