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1.
Eur J Clin Invest ; 35(2): 99-103, 2005 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15667580

RESUMO

BACKGROUND: Following cisplatin-based chemotherapy, survivors of testicular cancer have a high prevalence of cardiovascular risk factors and an increased risk of cardiovascular disease. Cardiac function has not been extensively studied and no comparisons have been made with men from the general population. DESIGN: Left ventricular and cardiac autonomic function were evaluated in chemotherapy-treated testicular cancer patients, in stage I patients after orchidectomy only, and in healthy men using Doppler echocardiography [wall motion score index, peak early (E) and atrial filling (A) velocities across the mitral valve, E/A-ratio, isovolumetric relaxation time, and deceleration time of the early peak flow] and measurements of N-terminal pro-brain natriuretic peptide and baroreflex sensitivity. Furthermore, 24-h ambulatory blood pressure was measured. RESULTS: Ninety chemotherapy-treated patients (median age 37 years, range 20-65; median follow up of 7 years, range 3-13) were compared with 44 stage I patients (median age 36 years, range 24-63) and 47 healthy controls (median age 37 years, range 22-55). Wall motion score index was less than 1.5 in all participants. Chemotherapy-treated patients had a higher peak A-wave and a lower E/A-ratio than stage I patients and controls. Isovolumetric relaxation and deceleration times did not differ between groups. Age, 24-h diastolic blood pressure and treatment with chemotherapy were significantly associated with E/A-ratio. Natriuretic peptide levels were normal. Baroreflex sensitivity was similar in the three groups. CONCLUSIONS: Chemotherapy-treated testicular cancer survivors have a lower E/A-ratio than healthy subjects from the general population, which may indicate impaired relaxation of the left ventricle and reflect the high prevalence of cardiovascular risk factors previously reported in these men.


Assuntos
Doenças do Sistema Nervoso Autônomo/induzido quimicamente , Cardiomiopatias/induzido quimicamente , Neoplasias Testiculares/tratamento farmacológico , Disfunção Ventricular Esquerda/induzido quimicamente , Adulto , Idoso , Antineoplásicos/efeitos adversos , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Doenças do Sistema Nervoso Autônomo/fisiopatologia , Barorreflexo , Bleomicina/administração & dosagem , Pressão Sanguínea/fisiologia , Cardiomiopatias/fisiopatologia , Cisplatino/administração & dosagem , Cisplatino/efeitos adversos , Ecocardiografia Doppler , Etoposídeo/administração & dosagem , Humanos , Masculino , Pessoa de Meia-Idade , Orquiectomia/métodos , Neoplasias Testiculares/cirurgia , Disfunção Ventricular Esquerda/fisiopatologia
2.
Eur J Cancer ; 40(5): 701-6, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15010071

RESUMO

Testicular cancer patients have an increased risk for coronary artery disease more than ten years after cisplatin-based chemotherapy. We investigated whether vascular changes, including endothelial dysfunction, are present earlier. Ninety chemotherapy-treated testicular cancer patients (median follow-up of seven years) were compared with 44 patients after orchidectomy only and 47 healthy men. Microalbuminuria was present in 10 (12%) chemotherapy patients, one stage I patient and none of the controls. Chemotherapy patients had higher levels of fibrinogen, C-reactive protein (hs-CRP), von Willebrand factor (vWF), plasminogen activator inhibitor (PAI-1), and tissue-type plasminogen activator (t-PA). Chemotherapy patients with elevated PAI-1 (25/90) showed clustering of cardiovascular risk factors resembling the metabolic syndrome. In conclusion, cured testicular cancer patients showed a high prevalence of microalbuminuria and increased plasma levels of endothelial and inflammatory marker proteins, which might progress to more severe endothelial dysfunction and overt atherosclerosis.


Assuntos
Albuminúria/induzido quimicamente , Antineoplásicos/efeitos adversos , Arteriosclerose/induzido quimicamente , Cisplatino/efeitos adversos , Fibrinólise/efeitos dos fármacos , Neoplasias Testiculares/tratamento farmacológico , Adulto , Idoso , Fatores de Coagulação Sanguínea/análise , Proteína C-Reativa/análise , Estudos Transversais , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Orquiectomia , Neoplasias Testiculares/sangue , Neoplasias Testiculares/cirurgia
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