Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/111879
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dc.contributorDepartment of Rehabilitation Sciences-
dc.creatorZhang, H-
dc.creatorChen, S-
dc.creatorXu, RH-
dc.creatorYu, S-
dc.creatorYu, J-
dc.creatorDong, D-
dc.date.accessioned2025-03-18T01:13:22Z-
dc.date.available2025-03-18T01:13:22Z-
dc.identifier.urihttp://hdl.handle.net/10397/111879-
dc.language.isoenen_US
dc.publisherPublic Library of Scienceen_US
dc.rights© 2024 Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.rightsThe following publication Zhang H, Chen S, Xu RH, Yu S, Yu J, Dong D (2024) Association between under-dose of enzyme replacement therapy and quality of life in adults with late-onset Pompe disease in China: A retrospective matched cohort study. PLoS ONE 19(9): e0310534 is available at https://doi.org/10.1371/journal.pone.0310534.en_US
dc.titleAssociation between under-dose of enzyme replacement therapy and quality of life in adults with late-onset Pompe disease in China : a retrospective matched cohort studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume19-
dc.identifier.issue9-
dc.identifier.doi10.1371/journal.pone.0310534-
dcterms.abstractBackground Due to the high cost of enzyme replacement therapy (ERT), most of adults with late-onset Pompe disease (LOPD) who received ERT used the medication with insufficient dosefs in China.-
dcterms.abstractObjective To compare the change in quality of life (QoL) between adults with LOPD receiving underdose ERT and no ERT, and identify factors associated with the change of QoL.-
dcterms.abstractMethods A retrospective matched cohort study was conducted among adult patients with LOPD in a nationwide Pompe registry in China. Eligible participants were those who completed two investigations, and didn’t expose to ERT at baseline or before. The treated group were those who used ERT during follow-up; the untreated group received general care. The treated and untreated group were matched with a ratio of 1:2. QoL was assessed by the SF-12 and EQ-5D-5L. The dose of ERT was evaluated by the ratio of actual vials patients used divided by the indicated vials patients should use. The treated patients were further classified into mild and severe under-dose users by the median ratio. Multivariate linear regression analyses were performed to estimate the average treatment effect in the treated groups and identify factors associated with the changes of QoL scores.-
dcterms.abstractResults The study sample included 5 mild under-dose users, 6 severe under-dose users, and 22 untreated participants. Compared with the untreated group, mild under-dose ERT had no significant effect on the changes of QoL scores. In contrast, severe under-dose ERT was associated with a decline of physical QoL (β = -6.19, p = 0.001), but an increase of overall health state (β = 19.69, p = 0.032). A higher score of physical QoL (β = -0.74, p = 0.001) and overall health state (β = -0.69, p<0.001) at baseline was associated with decline in corresponding scores at follow-up. Being female was a contributor to the worsening of the overall health state (β = -22.79, p = 0.002), while being employed or at school was a predictor of improvement in mental QoL (β = 5.83, p = 0.002).-
dcterms.abstractConclusions A Pompe-disease specific instrument based on patient experiences is warranted to closely monitor changes in QoL on a routine basis. It is desirable for patients with severe underdose ERT to discuss with physicians whether to adjust treatment strategies.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPLoS one, 2024, v. 19, no. 9, e0310534-
dcterms.isPartOfPLoS one-
dcterms.issued2024-
dc.identifier.scopus2-s2.0-85204301884-
dc.identifier.pmid39288112-
dc.identifier.eissn1932-6203-
dc.identifier.artne0310534-
dc.description.validate202503 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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