Decreased Cognition in Children with Risk Factors for Alzheimer's Disease

被引:51
作者
Bloss, Cinnamon S. [1 ,2 ]
Delis, Dean C. [3 ,4 ]
Salmon, David P. [5 ]
Bondi, Mark W. [3 ,4 ]
机构
[1] San Diego State Univ, San Diego, CA 92182 USA
[2] Univ Calif San Diego, Joint Doctoral Program Clin Psychol, San Diego, CA 92103 USA
[3] Univ Calif San Diego, VA San Diego Healthcare Syst, San Diego, CA 92103 USA
[4] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[5] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92103 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; apolipoprotein E; children; cognition; cognitive reserve; learning disorders;
D O I
10.1016/j.biopsych.2008.07.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: The epsilon 4 allele of the apolipoprotein E gene (APOE-epsilon 4) and a family history (+FH) of Alzheimer's disease (AD) are both risk factors for the development of AD. Although studies to identify a preclinical phase of AD have led to evidence of APOE-epsilon 4-and +FH-related differences in brain and cognitive functioning in healthy adults, the relative influence of these factors in children is unknown. Methods: To investigate this issue, school-age children (n = 109) received standardized achievement tests, the Rey-Osterrieth Complex Figure Test (Copy Condition; RCFT-CC), assessment of family medical history, and buccal swab testing to determine their APOE genotype. Results: Analyses revealed that, relative to children without these risk factors, children who possess both an APOE-epsilon 4 allele and a +FH of AD and/or significant memory problems (MID) obtained lower scores on nearly every cognitive test administered. Conclusions: Findings suggest that when both AD risk factors are present, cognition maybe adversely affected as early as childhood. Thus, risk factors for a disorder of pathological aging (i.e., AD) may have implications for the etiology of certain types of learning difficulties in children.
引用
收藏
页码:904 / 906
页数:3
相关论文
共 20 条
[1]   The distribution of apolipoprotein E alleles in Scottish perinatal deaths [J].
Becher, JC ;
Keeling, JW ;
McIntosh, N ;
Wyatt, B ;
Bell, J .
JOURNAL OF MEDICAL GENETICS, 2006, 43 (05) :414-418
[2]  
*CTB, 2001, TERRANOVA
[3]   Estimating risk curves for first-degree relatives of patients with Alzheimer's disease: The REVEAL study [J].
Cupples, LA ;
Farrer, LA ;
Sadovnick, AD ;
Relkin, N ;
Whitehouse, P ;
Green, RC .
GENETICS IN MEDICINE, 2004, 6 (04) :192-196
[4]   Ageing - Cognitive change and the APOE&4 allele [J].
Deary, IJ ;
Whiteman, MC ;
Pattie, A ;
Starr, JM ;
Hayward, C ;
Wright, AF ;
Carothers, A ;
Whalley, LJ .
NATURE, 2002, 418 (6901) :932-932
[5]   The influence of Alzheimer disease family history and apolipoprotein E ε4 on mesial temporal lobe activation [J].
Johnson, Sterling C. ;
Schmitz, Taylor W. ;
Trivedi, Mehul A. ;
Ries, Michele L. ;
Torgerson, Britta M. ;
Carlsson, Cynthia M. ;
Asthana, Sanjay ;
Hermann, Bruce P. ;
Sager, Mark A. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (22) :6069-6076
[6]  
Kolb B., 2017, Fundamentals of Human Neuropsychology, V7th
[7]   COGNITIVE CHANGES IN YOUNG-OLD ADULTS - EFFECT OF FAMILY HISTORY OF DEMENTIA [J].
LARUE, A ;
OHARA, R ;
MATSUYAMA, SS ;
JARVIK, LF .
JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY, 1995, 17 (01) :65-70
[8]  
Loring DW., 2004, NEUROPSYCHOLOGICAL A, P531
[9]  
Osterrieth P.A., 1944, ARCH PSYCHOL, V30, P206
[10]   ALLELIC ASSOCIATIONS BETWEEN 100 DNA MARKERS AND HIGH VERSUS LOW IQ [J].
PLOMIN, R ;
MCCLEARN, GE ;
SMITH, DL ;
SKUDER, P ;
VIGNETTI, S ;
CHORNEY, MJ ;
CHORNEY, K ;
KASARDA, S ;
THOMPSON, LA ;
DETTERMAN, DK ;
PETRILL, SA ;
DANIELS, J ;
OWEN, MJ ;
MCGUFFIN, P .
INTELLIGENCE, 1995, 21 (01) :31-48