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阿尔茨海默病的性别差异。

Sex differences in Alzheimer's disease.

机构信息

School of Life and Medical Sciences, University of Hertfordshire.

Hertfordshire Partnership University NHS Foundation Trust, Hatfield, Hertfordshire, UK.

出版信息

Curr Opin Psychiatry. 2018 Mar;31(2):133-139. doi: 10.1097/YCO.0000000000000401.

DOI:10.1097/YCO.0000000000000401
PMID:29324460
Abstract

PURPOSE OF REVIEW

Women are more impacted by Alzheimer's disease than men - they are at significantly greater risk of developing Alzheimer's disease, and recent research shows that they also appear to suffer a greater cognitive deterioration than men at the same disease stage. The purpose of this article is to review recent studies on examining sex differences in cognitive function in Alzheimer's disease.

RECENT FINDINGS

We searched electronically for articles, reviews and meta-analyses published between 1/2016 and 12/2017 and identified 298 articles on sex differences in cognition in Alzheimer's disease. The key themes to emerge were sex differences in cognitive function, risk factors, resilience, and cognitive reserve.

SUMMARY

Evidence is steadily and increasingly accumulating to confirm the poorer cognitive outcome for women than men with Alzheimer's disease. Although small in size, the effects occur across a broad range of cognitive domains including visuospatial, verbal, episodic memory, and semantic memory - some of which typically reveal a sex-related processing advantage for healthy women. Explanations have been linked to a variety of factors including differences in cognitive reserve, resilience, as well as genetics (apolipoprotein ε4) and functional and structural brain changes. Sex-related differences in risk factors, resilience, cognitive reserve, and rates of deterioration have implications for clinical practice.

摘要

目的综述:女性受阿尔茨海默病的影响大于男性——她们患阿尔茨海默病的风险明显更高,最近的研究还表明,在相同疾病阶段,女性的认知能力下降也比男性更为严重。本文旨在综述最近关于阿尔茨海默病认知功能性别差异的研究。

最新发现:我们检索了 2016 年 1 月至 2017 年 12 月期间发表的关于阿尔茨海默病认知性别差异的文章、综述和荟萃分析,共找到 298 篇文章。出现的关键主题包括认知功能、风险因素、韧性和认知储备方面的性别差异。

总结:越来越多的证据证实,女性在认知方面的结局比男性阿尔茨海默病患者更差。尽管规模较小,但这些影响发生在广泛的认知领域,包括视空间、语言、情景记忆和语义记忆,其中一些在健康女性中通常表现出与性别相关的处理优势。解释与多种因素有关,包括认知储备、韧性以及遗传因素(载脂蛋白 E4)和功能及结构脑变化的差异。与性别相关的风险因素、韧性、认知储备和恶化率的差异对临床实践具有重要意义。

相似文献

1
Sex differences in Alzheimer's disease.阿尔茨海默病的性别差异。
Curr Opin Psychiatry. 2018 Mar;31(2):133-139. doi: 10.1097/YCO.0000000000000401.
2
Greater cognitive deterioration in women than men with Alzheimer's disease: a meta analysis.女性阿尔茨海默病患者认知恶化程度大于男性:一项荟萃分析。
J Clin Exp Neuropsychol. 2012;34(9):989-98. doi: 10.1080/13803395.2012.712676. Epub 2012 Aug 23.
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Neuropsychological differences between men and women with Alzheimer's disease.患有阿尔茨海默病的男性和女性之间的神经心理学差异。
Int J Neurosci. 2018 Apr;128(4):342-348. doi: 10.1080/00207454.2017.1382492.
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Sex differences in cognitive impairment in Alzheimer's disease.阿尔茨海默病认知障碍的性别差异。
World J Psychiatry. 2016 Mar 22;6(1):54-65. doi: 10.5498/wjp.v6.i1.54.
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Fate of patients with questionable (very mild) Alzheimer's disease: longitudinal profiles of individual subjects' decline.可疑(非常轻度)阿尔茨海默病患者的转归:个体受试者衰退的纵向概况
Dement Geriatr Cogn Disord. 2000 Nov-Dec;11(6):342-9. doi: 10.1159/000017264.
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Gender-Specific Differences in Cognitive Profiles of Patients with Alzheimer's Disease: Results of the Prospective Dementia Registry Austria (PRODEM-Austria).阿尔茨海默病患者认知特征的性别差异:奥地利前瞻性痴呆登记研究(PRODEM-Austria)的结果
J Alzheimers Dis. 2015;46(3):631-7. doi: 10.3233/JAD-150188.
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Early- versus late-onset Alzheimer's disease in clinical practice: cognitive and global outcomes over 3 years.临床实践中的早发性与晚发性阿尔茨海默病:3 年的认知和总体结局。
Alzheimers Res Ther. 2017 Aug 31;9(1):70. doi: 10.1186/s13195-017-0294-2.
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Apolipoprotein E epsilon4 allele is unrelated to cognitive or functional decline in Alzheimer's disease: retrospective and prospective analysis.载脂蛋白E ε4等位基因与阿尔茨海默病的认知或功能衰退无关:回顾性和前瞻性分析。
Dement Geriatr Cogn Disord. 2006;22(1):73-82. doi: 10.1159/000093316. Epub 2006 May 12.
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Sex and gender differences in cognitive resilience to aging and Alzheimer's disease.衰老和阿尔茨海默病认知弹性的性别差异。
Alzheimers Dement. 2024 Aug;20(8):5695-5719. doi: 10.1002/alz.13844. Epub 2024 Jul 5.

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