活动能力受损和血管性脑损伤的 MRI 标记:社区动脉粥样硬化风险和英国生物数据库研究

IF 2.1 Q3 CLINICAL NEUROLOGY BMJ Neurology Open Pub Date : 2024-01-01 DOI:10.1136/bmjno-2023-000501
Richa Sharma, Adam de Havenon, Cyprien Rivier, Seyedmehdi Payabvash, Rachel Forman, Harlan Krumholz, Guido J Falcone, Kevin N Sheth, Walter N Kernan
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Quantitative biomarkers were categorised into tertiles. Mobility impairment outcomes were imbalance and slow walk in ARIC and recent fall and slow walk in UKB. Adjusted multivariable logistic regression analyses were performed. Results We included 1626 ARIC (mean age 76.2 years; 23.4% imbalance, 25.0% slow walk) and 40 098 UKB (mean age 55 years; 15.8% falls, 2.8% slow walk) participants. In ARIC, imbalance associated with four of five VBI measures (all p values<0.05), most strongly with WMH (adjusted OR, aOR 1.64; 95% CI 1.18 to 2.29). Slow walk associated with four of five VBI measures, most strongly with WMH (aOR 2.32; 95% CI 1.66 to 3.24). In UKB, falls associated with all VBI measures except WMH, most strongly with FA (aOR 1.16; 95% CI 1.08 to 1.24). Slow walking associated with WMH, FA and MD, most strongly with FA (aOR 1.57; 95% CI 1.32 to 1.87). Conclusions VBI is associated with mobility impairment in community-dwelling, clinically stroke-free cohorts. 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引用次数: 0

摘要

背景血管性脑损伤(VBI)可能是造成行动障碍的一个未被充分认识的因素。我们研究了磁共振成像血管性脑损伤生物标志物与行动障碍之间的关系。方法 我们分别分析了社区动脉粥样硬化风险(ARIC)和英国生物库(UKB)研究队列。纳入标准为无流行性临床中风、有脑磁共振成像和平衡与步态数据。MRI VBI 生物标志物包括(ARIC:脑室和白质高密度(WMH)体积、非腔隙性和腔隙性脑梗塞、微出血;UKB:脑室、脑和 WMH 体积、分数各向异性(FA)、平均扩散率(MD)、细胞内和各向同性自由水体积分数)。定量生物标志物分为三等分。ARIC的行动障碍结果为不平衡和行走缓慢,UKB的结果为近期跌倒和行走缓慢。进行了调整后的多变量逻辑回归分析。结果 我们纳入了1626名ARIC(平均年龄76.2岁;23.4%失衡,25.0%行走缓慢)和40 098名UKB(平均年龄55岁;15.8%跌倒,2.8%行走缓慢)参与者。在 ARIC 中,不平衡与五项 VBI 测量中的四项相关(所有 p 值均为 0.05)。这些数据的存储库--HLBI 生物样本和数据存储库 (BioLINCC)。再利用的任何条件(如许可、禁运、版权)-BioLINCC 注册数据是什么-英国生物库数据库。申请访问::.保存这些数据的存储库-英国生物样本库数据库以及任何再利用条件(如许可、禁售、版权)-英国生物样本库注册。
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Impaired mobility and MRI markers of vascular brain injury: Atherosclerosis Risk in Communities and UK Biobank studies
Background Vascular brain injury (VBI) may be an under-recognised contributor to mobility impairment. We examined associations between MRI VBI biomarkers and impaired mobility. Methods We separately analysed Atherosclerosis Risk in Communities (ARIC) and UK Biobank (UKB) study cohorts. Inclusion criteria were no prevalent clinical stroke, and available brain MRI and balance and gait data. MRI VBI biomarkers were (ARIC: ventricular and white matter hyperintensity (WMH) volumes, non-lacunar and lacunar infarctions, microhaemorrhage; UKB: ventricular, brain and WMH volumes, fractional anisotropy (FA), mean diffusivity (MD), intracellular and isotropic free water volume fractions). Quantitative biomarkers were categorised into tertiles. Mobility impairment outcomes were imbalance and slow walk in ARIC and recent fall and slow walk in UKB. Adjusted multivariable logistic regression analyses were performed. Results We included 1626 ARIC (mean age 76.2 years; 23.4% imbalance, 25.0% slow walk) and 40 098 UKB (mean age 55 years; 15.8% falls, 2.8% slow walk) participants. In ARIC, imbalance associated with four of five VBI measures (all p values<0.05), most strongly with WMH (adjusted OR, aOR 1.64; 95% CI 1.18 to 2.29). Slow walk associated with four of five VBI measures, most strongly with WMH (aOR 2.32; 95% CI 1.66 to 3.24). In UKB, falls associated with all VBI measures except WMH, most strongly with FA (aOR 1.16; 95% CI 1.08 to 1.24). Slow walking associated with WMH, FA and MD, most strongly with FA (aOR 1.57; 95% CI 1.32 to 1.87). Conclusions VBI is associated with mobility impairment in community-dwelling, clinically stroke-free cohorts. Consequences of VBI may extend beyond clinically apparent stroke to include mobility. Data are available in a public, open access repository. What the data are—Atherosclerosis Risk in Communities Study (ARIC). Apply for access at: . The repository where they are held—NHLBI Biologic Specimen and Data Repository (BioLINCC). Any conditions of reuse (eg, licence, embargo, copyright)—BioLINCC RegistrationWhat the data are—UK Biobank Database. Apply for access at: . The repository where they are held—UK Biobank DatabaseAnd any conditions of reuse (eg, licence, embargo, copyright)—UK Biobank Registration.
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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
期刊最新文献
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