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The Journal of Clinical Endocrinology & Metabolism Vol. 82, No. 2 438-443
Copyright © 1997 by The Endocrine Society


Clinical Studies

Mild Clinical Expression of Myasthenia Gravis Associated with Autoimmune Thyroid Diseases1

Michele Marinó, Roberta Ricciardi, Aldo Pinchera, Giuseppe Barbesino, Luca Manetti, Luca Chiovato, Lewis E. Braverman, Bruno Rossi, Alberto Muratorio and Stefano Mariotti

Institutes of Endocrinology (M.M., A.P., G.B., L.M., L.C.) and Neurology (R.R., B.R., A.M.), University of Pisa, Pisa; and the Institute of Internal Medicine, University of Cagliari (S.M.), Cagliari, Italy; and the Division of Endocrinology and Metabolism, University of Massachusetts (L.E.B.), Worcester, Massachusetts 01655

Address all correspondence and requests for reprints to: Aldo Pinchera, M.D., Institute of Endocrinology, University of Pisa, Viale del Tirreno 64, 56018 Tirrenia-Pisa, Italy.

Myasthenia gravis (MG) may occur in association with autoimmune thyroid diseases (AITD). The aim of this study was to evaluate the features of MG associated with AITD compared to those of MG without AITD. A total of 129 MG patients (34 men and 95 women; age range, 11–81 yr) were subdivided into: group A, 56 MG patients with AITD [25 with autoimmune thyroiditis and 31 with Graves’ disease (GD)]; group B, 21 MG patients with nonautoimmune thyroid diseases; and group C, 52 MG patients without thyroid disease. The severity of MG was ranked according to the Osserman score. Laboratory evaluation included assays for antithyroid and antiacetylcholine receptor (AchRAb) antibodies.

Ocular MG (Osserman’s class 1) was more frequent in group A (41.0%) than in group B (14.2%; P < 0.03) or C (21.4%; P < 0.03). Severe generalized MG (classes >=2B) was more frequent in groups B (57.1%; P < 0.03) and C (51.9%; P < 0.02) than in group A (28.5%). GD patients with clinical evidence of ophthalmopathy had a higher frequency (P = 0.05) of ocular MG (57.8%) than GD patients without clinical ophthalmopathy (16.6%). Thymic disease was less frequent in group A (26.7%) than in group B (71.4%; P = 0.001) or C (59.7%; P = 0.001). The prevalence of thymic hyperplasia was 17.8%, 38.0%, and 40.3% in groups A, B, and C, respectively; the prevalence of thymoma was 8.9%, 33.4%, and 19.4%. When only patients with generalized MG were considered, thymic disease was less frequent (P < 0.02) in group A (40.6%) than in the remaining groups (69.4%). AchRAb was more frequent in groups B (57.1%) and C (57.6%; P < 0.03) than in group A (35.7%).

In conclusion, MG associated with AITD has a mild clinical expression, with preferential ocular involvement and lower frequency of thymic disease and AchRAb. This supports the hypothesis that ocular and generalized MG are separate diseases with different spectra of associated diseases. Nonautoimmune thyroid diseases have no influence on the features of MG. The association of ocular MG and AITD might be due to a common autoimmune mechanism and/or a peculiar genetic background.




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