Pregnancy in Parkinson's disease: A review of the literature and a case report
Identifieur interne : 004F18 ( Main/Exploration ); précédent : 004F17; suivant : 004F19Pregnancy in Parkinson's disease: A review of the literature and a case report
Auteurs : Peter Hagell [Suède] ; Per Odin [Allemagne] ; Ellen Vinge [Suède]Source :
- Movement Disorders [ 0885-3185 ] ; 1998-01.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Abnormalities, Drug-Induced, Adjuvants, Pharmaceutic (therapeutic use), Adult, Amantadine (adverse effects), Animal, Animals, Antiparkinson Agents (therapeutic use), Antiparkinson agent, Aromatic Amino Acid Decarboxylase Inhibitors, Benserazide, Benserazide (therapeutic use), Bibliographic survey, Case study, Chemotherapy, Decarboxylase, Dopa decarboxylase inhibitors, Dopamine Agents (therapeutic use), Dopamine agonists, Enzyme Inhibitors (therapeutic use), Enzyme inhibitor, Female, Human, Humans, Levodopa, Levodopa (adverse effects), Mice, Parkinson Disease (drug therapy), Parkinson disease, Parkinson's disease, Pregnancy, Pregnancy Complications (drug therapy), Pregnancy Outcome, Rabbits, Rats, Selegiline, Selegiline (adverse effects), Treatment.
- MESH :
- chemical , adverse effects : Amantadine, Levodopa, Selegiline.
- chemical , therapeutic use : Adjuvants, Pharmaceutic, Antiparkinson Agents, Benserazide, Dopamine Agents, Enzyme Inhibitors.
- drug therapy : Parkinson Disease, Pregnancy Complications.
- Abnormalities, Drug-Induced, Adult, Animals, Aromatic Amino Acid Decarboxylase Inhibitors, Female, Humans, Mice, Pregnancy, Pregnancy Outcome, Rabbits, Rats.
Abstract
Pregnancy is rare in Parkinson's disease (PD). In the literature on studies of antiparkinsonian drugs in animals during pregnancy, there are reports on malformations of the skeletal and circulatory system. However, the majority of studies in animals have not shown any teratogenicity. Amantadine has been teratogenic in rats and selegiline has caused neurochemical and behavioral alterations in rats when coadministered with clorgyline. The published experience with humans consists of 35 pregnancies among 26 women suffering from PD, including this report, and a number of cases treated with antiparkinsonian agents for other reasons. With the exception of the majority of the cases where amantadine was used, complications have been rare. However, there are indications that suggest a possible risk of a woman's parkinsonism worsening in connection with pregnancy. We also report the case of a woman with PD who was treated with L‐dopa‐benserazide during an uncomplicated pregnancy and gave birth to a healthy boy without experiencing any worsening of her PD.
Url:
DOI: 10.1002/mds.870130110
Affiliations:
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Le document en format XML
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<term>Adult</term>
<term>Amantadine (adverse effects)</term>
<term>Animal</term>
<term>Animals</term>
<term>Antiparkinson Agents (therapeutic use)</term>
<term>Antiparkinson agent</term>
<term>Aromatic Amino Acid Decarboxylase Inhibitors</term>
<term>Benserazide</term>
<term>Benserazide (therapeutic use)</term>
<term>Bibliographic survey</term>
<term>Case study</term>
<term>Chemotherapy</term>
<term>Decarboxylase</term>
<term>Dopa decarboxylase inhibitors</term>
<term>Dopamine Agents (therapeutic use)</term>
<term>Dopamine agonists</term>
<term>Enzyme Inhibitors (therapeutic use)</term>
<term>Enzyme inhibitor</term>
<term>Female</term>
<term>Human</term>
<term>Humans</term>
<term>Levodopa</term>
<term>Levodopa (adverse effects)</term>
<term>Mice</term>
<term>Parkinson Disease (drug therapy)</term>
<term>Parkinson disease</term>
<term>Parkinson's disease</term>
<term>Pregnancy</term>
<term>Pregnancy Complications (drug therapy)</term>
<term>Pregnancy Outcome</term>
<term>Rabbits</term>
<term>Rats</term>
<term>Selegiline</term>
<term>Selegiline (adverse effects)</term>
<term>Treatment</term>
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<term>Levodopa</term>
<term>Selegiline</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Adjuvants, Pharmaceutic</term>
<term>Antiparkinson Agents</term>
<term>Benserazide</term>
<term>Dopamine Agents</term>
<term>Enzyme Inhibitors</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Parkinson Disease</term>
<term>Pregnancy Complications</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Abnormalities, Drug-Induced</term>
<term>Adult</term>
<term>Animals</term>
<term>Aromatic Amino Acid Decarboxylase Inhibitors</term>
<term>Female</term>
<term>Humans</term>
<term>Mice</term>
<term>Pregnancy</term>
<term>Pregnancy Outcome</term>
<term>Rabbits</term>
<term>Rats</term>
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<term>Antiparkinsonien</term>
<term>Bensérazide</term>
<term>Chimiothérapie</term>
<term>Decarboxylase</term>
<term>Etude cas</term>
<term>Gestation</term>
<term>Homme</term>
<term>Inhibiteur enzyme</term>
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<term>Parkinson maladie</term>
<term>Synthèse bibliographique</term>
<term>Traitement</term>
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<front><div type="abstract" xml:lang="en">Pregnancy is rare in Parkinson's disease (PD). In the literature on studies of antiparkinsonian drugs in animals during pregnancy, there are reports on malformations of the skeletal and circulatory system. However, the majority of studies in animals have not shown any teratogenicity. Amantadine has been teratogenic in rats and selegiline has caused neurochemical and behavioral alterations in rats when coadministered with clorgyline. The published experience with humans consists of 35 pregnancies among 26 women suffering from PD, including this report, and a number of cases treated with antiparkinsonian agents for other reasons. With the exception of the majority of the cases where amantadine was used, complications have been rare. However, there are indications that suggest a possible risk of a woman's parkinsonism worsening in connection with pregnancy. We also report the case of a woman with PD who was treated with L‐dopa‐benserazide during an uncomplicated pregnancy and gave birth to a healthy boy without experiencing any worsening of her PD.</div>
</front>
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