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High levels of IsoDGR-modified fibronectin are associated with higher levels of macrophages and other rupture-prone plaque characteristics in patients undergoing carotid endarterectomy 在接受颈动脉内膜切除术的患者中,高水平的 IsoDGR 修饰纤连蛋白与较高水平的巨噬细胞和其他易破裂斑块特征有关
Pub Date : 2024-09-03 DOI: 10.1101/2024.09.02.24312942
Tetiana Motsak, Barend M. Mol, Joost K.R. Hoekstra, Valentina Osorio Zuluaga, Saskia Rumpff-Derksen, Ioanna Paspali-Strik, Sofon Cam Ngan, Gerard Pasterkamp, Gert J. de Borst, Siu Kwan Sze, Dominique P.V. de Kleijn
Objective Deamidation of the NGR (Asn-Gly-Arg) motif to the isoDGR (isoAsp-Gly-Arg) motif in fibronectin (IsoDGR-fibronectin) enhances in vitro monocyte and endothelial cell activation. Blocking isoDGR reduces macrophage influx in murine tissues. Although macrophage influx is an important feature of human plaque destabilization, the role for plasma and plaque isoDGR-fibronectin in macrophage influx in the atherosclerotic plaque and thereby increasing plaque vulnerability has not been investigated in large human cohorts.
目的 将纤维粘连蛋白(IsoDGR-fibronectin)中的 NGR(Asn-Gly-Arg)基团脱氨为 isoDGR(isoAsp-Gly-Arg)基团可增强体外单核细胞和内皮细胞的活化。阻断 isoDGR 可减少小鼠组织中巨噬细胞的涌入。虽然巨噬细胞涌入是人类斑块失稳的一个重要特征,但血浆和斑块中的异DGR-纤连蛋白在巨噬细胞涌入动脉粥样硬化斑块从而增加斑块脆弱性方面的作用尚未在大型人类队列中进行研究。
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引用次数: 0
Triglyceride/High Density Lipoprotein Cholesterol Index and Future Cardiovascular Events in Diabetic Patients without Known Cardiovascular Disease 未患已知心血管疾病的糖尿病患者的甘油三酯/高密度脂蛋白胆固醇指数与未来心血管事件的关系
Pub Date : 2024-09-01 DOI: 10.1101/2024.08.30.24312870
Ryosuke Nakashima, Shota Ikeda, Keisuke Shinohara, Sho Matsumoto, Daisuke Yoshida, Yoshiyasu Ono, Hiroka Nakashima, Ryohei Miyamoto, Shouji Matsushima, Junji Kishimoto, Hiroshi Itoh, Issei Komuro, Hiroyuki Tsutsui, Shintaro Kinugawa, Kohtaro Abe
Background The triglyceride/high-density lipoprotein cholesterol (TG/HDL-C) index, calculated as TG levels divided by HDL-C levels, is suggested as a predictor of cardiovascular disease (CVD). We investigated the association between the TG/HDL-C index and initial CVD events in high-risk patients with type 2 diabetes mellitus (T2DM).
背景甘油三酯/高密度脂蛋白胆固醇(TG/HDL-C)指数(计算方法为甘油三酯水平除以高密度脂蛋白胆固醇水平)被认为是心血管疾病(CVD)的预测指标。我们研究了 2 型糖尿病(T2DM)高风险患者的 TG/HDL-C 指数与首次心血管疾病事件之间的关系。
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引用次数: 0
Large Language Models in Cardiology: A Systematic Review 心脏病学中的大型语言模型:系统回顾
Pub Date : 2024-09-01 DOI: 10.1101/2024.09.01.24312887
Moran Gendler, Girish N Nadkarni, Karin Sudri, Michal Cohen-Shelly, Benjamin S Glicksberg, Orly Efros, Shelly Soffer, Eyal Klang
Purpose This review analyzes the application of large language models (LLMs), in the field of cardiology, with a focus on evaluating their performances across various clinical tasks.
目的 本综述分析了大型语言模型(LLMs)在心脏病学领域的应用,重点是评估其在各种临床任务中的表现。
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引用次数: 0
Predicting thoracic aortic dissection in a diverse biobank using a polygenic risk score 利用多基因风险评分预测不同生物库中的胸主动脉夹层
Pub Date : 2024-09-01 DOI: 10.1101/2024.09.01.24312895
John DePaolo, Siavash Zamirpour, Sarah Abramowitz, Gina Biagetti, Renae Judy, Cameron Beeche, Jeffrey Duda, James Gee, Walter R. Witschey, Julio A. Chirinos, Nicholas J. Goel, Nimesh Desai, Wilson Y. Szeto, Dongchuan Guo, Dianna M. Milewicz, Michael G. Levin, James P. Pirruccello, Scott M. Damrauer
Background Thoracic aortic dissection is a life-threatening condition that often occurs in the presence of aortic dilation. Despite a known association between ascending aortic diameter (AscAoD) and dissection risk, predicting dissection risk remains challenging.
背景胸主动脉夹层是一种危及生命的疾病,通常发生在主动脉扩张的情况下。尽管升主动脉直径(AscAoD)与夹层风险之间存在已知的关联,但预测夹层风险仍具有挑战性。
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引用次数: 0
High Precision ECG Digitization Using Artificial Intelligence 利用人工智能实现高精度心电图数字化
Pub Date : 2024-09-01 DOI: 10.1101/2024.08.31.24312876
Anthony Demolder, Viera Kresnakova, Michal Hojcka, Vladimir Boza, Andrej Iring, Adam Rafajdus, Simon Rovder, Timotej Palus, Martin Herman, Felix Bauer, Viktor Jurasek, Robert Hatala, Jozef Bartunek, Boris Vavrik, Robert Herman
Background The digitization of electrocardiograms (ECGs) is an important process in modern healthcare, enabling the preservation, transmission, and advanced analysis of ECG data. Traditional methods for digitizing ECGs from paper formats face significant challenges, particularly in real-world scenarios with varying image quality, paper distortions, and overlapping signals. Existing solutions often require manual input and are limited by their dependence on high-quality images and standardized layouts.
背景心电图(ECG)数字化是现代医疗保健中的一项重要工作,可实现心电图数据的保存、传输和高级分析。将心电图从纸质格式数字化的传统方法面临着巨大的挑战,尤其是在现实世界中图像质量参差不齐、纸张失真和信号重叠的情况下。现有的解决方案通常需要手动输入,并且受限于对高质量图像和标准化布局的依赖。
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引用次数: 0
Children and Adolescent Patients with Variants in the ATP1A3-encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node Dysfunction ATP1A3编码的钠-钾ATP酶α-3亚基变异的儿童和青少年患者对心动过缓的QT反应受损,容易出现窦房结功能障碍
Pub Date : 2024-09-01 DOI: 10.1101/2024.08.31.24312446
Meredith K. Srour, Minu-Tshyeto K. Bidzimou, Padmapriya Muralidharan, Saige M. Mitchell, Mary E. Moya-Mendez, Lauren E. Parker, Gabriela Reyes Valenzuela, Roberto Caraballo, Giacomo Garone, Federico Vigevano, Sarah Weckhuysen, Charissa Millevert, Monica Troncoso, Mario Matamala, Simona Balestrini, Sanjay M. Sisodiya, Josephine Poole, Claudio Zucca, Eleni Panagiotakaki, Maria T. Papadopoulou, Sébile Tchaicha, Matthildi Athina Papathanasiou Terzi, Marta Zawadzka, Maria Mazurkiewicz-Bełdzińska, Carmen Fons, Jennifer Anticona, Elisa De Grandis, Ramona Cordani, Livia Pisciotta, Sergiu Groppa, Sandra Paryjas, Francesca Ragona, Elena Mangia, Tiziana Granata, Andrey Megvinov, Rosaria Vavassori, Mohamad A. Mikati, Andrew P. Landstrom
Background Alternating hemiplegia of childhood (AHC) is a rare disorder with both neurologic and cardiac manifestations. The ATP1A3-D801N variant is associated with a pathologically short QT interval and risk of ventricular arrhythmia following bradycardia; however, the mechanism of this remains unknown. We investigated the relationship between heart rate (HR), QT, and QTc, hypothesizing that individuals with ATP1A3-D801N have abnormal, impaired shortening of QT and QTc at lower HR leading to arrhythmia predisposition.
背景 儿童交替性偏瘫(AHC)是一种罕见的疾病,同时具有神经和心脏表现。ATP1A3-D801N变异与病理性短QT间期和心动过缓后室性心律失常的风险有关;然而,其机制仍不清楚。我们研究了心率(HR)、QT 和 QTc 之间的关系,假设 ATP1A3-D801N 基因携带者在心率较低时 QT 和 QTc 缩短异常、受损,从而导致心律失常倾向。
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引用次数: 0
Aortic root anatomy and impact on new-onset conduction abnormalities after transcatheter aortic valve implantation 主动脉根部解剖及其对经导管主动脉瓣植入术后新发传导异常的影响
Pub Date : 2024-08-31 DOI: 10.1101/2024.08.30.24312869
Habib Layoun, Joseph Kassab, Michel Chedid El Helou, Joseph El Dahdah, Odette Iskandar, Maryam Muhammad Ali Majeed Saidan, Abdelrahman Abushouk, Toshiaki Isogai, Grant Reed, Rishi Puri, Oussama M. Wazni, Amar Krishnaswamy, Serge Harb, Samir Kapadia
Background Angulation of virtual basal ring (VBR), also known as aortic annulus, in relation to sino-tubular joint (STJ) may lead to greater exposure of implanted stent to the conduction system, consequently increasing the risk of LBBB.
背景 虚拟基底环(VBR),又称主动脉瓣环,与声门-管状关节(STJ)的夹角可能会导致植入的支架更多地暴露于传导系统,从而增加发生 LBBB 的风险。
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引用次数: 0
Exploring associations between estrogen and gene candidates identified by coronary artery disease genome-wide association studies 探索雌激素与冠状动脉疾病全基因组关联研究确定的候选基因之间的关系
Pub Date : 2024-08-30 DOI: 10.1101/2024.08.29.24312812
Ava P. Aminbakhsh, Emilie T. Théberge, Elizabeth Burden, Cindy Kalenga Adejumo, Anna Lehman, Tara L. Sedlak
Introduction Coronary artery disease (CAD) is the leading cause of death around the world, with well-described epidemiological sex and gender differences in prevalence, pathophysiology and management outcomes. It has been hypothesized that sex steroids, like estrogen, may contribute to these sex differences. There is a relatively large genetic component to developing CAD, with heritability estimates ranging between 40-60%. In the last two decades, the computational methods, capabilities and scalability of genome-wide association studies (GWAS) have contributed substantially to advancing the understanding of which genetic candidates contribute to CAD. The aim of this study was to determine if genes discovered in CAD GWASs are affected by estrogen by means of direct modulation or indirect down-stream targets.
导言:冠状动脉疾病(CAD)是导致全球死亡的主要原因,在发病率、病理生理学和治疗效果方面存在着明显的流行病学性别差异。据推测,性类固醇(如雌激素)可能是造成这些性别差异的原因之一。CAD 的发病有相对较大的遗传因素,遗传率估计在 40-60% 之间。在过去二十年中,全基因组关联研究(GWAS)的计算方法、能力和可扩展性极大地促进了人们对哪些遗传候选基因会导致 CAD 的了解。本研究的目的是确定在 CAD 全基因组关联研究中发现的基因是否会受到雌激素的直接调节或间接下游靶点的影响。
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引用次数: 0
Advanced Echocardiographic Assessment in Transthyretin Amyloidosis: Early Phenotype Markers in Mutation Carriers 转甲状腺素淀粉样变性的高级超声心动图评估:突变携带者的早期表型标志物
Pub Date : 2024-08-29 DOI: 10.1101/2024.08.27.24311875
Lorena Squassante Capeline, Frederico José Neves Mancuso, Gardênia Silva Lobo Oishi, Marly Uellendahl, Fernando Naylor, Acary Souza Bulle Oliveira, Valdir Ambrósio Moises
Background Transthyretin cardiac amyloidosis (ATTR-CA) is a life-threatening heart condition due to mutations in the transthyretin (TTR) gene. This study aimed to investigate ventricular global longitudinal strain (GLS) and global circumferential strain (GCS) alongside traditional echocardiographic measures in TTR carries with preserved ejection fraction (EF).
背景 转甲状腺素心脏淀粉样变性病(ATTR-CA)是一种因转甲状腺素(TTR)基因突变而导致的危及生命的心脏疾病。本研究旨在对射血分数(EF)保留的TTR携带者进行心室整体纵向应变(GLS)和整体环向应变(GCS)以及传统超声心动图测量。
{"title":"Advanced Echocardiographic Assessment in Transthyretin Amyloidosis: Early Phenotype Markers in Mutation Carriers","authors":"Lorena Squassante Capeline, Frederico José Neves Mancuso, Gardênia Silva Lobo Oishi, Marly Uellendahl, Fernando Naylor, Acary Souza Bulle Oliveira, Valdir Ambrósio Moises","doi":"10.1101/2024.08.27.24311875","DOIUrl":"https://doi.org/10.1101/2024.08.27.24311875","url":null,"abstract":"<strong>Background</strong> Transthyretin cardiac amyloidosis (ATTR-CA) is a life-threatening heart condition due to mutations in the transthyretin (TTR) gene. This study aimed to investigate ventricular global longitudinal strain (GLS) and global circumferential strain (GCS) alongside traditional echocardiographic measures in TTR carries with preserved ejection fraction (EF).","PeriodicalId":501297,"journal":{"name":"medRxiv - Cardiovascular Medicine","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142218972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comorbidity trajectories before and after the diagnosis of heart failure: a UK Biobank cohort study 心力衰竭诊断前后的合并症轨迹:英国生物库队列研究
Pub Date : 2024-08-28 DOI: 10.1101/2024.08.28.24312712
Hugo MacGowan, Oliver Brown, Michael Drozd, Andrew Walker, Marilena Giannoudi, Sam Straw, Maria Paton, John Gierula, Melanie McGinlay, Kathryn Griffin, Klaus Witte, Mark Kearney, Richard Cubbon
Background: Heart Failure (HF) is frequently associated with multiple comorbidities. We aimed to define their trajectory of accrual to identify opportunities for disease prevention.Methods: We identified all participants in the UK Biobank cohort study diagnosed with HF prior to enrolment or during follow-up, who had disease occurrence data available from both primary and secondary care records (n=9,824). We established the time between diagnosis of HF and 16 common comorbidities to determine the rate and sequence of comorbidity accrual in relation to HF. Stratified analyses considered associations with sex and age at diagnosis of HF.Findings: In chronological sequence, HF was the median fourth diagnosis for men and women. As the age at HF diagnosis increased, HF came later in the sequence of diseases (median second in under 50s to fifth in those aged 80-90). In all age strata, comorbidities accumulated for over a decade before HF and this accelerated in the years immediately before HF. The median time between comorbidity and HF diagnoses ranged from depression preceding HF by 10.7 years to dementia proceeding HF by 0.7 years; all comorbidities presented earlier in women. Atrial fibrillation/flutter was the commonest disease to immediately precede HF, followed by hypertension, cancer, myocardial infarction and osteoarthritis.Interpretation: HF is most often diagnosed in people with established multimorbidity. There is a protracted window of opportunity during which interventions to prevent HF could be applied, often in disease contexts where this is not routine care, such as cancer and osteoarthritis.Funding: British Heart Foundation (RG/F/22/110076)
背景心力衰竭(HF)常常伴有多种并发症。我们的目的是确定他们的发病轨迹,从而发现疾病预防的机会:我们在英国生物库队列研究中确定了所有在入组前或随访期间被诊断为心力衰竭的参与者,他们都有初级和二级医疗记录中的疾病发生数据(n=9,824)。我们确定了心房颤动诊断与 16 种常见合并症之间的时间间隔,以确定与心房颤动相关的合并症发生率和顺序。分层分析考虑了与高血压诊断时的性别和年龄的关系:按时间顺序排列,男性和女性的第四次诊断中位数均为心房颤动。随着确诊心房颤动的年龄增加,心房颤动在疾病排序中出现的时间也越来越晚(50 岁以下的中位数为第二位,80-90 岁的中位数为第五位)。在所有年龄层中,合并症在心房颤动前都已积累了十多年,而在心房颤动前的几年中,合并症的积累速度加快。合并症与心房颤动诊断之间的中位时间从心房颤动前 10.7 年的抑郁症到心房颤动前 0.7 年的痴呆症不等;所有合并症在女性中均出现较早。心房颤动/扑动是心房颤动前最常见的疾病,其次是高血压、癌症、心肌梗塞和骨关节炎:心房颤动最常在已患有多种疾病的人群中被诊断出来。有一个长期的机会之窗,在此期间可以采取干预措施预防心房颤动,而这往往是在癌症和骨关节炎等非日常护理的疾病中:英国心脏基金会(RG/F/22/110076)
{"title":"Comorbidity trajectories before and after the diagnosis of heart failure: a UK Biobank cohort study","authors":"Hugo MacGowan, Oliver Brown, Michael Drozd, Andrew Walker, Marilena Giannoudi, Sam Straw, Maria Paton, John Gierula, Melanie McGinlay, Kathryn Griffin, Klaus Witte, Mark Kearney, Richard Cubbon","doi":"10.1101/2024.08.28.24312712","DOIUrl":"https://doi.org/10.1101/2024.08.28.24312712","url":null,"abstract":"Background: Heart Failure (HF) is frequently associated with multiple comorbidities. We aimed to define their trajectory of accrual to identify opportunities for disease prevention.\u0000Methods: We identified all participants in the UK Biobank cohort study diagnosed with HF prior to enrolment or during follow-up, who had disease occurrence data available from both primary and secondary care records (n=9,824). We established the time between diagnosis of HF and 16 common comorbidities to determine the rate and sequence of comorbidity accrual in relation to HF. Stratified analyses considered associations with sex and age at diagnosis of HF.\u0000Findings: In chronological sequence, HF was the median fourth diagnosis for men and women. As the age at HF diagnosis increased, HF came later in the sequence of diseases (median second in under 50s to fifth in those aged 80-90). In all age strata, comorbidities accumulated for over a decade before HF and this accelerated in the years immediately before HF. The median time between comorbidity and HF diagnoses ranged from depression preceding HF by 10.7 years to dementia proceeding HF by 0.7 years; all comorbidities presented earlier in women. Atrial fibrillation/flutter was the commonest disease to immediately precede HF, followed by hypertension, cancer, myocardial infarction and osteoarthritis.\u0000Interpretation: HF is most often diagnosed in people with established multimorbidity. There is a protracted window of opportunity during which interventions to prevent HF could be applied, often in disease contexts where this is not routine care, such as cancer and osteoarthritis.\u0000Funding: British Heart Foundation (RG/F/22/110076)","PeriodicalId":501297,"journal":{"name":"medRxiv - Cardiovascular Medicine","volume":"37 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142218969","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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medRxiv - Cardiovascular Medicine
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