Polymorphism modulates symptomatic response to antiarrhythmic drug therapy in patients with lone atrial fibrillation

scientific article

Polymorphism modulates symptomatic response to antiarrhythmic drug therapy in patients with lone atrial fibrillation is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.HRTHM.2007.02.006
P932PMC publication ID1948880
P698PubMed publication ID17556195
P5875ResearchGate publication ID6281079

P50authorMarylyn D. RitchieQ18631934
Dawood DarbarQ38327125
Alison Motsinger-ReifQ52448430
Dan RodenQ58973971
P2093author name stringJames V Gainer
P2860cites workKCNQ1 gain-of-function mutation in familial atrial fibrillationQ24338486
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillationQ24534117
Prognostic implications of echocardiographically determined left ventricular mass in the Framingham Heart StudyQ29614968
Electrical, morphological, and ultrastructural remodeling and reverse remodeling in a canine model of chronic atrial fibrillationQ30306103
ACC/AHA key data elements and definitions for measuring the clinical management and outcomes of patients with atrial fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Data Standards (WritiQ30940275
The natural history of lone atrial fibrillation. A population-based study over three decadesQ34186025
Characteristics and prognosis of lone atrial fibrillation. 30-year follow-up in the Framingham StudyQ34201000
Relations among impaired coronary flow reserve, left ventricular hypertrophy and thallium perfusion defects in hypertensive patients without obstructive coronary artery diseaseQ68408728
Echocardiographic criteria for left ventricular hypertrophy: the Framingham Heart StudyQ70026998
Angiotensin-converting enzyme in the human heart. Effect of the deletion/insertion polymorphismQ72034083
Angiotensin-converting enzyme DD genotype in patients with ischaemic or idiopathic dilated cardiomyopathyQ72235427
A prospective evaluation of an angiotensin-converting-enzyme gene polymorphism and the risk of ischemic heart diseaseQ72541490
Prevalence, age distribution, and gender of patients with atrial fibrillation. Analysis and implicationsQ72566134
Angiotensin II and aldosterone receptor binding in rat heart and kidney: response to chronic angiotensin II or aldosterone administrationQ72575475
Collagen metabolism in cultured adult rat cardiac fibroblasts: response to angiotensin II and aldosteroneQ72819723
Locus for atrial fibrillation maps to chromosome 6q14-16Q73469209
Pharmacogenetic interactions between beta-blocker therapy and the angiotensin-converting enzyme deletion polymorphism in patients with congestive heart failureQ73684390
Effects of atrial dilatation on refractory period and vulnerability to atrial fibrillation in the isolated Langendorff-perfused rabbit heartQ73744475
Increased expression of extracellular signal-regulated kinase and angiotensin-converting enzyme in human atria during atrial fibrillationQ73782374
Angiotensin II antagonist prevents electrical remodeling in atrial fibrillationQ73854861
Regulation of angiotensin II receptor subtypes during atrial fibrillation in humansQ73889054
C-reactive protein elevation in patients with atrial arrhythmias: inflammatory mechanisms and persistence of atrial fibrillationQ77337410
ACE (I/D) genotype as a predictor of the magnitude and duration of the response to an ACE inhibitor drug (enalaprilat) in humansQ77554983
Pharmacogenetic interactions between angiotensin-converting enzyme inhibitor therapy and the angiotensin-converting enzyme deletion polymorphism in patients with congestive heart failureQ80998610
An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levelsQ34262228
Renin-angiotensin system gene polymorphisms and atrial fibrillationQ34306157
Parental atrial fibrillation as a risk factor for atrial fibrillation in offspringQ34327141
Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac deathQ34335461
New ideas about atrial fibrillation 50 years on.Q34503407
Histological substrate of atrial biopsies in patients with lone atrial fibrillationQ34742809
Familial atrial fibrillation is a genetically heterogeneous disorder.Q35160348
The impact of renin-angiotensin system polymorphisms on physiological and pathophysiological processes in humansQ35748420
Mitogen-activated protein kinases p42mapk and p44mapk are required for fibroblast proliferationQ36525558
Echocardiographic determination of left ventricular mass in man. Anatomic validation of the methodQ39802766
PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1)Q40421372
Identification of a genetic locus for familial atrial fibrillationQ40900354
Ascorbate attenuates atrial pacing-induced peroxynitrite formation and electrical remodeling and decreases the incidence of postoperative atrial fibrillationQ43738125
Effects of angiotensin-converting enzyme inhibition on the development of the atrial fibrillation substrate in dogs with ventricular tachypacing-induced congestive heart failureQ43803594
C-reactive protein and paroxysmal atrial fibrillation: evidence of the implication of an inflammatory process in paroxysmal atrial fibrillationQ43854958
Pulmonary vein isolation for paroxysmal and persistent atrial fibrillationQ43904609
Influence of plasma aldosterone on left ventricular geometry and diastolic function in treated essential hypertensionQ43940854
Enalapril effects on atrial remodeling and atrial fibrillation in experimental congestive heart failureQ44025903
Quality of life improves with treatment in the Canadian Trial of Atrial FibrillationQ44035539
Use of irbesartan to maintain sinus rhythm in patients with long-lasting persistent atrial fibrillation: a prospective and randomized study.Q44064962
Angiotensin-converting enzyme (ACE) I/D genotype and renal ACE gene expressionQ44152987
Asymptomatic or "silent" atrial fibrillation: frequency in untreated patients and patients receiving azimilideQ44342393
Effects of angiotensin II type 1 receptor antagonist on electrical and structural remodeling in atrial fibrillationQ44487854
Quality of life variables in the selection of rate versus rhythm control in patients with atrial fibrillation: observations from the Canadian Trial of Atrial FibrillationQ44739491
A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarctionQ44836568
Relationship between C-reactive protein concentrations during glucocorticoid therapy and recurrent atrial fibrillationQ44961647
Association of angiotensin converting enzyme gene polymorphisms with left ventricular hypertrophyQ46683608
Left ventricular size, mass, and function in relation to angiotensin-converting enzyme gene polymorphism in humansQ47369600
Deletion polymorphism of the angiotensin-converting enzyme gene is independently associated with left ventricular mass and geometric remodeling in systemic hypertension.Q51027011
Symptomatic burden as an endpoint to evaluate interventions in patients with atrial fibrillation.Q51975703
Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.Q52429603
The impairment of health-related quality of life in patients with intermittent atrial fibrillation: implications for the assessment of investigational therapy.Q53510743
Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarctionQ57606113
P433issue6
P921main subjectAtrial FibrillationQ815819
P304page(s)743-749
P577publication date2007-02-09
P1433published inHeart RhythmQ2058605
P1476titlePolymorphism modulates symptomatic response to antiarrhythmic drug therapy in patients with lone atrial fibrillation
P478volume4

Reverse relations

cites work (P2860)
Q36280780A KCNJ8 mutation associated with early repolarization and atrial fibrillation
Q37730875A common angiotensin-converting enzyme polymorphism and preoperative angiotensin-converting enzyme inhibition modify risk of tachyarrhythmias after congenital heart surgery
Q37626276A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation.
Q35633271A common β1-adrenergic receptor polymorphism predicts favorable response to rate-control therapy in atrial fibrillation.
Q35549364A genetic contribution to risk for postoperative junctional ectopic tachycardia in children undergoing surgery for congenital heart disease
Q33993646A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation
Q37135895A genotype-dependent intermediate ECG phenotype in patients with persistent lone atrial fibrillation genotype ECG-phenotype correlation in atrial fibrillation
Q37339741ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: implications for electrical remodeling
Q38977861Association of the angiotensinogen M235T polymorphism with recurrence after catheter ablation of acquired atrial fibrillation
Q59136309Atrial Fibrillation Mechanisms and Implications for Catheter Ablation
Q56891140Atrial fibrillation symptom clusters and associated clinical characteristics and outcomes: A cross-sectional secondary data analysis
Q88386985Atrial fibrillation symptom profiles associated with healthcare utilization: A latent class regression analysis
Q36628071Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation
Q34182560Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans
Q36252497Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
Q37688211Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation.
Q36654218Common atrial fibrillation risk alleles at 4q25 predict recurrence after catheter-based atrial fibrillation ablation
Q33854824Common variants in KCNN3 are associated with lone atrial fibrillation
Q35108134Differential impact of race and risk factors on incidence of atrial fibrillation.
Q36683034Functional modeling in zebrafish demonstrates that the atrial-fibrillation-associated gene GREM2 regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm
Q36876093Genetic mechanisms of atrial fibrillation: impact on response to treatment
Q28607469Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)
Q34987142Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias
Q37099702Genetics of atrial fibrillation: rare mutations, common polymorphisms, and clinical relevance
Q38894994Genotype influence in responses to therapy for atrial fibrillation
Q37146274Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation
Q39300535Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy
Q35068272Lymphoblastoid cell lines models of drug response: successes and lessons from this pharmacogenomic model
Q60183578Mechanisms and Drug Development in Atrial Fibrillation
Q30156103Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation
Q33563000Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese
Q34976915Pharmacogenomics: the genetics of variable drug responses
Q37678692Prevalence and predictors of atrial fibrillation among patients undergoing bariatric surgery
Q36537035Relation of morbid obesity and female gender to risk of procedural complications in patients undergoing atrial fibrillation ablation.
Q36098696Relation of the severity of obstructive sleep apnea in response to anti-arrhythmic drugs in patients with atrial fibrillation or atrial flutter
Q38936967Rhythm control in atrial fibrillation
Q36315573Risk factors for bradycardia requiring pacemaker implantation in patients with atrial fibrillation.
Q33746384Role of inflammation and oxidative stress in atrial fibrillation
Q34735964SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation
Q36139922Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.
Q37469038The Role Of Renin Angiotensin System In Atrial Fibrillation
Q36264955The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight?
Q36853514The role of the renin-angiotensin system in atrial fibrillation and the therapeutic effects of ACE-Is and ARBS
Q33578278Whole blood gene expression and atrial fibrillation: the Framingham Heart Study
Q34217688Whole-exome sequencing in familial atrial fibrillation.

Search more.