帕金森病伴痴呆和路易体痴呆的性别差异

Lidadi L. Agbomi , Chika P. Onuoha , Samuel I. Nathaniel , Oreoluwa O. Coker-Ayo , Melissa J. Bailey-Taylor , Laurie Theriot Roley , Nicolas Poupore , Richard L. Goodwin , Thomas I. Nathaniel
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引用次数: 2

摘要

路易体痴呆(DLB)通常被认为是介于阿尔茨海默病(AD)、帕金森病(PD)和帕金森病伴痴呆(PDD)之间的一种中间疾病,其性别差异存在争议。本研究通过回顾性数据分析,利用人口学和药物治疗策略调查了DLB和PDD的性别差异。方法从PRISMA痴呆数据库登记处收集2015 - 2020年确诊的DLB和PDD病例数据。采用logistic回归分析对7594例PDD患者和608例DLB患者的数据进行分析,以确定与DLB和PDD患者相关的人口学和药理学因素。结果经校正分析,多奈哌齐、加兰他明、利瓦斯替明等中心乙酰胆碱酯酶抑制剂与DLB相关。第二代抗精神病药物(SGAs)如利培酮(奇比(OR)=1.900, 95%可信区间(CI), 1.191 ~ 3.030, P = 0.007)与女性DLB相关,阿立哌唑(OR=0.195,95% CI,0.06 ~ 0.631, P<0.006),选择性血清素受体抑制剂(SSRIs)包括艾司西酞普兰(OR=0.651, 95% CI,0.468 ~ 0.906, P = 0.011),人口统计学因素包括吸烟(OR=0.620, 95% CI,0.444 ~ 0.866, P<0.005)和年龄增长(OR= 1.042, 95% CI, 1.025 ~ 1.058),P<0.001),与患有PDD的女性相关。奥氮平(OR=2.871, 95%CI, 1.902-4.334, P<0.001)、艾司西酞普兰(OR=1.444, 95%CI, 1.079-1.932)和吸烟(OR=1.424, 95%CI, 1.075-1.887, P = 0.014)与男性DLB相关。使用过阿立哌唑(OR=0.581, 95%CI, 0.302-1.118)的非裔美国男性(OR= 0.249, 95%CI, 0.088-0.703, P = 0.009)与PDD相关(OR= 0.371, 95%CI, 0.260-0.531, P<0.001)。结论我们的研究结果揭示了与DLB和PDD相关的人口学和药理学因素的异同。在未来的研究中探讨已确定的因素对DLB或PDD的影响,有助于改善DLB和PDD患者的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gender differences in Parkinson's disease with dementia and dementia with Lewy bodies

Background

Gender differences for dementia with Lewy bodies (DLB), usually considered an intermediate disease between Alzheimer disease (AD), Parkinson disease (PD), and Parkinson disease with dementia (PDD), is controversial. The present study investigated gender differences in DLB and PDD using demographic and pharmacologic treatment strategies in a retrospective data analysis.

Method

Data of confirmed cases of DLB and PDD between 2015 and 2020 were collected from the PRISMA dementia data-base registry. Data from 7594 PDD patients and 608 DLB patients were analyzed using logistic regression analysis to determine demographic and pharmacologic factors associated with DLB and PDD patients.

Result

In the adjusted analysis, central acetylcholinesterase inhibitors (ChEIs) including donepezil, galantamine, rivastigmine were associated with DLB. Second generation antipsychotics (SGAs) such as risperidone (odd ratio(OR)=1.900, 95% confidence interval (CI),1.192–3.030, P = 0.007) was associated with females with DLB while aripiprazole (OR=0.195,95% CI,0.06–0.631, P<0.006), and a selective serotonin receptor inhibitor (SSRIs) including escitalopram (OR=0.651, 95% CI,0.468–0.906, P = 0.011), and demographic factors including tobacco use (OR=0.620, 95% CI,0.444–0.866, P<0.005) and increasing age (OR =1.042, 95% CI, 1.025–1.058, P<0.001), were associated with females that present with PDD. Olanzapine (OR=2.871, 95% CI, 1.902–4.334, P<0.001), escitalopram (OR=1.444, 95% CI, 1.079–1.932) and tobacco use (OR=1.424, 95%CI, 1.075–1.887, P = 0.014) were associated with males with DLB. African American males (OR= 0.249, 95% CI, 0.088–0.703, P = 0.009) with a history of ethyl alcohol (ETOH) use (OR= 0.371, 95% CI, 0.260–0.531, P<0.001) treated with aripiprazole (OR=0.581, 95%CI, (0.302–1.118), P = 0.004) were associated with PDD.

Conclusion

Our findings reveal similarities and differences in demographic and pharmacologic factors associated with DLB and PDD. Investigating the effect of identified factors on DLB or PDD in future studies can help improve the care of DLB and PDD patients.

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来源期刊
Aging and health research
Aging and health research Clinical Neurology, Public Health and Health Policy, Geriatrics and Gerontology
CiteScore
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