Adequate tacrolimus concentration for myasthenia gravis treatment.
Eur J Neurol
; 24(2): 270-275, 2017 02.
Article
em En
| MEDLINE
| ID: mdl-28102047
ABSTRACT
BACKGROUND AND PURPOSE:
A single, oral dose of 3 mg/day tacrolimus, approved for myasthenia gravis (MG) treatment in Japan, was shown to reduce steroid dose and anti-acetylcholine receptor (AChR) antibody titers as well as to improve MG symptoms. However, no studies have investigated the association between tacrolimus concentration and its clinical efficacy in MG. In this study, we aimed to determine the optimal tacrolimus concentration for MG treatment.METHODS:
The trough tacrolimus concentration in 51 patients with MG (positive for anti-AChR antibody, n = 48; negative for anti-AChR and anti-muscle-specific tyrosine kinase antibodies, n = 3) who received 3 mg/day tacrolimus for more than 1 year was measured using a chemiluminescent enzyme immunoassay. The clinical characteristics of patients with MG as well as the dose of prednisolone used before and after tacrolimus treatment were evaluated retrospectively.RESULTS:
The median trough tacrolimus concentration was 5.4 (range, 2.9-7.6) ng/mL, which was correlated with 'minimal manifestation or better status' (P = 0.0190, r = 0.3273) and the reduction in anti-AChR antibody 1 year after tacrolimus initiation (P = 0.0170, r = 0.3465). When the cut-off value for tacrolimus was defined as 4.8 ng/mL using a receiver operating characteristic curve, patients with adequate tacrolimus concentration (≥4.8 ng/mL) showed more reduction in anti-AChR antibody titers and more improvement in MG-related activities in daily life scores. More patients with adequate tacrolimus concentration achieved 'minimal manifestation or better status' compared with those with low tacrolimus concentration.CONCLUSIONS:
An adequate tacrolimus concentration is required for better MG prognosis.Palavras-chave
Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Prednisolona
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Tacrolimo
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Imunossupressores
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Miastenia Gravis
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article