Neuroimaging endophenotypes: Strategies for finding genes influencing brain structure and function

被引:201
作者
Glahn, David C.
Thompson, Paul M.
Blangero, John
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Psychiat, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Res Imaging Ctr, San Antonio, TX 78229 USA
[3] Univ Calif Los Angeles, Dept Neurol, Lab Neuro Imaging, Los Angeles, CA 90024 USA
[4] SW Fdn Biomed Res, Dept Genet, San Antonio, TX USA
关键词
genetics; neuroimaging; endophenotype; MRI; PET; anatomy; functional MRl; fMRI;
D O I
10.1002/hbm.20401
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is vitally important to identify the genetic determinants of complex brain-related disorders such as autism, dementia, mood disorders, and schizophrenia. However, the search for genes predisposing individuals to these illnesses has been hampered by their genetic and phenotypic complexity and by reliance upon phenomenologically based qualitative diagnostic systems. Neuroimaging endophenotypes are quantitative indicators of brain structure or function that index genetic liability for an illness. These indices will significantly improve gene discovery and help us to understand the functional consequences of specific genes at the level of systems neuroscience. Here, we review the feasibility of using neuroanatomic and neuropsychological measures as endophenotypes for brain-related disorders. Specifically, we examine specific indices of brain structure or function that are genetically influenced and associated with neurological and psychiatric illness. In addition, we review genetic approaches that capitalize on the use of quantitative traits, including those derived from brain images.
引用
收藏
页码:488 / 501
页数:14
相关论文
共 128 条
[81]   Longitudinal change in hippocampal volume as a function of apolipoprotein E genotype [J].
Moffat, SD ;
Szekely, CA ;
Zonderman, AB ;
Kabani, NJ ;
Resnick, SM .
NEUROLOGY, 2000, 55 (01) :134-136
[82]   Anatomical MRI abnormalities in bipolar disorder: do they exist and do they progress? [J].
Monkul, ES ;
Malhi, GS ;
Soares, JC .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2005, 39 (04) :222-226
[83]   Smaller prefrontal and premotor volumes in boys with attention-deficit/hyperactivity disorder [J].
Mostofsky, SH ;
Cooper, KL ;
Kates, WR ;
Denckla, MB ;
Kaufmann, WE .
BIOLOGICAL PSYCHIATRY, 2002, 52 (08) :785-794
[84]  
Narr KL, 2002, J NEUROSCI, V22, P3720
[85]   Preclinical models: Status of basic research in depression [J].
Nestler, EJ ;
Gould, E ;
Manji, H ;
Bucan, M ;
Duman, RS ;
Gershenfeld, HK ;
Hen, R ;
Koester, S ;
Lederhendler, I ;
Meaney, MJ ;
Robbins, T ;
Winsky, L ;
Zalcman, S .
BIOLOGICAL PSYCHIATRY, 2002, 52 (06) :503-528
[86]   The brain-derived neurotrophic factor val66met polymorphism and variation in human cortical morphology [J].
Pezawas, L ;
Verchinski, BA ;
Mattay, VS ;
Callicott, JH ;
Kolachana, BS ;
Straub, RE ;
Egan, MF ;
Meyer-Lindenberg, A ;
Weinberger, DR .
JOURNAL OF NEUROSCIENCE, 2004, 24 (45) :10099-10102
[87]   5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression [J].
Pezawas, L ;
Meyer-Lindenberg, A ;
Drabant, EM ;
Verchinski, BA ;
Munoz, KE ;
Kolachana, BS ;
Egan, MF ;
Mattay, VS ;
Hariri, AR ;
Weinberger, DR .
NATURE NEUROSCIENCE, 2005, 8 (06) :828-834
[88]   Morphological changes in aging brain structures are differentially affected by time-linked environmental influences despite strong genetic stability [J].
Pfefferbaum, A ;
Sullivan, EV ;
Carmelli, D .
NEUROBIOLOGY OF AGING, 2004, 25 (02) :175-183
[89]   Genetic regulation of regional microstructure of the corpus callosum in late life [J].
Pfefferbaum, A ;
Sullivan, EV ;
Carmelli, D .
NEUROREPORT, 2001, 12 (08) :1677-1681
[90]   Evidence for a cerebellar role in reduced exploration and stereotyped behavior in autism [J].
Pierce, K ;
Courchesne, E .
BIOLOGICAL PSYCHIATRY, 2001, 49 (08) :655-664