What is the impact of tacrolimus in myasthenia gravis?

Long-term efficacy and side effects of low-dose tacrolimus for the treatment of Myasthenia Gravis.

Tao X, Wang W, Jing F, et al.

Neurol Sci 2017; 38:325-330.



The study evaluated the efficacy of low-dose tacrolimus for treating Myasthenia Gravis (MG).


Data were collected from 97 patients treated with low-dose tacrolimus from February 2011 to April 2015. Metabolic analysis was performed to determine more accurate tacrolimus dosing and patients were followed-up within clinic every 6 months for up to 4 years. The myasthenia gravis-specific activities of daily living scale was used to assess MG symptoms and their effects on patients’ daily activities. All side effects and adverse reactions were thoroughly documented.


At the end of follow-up, 6 patients were in complete stable remission, 17 patients were in pharmacological remission, 26 patients were in minimal manifestation status, 32 patients were improved, 2 patients were unchanged, 11 patients had worsening symptoms, and 3 patients died. Side effects were reported and/or observed in 24 patients, of which 7 patients experienced elevated blood glucose, 2 patients developed neoplasms, 3 patients developed gastrointestinal symptoms, 3 showed mild increases in aminotransferases, 3 patients suffered from bone marrow suppression, 2 patients suffered from skin rashes and erythema, and 1 patient required discontinuation of therapy. Transient renal insufficiency was also observed in 1 patient and 3 other patients had minor miscellaneous side effects.


This study adds some knowledge on the efficacy and side effects of low-dose tacrolimus in the treatment of MG. Tacrolimus immunotherapy is a valid option for the management of MG, and can be gradually reduced in dose once symptoms are improved until complete withdrawal is achieved.


This reference is now included in the neurochecklist:

Myasthenia gravis (MG): medical treatment

Abstract link 1

Abstract link 2

By Doctor Jana – http://docjana.com/#/nmj, CC BY 4.0, Link

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