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dc.contributor.authorMaissen-Abgottspon, S.*
dc.contributor.authorMuri, R.*
dc.contributor.authorHochuli, M.*
dc.contributor.authorReismann, P.*
dc.contributor.authorBarta, A.G.*
dc.contributor.authorAlptekin, I.M.*
dc.contributor.authorHermida Ameijeiras, Alvaro *
dc.contributor.authorBurlina, A.P.*
dc.contributor.authorBurlina, A.B.*
dc.contributor.authorCazzorla, C.*
dc.contributor.authorCarretta, J.*
dc.contributor.authorTrepp, R.*
dc.contributor.authorEverts, R.*
dc.date.accessioned2025-09-09T12:31:39Z
dc.date.available2025-09-09T12:31:39Z
dc.date.issued2023
dc.identifier.citationMaissen-Abgottspon S, Muri R, Hochuli M, Reismann P, Barta AG, Alptekin IM, et al. Health-related quality of life in a european sample of adults with early-treated classical PKU. Orphanet Journal of Rare Diseases. 2023;18(1).
dc.identifier.issn1750-1172
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/6522c806ec1a10197ffd97b2
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21551
dc.description.abstractBackground: Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabolism of phenylalanine (Phe). To date, findings regarding health-related quality of life (HRQoL) in adults with early-treated classical PKU are discrepant. Moreover, little is known about metabolic, demographic, and cognitive factors associated with HRQoL. Hence, we aimed to investigate HRQoL and its association with demographic, metabolic, and cognitive characteristics in a large European sample of adults with early-treated classical PKU. Results: This cross-sectional study included 124 adults with early-treated classical PKU from Hungary, Italy, Spain, Switzerland, and Turkey. All participants prospectively completed the PKU quality of life questionnaire (PKU-QoL), a questionnaire specifically designed to evaluate the impact of PKU and its treatment on HRQoL in individuals with PKU. In addition, information about Phe levels (concurrent and past year), demographic (age and sex), and cognitive variables (intelligence quotient, IQ) were collected. Most domains revealed little or no impact of PKU on HRQoL and more than three-quarters of the patients rated their health status as good, very good, or excellent. Nevertheless, some areas of concern for patients were identified. Patients were worried about the guilt that they experience if they do not adhere to the dietary protein restriction and they were most concerned about high Phe levels during pregnancy. Further, tiredness was the most affected symptom, and the supplements' taste was considered a main issue for individuals with PKU. The overall impact of PKU on HRQoL was higher in women (U = 1315.5, p =.012) and in adults with a lower IQ (rs = ? 0.448, p =.005). The overall impact of dietary protein restriction was higher in adults with higher concurrent Phe levels (rs = 0.272, p =.007) and higher Phe levels during the past year (rs = 0.280, p =.009). Conclusion: The impact of PKU on most domains assessed in the PKU-QoL was considered to be low. These results likely reflect the successful implementation of the newborn screening resulting in the prevention of severe adverse long-term outcomes. However, a particular clinical focus should be given to patients with lower IQ, higher Phe levels, and women, as these variables were associated with a lower HRQoL.
dc.description.sponsorshipWe want to thank all participants that participated in the present study.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshInfant, Newborn *
dc.subject.meshPregnancy *
dc.subject.meshHumans *
dc.subject.meshAdult *
dc.subject.meshFemale *
dc.subject.meshQuality of Life *
dc.subject.meshCross-Sectional Studies *
dc.subject.meshPhenylketonurias *
dc.subject.meshHealth Status *
dc.subject.meshNeonatal Screening *
dc.subject.meshPhenylalanine *
dc.titleHealth-related quality of life in a european sample of adults with early-treated classical PKU
dc.typeArtigo
dc.authorsophosMaissen-Abgottspon, S.; Muri, R.; Hochuli, M.; Reismann, P.; Barta, A.G.; Alptekin, I.M.; Hermida-Ameijeiras, Á.; Burlina, A.P.; Burlina, A.B.; Cazzorla, C.; Carretta, J.; Trepp, R.; Everts, R.
dc.identifier.doi10.1186/s13023-023-02917-w
dc.identifier.sophos6522c806ec1a10197ffd97b2
dc.issue.number1
dc.journal.titleOrphanet Journal of Rare Diseases*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Santiago::Medicina interna
dc.relation.projectIDWe want to thank all participants that participated in the present study.
dc.relation.publisherversionhttps://doi.org/10.1186/s13023-023-02917-w
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Santiago
dc.subject.keywordCHUS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number18


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