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Heart-type fatty acid binding protein in elective cardioversion of atrial fibrillation
- Source :
- Clinical Biochemistry. 44:947-949
- Publication Year :
- 2011
- Publisher :
- Elsevier BV, 2011.
-
Abstract
- Objectives We sought to investigate whether heart-type fatty acid binding protein (H-FABP), a new marker of myocardial necrosis, increases in relation to elective cardioversion of atrial fibrillation (AF). Methods We studied 25 consecutive patients (61 ± 16 years old, 21 men) admitted to our hospital for elective cardioversion of AF. Peripheral venous samples were drawn immediately before cardioversion, one hour and 24 h after the procedure and assayed for H-FABP. Results A mean of 309 ± 183 J was used for cardioversion. Successful cardioversion in sinus rhythm was achieved in 18 patients (72%). Serum levels of H-FABP did not change significantly either in relation to the procedure [1385 (256–17,127) pg/mL at baseline, 1125 (290–15,238) pg/mL 1 h post and 1045.5 (66–2981) pg/mL 24 h post cardioversion, p = 0.37] or to the success of the procedure. Conclusion H-FABP does not significantly change following elective cardioversion for AF and we, therefore, speculate that myocardial necrosis does not occur during cardioversion.
- Subjects :
- Male
medicine.medical_specialty
medicine.medical_treatment
Post cardioversion
Clinical Biochemistry
Electric Countershock
Myocardial Infarction
Fatty Acid-Binding Proteins
Cardioversion
Fatty acid-binding protein
Necrosis
Internal medicine
Atrial Fibrillation
Creatine Kinase, MB Form
Humans
Medicine
Sinus rhythm
Aged
business.industry
Myocardium
Troponin I
Atrial fibrillation
General Medicine
Middle Aged
medicine.disease
Peripheral
Heart-type fatty acid binding protein
Cardiology
Female
Myocardial necrosis
business
Fatty Acid Binding Protein 3
Biomarkers
Subjects
Details
- ISSN :
- 00099120
- Volume :
- 44
- Database :
- OpenAIRE
- Journal :
- Clinical Biochemistry
- Accession number :
- edsair.doi.dedup.....9c7adde7e796646aecbc14e655519e73
- Full Text :
- https://doi.org/10.1016/j.clinbiochem.2011.05.029