Beneficial Effect of Growth Hormone Treatment on Health-Related Quality of Life in Children with Prader-Willi Syndrome: A Randomized Controlled Trial and Longitudinal Study

被引:22
作者
Bakker, Nienke E. [1 ,2 ]
Siemensma, Elbrich P. C. [1 ,2 ]
van Rijn, Marjon [1 ]
Festen, Dederieke A. M. [1 ]
Hokken-Koelega, Anita C. S. [1 ,2 ]
机构
[1] Erasmus Univ, Med Ctr, Sophia Childrens Hosp, Dutch Growth Res Fdn, NL-3016 AH Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Sophia Childrens Hosp, Dept Pediat,Subdiv Endocrinol, NL-3016 AH Rotterdam, Netherlands
来源
HORMONE RESEARCH IN PAEDIATRICS | 2015年 / 84卷 / 04期
关键词
Prader-Willi syndrome; Health-related quality of life; Growth hormone treatment; JAPANESE PATIENTS; QUESTIONNAIRE; ADOLESCENTS; DISORDER; PEOPLE; AGE;
D O I
10.1159/000437141
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Growth hormone (GH) treatment is beneficial for children with Prader-Willi syndrome (PWS), but data about health-related quality of life (HRQOL) and effects of GH treatment are scarce. We, therefore, investigated the effects of GH treatment on HRQOL in PWS children. Methods: In a randomized controlled GH trial including 26 PWS children and during an 11-year longitudinal GH study in 76 children, we annually assessed HRQOL recorded by patients and parents, using a generic questionnaire (DUX25), containing 4 subdomains (Physical, Home, Social, and Emotional) and a PWS-specific questionnaire (DUXPW). Results: At baseline, PWS children rated HRQOL similar to or higher than healthy and obese children. GH-treated children reported an increase in HRQOL in the Physical and Social subdomains and the DUXPW compared to untreated children. Parents reported an increase in the Physical and Emotional subdomains and borderline in the total DUX25 compared to parents of untreated children. During the 11 years of GH treatment, the Physical subdomain continued to improve, according to parents, whereas the Home, Social and Emotional subdomains, the total DUX25, and the DUXPW remained similar, according to children and parents. Conclusions: PWS children rated HRQOL equally to or better than healthy and obese children. HRQOL increased during GH treatment, in contrast to HRQOL of untreated children. This effect was sustained during long-term GH treatment. PWS children consider themselves quite happy, despite some difficulties related to the syndrome. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:231 / 239
页数:9
相关论文
共 39 条
  • [1] The European DISABKIDS project: Development of seven condition-specific modules to measure health related quality of life in children and adolescents
    Baars R.M.
    Atherton C.I.
    Koopman H.M.
    Bullinger M.
    Power M.
    Bullinger M.
    Schmidt S.
    Petersen C.
    Koopman H.
    Baars R.
    Hoare P.
    Power M.
    Atherton C.
    Simeoni M.C.
    Tsanakas J.
    Karagianni P.
    Hatziagorou E.
    Vidalis A.
    Chaplin J.E.
    Quittan M.
    Schuhfried O.
    Hachemian N.
    Thyen U.
    Müller-Godeffroy E.
    [J]. Health and Quality of Life Outcomes, 3 (1)
  • [2] Eight Years of Growth Hormone Treatment in Children With Prader-Willi Syndrome: Maintaining the Positive Effects
    Bakker, N. E.
    Kuppens, R. J.
    Siemensma, E. P. C.
    van Wijngaarden, R. F. A. Tummers-de Lind
    Festen, D. A. M.
    Bindels-de Heus, G. C. B.
    Bocca, G.
    Haring, D. A. J. P.
    Hoorweg-Nijman, J. J. G.
    Houdijk, E. C. A. M.
    Jira, P. E.
    Lunshof, L.
    Odink, R. J.
    Oostdijk, W.
    Rotteveel, J.
    Schroor, E. J.
    Van Alfen, A. A. E. M.
    Van Leeuwen, M.
    Van Pinxteren-Nagler, E.
    Van Wieringen, H.
    Vreuls, R. C. F. M.
    Zwaveling-Soonawala, N.
    de Ridder, M. A. J.
    Hokken-Koelega, A. C. S.
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 98 (10) : 4013 - 4022
  • [3] Quality of life in adolescents born small for gestational age: Does growth hormone make a difference?
    Bannink, EMN
    van Pareren, YK
    Theunissen, NCM
    Raat, H
    Mulder, PGM
    Hokken-Koelega, ACS
    [J]. HORMONE RESEARCH, 2005, 64 (04) : 166 - 174
  • [4] The Bt-DUX: Development of a Subjective Measure of Health-Related Quality of Life in Patients Who Underwent Surgery for Lower Extremity Malignant Bone Tumor
    Bekkering, W. Peter
    Vlieland, Theodora P. M. Vliet
    Koopman, Hendrik M.
    Schaap, Gerard R.
    Schreuder, H. W. Bart
    Beishuizen, Auke
    Tissing, Wim J. E.
    Hoogerbrugge, Peter M.
    Anninga, Jacob K.
    Taminiau, Antonie H. M.
    [J]. PEDIATRIC BLOOD & CANCER, 2009, 53 (03) : 348 - 355
  • [5] Quality of life and psychological well-being in GH-treated, adult PWS patients: a longitudinal study
    Bertella, L.
    Mori, I.
    Grugni, G.
    Pignatti, R.
    Ceriani, F.
    Molinari, E.
    Ceccarelli, A.
    Sartorio, A.
    Vettor, R.
    Semenza, C.
    [J]. JOURNAL OF INTELLECTUAL DISABILITY RESEARCH, 2007, 51 : 302 - 311
  • [6] Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy
    Boer, H
    Holland, A
    Whittington, J
    Butler, J
    Webb, T
    Clarke, D
    [J]. LANCET, 2002, 359 (9301) : 135 - 136
  • [7] Quality of life assessment in a sample of patients affected by Prader-Willi syndrome
    Caliandro, Pietro
    Grugni, Graziano
    Padua, Luca
    Kodra, Yllka
    Tonali, Pietro
    Gargantini, Luigi
    Ragusa, Letizia
    Crino, Antonino
    Taruscio, Domenica
    [J]. JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2007, 43 (12) : 826 - 830
  • [8] Prader-Willi syndrome
    Cassidy, SB
    [J]. JOURNAL OF MEDICAL GENETICS, 1997, 34 (11) : 917 - 923
  • [9] Latino Families with a Child with Prader-Willi Syndrome: Exploring Needs for Support
    Chaij, Carina
    Han, Meekyung
    Graziano, Lisa
    [J]. JOURNAL OF SOCIAL WORK IN DISABILITY & REHABILITATION, 2014, 13 (03) : 207 - 225
  • [10] Cronbach LJ, 1951, PSYCHOMETRIKA, V16, P297