In inflammatory myopathies, dropped head/bent spine syndrome is associated with scleromyositis: an international case–control study

Author:

Pijnenburg Luc,Giannini Margherita,Bouchard-Marmen Maude,Arnaud LaurentORCID,Barsotti Simone,Bellando-Randone Silvia,Bernardi Livio,Bini Paola,Blagojevic Jelena,Codullo VeronicaORCID,Couderc MarionORCID,De Moreuil Claire,Dernis Emanuelle,Diamanti Luca,Dubost Jean JacquesORCID,Duval Fanny,Emmi GiacomoORCID,Galempoix Jean-Marc,Geny Bernard,Gottenberg Jacques-EricORCID,Groza Monica,Guffroy Aurelien,Guichard Isabelle,Guilpain Philippe,Hervier BaptisteORCID,Hudson Marie,Iaccarino Luca,Iannone Florenzo,Lebrun Delphine,Marchioni Enrico,Mariampillai Kuberaka,Maurier Francois,Mosca Marta,Nadaj-Pakleza Aleksandra,Nannini Carlotta,Piot Jean-Maxime,Prieto-González Sergio,Poursac Nicolas,Rouanet Eglantine,Sellam Jérémie,Selva-O'Callaghan AlbertORCID,Séverac François,Sibilia Jean,Sole Guilhem,Soulages Antoine,Terrier BenjaminORCID,Tournadre AnneORCID,Troyanov Yves,Vernier Nathalie,Vesperini Veronique,Viallard Jean-François,Ziane Rahima,Cavagna Lorenzo,Meyer AlainORCID

Abstract

BackgroundSome myopathies can lead to dropped head or bent spine syndrome (DH/BS). The significance of this symptom has not been studied in inflammatory myopathies (IM).ObjectivesTo assess the significance of DH/BS in patients with IM.MethodsPractitioners from five IM networks were invited to report patients with IM suffering from DH/BS (without other known cause than IM). IM patients without DH/BS, randomly selected in each participating centre, were included as controls at a ratio of 2 to 1.Results49 DH/BS-IM patients (DH: 57.1%, BS: 42.9%) were compared with 98 control-IM patients. DH/BS-IM patients were older (65 years vs 53 years, p<0.0001) and the diagnosis of IM was delayed (6 months vs 3 months, p=0.009). Weakness prevailing in the upper limbs (42.9% vs 15.3%), dysphagia (57.1% vs 25.5%), muscle atrophy (65.3% vs 34.7%), weight loss (61.2% vs 23.5%) and loss of the ability to walk (24.5% vs 5.1%) were hallmarks of DH/BS-IM (p≤0.0005), for which the patients more frequently received intravenous immunoglobulins (65.3% vs 34.7%, p=0.0004). Moreover, DH/BS-IM patients frequently featured signs and/or complications of systemic sclerosis (SSc), fulfilling the American College of Rheumatology/European Alliance of Associations for Rheumatology criteria for this disease in 40.8% of the cases (vs 5.1%, p<0.0001). Distribution of the myopathy, its severity and its association with SSc were independently associated with DH/BS (p<0.05). Mortality was higher in the DH/BS-IM patients and loss of walking ability was independently associated with survival (p<0.05).ConclusionIn IM patients, DH/BS is a marker of severity and is associated with SSc (scleromyositis).

Publisher

BMJ

Subject

Immunology,Immunology and Allergy,Rheumatology

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