Suppr超能文献

与神经营养因子基因多态性相关的阿尔茨海默病风险中的性别差异:卡什县记忆研究

Sex Differences in Risk for Alzheimer's Disease Related to Neurotrophin Gene Polymorphisms: The Cache County Memory Study.

作者信息

Matyi Joshua, Tschanz JoAnn T, Rattinger Gail B, Sanders Chelsea, Vernon Elizabeth K, Corcoran Chris, Kauwe John S K, Buhusi Mona

机构信息

Department of Psychology, Utah State University.

Center for Epidemiologic Studies, Utah State University.

出版信息

J Gerontol A Biol Sci Med Sci. 2017 Nov 9;72(12):1607-1613. doi: 10.1093/gerona/glx092.

Abstract

Neurotrophins, including nerve-growth factor and brain-derived neurotrophic factor, have been implicated in Alzheimer's disease (AD). Associations between AD and neurotrophin signaling genes have been inconsistent, with few studies examining sex differences in risk. We examined four single-nucleotide polymorphisms (SNPs) involved in neurotrophin signaling (rs6265, rs56164415, rs2289656, rs2072446) and risk for AD by sex in a population-based sample of older adults. Three thousand four hundred and ninety-nine individuals without dementia at baseline [mean (standard deviation) age = 74.64 (6.84), 58% female] underwent dementia screening and assessment over four triennial waves. Cox regression was used to examine time to AD or right censoring for each SNP. Female carriers of the minor T allele for rs2072446 and rs56164415 had a 60% (hazard ratio [HR] = 1.60, 95% confidence interval [CI] = 1.02-2.51) and 93% (HR = 1.93, 95% CI = 1.30-2.84) higher hazard for AD, respectively, than male noncarriers of the T allele. Furthermore, male carriers of the T allele of rs2072446 had a 61% lower hazard (HR = 0.39, 95% CI = 0.14-1.06) than male noncarriers at trend-level significance (p = .07). The association between certain neurotrophin gene polymorphisms and AD differs by sex and may explain inconsistent findings in the literature.

摘要

神经营养因子,包括神经生长因子和脑源性神经营养因子,与阿尔茨海默病(AD)有关。AD与神经营养因子信号基因之间的关联并不一致,很少有研究考察风险中的性别差异。我们在一个基于人群的老年人样本中,按性别研究了参与神经营养因子信号传导的四个单核苷酸多态性(SNP,即rs6265、rs56164415、rs2289656、rs2072446)与AD风险的关系。3499名基线时无痴呆的个体[平均(标准差)年龄=74.64(6.84),58%为女性]在四个三年期随访中接受了痴呆筛查和评估。采用Cox回归分析每个SNP至AD发生或右侧删失的时间。rs2072446和rs56164415次要T等位基因的女性携带者发生AD的风险分别比T等位基因的男性非携带者高60%(风险比[HR]=1.60,95%置信区间[CI]=1.02 - 2.51)和93%(HR = 1.93,95% CI = 1.30 - 2.84)。此外,rs2072446的T等位基因男性携带者的风险比男性非携带者低61%(HR = 0.39,95% CI = 0.14 - 1.06),在趋势水平上具有显著性(p = 0.07)。某些神经营养因子基因多态性与AD之间的关联存在性别差异,这可能解释了文献中不一致的研究结果。

相似文献

1
Sex Differences in Risk for Alzheimer's Disease Related to Neurotrophin Gene Polymorphisms: The Cache County Memory Study.
J Gerontol A Biol Sci Med Sci. 2017 Nov 9;72(12):1607-1613. doi: 10.1093/gerona/glx092.
4
SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.
J Alzheimers Dis. 2008 Sep;15(1):61-70. doi: 10.3233/jad-2008-15105.
5
Association of rs2072446 in the NGFR gene with the risk of Alzheimer's disease and amyloid-β deposition in the brain.
CNS Neurosci Ther. 2022 Dec;28(12):2218-2229. doi: 10.1111/cns.13965. Epub 2022 Sep 8.
8
Brain derived neurotrophic factor Val66Met polymorphism and psychotic symptoms in Alzheimer's disease.
Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):356-62. doi: 10.1016/j.pnpbp.2010.10.020. Epub 2010 Oct 31.
9
SORL1 gene, plasma biomarkers, and the risk of Alzheimer's disease for the Han Chinese population in Taiwan.
Alzheimers Res Ther. 2016 Dec 30;8(1):53. doi: 10.1186/s13195-016-0222-x.
10
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.
Arch Neurol. 2008 Jan;65(1):45-53. doi: 10.1001/archneurol.2007.3. Epub 2007 Nov 12.

引用本文的文献

2
Cognitive Dysfunction and Exercise: From Epigenetic to Genetic Molecular Mechanisms.
Mol Neurobiol. 2024 Sep;61(9):6279-6299. doi: 10.1007/s12035-024-03970-7. Epub 2024 Jan 30.
3
The Nerve Growth Factor Receptor (NGFR/p75): A Major Player in Alzheimer's Disease.
Int J Mol Sci. 2023 Feb 6;24(4):3200. doi: 10.3390/ijms24043200.
4
Gene- and Gender-Related Decrease in Serum BDNF Levels in Alzheimer's Disease.
Int J Mol Sci. 2022 Nov 23;23(23):14599. doi: 10.3390/ijms232314599.
6
Alzheimer's pathogenic mechanisms and underlying sex difference.
Cell Mol Life Sci. 2021 Jun;78(11):4907-4920. doi: 10.1007/s00018-021-03830-w. Epub 2021 Apr 12.
7
Sex-dependent effect of on Alzheimer's disease and other age-related neurodegenerative disorders.
Dis Model Mech. 2020 Aug 27;13(8):dmm045211. doi: 10.1242/dmm.045211.
9
Nerve Growth Factor Pathobiology During the Progression of Alzheimer's Disease.
Front Neurosci. 2019 Jul 1;13:533. doi: 10.3389/fnins.2019.00533. eCollection 2019.
10
Sex differences in Alzheimer's disease: Understanding the molecular impact.
Brain Res. 2019 Sep 15;1719:194-207. doi: 10.1016/j.brainres.2019.05.031. Epub 2019 May 23.

本文引用的文献

1
Nerve growth factor: a neuroimmune crosstalk mediator for all seasons.
Immunology. 2017 May;151(1):1-15. doi: 10.1111/imm.12717. Epub 2017 Feb 21.
2
3
Neuromodulation of Aerobic Exercise-A Review.
Front Psychol. 2016 Jan 7;6:1890. doi: 10.3389/fpsyg.2015.01890. eCollection 2015.
6
2015 Alzheimer's disease facts and figures.
Alzheimers Dement. 2015 Mar;11(3):332-84. doi: 10.1016/j.jalz.2015.02.003.
7
Lack of an association of BDNF Val66Met polymorphism and plasma BDNF with hippocampal volume and memory.
Cogn Affect Behav Neurosci. 2015 Sep;15(3):625-43. doi: 10.3758/s13415-015-0343-x.
8
Population substructure in Cache County, Utah: the Cache County study.
BMC Bioinformatics. 2014;15 Suppl 7(Suppl 7):S8. doi: 10.1186/1471-2105-15-S7-S8. Epub 2014 May 28.
10
Nerve growth factor metabolic dysfunction in Down's syndrome brains.
Brain. 2014 Mar;137(Pt 3):860-72. doi: 10.1093/brain/awt372. Epub 2014 Feb 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验