Inflammatory myopathies

The clinical characteristics of pharyngeal and laryngeal lesions in anti-MDA5-positive dermatomyositis patients

Clin Exp RheumatolPublished Retrospective cohort study

Authors' conclusion

1. Pharyngeal and laryngeal lesions are not uncommon in anti-MDA5-positive DM, these patients have poorer nutritional status and more severe lung lesions; 2. Positive anti-Ro-52 antibodies and high serum ferritin levels are closely associated with pharyngeal and laryngeal involvement in anti-MDA5-positive DM; 3. Electronic laryngoscopy plays a crucial role in the diagnosis and evaluation of pharyngeal and laryngeal conditions.

Study context

Population
Patients with anti-MDA5-positive DM
Participants
131 patients
Exposure
Anti-MDA5-positive DM with vs without pharyngeal and laryngeal involvement
  • Pharyngeal/laryngeal involvementn = 35
Outcome
Clinical characteristics of pharyngeal and laryngeal lesions

Main finding

As reported in the abstract

Pharyngeal and laryngeal symptoms (prevalence)

Pharyngeal and laryngeal symptoms in anti-MDA5-positive DM patients

26.7%

Observational data: associations, not effects.

Further findings

Laboratory and lung features by involvement

Low haemoglobin, albumin, prealbumin, high-density lipoprotein and rapidly progressive ILD mainly in patients with involvement vs without

Mortality

No significant difference in mortality between the two groups

Anti-Ro-52 antibody status

Involvement significantly more frequent in anti-Ro-52-positive than anti-Ro-52-negative patients

Serum ferritin

Ferritin 1000–1500 ng/ml more likely to develop involvement vs ferritin < 500 ng/ml

Electronic laryngoscopy findings

Laryngoscopy assisted assessment of pharyngeal mucosa, arytenoid area, epiglottis and vocal cords; rare lesions incl. pharyngeal posterior wall fistulas, epiglottic ulcers, vocal cord white lesions

Original publication

The clinical characteristics of pharyngeal and laryngeal lesions in anti-MDA5-positive dermatomyositis patients. Clin Exp Rheumatol. Published 20 September 2024. doi:10.55563/clinexprheumatol/t0478a

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