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Statin-induced anti-HMGCR myopathy: successful therapeutic strategies for corticosteroid-free remission in 55 patients.
Meyer, Alain; Troyanov, Yves; Drouin, Julie; Oligny-Longpré, Geneviève; Landon-Cardinal, Océane; Hoa, Sabrina; Hervier, Baptiste; Bourré-Tessier, Josiane; Mansour, Anne-Marie; Hussein, Sara; Morin, Vincent; Rich, Eric; Goulet, Jean-Richard; Chartrand, Sandra; Hudson, Marie; Nehme, Jessica; Makhzoum, Jean-Paul; Zarka, Farah; Villeneuve, Edith; Raynauld, Jean-Pierre; Landry, Marianne; O'Ferrall, Erin K; Ferreira, Jose; Ellezam, Benjamin; Karamchandani, Jason; Larue, Sandrine; Massie, Rami; Isabelle, Catherine; Deschênes, Isabelle; Leclair, Valérie; Couture, Hélène; Targoff, Ira N; Fritzler, Marvin J; Senécal, Jean-Luc.
Afiliação
  • Meyer A; Faculté de médecine, Université de Strasbourg, Service de rhumatologie et Centre de références des maladies autoimmunes rares, Hôpitaux universitaires de Strasbourg, Strasbourg, France.
  • Troyanov Y; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Drouin J; Division of Rheumatology, Hôpital du Sacré-Coeur, Montreal, Québec, Canada.
  • Oligny-Longpré G; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Landon-Cardinal O; Division of Rheumatology, Centre hospitalier affilié universitaire régional de Trois-Rivières, Trois-Rivières, Québec, Canada.
  • Hoa S; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Hervier B; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • Bourré-Tessier J; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Mansour AM; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • Hussein S; CHUM Research Center, Montréal, Québec, Canada.
  • Morin V; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Rich E; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • Goulet JR; CHUM Research Center, Montréal, Québec, Canada.
  • Chartrand S; Service de médecine interne et immunologie clinique, Hôpital Pitié-Salpêtrière, Assistance publique Hôpitaux de Paris, Paris, France.
  • Hudson M; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Nehme J; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • Makhzoum JP; CHUM Research Center, Montréal, Québec, Canada.
  • Zarka F; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Villeneuve E; Division of Internal Medicine, Hôpital du Sacré-Coeur, Montréal, Québec, Canada.
  • Raynauld JP; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Landry M; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • O'Ferrall EK; Faculty of Pharmacy, Laval University, Québec City, Québec, Canada.
  • Ferreira J; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Ellezam B; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • Karamchandani J; CHUM Research Center, Montréal, Québec, Canada.
  • Larue S; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Massie R; Division of Rheumatology, Centre Hospitalier de l'Université de Montréal (CHUM), 264, Boulevard René-Lévesque Est, Montréal, Québec, H2X 1P1, Canada.
  • Isabelle C; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Deschênes I; Division of Rheumatology, Hôpital Maisonneuve-Rosemont, Montréal, Québec, Canada.
  • Leclair V; Department of Medicine, McGill University, Montreal, Canada.
  • Couture H; Division of Rheumatology, Jewish General Hospital, Montreal, Canada.
  • Targoff IN; Lady Davis Institute, Jewish General Hospital, Montreal, Canada.
  • Fritzler MJ; Department of Medicine, Faculty of Medicine, University of Montreal, Montreal, Québec, Canada.
  • Senécal JL; Division of Internal Medicine, Hôpital du Sacré-Coeur, Montréal, Québec, Canada.
Arthritis Res Ther ; 22(1): 5, 2020 01 08.
Article em En | MEDLINE | ID: mdl-31915059
ABSTRACT

OBJECTIVE:

To describe successful therapeutic strategies in statin-induced anti-HMGCR myopathy.

METHODS:

Retrospective data from a cohort of 55 patients with statin-induced anti-HMGCR myopathy, sequentially stratified by the presence of proximal weakness, early remission, and corticosteroid and IVIG use at treatment induction, were analyzed for optimal successful induction and maintenance of remission strategies.

RESULTS:

A total of 14 patients achieved remission with a corticosteroid-free induction strategy (25%). In 41 patients treated with corticosteroids, only 4 patients (10%) failed an initial triple steroid/IVIG/steroid-sparing immunosuppressant (SSI) induction strategy. Delay in treatment initiation was independently associated with lower odds of successful maintenance with immunosuppressant monotherapy (OR 0.92, 95% CI 0.85 to 0.97, P = 0.015). While 22 patients (40%) presented with normal strength, only 9 had normal strength at initiation of treatment.

CONCLUSION:

While corticosteroid-free treatment of anti-HMGCR myopathy is now a safe option in selected cases, initial triple steroid/IVIG/SSI was very efficacious in induction. Delays in treatment initiation and, as a corollary, delays in achieving remission decrease the odds of achieving successful maintenance with an SSI alone. Avoiding such delays, most notably in patients with normal strength, may reset the natural history of anti-HMGCR myopathy from a refractory entity to a treatable disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Inibidores de Hidroximetilglutaril-CoA Redutases / Imunossupressores / Miosite Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Inibidores de Hidroximetilglutaril-CoA Redutases / Imunossupressores / Miosite Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article