Clinical aspects and serodiagnosis of myasthenia gravis in Algerian patients: a prospective study on a small group of patients

Abstract

Introduction: Myasthenia gravis (MG) is a clinically heterogeneous disease and its diagnosis relies serologically on ELISA and RIPA. Here we report the clinical characteristics of a cohort of Algerian patients with MG and compare the diagnostic accuracy of ELISA and RIPA for anti-AChR and anti-MuSK autoantibodies in Algerian MG patients. Serological analyses were performed using ELISA-, RIPA- and cell-based (CBA) assays in a subset of 23 patients. The diagnostic accuracy of ELISA and RIPA for anti-AChR and anti-MuSK autoantibodies was compared in this subset of patients. Results: Algerian MG patients did not present with any specific clinical characteristics when compared to other populations. The ELISA and RIPA results showed a good correlation for anti-AChR and anti-MuSK autoantibodies. However, 100% of patients with generalized MG and none of those with ocular MG were positive for anti-AChR by ELISA, compared to 83.3% and 40% by RIPA, respectively. None of the 23 patients were anti-MuSK positive by RIPA or by an in-house CBA. Conclusions: The findings suggest that anti-AChR ELISA may be a useful diagnostic tool for MG in countries where RIPA is not available. The combination of clinical and electrophysiological findings with serological testing may improve the diagnosis of MG.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study was approved by the local ethical committee (The Thematic Agency for Health Science Research - Agence Thematique de Recherche en Science de la Sante)

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

留言 (0)

沒有登入
gif