Lack of association of the cholesterol 24-hydroxylase (CYP46) intron 2 polymorphism with Alzheimer's disease

被引:35
作者
Ingelsson, M
Jesneck, J
Irizarry, MC
Hyman, BT
Rebeck, GW
机构
[1] Georgetown Univ, Dept Neurosci, Washington, DC 20057 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Charlestown, MA 02129 USA
关键词
lipoprotein; genetics; LXR; efflux; APOE; neuropathology; amyloid;
D O I
10.1016/j.neulet.2004.06.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An association was recently reported between an increased risk of Alzheimer's disease and an intron 2 AA genotype of CYP46, the enzyme hydroxylating cholesterol to 24S-hydroxycholesterol. Moreover, CYP46 AA-carriers were found to have increased levels of amyloid-beta and tau in brain and cerebrospinal fluid. We determined the CYP46 intron 2 genotype in a cohort of 178 AD and 105 non-demented control subjects, but found no significant association with AD for any of the individual genotypes or alleles. Further, in an autopsy confirmed subset of this cohort, the proposed CYP46 risk genotype was not associated with any increase in the brain levels of amyloid-beta40, amyloid-beta42 or in the levels of amyloid plaques and neurofibrillary tangles. Despite growing evidence implicating cholesterol metabolism in AD risk and Abeta generation, our data does not support a robust genetic relationship between the CYP46 intron 2 polymorphism and AD risk or neuropathology. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:228 / 231
页数:4
相关论文
共 21 条
[1]  
Burns M, 2003, J NEUROSCI, V23, P5645
[2]   Exclusively targeting β-secretase to lipid rafts by GPI-anchor addition up-regulates β-site processing of the amyloid precursor protein [J].
Cordy, JM ;
Hussain, I ;
Dingwall, C ;
Hooper, NM ;
Turner, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) :11735-11740
[3]   Genetic variation in the cholesterol 24-hydroxylase (CYP46) gene and the risk of Alzheimer's disease [J].
Desai, P ;
DeKosky, ST ;
Kamboh, MI .
NEUROSCIENCE LETTERS, 2002, 328 (01) :9-12
[4]   Simvastatin strongly reduces levels of Alzheimer's disease β-amyloid peptides Aβ42 and Aβ40 in vitro and in vivo [J].
Fassbender, K ;
Simons, M ;
Bergmann, C ;
Stroick, M ;
Lütjohann, D ;
Keller, P ;
Runz, H ;
Kühl, S ;
Bertsch, T ;
von Bergmannn, K ;
Hennerici, M ;
Beyreuther, K ;
Hartmann, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (10) :5856-5861
[5]   Primary cultures of neuronal and non-neuronal rat brain cells secrete similar proportions of amyloid β peptides ending at Aβ40 and Aβ42 [J].
Fukumoto, H ;
Tomita, T ;
Matsunaga, H ;
Ishibashi, Y ;
Saido, TC ;
Iwatsubo, T .
NEUROREPORT, 1999, 10 (14) :2965-2969
[6]   β-secretase protein and activity are increased in the neocortex in Alzheimer disease [J].
Fukumoto, H ;
Cheung, BS ;
Hyman, BT ;
Irizarry, MC .
ARCHIVES OF NEUROLOGY, 2002, 59 (09) :1381-1389
[7]   THE LACK OF ACCUMULATION OF SENILE PLAQUES OR AMYLOID BURDEN IN ALZHEIMERS-DISEASE SUGGESTS A DYNAMIC BALANCE BETWEEN AMYLOID DEPOSITION AND RESOLUTION [J].
HYMAN, BT ;
MARZLOFF, K ;
ARRIAGADA, PV .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1993, 52 (06) :594-600
[8]   Editorial on consensus recommendations for the postmortem diagnosis of Alzheimer disease from the National Institute on Aging and the Reagan Institute working group on diagnostic criteria for the neuropathological assessment of Alzheimer disease [J].
Hyman, BT ;
Trojanowski, JQ .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1997, 56 (10) :1095-1097
[9]   Early Aβ accumulation and progressive synaptic loss, gliosis, and tangle formation in AD brain [J].
Ingelsson, M ;
Fukumoto, H ;
Newell, KL ;
Growdon, JH ;
Hedley-Whyte, ET ;
Frosch, MP ;
Albert, MS ;
Hyman, BT ;
Irizarry, MC .
NEUROLOGY, 2004, 62 (06) :925-931
[10]   Statins and the risk of dementia [J].
Jick, H ;
Zornberg, GL ;
Jick, SS ;
Seshadri, S ;
Drachman, DA .
LANCET, 2000, 356 (9242) :1627-1631