Health Related Quality of Life assessment among early -treated Hungarian adult PKU patients using the PKU-QOL adult questionnaire

被引:13
作者
Barta, Andras Gellert [1 ]
Sumanszki, Csaba [1 ]
Turgonyi, Zsofia [2 ]
Kiss, Erika [3 ]
Simon, Erika [3 ]
Serfozo, Csilla [4 ]
Reismann, Peter [1 ]
机构
[1] Semmelweis Univ, Dept Internal Med 2, Szentkiralyi St 46, H-1088 Budapest, Hungary
[2] Semmelweis Univ, Fac Med, Ulloi Ut 26, H-1085 Budapest, Hungary
[3] Semmelweis Univ, Dept Pediat 1, Bokay J St 53-54, H-1083 Budapest, Hungary
[4] Semmelweis Univ, Dept Ophthalmol, Maria St 39, H-1085 Budapest, Hungary
关键词
TETRAHYDROBIOPTERIN BH4; PHENYLKETONURIA; OUTCOMES; ADOLESCENTS; MANAGEMENT; DIAGNOSIS;
D O I
10.1016/j.ymgmr.2020.100589
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The implementation of neonatal screening and the early initiation of lifelong therapy have helped to prevent severe complications and enabled much more favorable outcomes for early-treated phenylketonuria (ETPKU) patients. However, PKU patients tend to develop subtle cognitive and psychosocial abnormalities and the strict dietary therapy can present financial and social burden. Thus, PKU is expected to affect the quality of life (QoL) of these patients. There is insufficient evidence regarding the relationship between metabolic control and Health-Related QoL (HRQoL). We aimed to assess the effect of short- and long-term therapy on QoL among Hungarian adult PKU patients using the standardized PKU-specific PKU-QoL questionnaire. Methods: We conducted a single-centre, cross-sectional, observational study in Hungary. We included adult PKU patients treated with diet and amino acid supplements only. Patients reported HRQoL using the standardized adult PKU-QoL questionnaire and mean blood Phe concentrations were assessed for three different time periods: the previous 10 years, the previous year and concentration at the time of completing the questionnaire. The correlation between patients’ QoL scores and their Phe levels was assessed. The classical PKU group was further divided into “good” and “suboptimal” adherence groups based on individual mean Phe levels in the examined time period. We evaluated differences in QoL among the two subgroups of classical PKU patients. QoL scores between classical and non-classical patients were also compared. Results: Data from 88 adult patients were analysed (66 had classical PKU). No median PKU-QoL score reached major or severe impact/frequent symptoms in any domain. The highest scores (meaning larger burden) were mostly related to emotional impact of PKU and disease management. When performing correlation analysis between Phe levels and QoL scores by all patients we found weak to fair positive correlation in several domains either short or long term. Patients with classical PKU reported greater financial impact of PKU than patients with less severe PKU. Classical PKU patients with good therapy adherence tended to report better HRQoL scores than patients with suboptimal adherence. Conclusion: We conclude that patients showed good HRQoL using the PKU-specific questionnaire. Our study demonstrates that suboptimal metabolic control is negatively associated with patients' HRQoL. © 2020 The Authors
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页数:7
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共 41 条
  • [1] Blood phenylalanine control in phenylketonuria: a survey of 10 European centres
    Ahring, K.
    Belanger-Quintana, A.
    Dokoupil, K.
    Gokmen-Ozel, H.
    Lammardo, A. M.
    MacDonald, A.
    Motzfeldt, K.
    Nowacka, M.
    Robert, M.
    van Rijn, M.
    [J]. EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2011, 65 (02) : 275 - 278
  • [2] The impact of phenylketonuria on PKU patients' quality of life: Using of the phenylketonuria-quality of life (PKU-QOL) questionnaires
    Alptekin, Ismail Mucahit
    Koc, Nevra
    Gunduz, Mehmet
    Cakiroglu, Funda Pinar
    [J]. CLINICAL NUTRITION ESPEN, 2018, 27 : 79 - 85
  • [3] Quality of life in noncompliant adults with phenylketonuria after resumption of the diet
    Bik-Multanowski, M.
    Didycz, B.
    Mozrzymas, R.
    Nowacka, M.
    Kaluzny, L.
    Cichy, W.
    Schneiberg, B.
    Amilkiewicz, J.
    Bilar, A.
    Gizewska, M.
    Lange, A.
    Starostecka, E.
    Chrobot, A.
    Wojcicka-Bartlomiejczyk, B. I.
    Milanowski, A.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : S415 - S418
  • [4] Living with phenylketonuria: Perspectives of patients and their families
    Bilginsoy, C
    Waitzman, N
    Leonard, CO
    Ernst, SL
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 (05) : 639 - 649
  • [5] Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies
    Blau, Nenad
    Hennermann, Julia B.
    Langenbeck, Ulrich
    Lichter-Konecki, Uta
    [J]. MOLECULAR GENETICS AND METABOLISM, 2011, 104 : S2 - S9
  • [6] Phenylketonuria
    Blau, Nenad
    van Spronsen, Francjan J.
    Levy, Harvey L.
    [J]. LANCET, 2010, 376 (9750) : 1417 - 1427
  • [7] The PKU & ME study: A qualitative exploration, through co -creative sessions, of attitudes and experience of the disease among adults with phenylketonuria in Italy
    Borghi, Lidia
    Moreschi, Carlotta
    Toscano, Alessandra
    Comber, Peter
    Vegni, Elena
    [J]. MOLECULAR GENETICS AND METABOLISM REPORTS, 2020, 23
  • [8] The course of life and quality of life of early and continuously treated Dutch patients with phenylketonuria
    Bosch, A. M.
    Tybout, W.
    van Spronsen, F. J.
    de Valk, H. W.
    Wijburg, F. A.
    Grootenhuis, M. A.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2007, 30 (01) : 29 - 34
  • [9] Assessment of the impact of phenylketonuria and its treatment on quality of life of patients and parents from seven European countries
    Bosch, Annet M.
    Burlina, Alberto
    Cunningham, Amy
    Bettiol, Esther
    Moreau-Stucker, Flavie
    Koledova, Ekaterina
    Benmedjahed, Khadra
    Regnault, Antoine
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2015, 10
  • [10] The neurological and psychological phenotype of adult patients with early-treated phenylketonuria: A systematic review
    Burlina, Alessandro P.
    Lachmann, Robin H.
    Manara, Renzo
    Cazzorla, Chiara
    Celato, Andrea
    van Spronsen, Francjan J.
    Burlina, Alberto
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2019, 42 (02) : 209 - 219