ABSTRACT
Indoleamine 2,3-dioxygenase (IDO) activity as determined by increases in serum kynurenine was measured in a group of hepatitis C patients treated with consensus interferon (IFN-con1). Kynurenine levels increased significantly within 2 days of initiation of treatment but returned to normal values by week 4 after treatment. Although IDO is normally induced by IFN-gamma, no such IFN was detected by ELISA or biologic assays. Thus, consensus IFN induces low levels of IDO in vivo without an IFN-gamma intermediate.
Subject(s)
Interferon Type I/administration & dosage , Tryptophan Oxygenase/biosynthesis , Enzyme Induction/drug effects , Enzyme Induction/immunology , Hepatitis C/drug therapy , Hepatitis C/immunology , Humans , Indoleamine-Pyrrole 2,3,-Dioxygenase , Interferon Type I/therapeutic use , Interferon-alpha , Interferon-gamma/biosynthesis , Interferon-gamma/blood , Kynurenine/pharmacology , Recombinant Proteins , Tryptophan/bloodABSTRACT
A prolonged rate-corrected QT interval (QTc) may be associated with an increased risk of developing ventricular arrhythmias and sudden death, particularly in patients with the hereditary long QT syndrome (LQTS), myocardial ischemia, or antiarrhythmic medication toxicity. It is known that there are some patients with LQTS who sometimes have a borderline or normal QTc (< or = 0.45 second). Although the QTc has been the standard measurement of ventricular repolarization, it includes both depolarization and repolarization and may not always be a sensitive indicator of the type of repolarization abnormalities seen in LQTS. Intraventricular conduction abnormalities complicate evaluation of the QTc interval. The rate-corrected JT interval (JTc) is a more accurate measurement of ventricular repolarization, and therefore may be a more sensitive means of assessing abnormalities. The QTc on a resting electrocardiogram was determined in 40 patients with LQTS and in 31 patients with right bundle branch block after tetralogy of Fallot repair. These were compared with 1,000 age-matched control subjects. The right bundle branch block group had normal JT and JTc measurements, despite having prolonged QT and QTc intervals compared with controls. The JTc identified 85% of patients affected with LQTS compared with only 58% identified using only the QTc as a marker for the syndrome. The JTc is a more specific measurement of ventricular repolarization than the QTc by eliminating QRS duration variability. It appears to be a more sensitive predictor of repolarization abnormalities, and may be helpful in identifying patients with LQTS who have borderline or normal QTc measurements on resting electrocardiograms.
Subject(s)
Bundle-Branch Block/physiopathology , Electrocardiography , Heart/physiology , Long QT Syndrome/diagnosis , Long QT Syndrome/physiopathology , Adolescent , Adult , Child , Child, Preschool , Electrocardiography/drug effects , Heart/physiopathology , Humans , Infant , Infant, Newborn , Long QT Syndrome/genetics , Membrane Potentials , Nadolol/pharmacology , Propranolol/pharmacology , Reference ValuesABSTRACT
Congenital junctional ectopic tachycardia (JET) is a difficult to treat arrhythmia with a variably poor response to pharmacologic intervention. We report on the successful treatment of a 17-day-old infant with JET via transcatheter radiofrequency ablation of the arrhythmogenic focus resulting in resolution of the tachycardia and maintenance of normal atrioventricular nodal function. Transcatheter radiofrequency ablation techniques should be considered in infants with life-threatening arrhythmia recalcitrant to standard forms of drug therapy.