Movement Disorders (revue)

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Long-Term Outcome of 32 Patients With Chorea and Systemic Lupus Erythematosus or Antiphospholipid Antibodies

Identifieur interne : 000339 ( PascalFrancis/Corpus ); précédent : 000338; suivant : 000340

Long-Term Outcome of 32 Patients With Chorea and Systemic Lupus Erythematosus or Antiphospholipid Antibodies

Auteurs : Peggy Reiner ; Damien Galanaud ; Gaëlle Leroux ; Marie Vidailhet ; Julien Haroche ; Du Le Thi Huong ; Camille Frances ; Thomas Papo ; Christian De Gennes ; Lucile Musset ; Bertrand Wechsler ; Zahir Amoura ; Jean-Charles Piette ; Nathalie Costedoat-Chalumeau

Source :

RBID : Pascal:12-0026980

Descripteurs français

English descriptors

Abstract

Objective: The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome. Methods: We retrospectively analyzed clinical features, laboratory findings, imaging characteristics, and outcome in a series of 32 patients. Results: Most patients were women (28 of 32), and mean age at onset of chorea was 20.6 (9-62) years. Chorea was inaugural for 28 patients. Improvement was observed with various treatments. During follow-up (12.2 ±11.3 years), severe manifestations of systemic lupus erythematosus were rare. Antiphospholipid antibodies were repeatedly positive for 90% of the patients. Twelve patients developed arterial thrombosis. Prophylactic treatment with antithrombotic therapy might reduce the risk of further thrombosis (8% versus 57%; P = 0.01). Cardiac valvulopathy occurred in 22 patients during follow-up. Chorea relapsed in 8 cases. Conclusions: Chorea had a good outcome in itself. This long-term follow-up shows, for the first time, that these patients have substantial risk for further arterial thrombosis.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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C01 01    ENG  @0 Objective: The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome. Methods: We retrospectively analyzed clinical features, laboratory findings, imaging characteristics, and outcome in a series of 32 patients. Results: Most patients were women (28 of 32), and mean age at onset of chorea was 20.6 (9-62) years. Chorea was inaugural for 28 patients. Improvement was observed with various treatments. During follow-up (12.2 ±11.3 years), severe manifestations of systemic lupus erythematosus were rare. Antiphospholipid antibodies were repeatedly positive for 90% of the patients. Twelve patients developed arterial thrombosis. Prophylactic treatment with antithrombotic therapy might reduce the risk of further thrombosis (8% versus 57%; P = 0.01). Cardiac valvulopathy occurred in 22 patients during follow-up. Chorea relapsed in 8 cases. Conclusions: Chorea had a good outcome in itself. This long-term follow-up shows, for the first time, that these patients have substantial risk for further arterial thrombosis.
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Format Inist (serveur)

NO : PASCAL 12-0026980 INIST
ET : Long-Term Outcome of 32 Patients With Chorea and Systemic Lupus Erythematosus or Antiphospholipid Antibodies
AU : REINER (Peggy); GALANAUD (Damien); LEROUX (Gaëlle); VIDAILHET (Marie); HAROCHE (Julien); THI HUONG (Du Le); FRANCES (Camille); PAPO (Thomas); DE GENNES (Christian); MUSSET (Lucile); WECHSLER (Bertrand); AMOURA (Zahir); PIETTE (Jean-Charles); COSTEDOAT-CHALUMEAU (Nathalie)
AF : Service de Neurologie, AP-HP, Hôpital Lariboisière/Paris/France (1 aut.); Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (3 aut., 5 aut., 6 aut., 9 aut., 11 aut., 12 aut., 13 aut., 14 aut.); Service de Neuroradiologie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (2 aut.); Fédération des Maladies du Système Nerveux Central, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (4 aut.); Service de Dermatologie, Hôpital Tenon, AP-HP/Paris/France (7 aut.); Service de Médecine Interne, AP-HP, Hôpital Bichat/Paris/France (8 aut.); Service d'Immunochimie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (10 aut.)
DT : Publication en série; Courte communication, note brève; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2011; Vol. 26; No. 13; Pp. 2422-2427; Bibl. 26 ref.
LA : Anglais
EA : Objective: The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome. Methods: We retrospectively analyzed clinical features, laboratory findings, imaging characteristics, and outcome in a series of 32 patients. Results: Most patients were women (28 of 32), and mean age at onset of chorea was 20.6 (9-62) years. Chorea was inaugural for 28 patients. Improvement was observed with various treatments. During follow-up (12.2 ±11.3 years), severe manifestations of systemic lupus erythematosus were rare. Antiphospholipid antibodies were repeatedly positive for 90% of the patients. Twelve patients developed arterial thrombosis. Prophylactic treatment with antithrombotic therapy might reduce the risk of further thrombosis (8% versus 57%; P = 0.01). Cardiac valvulopathy occurred in 22 patients during follow-up. Chorea relapsed in 8 cases. Conclusions: Chorea had a good outcome in itself. This long-term follow-up shows, for the first time, that these patients have substantial risk for further arterial thrombosis.
CC : 002B17; 002B17F
FD : Syndrome choréique; Lupus érythémateux disséminé; Syndrome des antiphospholipides; Thrombose; Pathologie du système nerveux; Long terme; Pronostic; Homme; Thrombocyte
FG : Pathologie de l'encéphale; Syndrome extrapyramidal; Mouvement involontaire; Pathologie du système nerveux central; Trouble neurologique; Maladie autoimmune; Maladie de système; Pathologie de la peau; Pathologie du tissu conjonctif; Immunopathologie; Pathologie de l'appareil circulatoire; Hémopathie; Pathologie des vaisseaux sanguins
ED : Chorea; Systemic lupus erythematosus; Antiphospholipid antibody syndrome; Thrombosis; Nervous system diseases; Long term; Prognosis; Human; Platelet
EG : Cerebral disorder; Extrapyramidal syndrome; Involuntary movement; Central nervous system disease; Neurological disorder; Autoimmune disease; Systemic disease; Skin disease; Connective tissue disease; Immunopathology; Cardiovascular disease; Hemopathy; Vascular disease
SD : Corea síndrome; Lupus eritematoso sistémico; Antifosfolípido síndrome; Trombosis; Sistema nervioso patología; Largo plazo; Pronóstico; Hombre; Trombocito
LO : INIST-20953.354000505925010190
ID : 12-0026980

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Pascal:12-0026980

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<name sortKey="Galanaud, Damien" sort="Galanaud, Damien" uniqKey="Galanaud D" first="Damien" last="Galanaud">Damien Galanaud</name>
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<name sortKey="Leroux, Gaelle" sort="Leroux, Gaelle" uniqKey="Leroux G" first="Gaëlle" last="Leroux">Gaëlle Leroux</name>
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<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
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<name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
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<s1>Fédération des Maladies du Système Nerveux Central, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
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</affiliation>
</author>
<author>
<name sortKey="Haroche, Julien" sort="Haroche, Julien" uniqKey="Haroche J" first="Julien" last="Haroche">Julien Haroche</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
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<sZ>13 aut.</sZ>
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<author>
<name sortKey="Thi Huong, Du Le" sort="Thi Huong, Du Le" uniqKey="Thi Huong D" first="Du Le" last="Thi Huong">Du Le Thi Huong</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
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<author>
<name sortKey="Frances, Camille" sort="Frances, Camille" uniqKey="Frances C" first="Camille" last="Frances">Camille Frances</name>
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<inist:fA14 i1="05">
<s1>Service de Dermatologie, Hôpital Tenon, AP-HP</s1>
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<sZ>7 aut.</sZ>
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<name sortKey="Papo, Thomas" sort="Papo, Thomas" uniqKey="Papo T" first="Thomas" last="Papo">Thomas Papo</name>
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<inist:fA14 i1="06">
<s1>Service de Médecine Interne, AP-HP, Hôpital Bichat</s1>
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<sZ>8 aut.</sZ>
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<name sortKey="De Gennes, Christian" sort="De Gennes, Christian" uniqKey="De Gennes C" first="Christian" last="De Gennes">Christian De Gennes</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
<s3>FRA</s3>
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<name sortKey="Musset, Lucile" sort="Musset, Lucile" uniqKey="Musset L" first="Lucile" last="Musset">Lucile Musset</name>
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<inist:fA14 i1="07">
<s1>Service d'Immunochimie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
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<s3>FRA</s3>
<sZ>10 aut.</sZ>
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</author>
<author>
<name sortKey="Wechsler, Bertrand" sort="Wechsler, Bertrand" uniqKey="Wechsler B" first="Bertrand" last="Wechsler">Bertrand Wechsler</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
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<sZ>9 aut.</sZ>
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</author>
<author>
<name sortKey="Amoura, Zahir" sort="Amoura, Zahir" uniqKey="Amoura Z" first="Zahir" last="Amoura">Zahir Amoura</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
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<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
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<sZ>11 aut.</sZ>
<sZ>12 aut.</sZ>
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<sZ>14 aut.</sZ>
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<name sortKey="Piette, Jean Charles" sort="Piette, Jean Charles" uniqKey="Piette J" first="Jean-Charles" last="Piette">Jean-Charles Piette</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
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<name sortKey="Costedoat Chalumeau, Nathalie" sort="Costedoat Chalumeau, Nathalie" uniqKey="Costedoat Chalumeau N" first="Nathalie" last="Costedoat-Chalumeau">Nathalie Costedoat-Chalumeau</name>
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<inist:fA14 i1="02">
<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
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<sZ>6 aut.</sZ>
<sZ>9 aut.</sZ>
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<sZ>13 aut.</sZ>
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<series>
<title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint>
<date when="2011">2011</date>
</imprint>
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<title level="j" type="main">Movement disorders</title>
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<term>Antiphospholipid antibody syndrome</term>
<term>Chorea</term>
<term>Human</term>
<term>Long term</term>
<term>Nervous system diseases</term>
<term>Platelet</term>
<term>Prognosis</term>
<term>Systemic lupus erythematosus</term>
<term>Thrombosis</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Syndrome choréique</term>
<term>Lupus érythémateux disséminé</term>
<term>Syndrome des antiphospholipides</term>
<term>Thrombose</term>
<term>Pathologie du système nerveux</term>
<term>Long terme</term>
<term>Pronostic</term>
<term>Homme</term>
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<div type="abstract" xml:lang="en">Objective: The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome. Methods: We retrospectively analyzed clinical features, laboratory findings, imaging characteristics, and outcome in a series of 32 patients. Results: Most patients were women (28 of 32), and mean age at onset of chorea was 20.6 (9-62) years. Chorea was inaugural for 28 patients. Improvement was observed with various treatments. During follow-up (12.2 ±11.3 years), severe manifestations of systemic lupus erythematosus were rare. Antiphospholipid antibodies were repeatedly positive for 90% of the patients. Twelve patients developed arterial thrombosis. Prophylactic treatment with antithrombotic therapy might reduce the risk of further thrombosis (8% versus 57%; P = 0.01). Cardiac valvulopathy occurred in 22 patients during follow-up. Chorea relapsed in 8 cases. Conclusions: Chorea had a good outcome in itself. This long-term follow-up shows, for the first time, that these patients have substantial risk for further arterial thrombosis.</div>
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<s1>Long-Term Outcome of 32 Patients With Chorea and Systemic Lupus Erythematosus or Antiphospholipid Antibodies</s1>
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<s1>Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
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<s1>Service de Neuroradiologie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
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<s1>Fédération des Maladies du Système Nerveux Central, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
<s2>Paris</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
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<s1>Service d'Immunochimie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière</s1>
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<s0>12-0026980</s0>
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<s0>Objective: The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome. Methods: We retrospectively analyzed clinical features, laboratory findings, imaging characteristics, and outcome in a series of 32 patients. Results: Most patients were women (28 of 32), and mean age at onset of chorea was 20.6 (9-62) years. Chorea was inaugural for 28 patients. Improvement was observed with various treatments. During follow-up (12.2 ±11.3 years), severe manifestations of systemic lupus erythematosus were rare. Antiphospholipid antibodies were repeatedly positive for 90% of the patients. Twelve patients developed arterial thrombosis. Prophylactic treatment with antithrombotic therapy might reduce the risk of further thrombosis (8% versus 57%; P = 0.01). Cardiac valvulopathy occurred in 22 patients during follow-up. Chorea relapsed in 8 cases. Conclusions: Chorea had a good outcome in itself. This long-term follow-up shows, for the first time, that these patients have substantial risk for further arterial thrombosis.</s0>
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<s5>49</s5>
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<s5>50</s5>
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<s5>50</s5>
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<NO>PASCAL 12-0026980 INIST</NO>
<ET>Long-Term Outcome of 32 Patients With Chorea and Systemic Lupus Erythematosus or Antiphospholipid Antibodies</ET>
<AU>REINER (Peggy); GALANAUD (Damien); LEROUX (Gaëlle); VIDAILHET (Marie); HAROCHE (Julien); THI HUONG (Du Le); FRANCES (Camille); PAPO (Thomas); DE GENNES (Christian); MUSSET (Lucile); WECHSLER (Bertrand); AMOURA (Zahir); PIETTE (Jean-Charles); COSTEDOAT-CHALUMEAU (Nathalie)</AU>
<AF>Service de Neurologie, AP-HP, Hôpital Lariboisière/Paris/France (1 aut.); Service de Médecine Interne, Centre de Reference National pour le Lupus Systémique et le Syndrome des Antiphospholipides, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (3 aut., 5 aut., 6 aut., 9 aut., 11 aut., 12 aut., 13 aut., 14 aut.); Service de Neuroradiologie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (2 aut.); Fédération des Maladies du Système Nerveux Central, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (4 aut.); Service de Dermatologie, Hôpital Tenon, AP-HP/Paris/France (7 aut.); Service de Médecine Interne, AP-HP, Hôpital Bichat/Paris/France (8 aut.); Service d'Immunochimie, AP-HP, Centre Hospitalier Universitaire Pitié-Salpêtrière/Paris/France (10 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2011; Vol. 26; No. 13; Pp. 2422-2427; Bibl. 26 ref.</SO>
<LA>Anglais</LA>
<EA>Objective: The aim of this work was to describe chorea during systemic lupus erythematosus or antiphospholipid antibodies and its long-term outcome. Methods: We retrospectively analyzed clinical features, laboratory findings, imaging characteristics, and outcome in a series of 32 patients. Results: Most patients were women (28 of 32), and mean age at onset of chorea was 20.6 (9-62) years. Chorea was inaugural for 28 patients. Improvement was observed with various treatments. During follow-up (12.2 ±11.3 years), severe manifestations of systemic lupus erythematosus were rare. Antiphospholipid antibodies were repeatedly positive for 90% of the patients. Twelve patients developed arterial thrombosis. Prophylactic treatment with antithrombotic therapy might reduce the risk of further thrombosis (8% versus 57%; P = 0.01). Cardiac valvulopathy occurred in 22 patients during follow-up. Chorea relapsed in 8 cases. Conclusions: Chorea had a good outcome in itself. This long-term follow-up shows, for the first time, that these patients have substantial risk for further arterial thrombosis.</EA>
<CC>002B17; 002B17F</CC>
<FD>Syndrome choréique; Lupus érythémateux disséminé; Syndrome des antiphospholipides; Thrombose; Pathologie du système nerveux; Long terme; Pronostic; Homme; Thrombocyte</FD>
<FG>Pathologie de l'encéphale; Syndrome extrapyramidal; Mouvement involontaire; Pathologie du système nerveux central; Trouble neurologique; Maladie autoimmune; Maladie de système; Pathologie de la peau; Pathologie du tissu conjonctif; Immunopathologie; Pathologie de l'appareil circulatoire; Hémopathie; Pathologie des vaisseaux sanguins</FG>
<ED>Chorea; Systemic lupus erythematosus; Antiphospholipid antibody syndrome; Thrombosis; Nervous system diseases; Long term; Prognosis; Human; Platelet</ED>
<EG>Cerebral disorder; Extrapyramidal syndrome; Involuntary movement; Central nervous system disease; Neurological disorder; Autoimmune disease; Systemic disease; Skin disease; Connective tissue disease; Immunopathology; Cardiovascular disease; Hemopathy; Vascular disease</EG>
<SD>Corea síndrome; Lupus eritematoso sistémico; Antifosfolípido síndrome; Trombosis; Sistema nervioso patología; Largo plazo; Pronóstico; Hombre; Trombocito</SD>
<LO>INIST-20953.354000505925010190</LO>
<ID>12-0026980</ID>
</server>
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