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[The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]. / A késoi kezdetu Pompe-kórban szenvedok enzimpótló kezelésének hosszú távú követése.
Molnár, Mária Judit; Borsos, Beáta; Várdi, Katalin Visy; Grosz, Zoltán; Sebok, Ágnes; Dézsi, Lívia; Almássy, Zsuzsanna; Kerényi, Levente; Jobbágy, Zita; Jávor, László; Bidló, Judit.
Afiliação
  • Molnár MJ; Semmelweis Egyetem, Genomikai Medicina és Ritka Betegségek Intézete, ERN NMD, Budapest.
  • Borsos B; Semmelweis Egyetem, Genomikai Medicina és Ritka Betegségek Intézete, ERN NMD, Budapest.
  • Várdi KV; InspiroMed, Budapest.
  • Grosz Z; Semmelweis Egyetem, Genomikai Medicina és Ritka Betegségek Intézete, ERN NMD, Budapest.
  • Sebok Á; Pécsi Tudományegyetem, Neurológiai Klinika, ERN NMD, Pécs.
  • Dézsi L; Szegedi Tudományegyetem, Neurológiai Klinika, Szeged.
  • Almássy Z; Heim Pál Országos Gyermekgyógyászati Intézet, Gyermekkórház, Budapest.
  • Kerényi L; Fejér Megyei Szent György Egyetemi Oktató Kórház, Neurológiai Osztály, Székesfehérvár.
  • Jobbágy Z; Bács-Kiskun Megyei Kórház, Neurológiai Osztály, Kecskemét.
  • Jávor L; Petz Aladár Megyei Oktató Kórház, Neurológiai Osztály, Gyôr.
  • Bidló J; Nemzeti Egészségbiztosítási Alapkezelô, Budapest.
Ideggyogy Sz ; 73(05-06): 151-159, 2020 05 30.
Article em Hu | MEDLINE | ID: mdl-32579304
ABSTRACT
Pompe disease (PD) is a rare lysosomal disease caused by the deficient activity of acid alpha-glucosidase (GAA) enzyme due to mutations in the GAA gene. The enzymatic deficiency leads to the accumulation of glycogen within the lysosomes. Clinically, the disease has been classically classified in infantile and childhood/adult forms. Presently cc. close to 600 mutations distributed throughout the whole gene have been reported. The c.-32-13T>G splice mutation that is very common in patients of Caucasian origin affected by the childhood/adult form of the disease, with an allelic frequency close to 70%. Enzyme replacement treatment (ERT) is available for the patients with Pompe disease (Myozyme). In this paper, we are presenting the long term follow up of 13 adult onset cases treated more than 5 years. The longest follow up was 15 years. To evaluate the treatment efficacy, the 6 minutes walking test (6MWT) and the respiratory functions were monitored annually. The analysis revealed that at the beginning of ERT for 3-4 years the 6MWT had been generally increasing, then it declined, and after 10 years it was lower in 77% of the cases than it had been at the start of the treatment. In 23% of the cases the 6MWT increased during the follow up time. Only one of the patients become wheelchair dependent during the follow-up period. The respiratory function showed similar results especially in supine position. A high degree of variability was observed among patients in their responses to the treatment, which only partially associated with the antibody titer against the therapeutic protein. The efficacy of the ERT was associated with the type of the disease causing mutation, the baseline status of the disease, the lifestyle and the diet of the patient. The long-term follow up of the patients with innovative orphan drugs is necessary to really understand the value of the treatment and the need of the patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Depósito de Glicogênio Tipo II / Alfa-Glucosidases / Terapia de Reposição de Enzimas Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Child / Humans Idioma: Hu Revista: Ideggyogy Sz Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Depósito de Glicogênio Tipo II / Alfa-Glucosidases / Terapia de Reposição de Enzimas Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Child / Humans Idioma: Hu Revista: Ideggyogy Sz Ano de publicação: 2020 Tipo de documento: Article