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Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy

BACKGROUND: Enzyme replacement therapy (ERT) has deeply modified the clinical history of Infantile Onset Pompe Disease (IOPD). However, its long-term effectiveness is still not completely defined. Available data shows a close relationship between clinical outcome and patients’ cross-reactive immunol...

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Autores principales: Parini, Rossella, De Lorenzo, Paola, Dardis, Andrea, Burlina, Alberto, Cassio, Alessandra, Cavarzere, Paolo, Concolino, Daniela, Della Casa, Roberto, Deodato, Federica, Donati, Maria Alice, Fiumara, Agata, Gasperini, Serena, Menni, Francesca, Pagliardini, Veronica, Sacchini, Michele, Spada, Marco, Taurisano, Roberta, Valsecchi, Maria Grazia, Di Rocco, Maja, Bembi, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806382/
https://www.ncbi.nlm.nih.gov/pubmed/29422078
http://dx.doi.org/10.1186/s13023-018-0771-0
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author Parini, Rossella
De Lorenzo, Paola
Dardis, Andrea
Burlina, Alberto
Cassio, Alessandra
Cavarzere, Paolo
Concolino, Daniela
Della Casa, Roberto
Deodato, Federica
Donati, Maria Alice
Fiumara, Agata
Gasperini, Serena
Menni, Francesca
Pagliardini, Veronica
Sacchini, Michele
Spada, Marco
Taurisano, Roberta
Valsecchi, Maria Grazia
Di Rocco, Maja
Bembi, Bruno
author_facet Parini, Rossella
De Lorenzo, Paola
Dardis, Andrea
Burlina, Alberto
Cassio, Alessandra
Cavarzere, Paolo
Concolino, Daniela
Della Casa, Roberto
Deodato, Federica
Donati, Maria Alice
Fiumara, Agata
Gasperini, Serena
Menni, Francesca
Pagliardini, Veronica
Sacchini, Michele
Spada, Marco
Taurisano, Roberta
Valsecchi, Maria Grazia
Di Rocco, Maja
Bembi, Bruno
author_sort Parini, Rossella
collection PubMed
description BACKGROUND: Enzyme replacement therapy (ERT) has deeply modified the clinical history of Infantile Onset Pompe Disease (IOPD). However, its long-term effectiveness is still not completely defined. Available data shows a close relationship between clinical outcome and patients’ cross-reactive immunological status (CRIM), being CRIM-negative status a negative prognostic factor. At the same time limited data are available on the long-term treatment in CRIM-positive infants. METHODS: A retrospective multicentre observational study was designed to analyse the long-term effectiveness of ERT in IOPD. Thirteen Italian centres spread throughout the country were involved and a cohort of 28 patients (15 females, 13 males, born in the period: February 2002–January 2013) was enrolled. IOPD diagnosis was based on clinical symptoms, enzymatic and molecular analysis. All patients received ERT within the first year of life. Clinical, laboratory, and functional data (motor, cardiac and respiratory) were collected and followed for a median period of 71 months (5 years 11 months). RESULTS: Median age at onset, diagnosis and start of ERT were 2, 3 and 4 months, respectively. CRIM status was available for 24/28 patients: 17/24 (71%) were CRIM-positive. Nineteen patients (67%) survived > 2 years: 4 were CRIM-negative, 14 CRIM-positive and one unknown. Six patients (5 CRIM-positive and one unknown) never needed ventilation support (21,4%) and seven (6 CRIM-positive and one unknown: 25%) developed independent ambulation although one subsequently lost this function. Brain imaging study was performed in 6 patients and showed peri-ventricular white matter abnormalities in all of them. Clinical follow-up confirmed the better prognosis for CRIM-positive patients, though a slow, progressive worsening of motor and/or respiratory functions was detected in 8 patients. CONCLUSIONS: These data are the result of the longest independent retrospective study on ERT in IOPD reported so far outside clinical trials. The data obtained confirmed the better outcome of the CRIM-positive patients but at the same time, showed the inability of the current therapeutic approach to reverse or stabilize the disease progression. The results also evidenced the involvement of central nervous system in Pompe disease. To better understand the disease clinical history and to improve treatment efficacy larger multicentre studies are needed as well as the development of new therapeutic approaches.
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spelling pubmed-58063822018-02-15 Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy Parini, Rossella De Lorenzo, Paola Dardis, Andrea Burlina, Alberto Cassio, Alessandra Cavarzere, Paolo Concolino, Daniela Della Casa, Roberto Deodato, Federica Donati, Maria Alice Fiumara, Agata Gasperini, Serena Menni, Francesca Pagliardini, Veronica Sacchini, Michele Spada, Marco Taurisano, Roberta Valsecchi, Maria Grazia Di Rocco, Maja Bembi, Bruno Orphanet J Rare Dis Research BACKGROUND: Enzyme replacement therapy (ERT) has deeply modified the clinical history of Infantile Onset Pompe Disease (IOPD). However, its long-term effectiveness is still not completely defined. Available data shows a close relationship between clinical outcome and patients’ cross-reactive immunological status (CRIM), being CRIM-negative status a negative prognostic factor. At the same time limited data are available on the long-term treatment in CRIM-positive infants. METHODS: A retrospective multicentre observational study was designed to analyse the long-term effectiveness of ERT in IOPD. Thirteen Italian centres spread throughout the country were involved and a cohort of 28 patients (15 females, 13 males, born in the period: February 2002–January 2013) was enrolled. IOPD diagnosis was based on clinical symptoms, enzymatic and molecular analysis. All patients received ERT within the first year of life. Clinical, laboratory, and functional data (motor, cardiac and respiratory) were collected and followed for a median period of 71 months (5 years 11 months). RESULTS: Median age at onset, diagnosis and start of ERT were 2, 3 and 4 months, respectively. CRIM status was available for 24/28 patients: 17/24 (71%) were CRIM-positive. Nineteen patients (67%) survived > 2 years: 4 were CRIM-negative, 14 CRIM-positive and one unknown. Six patients (5 CRIM-positive and one unknown) never needed ventilation support (21,4%) and seven (6 CRIM-positive and one unknown: 25%) developed independent ambulation although one subsequently lost this function. Brain imaging study was performed in 6 patients and showed peri-ventricular white matter abnormalities in all of them. Clinical follow-up confirmed the better prognosis for CRIM-positive patients, though a slow, progressive worsening of motor and/or respiratory functions was detected in 8 patients. CONCLUSIONS: These data are the result of the longest independent retrospective study on ERT in IOPD reported so far outside clinical trials. The data obtained confirmed the better outcome of the CRIM-positive patients but at the same time, showed the inability of the current therapeutic approach to reverse or stabilize the disease progression. The results also evidenced the involvement of central nervous system in Pompe disease. To better understand the disease clinical history and to improve treatment efficacy larger multicentre studies are needed as well as the development of new therapeutic approaches. BioMed Central 2018-02-08 /pmc/articles/PMC5806382/ /pubmed/29422078 http://dx.doi.org/10.1186/s13023-018-0771-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Parini, Rossella
De Lorenzo, Paola
Dardis, Andrea
Burlina, Alberto
Cassio, Alessandra
Cavarzere, Paolo
Concolino, Daniela
Della Casa, Roberto
Deodato, Federica
Donati, Maria Alice
Fiumara, Agata
Gasperini, Serena
Menni, Francesca
Pagliardini, Veronica
Sacchini, Michele
Spada, Marco
Taurisano, Roberta
Valsecchi, Maria Grazia
Di Rocco, Maja
Bembi, Bruno
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
title Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
title_full Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
title_fullStr Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
title_full_unstemmed Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
title_short Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy
title_sort long term clinical history of an italian cohort of infantile onset pompe disease treated with enzyme replacement therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806382/
https://www.ncbi.nlm.nih.gov/pubmed/29422078
http://dx.doi.org/10.1186/s13023-018-0771-0
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