» Articles » PMID: 37666644

In Inflammatory Myopathies, Dropped Head/bent Spine Syndrome is Associated with Scleromyositis: an International Case-control Study

Abstract

Background: Some 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).

Objectives: To assess the significance of DH/BS in patients with IM.

Methods: Practitioners 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.

Results: 49 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).

Conclusion: In IM patients, DH/BS is a marker of severity and is associated with SSc (scleromyositis).

Citing Articles

Case report: A patient with brachio-cervical inflammatory myopathy was misdiagnosed as flail arm syndrome.

Sun H, Wei X, Han Y, Wang Y, Wang Z, Yu X Front Immunol. 2024; 15:1378130.

PMID: 39021570 PMC: 11251991. DOI: 10.3389/fimmu.2024.1378130.


Systemic sclerosis associated myopathy: how to treat.

Selva-OCallaghan A, Guillen-Del-Castillo A, Gil-Vila A, Trallero-Araguas E, Matas-Garcia A, Milisenda J Curr Treatm Opt Rheumatol. 2024; 9(4):151-167.

PMID: 38737329 PMC: 11086655. DOI: 10.1007/s40674-023-00206-y.

References
1.
Lloyd T, Mammen A, Amato A, Weiss M, Needham M, Greenberg S . Evaluation and construction of diagnostic criteria for inclusion body myositis. Neurology. 2014; 83(5):426-33. PMC: 4132572. DOI: 10.1212/WNL.0000000000000642. View

2.
De Lorenzo R, Pinal-Fernandez I, Huang W, Albayda J, Tiniakou E, Johnson C . Muscular and extramuscular clinical features of patients with anti-PM/Scl autoantibodies. Neurology. 2018; 90(23):e2068-e2076. PMC: 5993182. DOI: 10.1212/WNL.0000000000005638. View

3.
Meyer A, Scire C, Talarico R, Alexander T, Amoura Z, Avcin T . Idiopathic inflammatory myopathies: state of the art on clinical practice guidelines [corrected]. RMD Open. 2019; 4(Suppl 1):e000784. PMC: 6397434. DOI: 10.1136/rmdopen-2018-000784. View

4.
Ghosh P, Milone M . Camptocormia as presenting manifestation of a spectrum of myopathic disorders. Muscle Nerve. 2015; 52(6):1008-12. DOI: 10.1002/mus.24689. View

5.
Ellezam B, Leclair V, Troyanov Y, Meyer A, Hudson M, Landon-Cardinal O . Capillary basement membrane reduplication in myositis patients with mild clinical features of systemic sclerosis supports the concept of 'scleromyositis'. Acta Neuropathol. 2021; 142(2):395-397. DOI: 10.1007/s00401-021-02335-x. View