Sandro Marini, Tamara N Kimball, Ernst Mayerhofer, Reinier W P Tack, Jasper R Senff, Savvina Prapiadou, Cyprien A Rivier, Jonathan Duskin, Christina Kourkoulis, Guido J Falcone, Nirupama Yechoor, Rudolph E Tanzi, Jonathan Rosand, Sanjula Singh, Livia Parodi, Christopher D Anderson
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We aimed to investigate whether the associations between BCS and stroke, LLD, and dementia risks are independent of genetic predisposition for these conditions and quantify the effect of healthy lifestyle across genetic risk distributions for these outcomes.</p><p><strong>Methods: </strong>Using the UK Biobank (UKB) prospective cohort study, we computed baseline BCSs and polygenic scores to estimate genetic predisposition for stroke and LLD and <i>APOE</i> ε allele status to stratify dementia risk. As for outcomes again in UKB, we measured incidence of stroke, LLD, and dementia. We used multivariate Cox proportional hazard models to assess associations between BCS, genetic predisposition, and these outcomes. We also conducted stratified and interaction analyses to estimate the incidence of these outcomes across quartiles of genetic risk and BCS.</p><p><strong>Results: </strong>We included 368,340 UKB participants (median age 58 years (interquartile range 51-63 years), 46.3% male). Independent of genetic risk, a 5-point increase in BCS corresponded to lowered hazards of stroke (hazard ratio [HR] 0.70, 95% CI 0.68-0.73), LLD (HR 0.65, 95% CI 0.63-0.67), and dementia (HR 0.82, 95% CI 0.78-0.85). Incidences of all 3 outcomes were higher among participants with high genetic risk of these outcomes. However, these increased risks were offset for individuals with a higher BCS (incidence rates per 1,000 person-years were 2.76 vs 1.19 for stroke, 7.34 vs 4.46 for LLD, and 3.64 vs 2.05 for dementia, when comparing low and high BCS).</p><p><strong>Discussion: </strong>Across different genetic predispositions for stroke, LLD, and dementia, healthier lifestyle behaviors are protective for brain health, demonstrating the nondeterminism of genetic risk. Furthermore, differences in BCS behave as aggregate risk estimators of all 3 outcomes. Further work is needed to prospectively investigate the utility and performance of the BCS as a targeted intervention in populations at elevated genetic risk of age-related brain disease.</p>","PeriodicalId":19256,"journal":{"name":"Neurology","volume":"103 10","pages":"e210014"},"PeriodicalIF":7.7000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Health-Related Behaviors and Risk of Common Age-Related Brain Diseases Across Severities of Genetic Risk.\",\"authors\":\"Sandro Marini, Tamara N Kimball, Ernst Mayerhofer, Reinier W P Tack, Jasper R Senff, Savvina Prapiadou, Cyprien A Rivier, Jonathan Duskin, Christina Kourkoulis, Guido J Falcone, Nirupama Yechoor, Rudolph E Tanzi, Jonathan Rosand, Sanjula Singh, Livia Parodi, Christopher D Anderson\",\"doi\":\"10.1212/WNL.0000000000210014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objectives: </strong>The 21-point Brain Care Score (BCS) is an index that ranks behaviors and clinical measurements with the aim of encouraging lifestyle adjustments to lower the incidence of age-related brain disease, including stroke, late-life depression (LLD), and dementia. A higher BCS at baseline is associated with a lower risk of these outcomes. We aimed to investigate whether the associations between BCS and stroke, LLD, and dementia risks are independent of genetic predisposition for these conditions and quantify the effect of healthy lifestyle across genetic risk distributions for these outcomes.</p><p><strong>Methods: </strong>Using the UK Biobank (UKB) prospective cohort study, we computed baseline BCSs and polygenic scores to estimate genetic predisposition for stroke and LLD and <i>APOE</i> ε allele status to stratify dementia risk. As for outcomes again in UKB, we measured incidence of stroke, LLD, and dementia. We used multivariate Cox proportional hazard models to assess associations between BCS, genetic predisposition, and these outcomes. We also conducted stratified and interaction analyses to estimate the incidence of these outcomes across quartiles of genetic risk and BCS.</p><p><strong>Results: </strong>We included 368,340 UKB participants (median age 58 years (interquartile range 51-63 years), 46.3% male). Independent of genetic risk, a 5-point increase in BCS corresponded to lowered hazards of stroke (hazard ratio [HR] 0.70, 95% CI 0.68-0.73), LLD (HR 0.65, 95% CI 0.63-0.67), and dementia (HR 0.82, 95% CI 0.78-0.85). Incidences of all 3 outcomes were higher among participants with high genetic risk of these outcomes. However, these increased risks were offset for individuals with a higher BCS (incidence rates per 1,000 person-years were 2.76 vs 1.19 for stroke, 7.34 vs 4.46 for LLD, and 3.64 vs 2.05 for dementia, when comparing low and high BCS).</p><p><strong>Discussion: </strong>Across different genetic predispositions for stroke, LLD, and dementia, healthier lifestyle behaviors are protective for brain health, demonstrating the nondeterminism of genetic risk. Furthermore, differences in BCS behave as aggregate risk estimators of all 3 outcomes. 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引用次数: 0
摘要
背景和目标:21 分护脑评分(BCS)是一项对行为和临床测量进行排名的指数,旨在鼓励人们调整生活方式,以降低中风、晚年抑郁(LLD)和痴呆等老年性脑部疾病的发病率。基线 BCS 越高,发生这些结果的风险越低。我们旨在研究 BCS 与中风、晚年抑郁症和痴呆症风险之间的关联是否与这些疾病的遗传易感性无关,并量化健康生活方式对这些结果的遗传风险分布的影响:利用英国生物库(UKB)前瞻性队列研究,我们计算了基线BCS和多基因评分,以估计中风和LLD的遗传易感性,并计算了APOE ε等位基因状态,以对痴呆风险进行分层。至于结果,我们再次在 UKB 中测量了脑卒中、LLD 和痴呆症的发病率。我们使用多变量 Cox 比例危险模型来评估 BCS、遗传易感性和这些结果之间的关联。我们还进行了分层和交互分析,以估计遗传风险和 BCS 四分位数中这些结果的发生率:我们纳入了 368,340 名 UKB 参与者(中位年龄 58 岁(四分位间范围 51-63 岁),46.3% 为男性)。与遗传风险无关,BCS 每增加 5 分,中风(危险比 [HR] 0.70,95% CI 0.68-0.73)、低密度脂蛋白血症(HR 0.65,95% CI 0.63-0.67)和痴呆(HR 0.82,95% CI 0.78-0.85)的危险性相应降低。在这些结果的高遗传风险参与者中,所有 3 种结果的发生率都较高。然而,这些增加的风险在 BCS 较高的个体中被抵消了(比较低 BCS 和高 BCS,中风的每千人年发病率分别为 2.76 vs 1.19,LLD 的每千人年发病率分别为 7.34 vs 4.46,痴呆的每千人年发病率分别为 3.64 vs 2.05):讨论:在不同的中风、低密度脂蛋白血症和痴呆症遗传倾向中,更健康的生活方式行为对大脑健康具有保护作用,这表明遗传风险具有非决定性。此外,BCS的差异还可作为所有3种结果的总体风险估计因子。需要进一步开展工作,前瞻性地研究 BCS 作为一种有针对性的干预措施,在老年性脑部疾病遗传风险较高的人群中的效用和表现。
Health-Related Behaviors and Risk of Common Age-Related Brain Diseases Across Severities of Genetic Risk.
Background and objectives: The 21-point Brain Care Score (BCS) is an index that ranks behaviors and clinical measurements with the aim of encouraging lifestyle adjustments to lower the incidence of age-related brain disease, including stroke, late-life depression (LLD), and dementia. A higher BCS at baseline is associated with a lower risk of these outcomes. We aimed to investigate whether the associations between BCS and stroke, LLD, and dementia risks are independent of genetic predisposition for these conditions and quantify the effect of healthy lifestyle across genetic risk distributions for these outcomes.
Methods: Using the UK Biobank (UKB) prospective cohort study, we computed baseline BCSs and polygenic scores to estimate genetic predisposition for stroke and LLD and APOE ε allele status to stratify dementia risk. As for outcomes again in UKB, we measured incidence of stroke, LLD, and dementia. We used multivariate Cox proportional hazard models to assess associations between BCS, genetic predisposition, and these outcomes. We also conducted stratified and interaction analyses to estimate the incidence of these outcomes across quartiles of genetic risk and BCS.
Results: We included 368,340 UKB participants (median age 58 years (interquartile range 51-63 years), 46.3% male). Independent of genetic risk, a 5-point increase in BCS corresponded to lowered hazards of stroke (hazard ratio [HR] 0.70, 95% CI 0.68-0.73), LLD (HR 0.65, 95% CI 0.63-0.67), and dementia (HR 0.82, 95% CI 0.78-0.85). Incidences of all 3 outcomes were higher among participants with high genetic risk of these outcomes. However, these increased risks were offset for individuals with a higher BCS (incidence rates per 1,000 person-years were 2.76 vs 1.19 for stroke, 7.34 vs 4.46 for LLD, and 3.64 vs 2.05 for dementia, when comparing low and high BCS).
Discussion: Across different genetic predispositions for stroke, LLD, and dementia, healthier lifestyle behaviors are protective for brain health, demonstrating the nondeterminism of genetic risk. Furthermore, differences in BCS behave as aggregate risk estimators of all 3 outcomes. Further work is needed to prospectively investigate the utility and performance of the BCS as a targeted intervention in populations at elevated genetic risk of age-related brain disease.
期刊介绍:
Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology.
As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content.
Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.