RESUMO
We evaluated whether the paralytic attacks in thyrotoxic periodic paralysis (TPP) are primarily due to the abnormal excitability of the muscle membrane caused by a preexisting latent abnormality or to the effects of thyroid hormone. The prolonged exercise (PE) test was used to evaluate muscle membrane excitability in 21 patients with TPP and 11 patients with thyrotoxicosis without paralytic attacks (Tw/oPP) in the hyperthyroid state. The PE tests were compared between the hyperthyroid and euthyroid states in five of the TPP and three of the Tw/oPP patients. Compared to 20 healthy subjects, a significant increase in compound muscle action potential (CMAP) amplitudes immediately after exercise and a significant time-dependent gradual decline in CMAP amplitudes starting from 20 min after exercise were observed in the TPP patients. A significant decline in CMAP amplitudes was also observed in the Tw/oPP patients but only at 50 min after exercise. All of the TPP and Tw/oPP patients had a tendency to improve in the euthyroid state; the PE tests remained abnormal only in the TPP patients. Paralytic attacks in TPP patients are due primarily to a preexisting latent abnormal excitability of the muscle membrane, possibly genetic in origin.
Assuntos
Membrana Celular/metabolismo , Músculo Esquelético/fisiopatologia , Paralisias Periódicas Familiares/diagnóstico , Paralisias Periódicas Familiares/fisiopatologia , Tireotoxicose/diagnóstico , Tireotoxicose/fisiopatologia , Potenciais de Ação/genética , Adolescente , Adulto , Idoso , Membrana Celular/genética , Análise Mutacional de DNA , Exercício Físico/fisiologia , Teste de Esforço/efeitos adversos , Tolerância ao Exercício/fisiologia , Feminino , Predisposição Genética para Doença/genética , Humanos , Canais Iônicos/genética , Masculino , Pessoa de Meia-Idade , Contração Muscular/genética , Músculo Esquelético/metabolismo , Paralisias Periódicas Familiares/metabolismo , Polimorfismo de Nucleotídeo Único/genética , Sarcômeros/genética , Sarcômeros/metabolismo , Tireotoxicose/metabolismoRESUMO
A Japanese man with a negative family history of paramyotonia congenita (PMC) was evaluated for symptoms of cold-induced weakness and stiffness. Exercise testing revealed findings characteristic of PMC, and a genetic analysis was therefore performed. A well-known sodium channel mutation for PMC (T1313M) was identified in the patient, but was absent in his biological parents. These data demonstrate the occurrence of a de novo mutation, suggesting that evaluation for PMC should be performed in patients with typical symptoms even if the family history is negative.