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CALHM1 P86L 多态性不会改变脑脊液中的淀粉样蛋白-β或tau。

CALHM1 P86L polymorphism does not alter amyloid-beta or tau in cerebrospinal fluid.

机构信息

Uppsala University, Department of Public Health/Geriatrics, Rudbeck Laboratory, Uppsala, Sweden.

出版信息

Neurosci Lett. 2010 Jan 22;469(2):265-7. doi: 10.1016/j.neulet.2009.12.011. Epub 2009 Dec 23.

DOI:10.1016/j.neulet.2009.12.011
PMID:20005921
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2860374/
Abstract

Recently, the P86L alteration in CALHM1 (calcium homeostasis modulator-1) was reported to be associated with Alzheimer's disease (AD). Moreover, the risk allele increased amyloid-beta (A beta) levels in conditioned media from cultured cells. Therefore, we hypothesized that CALHM1 P86L may modulate A beta or tau levels in cerebrospinal fluid (CSF). Nearly 200 individuals with AD or other cognitive disorders were included for CSF analysis and CALHM1 genotyping. No significant differences in CSF levels of A beta 42, tau or phospho-tau were found across the various CALHM1 genotypes. In conclusion, we found no evidence that CALHM1 P86L is associated with altered CSF levels of the investigated AD biomarkers.

摘要

最近,CALHM1(钙稳态调节剂-1)中的 P86L 改变与阿尔茨海默病(AD)有关。此外,风险等位基因增加了培养细胞条件培养基中的淀粉样蛋白-β(Aβ)水平。因此,我们假设 CALHM1 P86L 可能调节脑脊液(CSF)中的 Aβ或 tau 水平。将近 200 名患有 AD 或其他认知障碍的个体被纳入 CSF 分析和 CALHM1 基因分型。在不同的 CALHM1 基因型中,Aβ42、tau 或磷酸化 tau 的 CSF 水平没有显著差异。总之,我们没有发现证据表明 CALHM1 P86L 与所研究的 AD 生物标志物的 CSF 水平改变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6590/2860374/b011b0a38868/nihms188860f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6590/2860374/b011b0a38868/nihms188860f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6590/2860374/b011b0a38868/nihms188860f1.jpg

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Neurosci Lett. 2010 Jan 22;469(2):265-7. doi: 10.1016/j.neulet.2009.12.011. Epub 2009 Dec 23.
2
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本文引用的文献

1
No association between CALHM1 and risk for Alzheimer dementia in a Belgian population.在比利时人群中,CALHM1与阿尔茨海默病痴呆风险之间无关联。
Hum Mutat. 2009 Apr;30(4):E570-4. doi: 10.1002/humu.20990.
2
No association between CALHM1 variation and risk of Alzheimer disease.CALHM1基因变异与阿尔茨海默病风险之间无关联。
Hum Mutat. 2009 Apr;30(4):E566-9. doi: 10.1002/humu.20989.
3
No association between CALHM1 and Alzheimer's disease risk.CALHM1与阿尔茨海默病风险之间无关联。
Cell. 2008 Dec 12;135(6):993-4; author reply 994-6. doi: 10.1016/j.cell.2008.11.030.
4
A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk.CALHM1基因的多态性影响钙离子稳态、β淀粉样蛋白水平及阿尔茨海默病风险。
Cell. 2008 Jun 27;133(7):1149-61. doi: 10.1016/j.cell.2008.05.048.
5
PET amyloid ligand [11C]PIB uptake is increased in mild cognitive impairment.正电子发射断层扫描淀粉样蛋白配体[11C]匹兹堡化合物B摄取在轻度认知障碍中增加。
Neurology. 2007 May 8;68(19):1603-6. doi: 10.1212/01.wnl.0000260969.94695.56.
6
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.阿尔茨海默病遗传关联研究的系统荟萃分析:AlzGene数据库
Nat Genet. 2007 Jan;39(1):17-23. doi: 10.1038/ng1934.
7
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Biol Psychiatry. 2004 Nov 1;56(9):670-6. doi: 10.1016/j.biopsych.2004.07.021.
8
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Hum Genet. 2004 May;114(6):581-7. doi: 10.1007/s00439-004-1107-9. Epub 2004 Mar 18.
9
Relationship between apoE genotype and CSF beta-amyloid (1-42) and tau in patients with probable and definite Alzheimer's disease.可能及确诊的阿尔茨海默病患者中载脂蛋白E基因型与脑脊液β-淀粉样蛋白(1-42)及tau蛋白的关系。
Neurobiol Aging. 2000 Sep-Oct;21(5):735-40. doi: 10.1016/s0197-4580(00)00164-0.
10
High cerebrospinal fluid tau and low amyloid beta42 levels in the clinical diagnosis of Alzheimer disease and relation to apolipoprotein E genotype.脑脊液中tau蛋白水平升高和β淀粉样蛋白42水平降低在阿尔茨海默病临床诊断中的意义及与载脂蛋白E基因型的关系
Arch Neurol. 1998 Jul;55(7):937-45. doi: 10.1001/archneur.55.7.937.