Abstract

BackgroundRecently different subtypes of myasthenia gravis (MG) have been described. They differ for clinical features and pathogenesis but the prognosis and response to treatment is less clear. The aim of the study was to evaluate outcome and treatment effectiveness including side effects in late onset MG (LOMG) compared with early onset MG (EOMG).MethodsWe analysed retrospectively 208 MG patients. Clinical features were recorded as well as treatment and side effects. Outcome at the last follow-up was evaluated with MGSTI and MGPIS scales.ResultsThe 208 patients included were classified as follow: 36 ocular MG, 40 EOMG, 72 LOMG, 25 thymoma-associated, 14 anti-MuSK and 21 double seronegative. Similar positive outcome was achieved in either early and late onset subgroup. We found pharmacological remission and minimal manifestations at the MGFA-PIS in the 95% and 94,4% of EOMG and LOMG respectively but in LOMG a lower dose of immunosuppressors (MGSTI< 2) was required compared to EOMG (p = 0,048). Severe side effects were present in a small percentage of patients in both group but diabetes was more frequent in LOMG vs EOMG (2,2% vs 5%, p = 0.017).ConclusionsDespite LOMG has more comorbidities that might interfere with treatment and outcome, therapeutic management does not seem to differ between EOMG and LOMG. A similar positive outcome was seen in both subgroups but LOMG group seems to require lower doses of medication to control symptoms.

Highlights

  • Myasthenia gravis (MG) is an autoimmune disorder due to antibodies against post-synaptic membrane proteins

  • M Males (Females) were prevalent in the first peak whereas males in the second one

  • When we evaluate the severity of the course of the disease measured by the number of acute intravenous immunoglobulin (IVIG) or PLEX cycles no significant difference between early onset myasthenia gravis (MG) (EOMG) and late onset MG (LOMG) was found as well as with other subgroups but ocular and seronegative MG (p < 0, 0001)

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Summary

Introduction

Myasthenia gravis (MG) is an autoimmune disorder due to antibodies against post-synaptic membrane proteins. The most accepted classification divides myasthenia gravis into the following subgroups: ocular; thymoma-associated; early onset and late-onset generalized with antibodies against acetylcholine receptor (AChR), anti-muscle specific tyrosine kinase (MuSK) positive and double seronegative [1]. They differ for clinical features and probably pathogenesis. Different subtypes of myasthenia gravis (MG) have been described They differ for clinical features and pathogenesis but the prognosis and response to treatment is less clear. The aim of the study was to evaluate outcome and treatment effectiveness including side effects in late onset MG (LOMG) compared with early onset MG (EOMG)

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