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Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride

BACKGROUND: Sapropterin dihydrochloride effectively lowers plasma phenylalanine (Phe) for at least a third of phenylketonuria (PKU) patients, with potential for increased dietary Phe tolerance and decreased medical food requirement. OBJECTIVE: To investigate long-term quality of life (QOL) in patien...

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Autores principales: Douglas, Teresa D, Ramakrishnan, Usha, Kable, Julie A, Singh, Rani H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880979/
https://www.ncbi.nlm.nih.gov/pubmed/24373161
http://dx.doi.org/10.1186/1477-7525-11-218
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author Douglas, Teresa D
Ramakrishnan, Usha
Kable, Julie A
Singh, Rani H
author_facet Douglas, Teresa D
Ramakrishnan, Usha
Kable, Julie A
Singh, Rani H
author_sort Douglas, Teresa D
collection PubMed
description BACKGROUND: Sapropterin dihydrochloride effectively lowers plasma phenylalanine (Phe) for at least a third of phenylketonuria (PKU) patients, with potential for increased dietary Phe tolerance and decreased medical food requirement. OBJECTIVE: To investigate long-term quality of life (QOL) in patients with phenylketonuria (PKU) who took sapropterin (BH4, Kuvan®) for up to one year. METHODS: 37 PKU patients, ages 10–49 years, were asked to complete a PKU-specific self-report QOL questionnaire (QOLQ) at baseline, 1, 4, 8, and 12 months. Questions were scored on a 5-point Likert scale under 5 sub-sections measuring Impact, Worries, Satisfaction, Support, and General wellbeing in relation to PKU. Responders with a plasma Phe decrease ≥ 15% after 1 month on sapropterin remained on the drug; Nonresponders ceased sapropterin after the trial month. Responders able to relax medical diet and maintain plasma Phe control were classified as Definitive; Responders unable to relax medical diet were classified as Provisional. All patients were routinely monitored by a registered dietitian. Data was analyzed in SPSS 19.0 using regression techniques. RESULTS: Of 17 Responders, 11 could maintain adequate Phe control on a less restrictive diet. One year mean Impact sub-score trends improved significantly for all sapropterin response groups, with greatest improvement among Definitive Responders (p < 0.0001). Satisfaction sub-scores also improved for Definitive Responders (p = 0.001). Trends for Total QOL score improved significantly over time for both Definitive (p = 0.001) and Provisional Responders (p = 0.028). Improvements in Definitive Responder scores were associated with increased Phe tolerance (Impact: p < 0.0001, Satisfaction: p = 0.022, Total QOL: p = 0.005) and MF adjustment (Satisfaction: p = 0.014, Total QOL: p = 0.026). Other sub-section scores remained steady, unaffected by sapropterin response or diet modification. CONCLUSION: Increased Phe tolerance and reduced MF requirement in sapropterin Definitive Responders improves QOL perception across one year, specifically for life impact and satisfaction.
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spelling pubmed-38809792014-01-07 Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride Douglas, Teresa D Ramakrishnan, Usha Kable, Julie A Singh, Rani H Health Qual Life Outcomes Research BACKGROUND: Sapropterin dihydrochloride effectively lowers plasma phenylalanine (Phe) for at least a third of phenylketonuria (PKU) patients, with potential for increased dietary Phe tolerance and decreased medical food requirement. OBJECTIVE: To investigate long-term quality of life (QOL) in patients with phenylketonuria (PKU) who took sapropterin (BH4, Kuvan®) for up to one year. METHODS: 37 PKU patients, ages 10–49 years, were asked to complete a PKU-specific self-report QOL questionnaire (QOLQ) at baseline, 1, 4, 8, and 12 months. Questions were scored on a 5-point Likert scale under 5 sub-sections measuring Impact, Worries, Satisfaction, Support, and General wellbeing in relation to PKU. Responders with a plasma Phe decrease ≥ 15% after 1 month on sapropterin remained on the drug; Nonresponders ceased sapropterin after the trial month. Responders able to relax medical diet and maintain plasma Phe control were classified as Definitive; Responders unable to relax medical diet were classified as Provisional. All patients were routinely monitored by a registered dietitian. Data was analyzed in SPSS 19.0 using regression techniques. RESULTS: Of 17 Responders, 11 could maintain adequate Phe control on a less restrictive diet. One year mean Impact sub-score trends improved significantly for all sapropterin response groups, with greatest improvement among Definitive Responders (p < 0.0001). Satisfaction sub-scores also improved for Definitive Responders (p = 0.001). Trends for Total QOL score improved significantly over time for both Definitive (p = 0.001) and Provisional Responders (p = 0.028). Improvements in Definitive Responder scores were associated with increased Phe tolerance (Impact: p < 0.0001, Satisfaction: p = 0.022, Total QOL: p = 0.005) and MF adjustment (Satisfaction: p = 0.014, Total QOL: p = 0.026). Other sub-section scores remained steady, unaffected by sapropterin response or diet modification. CONCLUSION: Increased Phe tolerance and reduced MF requirement in sapropterin Definitive Responders improves QOL perception across one year, specifically for life impact and satisfaction. BioMed Central 2013-12-30 /pmc/articles/PMC3880979/ /pubmed/24373161 http://dx.doi.org/10.1186/1477-7525-11-218 Text en Copyright © 2013 Douglas et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Douglas, Teresa D
Ramakrishnan, Usha
Kable, Julie A
Singh, Rani H
Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
title Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
title_full Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
title_fullStr Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
title_full_unstemmed Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
title_short Longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
title_sort longitudinal quality of life analysis in a phenylketonuria cohort provided sapropterin dihydrochloride
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880979/
https://www.ncbi.nlm.nih.gov/pubmed/24373161
http://dx.doi.org/10.1186/1477-7525-11-218
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