Alteration of serum biomarkers in patients with hypertrophic cardiomyopathy with and without atrial fibrillation.
Munevver SariHayrullah YazarIbrahim KocayiğitAli KaragözMehmet AyturkSerdar FidanUgur ArslantasEnder Özgün ÇakmakGökhan AlıcıBirol OzkanPublished in: Biomarkers in medicine (2021)
Aim: We sought to determine the relationship between presence of atrial fibrillation (AF) and serum biomarkers, including native thiol (antioxidant), disulphide/native thiol ratio, Hs-CRP and high-sensitivity Troponin-I (Hs-TnI) in hypertrophic cardiomyopathy (HCM). Materials & methods: We enrolled consecutive 121 HCM outpatients without AF and 40 HCM outpatients with AF. A 12-lead electrocardiogram, transthoracic echocardiography and 24/48-h ambulatory rhythm monitoring were performed for all patients. Fasting venous blood samples were taken from all study patients to measure serum thiol-disulphide homeostasis, Hs-CRP and Hs-TnI. Results: Serum-native thiol was lower and disulphide/native thiol ratio was more oxidized in HCM patients with AF (p < 0.001). Also, HCM patients with AF had higher Hs-TnI and Hs-CRP than no-AF HCM patients. Disulphide/native thiol ratio, serum-native thiol, age, NYHA functional class≥III, and advanced diastolic dysfunction were independently associated with the presence of AF in HCM. Conclusion: In addition to clinical and echocardiographic findings, oxidative stress is also associated with AF in HCM patients.
Keyphrases
- hypertrophic cardiomyopathy
- atrial fibrillation
- left ventricular
- end stage renal disease
- ejection fraction
- oxidative stress
- newly diagnosed
- chronic kidney disease
- heart failure
- prognostic factors
- blood pressure
- left atrial
- peritoneal dialysis
- type diabetes
- coronary artery disease
- left atrial appendage
- catheter ablation
- patient reported outcomes
- dna damage
- ischemia reperfusion injury
- percutaneous coronary intervention
- adipose tissue
- endoplasmic reticulum stress
- acute coronary syndrome
- direct oral anticoagulants
- induced apoptosis
- diabetic rats
- heat shock protein