不同民族文化的老年人神经认知障碍中的精神病。

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-06-01 Epub Date: 2025-04-25 DOI:10.1212/CPJ.0000000000200467
Estevana Isaac, Carolyn Wei Zhu, Monica Rivera Mindt, Albert L Siu, Alex Federman, Kristine Yaffe, Barbara G Vickrey, Jenifer Voeks, Parul Agarwal, Derrick Brooks, Ombolanle Ayo, Mary Sano
{"title":"不同民族文化的老年人神经认知障碍中的精神病。","authors":"Estevana Isaac, Carolyn Wei Zhu, Monica Rivera Mindt, Albert L Siu, Alex Federman, Kristine Yaffe, Barbara G Vickrey, Jenifer Voeks, Parul Agarwal, Derrick Brooks, Ombolanle Ayo, Mary Sano","doi":"10.1212/CPJ.0000000000200467","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>There is longstanding evidence that the presence of psychosis in neurocognitive disorders (NCDs) is associated with faster cognitive and functional decline. The goal of this study was to examine how clinician-diagnosed psychosis differs among ethnoracial groups with NCDs (including early onset) and to explore whether these differences exist even for those without advanced dementia.</p><p><strong>Method: </strong>This is an IRB-approved retrospective analysis. Data are from the National Alzheimer's Coordinating Center Uniform Dataset from 42 Alzheimer's Disease Research Centers. Participants aged 40-95 years as of June 2023 with mild cognitive impairment (MCI) or dementia on baseline evaluation were included. Psychosis was defined as clinician-diagnosed visual or auditory hallucinations or delusions manifesting at the time of baseline evaluation. Ethnoracial groups were self-reported. Associations between ethnoracial groups and psychosis in NCDs were estimated using adjusted multivariable logistic regression with dichotomous measures of outcomes. Covariates included age, sex, years of education, severity of cognitive impairment (Clinical Dementia Rating scale), and presence or absence of any self-reported preexisting psychiatric illness. An analysis by age younger than 65 years was also conducted. Exploratory multivariable logistic regression analyses were performed for participants with milder stages of dementia (Clinical Dementia Rating 0.5 or 1) and for the subset of participants diagnosed with MCI.</p><p><strong>Results: </strong>A total of 22,854 participants were included. The mean age was 73 + 9.7 years, and 50% were women. A total of 8,352 (37%) had MCI and 14,502 (63%) had dementia. In adjusted analysis, American Indian/Alaska Native (AI/AN) (OR 2.70, 1.75-4.17, <i>p</i> < 0.0001), Black-Latino (OR 2.33, 1.25-4.35, <i>p</i> = 0.0076), Other-Latino (OR 1.82, 1.42-2.33, <i>p</i> < 0.0001), Black, non-Latino (NL) (OR 1.66,1.47-1.87, <i>p</i> < 0.0001), and White-Latino (OR 1.42, 1.21-1.67, <i>p</i> < 0.0001) participants had greater odds of any psychotic symptom than White-NL participants. For age groups 40 to younger than 65 years, only Black-NL participants (OR 1.56, 1.13-2.14, <i>p</i> = 0.0064) were more likely to be diagnosed with any psychotic symptoms. For milder stages of dementia, Black-Latino (OR 3.44, 1.58-7.48, <i>p</i> = 0.0018), AI/AN (OR 2.73, 1.66-4.48, <i>p</i> < 0.0001), Other-Latino (OR 2.38, 1.72-3.30, <i>p</i> < 0.0001), Black-NL (OR 2.08,1.77-2.45, <i>p</i> < 0.0001), and White-Latino (OR 1.55, 1.23-1.95, <i>p</i> = 0.0002) participants had greater odds of psychosis in NCDs when compared with White-NL participants. For MCI alone, there were no significant differences.</p><p><strong>Discussion: </strong>Black-NL, Latino, and AI/AN individuals were more likely to be diagnosed with psychosis in NCDs when compared with White-NL participants. More research is needed to explore sociocultural, psychosocial, and neuropathologic factors involved.</p>","PeriodicalId":19136,"journal":{"name":"Neurology. Clinical practice","volume":"15 3","pages":"e200467"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12048866/pdf/","citationCount":"0","resultStr":"{\"title\":\"Psychosis in Neurocognitive Disorder Among Ethnoculturally Diverse Older Persons.\",\"authors\":\"Estevana Isaac, Carolyn Wei Zhu, Monica Rivera Mindt, Albert L Siu, Alex Federman, Kristine Yaffe, Barbara G Vickrey, Jenifer Voeks, Parul Agarwal, Derrick Brooks, Ombolanle Ayo, Mary Sano\",\"doi\":\"10.1212/CPJ.0000000000200467\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objectives: </strong>There is longstanding evidence that the presence of psychosis in neurocognitive disorders (NCDs) is associated with faster cognitive and functional decline. The goal of this study was to examine how clinician-diagnosed psychosis differs among ethnoracial groups with NCDs (including early onset) and to explore whether these differences exist even for those without advanced dementia.</p><p><strong>Method: </strong>This is an IRB-approved retrospective analysis. Data are from the National Alzheimer's Coordinating Center Uniform Dataset from 42 Alzheimer's Disease Research Centers. Participants aged 40-95 years as of June 2023 with mild cognitive impairment (MCI) or dementia on baseline evaluation were included. Psychosis was defined as clinician-diagnosed visual or auditory hallucinations or delusions manifesting at the time of baseline evaluation. Ethnoracial groups were self-reported. Associations between ethnoracial groups and psychosis in NCDs were estimated using adjusted multivariable logistic regression with dichotomous measures of outcomes. Covariates included age, sex, years of education, severity of cognitive impairment (Clinical Dementia Rating scale), and presence or absence of any self-reported preexisting psychiatric illness. An analysis by age younger than 65 years was also conducted. Exploratory multivariable logistic regression analyses were performed for participants with milder stages of dementia (Clinical Dementia Rating 0.5 or 1) and for the subset of participants diagnosed with MCI.</p><p><strong>Results: </strong>A total of 22,854 participants were included. The mean age was 73 + 9.7 years, and 50% were women. A total of 8,352 (37%) had MCI and 14,502 (63%) had dementia. In adjusted analysis, American Indian/Alaska Native (AI/AN) (OR 2.70, 1.75-4.17, <i>p</i> < 0.0001), Black-Latino (OR 2.33, 1.25-4.35, <i>p</i> = 0.0076), Other-Latino (OR 1.82, 1.42-2.33, <i>p</i> < 0.0001), Black, non-Latino (NL) (OR 1.66,1.47-1.87, <i>p</i> < 0.0001), and White-Latino (OR 1.42, 1.21-1.67, <i>p</i> < 0.0001) participants had greater odds of any psychotic symptom than White-NL participants. For age groups 40 to younger than 65 years, only Black-NL participants (OR 1.56, 1.13-2.14, <i>p</i> = 0.0064) were more likely to be diagnosed with any psychotic symptoms. For milder stages of dementia, Black-Latino (OR 3.44, 1.58-7.48, <i>p</i> = 0.0018), AI/AN (OR 2.73, 1.66-4.48, <i>p</i> < 0.0001), Other-Latino (OR 2.38, 1.72-3.30, <i>p</i> < 0.0001), Black-NL (OR 2.08,1.77-2.45, <i>p</i> < 0.0001), and White-Latino (OR 1.55, 1.23-1.95, <i>p</i> = 0.0002) participants had greater odds of psychosis in NCDs when compared with White-NL participants. For MCI alone, there were no significant differences.</p><p><strong>Discussion: </strong>Black-NL, Latino, and AI/AN individuals were more likely to be diagnosed with psychosis in NCDs when compared with White-NL participants. More research is needed to explore sociocultural, psychosocial, and neuropathologic factors involved.</p>\",\"PeriodicalId\":19136,\"journal\":{\"name\":\"Neurology. Clinical practice\",\"volume\":\"15 3\",\"pages\":\"e200467\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12048866/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurology. Clinical practice\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1212/CPJ.0000000000200467\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurology. Clinical practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1212/CPJ.0000000000200467","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/25 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景和目的:长期以来有证据表明,神经认知障碍(ncd)中精神病的存在与认知和功能衰退的加速有关。本研究的目的是研究临床诊断的精神病在非传染性疾病(包括早期发病)的种族群体之间的差异,并探讨这些差异是否存在于那些没有晚期痴呆的人身上。方法:这是一项irb批准的回顾性分析。数据来自国家阿尔茨海默病协调中心统一数据集,来自42个阿尔茨海默病研究中心。截至2023年6月,年龄在40-95岁之间,基线评估为轻度认知障碍(MCI)或痴呆。精神病被定义为临床医生诊断的视觉或听觉幻觉或在基线评估时表现的妄想。种族组是自我报告的。使用校正多变量logistic回归对结果进行二分类测量,估计非传染性疾病中种族群体与精神病之间的关联。协变量包括年龄、性别、受教育年限、认知障碍严重程度(临床痴呆评定量表)以及是否存在任何自我报告的先前存在的精神疾病。对年龄小于65岁的人也进行了分析。对轻度痴呆患者(临床痴呆评分0.5或1)和轻度认知障碍患者进行探索性多变量logistic回归分析。结果:共纳入22,854名受试者。平均年龄73 + 9.7岁,女性占50%。共有8352人(37%)患有轻度认知障碍,14502人(63%)患有痴呆症。在调整分析中,美国印第安人/阿拉斯加原住民(AI/AN) (OR 2.70, 1.75-4.17, p < 0.0001)、黑人拉丁裔(OR 2.33, 1.25-4.35, p = 0.0076)、其他拉丁裔(OR 1.82, 1.42-2.33, p < 0.0001)、黑人、非拉丁裔(NL) (OR 1.66,1.47-1.87, p < 0.0001)和白人拉丁裔(OR 1.42, 1.21-1.67, p < 0.0001)参与者出现任何精神病症状的几率高于白人-NL参与者。在40岁到65岁以下的年龄组中,只有Black-NL参与者(OR为1.56,1.13-2.14,p = 0.0064)更有可能被诊断为任何精神病症状。对于轻度痴呆,黑人-拉丁裔(OR 3.44, 1.58-7.48, p = 0.0018)、AI/AN (OR 2.73, 1.66-4.48, p < 0.0001)、其他-拉丁裔(OR 2.38, 1.72-3.30, p < 0.0001)、黑人- nl (OR 2.08,1.77-2.45, p < 0.0001)和白人-拉丁裔(OR 1.55, 1.23-1.95, p = 0.0002)参与者与白人- nl参与者相比,在非传染性疾病中出现精神病的几率更高。单独MCI,无显著性差异。讨论:与白人- nl参与者相比,黑人- nl、拉丁裔和AI/AN个体在非传染性疾病中更容易被诊断为精神病。需要更多的研究来探索所涉及的社会文化、心理社会和神经病理因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Psychosis in Neurocognitive Disorder Among Ethnoculturally Diverse Older Persons.

Background and objectives: There is longstanding evidence that the presence of psychosis in neurocognitive disorders (NCDs) is associated with faster cognitive and functional decline. The goal of this study was to examine how clinician-diagnosed psychosis differs among ethnoracial groups with NCDs (including early onset) and to explore whether these differences exist even for those without advanced dementia.

Method: This is an IRB-approved retrospective analysis. Data are from the National Alzheimer's Coordinating Center Uniform Dataset from 42 Alzheimer's Disease Research Centers. Participants aged 40-95 years as of June 2023 with mild cognitive impairment (MCI) or dementia on baseline evaluation were included. Psychosis was defined as clinician-diagnosed visual or auditory hallucinations or delusions manifesting at the time of baseline evaluation. Ethnoracial groups were self-reported. Associations between ethnoracial groups and psychosis in NCDs were estimated using adjusted multivariable logistic regression with dichotomous measures of outcomes. Covariates included age, sex, years of education, severity of cognitive impairment (Clinical Dementia Rating scale), and presence or absence of any self-reported preexisting psychiatric illness. An analysis by age younger than 65 years was also conducted. Exploratory multivariable logistic regression analyses were performed for participants with milder stages of dementia (Clinical Dementia Rating 0.5 or 1) and for the subset of participants diagnosed with MCI.

Results: A total of 22,854 participants were included. The mean age was 73 + 9.7 years, and 50% were women. A total of 8,352 (37%) had MCI and 14,502 (63%) had dementia. In adjusted analysis, American Indian/Alaska Native (AI/AN) (OR 2.70, 1.75-4.17, p < 0.0001), Black-Latino (OR 2.33, 1.25-4.35, p = 0.0076), Other-Latino (OR 1.82, 1.42-2.33, p < 0.0001), Black, non-Latino (NL) (OR 1.66,1.47-1.87, p < 0.0001), and White-Latino (OR 1.42, 1.21-1.67, p < 0.0001) participants had greater odds of any psychotic symptom than White-NL participants. For age groups 40 to younger than 65 years, only Black-NL participants (OR 1.56, 1.13-2.14, p = 0.0064) were more likely to be diagnosed with any psychotic symptoms. For milder stages of dementia, Black-Latino (OR 3.44, 1.58-7.48, p = 0.0018), AI/AN (OR 2.73, 1.66-4.48, p < 0.0001), Other-Latino (OR 2.38, 1.72-3.30, p < 0.0001), Black-NL (OR 2.08,1.77-2.45, p < 0.0001), and White-Latino (OR 1.55, 1.23-1.95, p = 0.0002) participants had greater odds of psychosis in NCDs when compared with White-NL participants. For MCI alone, there were no significant differences.

Discussion: Black-NL, Latino, and AI/AN individuals were more likely to be diagnosed with psychosis in NCDs when compared with White-NL participants. More research is needed to explore sociocultural, psychosocial, and neuropathologic factors involved.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信