La maladie de Parkinson au Canada (serveur d'exploration)

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Risk of heart failure following treatment with dopamine agonists in Parkinson's disease patients

Identifieur interne : 000031 ( PascalFrancis/Corpus ); précédent : 000030; suivant : 000032

Risk of heart failure following treatment with dopamine agonists in Parkinson's disease patients

Auteurs : Santiago Perez-Lloret ; María Ver Nica Rey ; James Crispo ; Daniel Krewski ; Marise Lapeyre-Mestre ; Jean-Louis Montastruc ; Olivier Rascol

Source :

RBID : Pascal:14-0095204

Descripteurs français

English descriptors

Abstract

Introduction: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. Areas covered: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. Expert opinion: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A11 02  1    @1 REY (María Verónica)
A11 03  1    @1 CRISPO (James)
A11 04  1    @1 KREWSKI (Daniel)
A11 05  1    @1 LAPEYRE-MESTRE (Marise)
A11 06  1    @1 MONTASTRUC (Jean-Louis)
A11 07  1    @1 RASCOL (Olivier)
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A14 03      @1 Faculty of Medicine, Department of Clinical Pharmacology, 37 Allées Jules Guesde @2 31000, Toulouse @3 FRA @Z 7 aut.
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C01 01    ENG  @0 Introduction: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. Areas covered: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. Expert opinion: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.
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Format Inist (serveur)

NO : PASCAL 14-0095204 INIST
ET : Risk of heart failure following treatment with dopamine agonists in Parkinson's disease patients
AU : PEREZ-LLORET (Santiago); REY (María Verónica); CRISPO (James); KREWSKI (Daniel); LAPEYRE-MESTRE (Marise); MONTASTRUC (Jean-Louis); RASCOL (Olivier)
AF : Hospital and University Paul Sabatier of Toulouse, France and INSERM CIC9023 and UMR 825, Department of Clinical Pharmacology and Neurosciences/Toulouse/France (1 aut., 2 aut., 5 aut., 6 aut., 7 aut.); University of Ottawa, McLaughlin Centre for Population Health Risk Assessment, 1 Stewart Street/Ottawa, Ontario, K1N 6N5/Canada (3 aut., 4 aut.); Faculty of Medicine, Department of Clinical Pharmacology, 37 Allées Jules Guesde/31000, Toulouse/France (7 aut.)
DT : Publication en série; Niveau analytique
SO : Expert opinion on drug safety; ISSN 1474-0338; Royaume-Uni; Da. 2014; Vol. 13; No. 3; Pp. 351-360; Bibl. 61 ref.
LA : Anglais
EA : Introduction: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. Areas covered: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. Expert opinion: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.
CC : 002B02U; 002B12A01; 002B17G; 002B17A01
FD : Facteur risque; Insuffisance cardiaque; Traitement; Stimulant dopaminergique; Maladie de Parkinson; Homme; Toxicité; Médicament; Pathologie de l'appareil circulatoire; Pharmacovigilance; Pramipexole; Article synthèse; Revue bibliographique; Antiparkinsonien; Neuroprotecteur
FG : Cardiopathie; Maladie dégénérative; Pathologie du système nerveux; Pathologie de l'encéphale; Syndrome extrapyramidal; Pathologie du système nerveux central; Agoniste; Récepteur dopaminergique D2
ED : Risk factor; Heart failure; Treatment; Dopamine agonist; Parkinson disease; Human; Toxicity; Drug; Cardiovascular disease; Pharmacovigilance; Pramipexole; Review; Bibliographic review; Antiparkinson agent; Neuroprotective agent
EG : Heart disease; Degenerative disease; Nervous system diseases; Cerebral disorder; Extrapyramidal syndrome; Central nervous system disease; Agonist; D2 Dopamine receptor
SD : Factor riesgo; Insuficiencia cardíaca; Tratamiento; Estimulante dopaminérgico; Parkinson enfermedad; Hombre; Toxicidad; Medicamento; Aparato circulatorio patología; Farmacovigilancia; Pramipexol; Artículo síntesis; Revista bibliográfica; Antiparkinsoniano; Neuroprotector
LO : INIST-28166.354000501182730090
ID : 14-0095204

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Pascal:14-0095204

Le document en format XML

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<term>Facteur risque</term>
<term>Insuffisance cardiaque</term>
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<term>Stimulant dopaminergique</term>
<term>Maladie de Parkinson</term>
<term>Homme</term>
<term>Toxicité</term>
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<div type="abstract" xml:lang="en">Introduction: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. Areas covered: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. Expert opinion: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.</div>
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<s0>Introduction: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. Areas covered: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. Expert opinion: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.</s0>
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<ET>Risk of heart failure following treatment with dopamine agonists in Parkinson's disease patients</ET>
<AU>PEREZ-LLORET (Santiago); REY (María Verónica); CRISPO (James); KREWSKI (Daniel); LAPEYRE-MESTRE (Marise); MONTASTRUC (Jean-Louis); RASCOL (Olivier)</AU>
<AF>Hospital and University Paul Sabatier of Toulouse, France and INSERM CIC9023 and UMR 825, Department of Clinical Pharmacology and Neurosciences/Toulouse/France (1 aut., 2 aut., 5 aut., 6 aut., 7 aut.); University of Ottawa, McLaughlin Centre for Population Health Risk Assessment, 1 Stewart Street/Ottawa, Ontario, K1N 6N5/Canada (3 aut., 4 aut.); Faculty of Medicine, Department of Clinical Pharmacology, 37 Allées Jules Guesde/31000, Toulouse/France (7 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Expert opinion on drug safety; ISSN 1474-0338; Royaume-Uni; Da. 2014; Vol. 13; No. 3; Pp. 351-360; Bibl. 61 ref.</SO>
<LA>Anglais</LA>
<EA>Introduction: Dopamine agonists (DAs) are frequently used to treat early or advanced Parkinson's disease (PD) patients. They have been shown to be efficacious for the treatment of motor symptoms and for delaying levodopa-induced dyskinesias. However, their utilization is limited by the risk of adverse drug reactions, some of which affect the cardiovascular system. Recently, the US FDA identified a possible association between exposure to pramipexole and the risk of heart failure. Areas covered: This article begins by reviewing the pharmacodynamic and cardiovascular effects of DAs on PD patients. Pharmacoepidemiological studies about the association between DAs and heart failure are then evaluated. Expert opinion: Four nested case-control studies were reviewed. In general, results showed higher heart failure risk following use of pramipexole or cabergoline. Although the effects of cabergoline may be explained by the induction of cardiac valve fibrosis, the basis for the significantly increased risk associated with pramipexole is unclear. It remains to be determined if these are dose-related effects, at what point they occur during the course of treatment, and if the risk is the same for all patients irrespective of other potential modifying factors, such as age and sex.</EA>
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<ED>Risk factor; Heart failure; Treatment; Dopamine agonist; Parkinson disease; Human; Toxicity; Drug; Cardiovascular disease; Pharmacovigilance; Pramipexole; Review; Bibliographic review; Antiparkinson agent; Neuroprotective agent</ED>
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