Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/68587
Type: Artigo de periódico
Title: Haptoglobin study in myasthenia gravis
Author: Oliveira, LHM
Franca, MC
Nucci, A
de Oliveira, DM
Kimura, EM
Sonati, MD
Abstract: Objective: A cross-sectional study of haptoglobin (Hp) in myasthenia gravis (MG) was designed, with, the objective to identify its values and correlate them with different disease status. Method: 46 patients were enrolled in the study, all having disease severity established according to the quantitative myasthenia gravis strength scores (QMGSS). Based on the functional scale determined by Myasthenia Gravis Foundation of America (MGFA) recommendations, patients were classified as having: complete stable remission (CSR; n=10); minimal manifestations-O (MMO; n=6), minimal manifestations-1 (MM1; n=4); pharmacological remission (PR; n=6). Two other groups participated: thymomatous patients (T; n=10) and patients without imunosuppression or thymectomy, until the assessment for Hp (WIT; n=10). Hp dosage was done by immunonephelometry, blindly to clinical data. Student's t-test, Anova test and linear regression were employed for statistical analyses. Results: Statistically significant differences occurred between CSR+MMOxWIT groups (86.62x157.57, p < 0.001) and PR+MM1xWIT groups (73.93x157.57, p < 0.001). Linear regression showed correlation between Hp levels and QMGSS (r=0.759, p < 0.001). Conclusion: Our results suggest that Hp may be useful in clinical practice as a disease severity marker in MG.
Subject: haptoglobin
acute phase response
myasthenia gravis
immune disorders
Country: Brasil
Editor: Assoc Arquivos Neuro- Psiquiatria
Rights: aberto
Identifier DOI: 10.1590/S0004-282X2008000200017
Date Issue: 2008
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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