Lina Rydén, Nazib M Seidu, Hanna Wetterberg, Jenna Najar, Margda Waern, Silke Kern, Kaj Blennow, Henrik Zetterberg, Ingmar Skoog, Anna Zettergren
{"title":"房颤和心力衰竭以及中风和痴呆风险的多基因风险评分。","authors":"Lina Rydén, Nazib M Seidu, Hanna Wetterberg, Jenna Najar, Margda Waern, Silke Kern, Kaj Blennow, Henrik Zetterberg, Ingmar Skoog, Anna Zettergren","doi":"10.1093/braincomms/fcae477","DOIUrl":null,"url":null,"abstract":"<p><p>Atrial fibrillation and heart failure have both been suggested to increase stroke and dementia risk. However, in observational studies, reversed causation and unmeasured confounding may occur. To mitigate these issues, this study aims to investigate if higher genetic risk for atrial fibrillation and heart failure increases dementia and stroke risk. Data were obtained from the population-based Gothenburg H70 Birth Cohort Studies in Sweden. Participants (<i>N</i> = 984) were born in 1930 with baseline examinations at age 70, 75, 79 or 85 and follow-ups until age 88-89. Polygenic risk scores at the 5 × 10<sup>-8</sup>, 1 × 10<sup>-5</sup>, 1 × 10<sup>-3</sup> and 1 × 10<sup>-1</sup> thresholds were generated for atrial fibrillation and heart failure. Stroke was diagnosed based on self-reports, close-informant interviews, and the National Patient Register. Dementia was diagnosed based on neuropsychiatric examinations, close-informant interviews, and the National Patient Register. Cox regression analyses were performed, adjusted for sex, age at baseline and the first five principal components to correct for population stratification. Those within the highest atrial fibrillation-polygenic risk score tertile had a 1.5 (95% CI 1.09-2.03) increased risk of dementia (at the 1 × 10<sup>-5</sup> threshold) and a 1.5 (95% CI 1.07-2.03) increased risk of stroke (at the 1 × 10<sup>-3</sup> threshold) compared to the lowest tertile. Those within the highest heart failure-polygenic risk score tertile had a 1.6 (95% CI 1.19-2.27) increased risk of dementia (at the 5 × 10<sup>-8</sup> threshold), but no increased risk of stroke (HR 1.2; 95% CI 0.83-1.60 at the 1 × 10<sup>-5</sup> threshold), compared to the lowest tertile. When analysing the polygenic risk scores as a continuous variable, the associations were in the same direction, although weaker. This study, investigating genetic risk of atrial fibrillation and heart failure in relation to stroke and dementia, supports the increasing body of evidence suggesting that atrial fibrillation is associated with both stroke and dementia risk. Whether heart failure increases dementia risk is less established, but the present study found that genetic risk of heart failure increased dementia risk. The finding that genetic risk for heart failure did not increase stroke risk needs to be interpreted with caution, as it may be due to a lack of statistical power. There are guidelines on how to best treat atrial fibrillation to prevent stroke, but more knowledge is needed on how to treat atrial fibrillation and heart failure to prevent dementia.</p>","PeriodicalId":93915,"journal":{"name":"Brain communications","volume":"7 1","pages":"fcae477"},"PeriodicalIF":4.1000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11748287/pdf/","citationCount":"0","resultStr":"{\"title\":\"Polygenic risk scores for atrial fibrillation and heart failure and the risk of stroke and dementia.\",\"authors\":\"Lina Rydén, Nazib M Seidu, Hanna Wetterberg, Jenna Najar, Margda Waern, Silke Kern, Kaj Blennow, Henrik Zetterberg, Ingmar Skoog, Anna Zettergren\",\"doi\":\"10.1093/braincomms/fcae477\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Atrial fibrillation and heart failure have both been suggested to increase stroke and dementia risk. However, in observational studies, reversed causation and unmeasured confounding may occur. To mitigate these issues, this study aims to investigate if higher genetic risk for atrial fibrillation and heart failure increases dementia and stroke risk. Data were obtained from the population-based Gothenburg H70 Birth Cohort Studies in Sweden. Participants (<i>N</i> = 984) were born in 1930 with baseline examinations at age 70, 75, 79 or 85 and follow-ups until age 88-89. Polygenic risk scores at the 5 × 10<sup>-8</sup>, 1 × 10<sup>-5</sup>, 1 × 10<sup>-3</sup> and 1 × 10<sup>-1</sup> thresholds were generated for atrial fibrillation and heart failure. Stroke was diagnosed based on self-reports, close-informant interviews, and the National Patient Register. Dementia was diagnosed based on neuropsychiatric examinations, close-informant interviews, and the National Patient Register. Cox regression analyses were performed, adjusted for sex, age at baseline and the first five principal components to correct for population stratification. Those within the highest atrial fibrillation-polygenic risk score tertile had a 1.5 (95% CI 1.09-2.03) increased risk of dementia (at the 1 × 10<sup>-5</sup> threshold) and a 1.5 (95% CI 1.07-2.03) increased risk of stroke (at the 1 × 10<sup>-3</sup> threshold) compared to the lowest tertile. Those within the highest heart failure-polygenic risk score tertile had a 1.6 (95% CI 1.19-2.27) increased risk of dementia (at the 5 × 10<sup>-8</sup> threshold), but no increased risk of stroke (HR 1.2; 95% CI 0.83-1.60 at the 1 × 10<sup>-5</sup> threshold), compared to the lowest tertile. When analysing the polygenic risk scores as a continuous variable, the associations were in the same direction, although weaker. This study, investigating genetic risk of atrial fibrillation and heart failure in relation to stroke and dementia, supports the increasing body of evidence suggesting that atrial fibrillation is associated with both stroke and dementia risk. Whether heart failure increases dementia risk is less established, but the present study found that genetic risk of heart failure increased dementia risk. The finding that genetic risk for heart failure did not increase stroke risk needs to be interpreted with caution, as it may be due to a lack of statistical power. There are guidelines on how to best treat atrial fibrillation to prevent stroke, but more knowledge is needed on how to treat atrial fibrillation and heart failure to prevent dementia.</p>\",\"PeriodicalId\":93915,\"journal\":{\"name\":\"Brain communications\",\"volume\":\"7 1\",\"pages\":\"fcae477\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11748287/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/braincomms/fcae477\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/braincomms/fcae477","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
心房颤动和心力衰竭都被认为会增加中风和痴呆的风险。然而,在观察性研究中,可能会出现反向因果关系和未测量的混淆。为了缓解这些问题,本研究旨在调查心房颤动和心力衰竭的较高遗传风险是否会增加痴呆和中风的风险。数据来自瑞典以人群为基础的哥德堡H70出生队列研究。参与者(N = 984)出生于1930年,在70岁、75岁、79岁或85岁时进行基线检查,并随访至88-89岁。心房颤动和心力衰竭的多基因风险评分分别为5 × 10-8、1 × 10-5、1 × 10-3和1 × 10-1阈值。中风的诊断是基于自我报告、近距离访谈和国家患者登记。痴呆的诊断是基于神经精神病学检查、密切的知情访谈和国家患者登记册。进行Cox回归分析,调整性别、基线年龄和前五个主要成分以校正人口分层。与最低分位数相比,房颤-多基因风险评分最高分位数的患者痴呆风险增加1.5 (95% CI 1.09-2.03) (1 × 10-5阈值),卒中风险增加1.5 (95% CI 1.07-2.03) (1 × 10-3阈值)。心力衰竭-多基因风险评分最高的患者痴呆风险增加1.6 (95% CI 1.19-2.27) (5 × 10-8阈值),但卒中风险未增加(HR 1.2;95% CI 0.83-1.60 (1 × 10-5阈值),与最低分位数相比。当将多基因风险评分作为一个连续变量进行分析时,相关性虽然较弱,但方向相同。这项研究调查了心房颤动和心力衰竭与中风和痴呆的遗传风险,支持越来越多的证据表明心房颤动与中风和痴呆风险相关。心力衰竭是否会增加患痴呆症的风险尚不确定,但目前的研究发现,心力衰竭的遗传风险会增加患痴呆症的风险。心力衰竭的遗传风险不会增加中风的风险,这一发现需要谨慎解释,因为这可能是由于缺乏统计能力。有关于如何最好地治疗房颤以预防中风的指南,但如何治疗房颤和心力衰竭以预防痴呆需要更多的知识。
Polygenic risk scores for atrial fibrillation and heart failure and the risk of stroke and dementia.
Atrial fibrillation and heart failure have both been suggested to increase stroke and dementia risk. However, in observational studies, reversed causation and unmeasured confounding may occur. To mitigate these issues, this study aims to investigate if higher genetic risk for atrial fibrillation and heart failure increases dementia and stroke risk. Data were obtained from the population-based Gothenburg H70 Birth Cohort Studies in Sweden. Participants (N = 984) were born in 1930 with baseline examinations at age 70, 75, 79 or 85 and follow-ups until age 88-89. Polygenic risk scores at the 5 × 10-8, 1 × 10-5, 1 × 10-3 and 1 × 10-1 thresholds were generated for atrial fibrillation and heart failure. Stroke was diagnosed based on self-reports, close-informant interviews, and the National Patient Register. Dementia was diagnosed based on neuropsychiatric examinations, close-informant interviews, and the National Patient Register. Cox regression analyses were performed, adjusted for sex, age at baseline and the first five principal components to correct for population stratification. Those within the highest atrial fibrillation-polygenic risk score tertile had a 1.5 (95% CI 1.09-2.03) increased risk of dementia (at the 1 × 10-5 threshold) and a 1.5 (95% CI 1.07-2.03) increased risk of stroke (at the 1 × 10-3 threshold) compared to the lowest tertile. Those within the highest heart failure-polygenic risk score tertile had a 1.6 (95% CI 1.19-2.27) increased risk of dementia (at the 5 × 10-8 threshold), but no increased risk of stroke (HR 1.2; 95% CI 0.83-1.60 at the 1 × 10-5 threshold), compared to the lowest tertile. When analysing the polygenic risk scores as a continuous variable, the associations were in the same direction, although weaker. This study, investigating genetic risk of atrial fibrillation and heart failure in relation to stroke and dementia, supports the increasing body of evidence suggesting that atrial fibrillation is associated with both stroke and dementia risk. Whether heart failure increases dementia risk is less established, but the present study found that genetic risk of heart failure increased dementia risk. The finding that genetic risk for heart failure did not increase stroke risk needs to be interpreted with caution, as it may be due to a lack of statistical power. There are guidelines on how to best treat atrial fibrillation to prevent stroke, but more knowledge is needed on how to treat atrial fibrillation and heart failure to prevent dementia.