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The complete sequence of a human Y chromosome.人类 Y 染色体的完整序列。
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Donanemab in Early Symptomatic Alzheimer Disease: The TRAILBLAZER-ALZ 2 Randomized Clinical Trial.多奈哌齐治疗早期症状性阿尔茨海默病的随机临床试验。
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Single-cell RNA sequencing analysis of human Alzheimer's disease brain samples reveals neuronal and glial specific cells differential expression.单细胞 RNA 测序分析人类阿尔茨海默病脑样本揭示神经元和神经胶质细胞特异性差异表达。
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Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.孟德尔随机化证实了 Y 染色体丢失在男性阿尔茨海默病发病机制中的作用。
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Lecanemab in Early Alzheimer's Disease.早期阿尔茨海默病中的lecanemab
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X-linked ubiquitin-specific peptidase 11 increases tauopathy vulnerability in women.X 连锁泛素特异性肽酶 11 增加女性 tau 病易感性。
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Modifiable Risk Factors for Alzheimer Disease and Related Dementias Among Adults Aged ≥45 Years - United States, 2019.45 岁及以上成年人阿尔茨海默病和相关痴呆可改变的风险因素 - 美国,2019 年。
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Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease.阿尔茨海默病认知弹性的遗传结构中的性别差异。
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Advances in the development of new biomarkers for Alzheimer's disease.阿尔茨海默病新型生物标志物的研究进展。
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Mechanisms of Choice in X-Chromosome Inactivation.X 染色体失活中的选择机制。
Cells. 2022 Feb 3;11(3):535. doi: 10.3390/cells11030535.

追寻线索:探究X染色体在晚发性阿尔茨海默病中的作用机制

Chasing shadows: Investigating X chromosome mediation in late-onset Alzheimer's disease.

作者信息

Armon Carmel, Cannon-Albright Lisa A, Allen-Brady Kristina, Wolfson Sharon

机构信息

Department of Neurology, Loma Linda University School of Medicine, Loma Linda, California, United States of America.

Department of Neurology, Tel Aviv University School of Medicine and Shamir (Assaf Harofeh) Medical Center, Zerifin, Israel.

出版信息

Adv Neurol (Singap). 2024;3(2). doi: 10.36922/an.3122. Epub 2024 Jun 14.

DOI:10.36922/an.3122
PMID:39634155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11616353/
Abstract

Alzheimer's disease (AD) is a major cause of dementia. While maternal inheritance has been recognized for late-onset AD (LOAD), risk factors have not been identified consistently on the X chromosome. We recently developed a new method to identify an apparent risk of 70% mediated by the X chromosome in newly-presenting cognitive disorders clinic patients with amnestic mild cognitive impairment (aMCI) or early LOAD with unilateral parental lineage for AD or dementia. We sought to confirm our preliminary findings in the Utah Population Database (UPDB). We obtained previously published aggregate data on the risk of AD in the UPDB based on family history, stratified the data by the sex of the proband, and analyzed them using the new method. The X chromosome-attributable relative risk was estimated by calculating the following: Odds ratio (OR) = (women with paternal lineage: Women with maternal lineage)/(men with paternal lineage: Men with maternal lineage). The proportion of genetic risk attributable to the X chromosome is equal to (OR-1)/OR. The analysis did not reveal any risk mediated by the X chromosome, and the null result could be attributed to methodological limitations. Factors that impact the initial or early presentation (incidence) of LOAD, which are appropriate for consideration as risk factors, may not be detectable in a (prevalent) population of deceased individuals. Thus, epidemiological evidence for the contribution of the X chromosome to the development of LOAD will need to be sought prospectively in incident patient populations with newly diagnosed, biologically-confirmed aMCI or LOAD.

摘要

阿尔茨海默病(AD)是痴呆的主要病因。虽然母系遗传已被认为与晚发性阿尔茨海默病(LOAD)有关,但X染色体上的风险因素尚未得到一致确认。我们最近开发了一种新方法,用于确定在新出现认知障碍的门诊患者中,由X染色体介导的明显风险,这些患者患有遗忘型轻度认知障碍(aMCI)或有AD或痴呆单侧亲本谱系的早期LOAD。我们试图在犹他州人口数据库(UPDB)中证实我们的初步发现。我们根据家族病史获得了UPDB中先前发表的关于AD风险的汇总数据,按先证者性别对数据进行分层,并使用新方法进行分析。通过计算以下内容来估计X染色体归因相对风险:优势比(OR)=(有父系谱系的女性:有母系谱系的女性)/(有父系谱系的男性:有母系谱系的男性)。X染色体可归因的遗传风险比例等于(OR - 1)/OR。分析未发现X染色体介导的任何风险,而无效结果可能归因于方法学上的局限性。影响LOAD初始或早期表现(发病率)的因素,这些因素适合作为风险因素考虑,但在已死亡个体的(现患)人群中可能无法检测到。因此,需要在新诊断、经生物学确认患有aMCI或LOAD的新发患者人群中前瞻性地寻找X染色体对LOAD发展贡献的流行病学证据。