keyword
https://read.qxmd.com/read/38505024/transcriptomic-analysis-reveals-the-potential-crosstalk-genes-and-immune-relationship-between-crohn-s-disease-and-atrial-fibrillation
#21
JOURNAL ARTICLE
Xiaohan Qiu, Junlin Teng, Ning Wang, Luying Cao, Congyi Cheng, Cong Su, Youran Dong, Fen Wang, Wenqiang Chen
BACKGROUND: At present, there is a paucity of research on the link between Crohn's disease (CD) and atrial fibrillation (AF). Nevertheless, both ailments are thought to entail inflammatory and autoimmune processes, and emerging evidence indicates that individuals with CD may face an elevated risk of AF. To shed light on this issue, our study seeks to explore the possibility of shared genes, pathways, and immune cells between these two conditions. METHODS: We retrieved the gene expression profiles of both CD and AF from the Gene Expression Omnibus (GEO) database and subjected them to analysis...
February 29, 2024: Journal of Thoracic Disease
https://read.qxmd.com/read/38496712/stroke-emboli-from-patients-with-atrial-fibrillation-enriched-with-neutrophil-extracellular-traps
#22
JOURNAL ARTICLE
Sajal Medha K Akkipeddi, Redi Rahmani, Derrek Schartz, Siddharth Chittaranjan, Nathaniel R Ellens, Gurkirat S Kohli, Tarun Bhalla, Thomas K Mattingly, Kevin Welle, Craig N Morrell, Matthew T Bender
BACKGROUND: Recent literature has demonstrated remarkable heterogeneity in the composition of acute ischemic stroke (AIS) emboli, which may impact susceptibility to therapy. OBJECTIVES: In this study, we explored differences in proteomic composition of retrieved embolic material from patients with stroke with and without atrial fibrillation (AF) (AF+ and AF-, respectively). METHODS: The full proteome of retrieved thromboembolic material from 24 patients with AIS was obtained by mass spectrometry...
February 2024: Research and Practice in Thrombosis and Haemostasis
https://read.qxmd.com/read/38492543/utilizing-rna-sequencing-to-identify-gene-expression-markers-of-stroke-causing-thrombi-origin-a-pilot-study
#23
JOURNAL ARTICLE
Kunakorn Atchaneeyasakul, Karen E Bates, Alyssa Toledo, Anthony J Griswold, Kevin Ramdas, Mitsuyoshi Watanabe, Meghana Shownkeen, Luis Guada, Dileep Yavagal
INTRODUCTION: Stroke embolic source have an unknown origin in 30-40% of cases. Mechanical thrombectomy for acute large vessel occlusion stroke has provided us with a method to directly retrieve the thrombi from patients for analysis. By collecting stroke-causing thrombi from known sources, we can then use high-throughput RNA sequencing (RNAseq) technology to directly measure the gene expression signatures of these clots. This may allow us to identify genetic markers to predict the cause of cryptogenic embolism...
March 15, 2024: Journal of Stroke and Cerebrovascular Diseases: the Official Journal of National Stroke Association
https://read.qxmd.com/read/38479924/red-and-processed-meat-intake-and-risk-of-cardiovascular-disease-a%C3%A2-two-sample-mendelian-randomization-study
#24
JOURNAL ARTICLE
Bing Hu, Xin He, Hao Sun, Yongyi Hu, Fei Li, Yanxiang Sun, Jie Sun, Li Feng
BACKGROUND & AIMS: Previous observational studies have yielded inconsistent findings regarding associations between red/processed meat intake and the risk of cardiovascular disease (CVD). Some studies have suggested positive relationships, while others have demonstrated no significant associations. However, causal effects remain uncertain. This 2023 Mendelianrandomization (MR) study investigated the causal relationship between red and processed meat (porkmeat, mutton meat, beef meat)intake and CVD risk by analyzing summary data from the UK Biobank (exposure), CARDIoGRAMplusC4D (coronary artery disease [CAD]), MEGASTROKE (stroke), Nielsen et al...
April 2024: Clinical Nutrition ESPEN
https://read.qxmd.com/read/38476290/the-role-of-detailed-medical-history-for-the-early-diagnosis-of-familial-bradycardia-in-a-patient-with-associated-atrial-fibrillation-case-report
#25
Andreea Ciacaru, Anna Tusa, Annamaria Magdas, Cristian Podoleanu
BACKGROUND: Bradycardia represents a frequent reason for medical presentation and has a complex aetiology, including genetic disorders, like LMNA mutation. LMNA mutation is responsible for laminopathies, including LMNA -cardiomyopathy. Cardiac involvement is prevalent and is linked to dilated cardiomyopathy associated with conduction block, which is anticipated by bradyarrhythmia and supraventricular tachyarrhythmia. LMNA mutation carriers have higher risk for sudden cardiac death (SCD), malignant ventricular tachycardia, and extreme bradycardia...
March 2024: European Heart Journal. Case Reports
https://read.qxmd.com/read/38474722/high-dietary-intake-of-iron-might-be-harmful-to-atrial-fibrillation-and-modified-by-genetic-diversity-a-prospective-cohort-study
#26
JOURNAL ARTICLE
Zierdi Habudele, Ge Chen, Samantha E Qian, Michael G Vaughn, Junguo Zhang, Hualiang Lin
Some studies suggest an association between iron overload and cardiovascular diseases (CVDs). However, the relationship between dietary iron intake and atrial fibrillation (AF) remains uncertain, as does the role of genetic loci on this association. The study involved 179,565 participants from UK Biobank, tracking incident atrial fibrillation (AF) cases. Iron intake was categorized into low, moderate, and high groups based on dietary surveys conducted from 2009 to 2012. The Cox regression model was used to estimate the risk of AF in relation to iron intake, assessing the hazard ratio (HR) and 95% confidence interval (95% CI)...
February 22, 2024: Nutrients
https://read.qxmd.com/read/38452746/upregulated-genes-in-atrial-fibrillation-blood-and-the-left-atrium
#27
JOURNAL ARTICLE
Takahiro Kamihara, Tomoyasu Kinoshita, Reo Kawano, Seiya Tanaka, Ayano Toda, Fumiya Ohara, Akihiro Hirashiki, Manabu Kokubo, Atsuya Shimizu
INTRODUCTION: Atrial fibrillation (AF) is a common arrhythmia associated with aging. Many known risk factors are associated with AF, but many senior individuals do not develop AF despite having multiple risk factors. This finding suggests that other factors may be involved in AF onset. This study aimed to identify upregulated genes in the peripheral blood and left atrium of patients with AF. These genes may serve as potential biomarkers to predict AF onset risk and its complications. METHODS: Gene expression data was analyzed from blood (n = 3) and left atrial samples (n = 15) of patients with AF and sinus rhythm...
March 7, 2024: Cardiology
https://read.qxmd.com/read/38437179/sex-specific-and-polygenic-effects-underlying-resting-heart-rate-and-associated-risk-of-cardiovascular-disease
#28
JOURNAL ARTICLE
Ada N Nordeidet, Marie Klevjer, Karsten Øvretveit, Erik Madssen, Ulrik Wisløff, Ben M Brumpton, Anja Bye
AIMS: Resting heart rate (RHR) is associated with cardiovascular disease (CVD) and mortality. This study aimed to identify genetic loci associated with RHR, develop a genome-wide polygenic risk score (PRS) for RHR, and assess associations between the RHR PRS and CVD outcomes, to better understand the biological mechanisms linking RHR to disease. Sex-specific analyses were conducted to potentially elucidate different pathways between the sexes. METHODS: We performed a genome-wide meta-analysis of RHR (n=550,467) using two independent study populations, The Trøndelag Health Study (HUNT) and the UK Biobank (UKB), comprising 69,155 and 481,312 participants, respectively...
March 4, 2024: European Journal of Preventive Cardiology
https://read.qxmd.com/read/38435380/implantable-loop-recorder-in-brugada-syndrome-insights-from-a-single-center-experience
#29
JOURNAL ARTICLE
Gianmarco Arabia, Manuel Cerini, Angelica Cersosimo, Paolo Vinciguerra, Emiliano Calvi, Gianfranco Mitacchione, Mohamed Aboelhassan, Daniele Giacopelli, Antonio Curnis
BACKGROUND: This study aimed to investigate the characteristics and outcomes of patients diagnosed with Brugada syndrome (BrS) who underwent implantable loop recorder (ILR) insertion during routine clinical activity. METHODS: We conducted a comprehensive screening of all consecutive patients diagnosed with BrS at our institution. We analyzed baseline clinical characteristics, arrhythmic findings, and outcomes. RESULTS: Out of 147 BrS patients, 42 (29 %) received an ILR, 13 (9 %) underwent implantable cardioverter-defibrillator (ICD) placement, and 92 patients (63 %) continued regular cardiological follow-up...
April 2024: IJC Heart & Vasculature
https://read.qxmd.com/read/38432398/coexistent-hcn4-and-gata5-rare-variants-and-atrial-fibrillation-in-a-large-spanish-family
#30
JOURNAL ARTICLE
Alfonso Fraile, Jorge Cebrián, Israel Thuissard-Vasallo, Sara Pérez-Martín, Raquel Casado, Belen Gil-Fournier, Joaquín Alonso-Martín, Juan Tamargo, Ricardo Caballero, Eva Delpón, Francisco G Cosío
BACKGROUND: Familial association of atrial fibrillation (AF) can involve single gene variants related to known arrhythmogenic mechanisms; however, genome-wide association studies often disclose complex genetic variants in familial and non-familial AF, making it difficult to relate to known pathogenetic mechanisms. METHODS: The finding of 4 siblings with AF led to studying 47 members of a family. Long-term Holter monitoring (298 hours average) ruled out silent AFWhole-exome sequencing was performed and variants shared by the index cases were filtered and prioritized according to current recommendations...
March 1, 2024: Canadian Journal of Cardiology
https://read.qxmd.com/read/38428890/variations-in-serum-low-density-lipoprotein-and-sst2-among-heart-failure-patients-with-different-ejection-fraction-groups-and-their-clinical-significance
#31
JOURNAL ARTICLE
Yuanzhi Liu, Lijian Gao, Guangxian Zhao, Wenchen Zhang, Chuan Du, Wenjing Sun, Lei Jin, Hongyu Lu, He Zhou
OBJECTIVE: This study aimed to examine the changes in serum Low Density Lipoprotein Cholesterol (LDL-C) and Soluble Growth Stimulating Expressed Gene 2 Protein (sST2) among Heart Failure (HF) patients with varying ejection fractions and their clinical significance, providing a reference for the clinical assessment of HF severity. METHODS: A total of 238 HF patients treated in our hospital's cardiology department from September 2019 to December 2021 were selected; 68 patients hospitalized in the same period were selected as the control group...
March 1, 2024: Medicine (Baltimore)
https://read.qxmd.com/read/38411625/blood-pressure-elevation-in-erenumab-treated-patients-with-migraine-a-retrospective-real-world-experience
#32
JOURNAL ARTICLE
Nikita Chhabra, Carolyn Mead-Harvey, Christopher A Dodoo, Courtney Iser, Hallie Taylor, Hira Chaudhary, Aimen Vanood, David W Dodick
BACKGROUND: Erenumab is a monoclonal antibody that targets the calcitonin gene-related peptide (CGRP) receptor and is approved for the preventative treatment of migraine in adults. CGRP is involved in the regulation of vasomotor tone under physiologic and pathologic conditions, including hypertension. While there has not been evidence of hypertension in preclinical models or clinical trials, post-marketing data suggest erenumab may be associated with hypertension. This led to a warning in the United States Food and Drug Administration prescribing information for erenumab...
March 2024: Headache
https://read.qxmd.com/read/38402495/cardiovascular-adverse-drug-reactions-of-anti-calcitonin-gene-related-peptide-monoclonal-antibodies-for-migraine-prevention-an-analysis-from-the-european-spontaneous-adverse-event-reporting-system
#33
JOURNAL ARTICLE
Emanuela Elisa Sorbara, Maria Antonietta Barbieri, Giulia Russo, Giuseppe Cicala, Edoardo Spina
INTRODUCTION: Anti-calcitonin gene-related peptide monoclonal antibodies (anti-CGRP-mAbs) have recently been approved for the prevention of migraine, and their safety profile is not fully characterized. OBJECTIVE: The aim of this study was to evaluate the adverse drug reactions (ADRs) of anti-CGRP-mAbs through the analysis of individual case safety reports (ICSRs) collected in the EudraVigilance (EV) database, with a specific focus on cardiovascular (CV) ADRs. METHODS: Data on ICSRs recorded between July 2018 and December 2022 in the EV database, involving one of the anti-CGRP-mAbs for migraine prevention-erenumab (ERE), galcanezumab (GMB), fremanezumab (FMB), and eptinezumab (EPT)-were included in the analysis...
March 2024: BioDrugs: Clinical Immunotherapeutics, Biopharmaceuticals and Gene Therapy
https://read.qxmd.com/read/38398612/revealing-medicinal-constituents-of-bistorta-vivipara-based-on-non-targeted-metabolomics-and-16s-rdna-gene-sequencing-technology
#34
JOURNAL ARTICLE
Hui He, Chuyu Tang, Zhengfei Cao, Tao Wang, Min He, Mengjun Xiao, Licheng Xiao, Yuling Li, Xiuzhang Li
Bistorta vivipara is a medicinal plant with a long history, but there are few studies on the effects of its medicinal components and endophytic bacteria on the accumulation of secondary metabolites. Therefore, in this study, non-targeted metabolomics techniques and 16s rDNA techniques were used to study B. vivipara from different regions. A total of 1290 metabolites and 437 differential metabolites were identified from all samples. Among them, flavonoids, isoflavonoids, and benzopyrans are the main medicinal components of B...
February 15, 2024: Molecules: a Journal of Synthetic Chemistry and Natural Product Chemistry
https://read.qxmd.com/read/38398418/genetic-susceptibility-to-arrhythmia-phenotypes-in-a-middle-eastern-cohort-of-14-259-whole-genome-sequenced-individuals
#35
JOURNAL ARTICLE
Fatima Qafoud, Mohamed Elshrif, Khalid Kunji, Asma Althani, Amar Salam, Jassim Al Suwaidi, Nidal Asaad, Dawood Darbar, Mohamad Saad
Background: The current study explores the genetic underpinnings of cardiac arrhythmia phenotypes within Middle Eastern populations, which are under-represented in genomic medicine research. Methods: Whole-genome sequencing data from 14,259 individuals from the Qatar Biobank were used and contained 47.8% of Arab ancestry, 18.4% of South Asian ancestry, and 4.6% of African ancestry. The frequency of rare functional variants within a set of 410 candidate genes for cardiac arrhythmias was assessed. Polygenic risk score (PRS) performance for atrial fibrillation (AF) prediction was evaluated...
February 15, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/38397190/polymorphic-variants-of-scn5a-gene-rs41312433-and-rs1805124-associated-with-coronary-artery-affliction-in-patients-with-severe-arrhythmias
#36
JOURNAL ARTICLE
Anna Vašků, Tomáš Novotný, Jindřich Špinar
UNLABELLED: Several mutations in this gene for the α subunit of the cardiac sodium channel have been identified in a heterogeneous subset of cardiac rhythm syndromes, including Brugada syndrome, progressive cardiac conduction defect, sick sinus node syndrome, atrial fibrillation and dilated cardiomyopathy. The aim of our study was to associate some SCN5A polymorphic variants directly with confirmed coronary stenoses in patients with non-LQTS ventricular fibrillation/flutter treated by an implantable cardioverter defibrillator...
February 2, 2024: Genes
https://read.qxmd.com/read/38390584/rare-variant-collapsing-and-bioinformatic-analyses-for-different-types-of-cardiac-arrhythmias-in-the-uk-biobank-reveal-novel-susceptibility-loci-and-candidate-amyloid-forming-proteins
#37
JOURNAL ARTICLE
Bengt Zöller, Eric Manderstedt, Christina Lind-Halldén, Christer Halldén
BACKGROUND: Cardiac arrhythmias are a common health problem. Both common and rare genetic risk factors exist for cardiac arrhythmias. Cardiac amyloidosis is a rare disease that may manifest various arrhythmias. Few large-scale whole exome sequencing studies elucidating the contribution of rare variations to arrhythmias have been published. OBJECTIVE: To access gene collapsing analysis of rare variations for different types of cardiac arrhythmias in UK Biobank. Identified genes were analyzed in silico for probability to form amyloid fibrils...
February 2024: Cardiovascular digital health journal
https://read.qxmd.com/read/38372174/dilated-cardiomyopathy-with-concomitant-salt-losing-renal-tubulopathy-caused-by-heterozygous-rragd-gene-variant
#38
JOURNAL ARTICLE
Fernando de Frutos, Carles Diez-Lopez, Elena García-Romero, Leire Gondra, Leire Madariaga, Gema Ariceta, Alejandro García-Castaño, Edoardo Melilli, Lorena Herrador, Laura Triguero-Llonch, Ferran Gran, Laia Rosenfeld, Roger Llatjos, Josep Comin-Colet, José González-Costello
No abstract text is available yet for this article.
February 19, 2024: Circulation. Genomic and Precision Medicine
https://read.qxmd.com/read/38368363/long-noncoding-rna-and-messenger-rna-profiling-in-epicardial-adipose-tissue-of-patients-with-new-onset-postoperative-atrial-fibrillation-after-coronary-artery-bypass-grafting
#39
JOURNAL ARTICLE
Yuanshu Peng, Pixiong Su, Lei Zhao
BACKGROUND: Postoperative atrial fibrillation (POAF) constitutes a significant complication following coronary artery bypass graft surgery (CABG), potentially linked to epicardial adipose tissue (EAT). This investigation seeks to elucidate the association between POAF and EAT at the genetic level. METHODS: EAT and clinical data from patients undergoing CABG were systematically acquired, adhering to established inclusion and exclusion criteria. Patients were categorized into POAF and Non-POAF groups based on the presence or absence of POAF...
February 17, 2024: European Journal of Medical Research
https://read.qxmd.com/read/38352455/decreased-left-atrial-cardiomyocyte-fgf13-expression-increases-vulnerability-to-postoperative-atrial-fibrillation-in-humans
#40
Matthew A Fischer, Adrian Arrieta, Marina Angelini, Elizabeth Soehalim, Douglas J Chapski, Richard J Shemin, Thomas M Vondriska, Riccardo Olcese
Postoperative atrial fibrillation (POAF) is the most common complication after cardiac surgery and a significant cause of increased morbidity and mortality. The development of novel POAF therapeutics has been limited by an insufficient understanding of molecular mechanisms promoting atrial fibrillation. In this observational cohort study, we enrolled 28 patients without a history of atrial fibrillation that underwent mitral valve surgery for degenerative mitral regurgitation and obtained left atrial tissue samples along the standard atriotomy incision in proximity to the right pulmonary veins...
January 31, 2024: bioRxiv
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