脑小血管疾病进展与痴呆症风险:14年随访研究

IF 14.7 1区 医学 Q1 PSYCHIATRY
American Journal of Psychiatry Pub Date : 2023-07-01 Epub Date: 2023-04-19 DOI:10.1176/appi.ajp.20220380
Mina A Jacob, Mengfei Cai, Vera van de Donk, Mayra Bergkamp, José Marques, David G Norris, Roy P C Kessels, Jurgen A H R Claassen, Marco Duering, Anil M Tuladhar, Frank-Erik de Leeuw
{"title":"脑小血管疾病进展与痴呆症风险:14年随访研究","authors":"Mina A Jacob, Mengfei Cai, Vera van de Donk, Mayra Bergkamp, José Marques, David G Norris, Roy P C Kessels, Jurgen A H R Claassen, Marco Duering, Anil M Tuladhar, Frank-Erik de Leeuw","doi":"10.1176/appi.ajp.20220380","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Cerebral small vessel disease (SVD) is considered the most important vascular contributor to cognitive decline and dementia, although a causal relation between its MRI markers and dementia still needs to be established. The authors investigated the relation between baseline SVD severity as well as SVD progression on MRI markers and incident dementia, by subtype, in individuals with sporadic SVD over a follow-up period of 14 years.</p><p><strong>Methods: </strong>The study included 503 participants with sporadic SVD, and without dementia, from the prospective Radboud University Nijmegen Diffusion Tensor and Magnetic Resonance Cohort (RUN DMC) study, with screening for baseline inclusion conducted in 2006. Follow-ups in 2011, 2015, and 2020 included cognitive assessments and MRI scans. Dementia was diagnosed according to DSM-5 criteria and stratified into Alzheimer's dementia and vascular dementia.</p><p><strong>Results: </strong>Dementia as an endpoint was available for 498 participants (99.0%) and occurred in 108 participants (21.5%) (Alzheimer's dementia, N=38; vascular dementia, N=34; mixed-etiology Alzheimer's dementia/vascular dementia, N=26), with a median follow-up time of 13.2 years (interquartile range, 8.8-13.8). Higher baseline white matter hyperintensity (WMH) volume (hazard ratio=1.31 per 1-SD increase, 95% CI=1.02-1.67), presence of diffusion-weighted-imaging-positive lesions (hazard ratio=2.03, 95% CI=1.01-4.04), and higher peak width of skeletonized mean diffusivity (hazard ratio=1.24 per 1-SD increase, 95% CI=1.02-1.51) were independently associated with all-cause dementia and vascular dementia. WMH progression predicted incident all-cause dementia (hazard ratio=1.76 per 1-SD increase, 95% CI=1.18-2.63).</p><p><strong>Conclusions: </strong>Both baseline SVD severity and SVD progression were independently associated with an increase in risk of all-cause dementia over a follow-up of 14 years. The results suggest that SVD progression precedes dementia and may causally contribute to its development. Slowing SVD progression may delay dementia onset.</p>","PeriodicalId":7656,"journal":{"name":"American Journal of Psychiatry","volume":"180 7","pages":"508-518"},"PeriodicalIF":14.7000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Cerebral Small Vessel Disease Progression and the Risk of Dementia: A 14-Year Follow-Up Study.\",\"authors\":\"Mina A Jacob, Mengfei Cai, Vera van de Donk, Mayra Bergkamp, José Marques, David G Norris, Roy P C Kessels, Jurgen A H R Claassen, Marco Duering, Anil M Tuladhar, Frank-Erik de Leeuw\",\"doi\":\"10.1176/appi.ajp.20220380\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Cerebral small vessel disease (SVD) is considered the most important vascular contributor to cognitive decline and dementia, although a causal relation between its MRI markers and dementia still needs to be established. The authors investigated the relation between baseline SVD severity as well as SVD progression on MRI markers and incident dementia, by subtype, in individuals with sporadic SVD over a follow-up period of 14 years.</p><p><strong>Methods: </strong>The study included 503 participants with sporadic SVD, and without dementia, from the prospective Radboud University Nijmegen Diffusion Tensor and Magnetic Resonance Cohort (RUN DMC) study, with screening for baseline inclusion conducted in 2006. Follow-ups in 2011, 2015, and 2020 included cognitive assessments and MRI scans. Dementia was diagnosed according to DSM-5 criteria and stratified into Alzheimer's dementia and vascular dementia.</p><p><strong>Results: </strong>Dementia as an endpoint was available for 498 participants (99.0%) and occurred in 108 participants (21.5%) (Alzheimer's dementia, N=38; vascular dementia, N=34; mixed-etiology Alzheimer's dementia/vascular dementia, N=26), with a median follow-up time of 13.2 years (interquartile range, 8.8-13.8). Higher baseline white matter hyperintensity (WMH) volume (hazard ratio=1.31 per 1-SD increase, 95% CI=1.02-1.67), presence of diffusion-weighted-imaging-positive lesions (hazard ratio=2.03, 95% CI=1.01-4.04), and higher peak width of skeletonized mean diffusivity (hazard ratio=1.24 per 1-SD increase, 95% CI=1.02-1.51) were independently associated with all-cause dementia and vascular dementia. WMH progression predicted incident all-cause dementia (hazard ratio=1.76 per 1-SD increase, 95% CI=1.18-2.63).</p><p><strong>Conclusions: </strong>Both baseline SVD severity and SVD progression were independently associated with an increase in risk of all-cause dementia over a follow-up of 14 years. The results suggest that SVD progression precedes dementia and may causally contribute to its development. Slowing SVD progression may delay dementia onset.</p>\",\"PeriodicalId\":7656,\"journal\":{\"name\":\"American Journal of Psychiatry\",\"volume\":\"180 7\",\"pages\":\"508-518\"},\"PeriodicalIF\":14.7000,\"publicationDate\":\"2023-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Psychiatry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1176/appi.ajp.20220380\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/4/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1176/appi.ajp.20220380","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/4/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 1

摘要

目的:脑小血管病(SVD)被认为是导致认知功能下降和痴呆的最重要的血管因素,但其磁共振成像标记物与痴呆之间的因果关系仍有待确定。作者研究了散发性 SVD 患者在 14 年的随访期内基线 SVD 严重程度以及 SVD 在 MRI 标记上的进展与亚型痴呆事件之间的关系:该研究纳入了503名散发性SVD患者,他们均未患有痴呆症,这些患者来自奈梅亨大学扩散张量和磁共振队列(RUN DMC)前瞻性研究,2006年进行了基线纳入筛选。2011年、2015年和2020年的随访包括认知评估和核磁共振扫描。痴呆的诊断依据DSM-5标准,并分为阿尔茨海默氏症痴呆和血管性痴呆:498名参与者(99.0%)的终点为痴呆,108名参与者(21.5%)的终点为痴呆(阿尔茨海默氏痴呆,38人;血管性痴呆,34人;阿尔茨海默氏痴呆/血管性痴呆混合病因,26人),中位随访时间为13.2年(四分位间范围为8.8-13.8)。较高的基线白质高密度(WMH)体积(每增加1SD,危险比=1.31,95% CI=1.02-1.67)、弥散加权成像阳性病变的存在(危险比=2.03,95% CI=1.01-4.04)以及较高的骨架平均弥散度峰值宽度(每增加1SD,危险比=1.24,95% CI=1.02-1.51)与全因痴呆和血管性痴呆独立相关。WMH进展预示着全因痴呆的发生(每增加1个标准差,危险比=1.76,95% CI=1.18-2.63):结论:在14年的随访中,基线SVD严重程度和SVD进展均与全因痴呆风险的增加独立相关。研究结果表明,SVD进展先于痴呆症,可能是痴呆症发展的诱因。减缓心血管疾病的进展可能会推迟痴呆症的发病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebral Small Vessel Disease Progression and the Risk of Dementia: A 14-Year Follow-Up Study.

Objective: Cerebral small vessel disease (SVD) is considered the most important vascular contributor to cognitive decline and dementia, although a causal relation between its MRI markers and dementia still needs to be established. The authors investigated the relation between baseline SVD severity as well as SVD progression on MRI markers and incident dementia, by subtype, in individuals with sporadic SVD over a follow-up period of 14 years.

Methods: The study included 503 participants with sporadic SVD, and without dementia, from the prospective Radboud University Nijmegen Diffusion Tensor and Magnetic Resonance Cohort (RUN DMC) study, with screening for baseline inclusion conducted in 2006. Follow-ups in 2011, 2015, and 2020 included cognitive assessments and MRI scans. Dementia was diagnosed according to DSM-5 criteria and stratified into Alzheimer's dementia and vascular dementia.

Results: Dementia as an endpoint was available for 498 participants (99.0%) and occurred in 108 participants (21.5%) (Alzheimer's dementia, N=38; vascular dementia, N=34; mixed-etiology Alzheimer's dementia/vascular dementia, N=26), with a median follow-up time of 13.2 years (interquartile range, 8.8-13.8). Higher baseline white matter hyperintensity (WMH) volume (hazard ratio=1.31 per 1-SD increase, 95% CI=1.02-1.67), presence of diffusion-weighted-imaging-positive lesions (hazard ratio=2.03, 95% CI=1.01-4.04), and higher peak width of skeletonized mean diffusivity (hazard ratio=1.24 per 1-SD increase, 95% CI=1.02-1.51) were independently associated with all-cause dementia and vascular dementia. WMH progression predicted incident all-cause dementia (hazard ratio=1.76 per 1-SD increase, 95% CI=1.18-2.63).

Conclusions: Both baseline SVD severity and SVD progression were independently associated with an increase in risk of all-cause dementia over a follow-up of 14 years. The results suggest that SVD progression precedes dementia and may causally contribute to its development. Slowing SVD progression may delay dementia onset.

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
American Journal of Psychiatry
American Journal of Psychiatry 医学-精神病学
CiteScore
22.30
自引率
2.80%
发文量
157
审稿时长
4-8 weeks
期刊介绍: The American Journal of Psychiatry, dedicated to keeping psychiatry vibrant and relevant, publishes the latest advances in the diagnosis and treatment of mental illness. The journal covers the full spectrum of issues related to mental health diagnoses and treatment, presenting original articles on new developments in diagnosis, treatment, neuroscience, and patient populations.
×
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