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1.
Chin Med J (Engl) ; 132(12): 1406-1413, 2019 Jun 20.
Article de Anglais | MEDLINE | ID: mdl-31205097

RÉSUMÉ

BACKGROUND: The long-term predicted value of microvolt T-wave alternans (MTWA) for ventricular tachyarrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) remains unclear. Our study explored the characteristics of MTWA and its prognostic value when combined with an electrophysiologic study (EPS) in patients with ARVC. METHODS: All patients underwent non-invasive MTWA examination with modified moving average (MMA) analysis and an EPS. A positive event was defined as the first occurrence of sudden cardiac death, documented sustained ventricular tachycardia (VT), ventricular fibrillation, or the administration of appropriate implantable cardioverter defibrillator therapy including shock or anti-tachycardia pacing. RESULTS: Thirty-five patients with ARVC (age 38.6 ±â€Š11.0 years; 28 males) with preserved left ventricular (LV) function were recruited. The maximal TWA value (MaxValt) was 17.0 (11.0-27.0) µV. Sustained VT was induced in 22 patients by the EPS. During a median follow-up of 99.9 ±â€Š7.7 months, 15 patients had positive clinical events. When inducible VT was combined with the MaxValt, the area under the curve improved from 0.739 to 0.797. The receiver operating characteristic curve showed that a MaxValt of 23.5 µV was the optimal cutoff value to identify positive events. The multivariate Cox regression model for survival showed that MTWA (MaxValt, hazard ratio [HR], 1.06; 95% confidence interval [CI], 1.01-1.11; P = 0.01) and inducible VT (HR, 5.98; 95% CI, 1.33-26.8; P = 0.01) independently predicted positive events in patients with ARVC. CONCLUSIONS: MTWA assessment with MMA analysis complemented by an EPS might provide improved prognostic ability in patients with ARVC with preserved LV function during long-term follow-up.


Sujet(s)
Troubles du rythme cardiaque/diagnostic , Dysplasie ventriculaire droite arythmogène/diagnostic , Électrocardiographie/méthodes , Électrophysiologie/méthodes , Tachycardie ventriculaire/diagnostic , Adulte , Épreuve d'effort , Femelle , Études de suivi , Humains , Mâle , Adulte d'âge moyen , Fonction ventriculaire gauche/physiologie
2.
Toxicol Ind Health ; 28(2): 152-61, 2012 Mar.
Article de Anglais | MEDLINE | ID: mdl-21632572

RÉSUMÉ

The purpose of this study was to investigate the effects of vitamin E on reproductive hormones and testis structure in mice treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Five experimental groups of a combination of TCDD and vitamin E were designed as follows: 0 ng/kg/d and 0 mg/kg/d (control group), 100 ng/kg/d and 0 mg/kg/d (Group I), 100 ng/kg/d and 20 mg/kg/d (Group II), 100 ng/kg/d and 100 mg/kg/d (Group III), and 100 ng/kg/d and 500 mg/kg/d (Group IV) respectively. Vitamin E and TCDD were given by oral gavage for 7 weeks. The results demonstrated that TCDD decreased the levels of brain gonadotropin releasing hormone (GnRH), testis luteinizing hormone (LH) and follicle stimulating hormone (FSH), serum testosterone and testis spermatozoa number, and damaged testis structure. Vitamin E at 20 mg/kg alleviated the decrease of GnRH; vitamin E at 20, 100, and 500 mg/kg antagonized the decline of LH and FSH; vitamin E at 20 and 100 mg/kg reversed the decrease of testosterone and spermatozoa number; and vitamin E at 100 mg/kg decreased the damage of the testis structure caused by TCDD. The results indicate that vitamin E antagonizes the reproductive endocrine toxicity and alleviates the changes in testicular structure caused by TCDD.


Sujet(s)
Antioxydants/pharmacologie , Hormone de libération des gonadotrophines/métabolisme , Dibenzodioxines polychlorées/toxicité , Testicule/effets des médicaments et des substances chimiques , Testostérone/sang , Vitamine E/pharmacologie , Analyse de variance , Animaux , Chimie du cerveau , Hormone folliculostimulante/sang , Histocytochimie , Hormone lutéinisante/sang , Mâle , Souris , Spermatozoïdes/effets des médicaments et des substances chimiques , Testicule/anatomopathologie , Tests de toxicité chronique
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