Dinithi Mudalige, Dylan X Guan, Maryam Ghahremani, Zahinoor Ismail
{"title":"轻度行为障碍、睡眠障碍与痴呆症进展之间的纵向联系。","authors":"Dinithi Mudalige, Dylan X Guan, Maryam Ghahremani, Zahinoor Ismail","doi":"10.3233/ADR-230086","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Clinical guidelines recommend incorporating non-cognitive markers like mild behavioral impairment (MBI) and sleep disturbance (SD) into dementia screening to improve detection.</p><p><strong>Objective: </strong>We investigated the longitudinal associations between MBI, SD, and incident dementia.</p><p><strong>Methods: </strong>Participant data were from the National Alzheimer's Coordinating Center in the United States. MBI was derived from the Neuropsychiatric Inventory Questionnaire (NPI-Q) using a published algorithm. SD was determined using the NPI-Q nighttime behaviors item. Cox proportional hazard regressions with time-dependant variables for MBI, SD, and cognitive diagnosis were used to model associations between baseline 1) MBI and incident SD (<i>n</i> = 11,277); 2) SD and incident MBI (<i>n</i> = 10,535); 3) MBI with concurrent SD and incident dementia (<i>n</i> = 13,544); and 4) MBI without concurrent SD and incident dementia (<i>n</i> = 11,921). Models were adjusted for first-visit age, sex, education, cognitive diagnosis, race, and for multiple comparisons using the Benjamini-Hochberg method.</p><p><strong>Results: </strong>The rate of developing SD was 3.1-fold higher in older adults with MBI at baseline compared to those without MBI (95% CI: 2.8-3.3). The rate of developing MBI was 1.5-fold higher in older adults with baseline SD than those without SD (95% CI: 1.3-1.8). The rate of developing dementia was 2.2-fold greater in older adults with both MBI and SD, as opposed to SD alone (95% CI:1.9-2.6).</p><p><strong>Conclusions: </strong>There is a bidirectional relationship between MBI and SD. Older adults with SD develop dementia at higher rates when co-occurring with MBI. Future studies should explore the mechanisms underlying these relationships, and dementia screening may be improved by assessing for both MBI and SD.</p>","PeriodicalId":73594,"journal":{"name":"Journal of Alzheimer's disease reports","volume":"7 1","pages":"1323-1334"},"PeriodicalIF":2.8000,"publicationDate":"2023-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10741901/pdf/","citationCount":"0","resultStr":"{\"title\":\"Longitudinal Associations Between Mild Behavioral Impairment, Sleep Disturbance, and Progression to Dementia.\",\"authors\":\"Dinithi Mudalige, Dylan X Guan, Maryam Ghahremani, Zahinoor Ismail\",\"doi\":\"10.3233/ADR-230086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Clinical guidelines recommend incorporating non-cognitive markers like mild behavioral impairment (MBI) and sleep disturbance (SD) into dementia screening to improve detection.</p><p><strong>Objective: </strong>We investigated the longitudinal associations between MBI, SD, and incident dementia.</p><p><strong>Methods: </strong>Participant data were from the National Alzheimer's Coordinating Center in the United States. MBI was derived from the Neuropsychiatric Inventory Questionnaire (NPI-Q) using a published algorithm. SD was determined using the NPI-Q nighttime behaviors item. Cox proportional hazard regressions with time-dependant variables for MBI, SD, and cognitive diagnosis were used to model associations between baseline 1) MBI and incident SD (<i>n</i> = 11,277); 2) SD and incident MBI (<i>n</i> = 10,535); 3) MBI with concurrent SD and incident dementia (<i>n</i> = 13,544); and 4) MBI without concurrent SD and incident dementia (<i>n</i> = 11,921). Models were adjusted for first-visit age, sex, education, cognitive diagnosis, race, and for multiple comparisons using the Benjamini-Hochberg method.</p><p><strong>Results: </strong>The rate of developing SD was 3.1-fold higher in older adults with MBI at baseline compared to those without MBI (95% CI: 2.8-3.3). The rate of developing MBI was 1.5-fold higher in older adults with baseline SD than those without SD (95% CI: 1.3-1.8). The rate of developing dementia was 2.2-fold greater in older adults with both MBI and SD, as opposed to SD alone (95% CI:1.9-2.6).</p><p><strong>Conclusions: </strong>There is a bidirectional relationship between MBI and SD. Older adults with SD develop dementia at higher rates when co-occurring with MBI. Future studies should explore the mechanisms underlying these relationships, and dementia screening may be improved by assessing for both MBI and SD.</p>\",\"PeriodicalId\":73594,\"journal\":{\"name\":\"Journal of Alzheimer's disease reports\",\"volume\":\"7 1\",\"pages\":\"1323-1334\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2023-12-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10741901/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Alzheimer's disease reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3233/ADR-230086\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's disease reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3233/ADR-230086","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
背景:临床指南建议将轻度行为障碍(MBI)和睡眠障碍(SD)等非认知标记纳入痴呆症筛查,以提高发现率:我们研究了 MBI、SD 与痴呆症事件之间的纵向关联:参与者数据来自美国国家阿尔茨海默氏症协调中心。MBI通过神经精神量表问卷(NPI-Q)得出,采用的是一种已公布的算法。SD通过NPI-Q夜间行为项目确定。利用MBI、SD和认知诊断的时间依赖变量进行Cox比例危险回归,以建立基线1)MBI和事件SD(n = 11,277);2)SD和事件MBI(n = 10,535);3)并发SD的MBI和事件痴呆(n = 13,544);4)不并发SD的MBI和事件痴呆(n = 11,921)之间的关联模型。模型根据首次就诊的年龄、性别、教育程度、认知诊断、种族进行了调整,并使用本杰明-霍奇伯格方法进行了多重比较:基线时患有 MBI 的老年人的 SD 患病率是未患有 MBI 的老年人的 3.1 倍(95% CI:2.8-3.3)。基线值为 SD 的老年人患 MBI 的比例是未患 SD 的老年人的 1.5 倍(95% CI:1.3-1.8)。同时患有MBI和SD的老年人患痴呆症的比例是单独患有SD的老年人的2.2倍(95% CI:1.9-2.6):结论:MBI和SD之间存在双向关系。结论:MBI和SD之间存在双向关系,当SD与MBI同时存在时,患有SD的老年人患痴呆症的比例更高。未来的研究应探索这些关系的内在机制,同时评估MBI和SD可能会改善痴呆症筛查。
Longitudinal Associations Between Mild Behavioral Impairment, Sleep Disturbance, and Progression to Dementia.
Background: Clinical guidelines recommend incorporating non-cognitive markers like mild behavioral impairment (MBI) and sleep disturbance (SD) into dementia screening to improve detection.
Objective: We investigated the longitudinal associations between MBI, SD, and incident dementia.
Methods: Participant data were from the National Alzheimer's Coordinating Center in the United States. MBI was derived from the Neuropsychiatric Inventory Questionnaire (NPI-Q) using a published algorithm. SD was determined using the NPI-Q nighttime behaviors item. Cox proportional hazard regressions with time-dependant variables for MBI, SD, and cognitive diagnosis were used to model associations between baseline 1) MBI and incident SD (n = 11,277); 2) SD and incident MBI (n = 10,535); 3) MBI with concurrent SD and incident dementia (n = 13,544); and 4) MBI without concurrent SD and incident dementia (n = 11,921). Models were adjusted for first-visit age, sex, education, cognitive diagnosis, race, and for multiple comparisons using the Benjamini-Hochberg method.
Results: The rate of developing SD was 3.1-fold higher in older adults with MBI at baseline compared to those without MBI (95% CI: 2.8-3.3). The rate of developing MBI was 1.5-fold higher in older adults with baseline SD than those without SD (95% CI: 1.3-1.8). The rate of developing dementia was 2.2-fold greater in older adults with both MBI and SD, as opposed to SD alone (95% CI:1.9-2.6).
Conclusions: There is a bidirectional relationship between MBI and SD. Older adults with SD develop dementia at higher rates when co-occurring with MBI. Future studies should explore the mechanisms underlying these relationships, and dementia screening may be improved by assessing for both MBI and SD.