标题:Health-related quality of life in children with osteogenesis imperfecta: a large-sample study
作者:Song, Y.; Zhao, D.; Li, L.; Lv, F.; Wang, O.; Jiang, Y.; Xia, W.; Xing, X.; Li, M.
作者机构:[Song, Y.; Zhao, D.; Li, L.; Lv, F.; Wang, O.; Jiang, Y.; Xia, W.; Xing, X.; Li, M.] Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist 更多
通讯作者:Li, M;Li, M
通讯作者地址:[Li, M]Chinese Acad Med Sci, Dept Endocrinol, Key Lab Endocrinol, Minist Hlth,Natl Hlth & Family Planning Commiss,P, Shuaifuyuan 1, Beijing 100730, Pe 更多
来源:OSTEOPOROSIS INTERNATIONAL
出版年:2019
卷:30
期:2
页码:461-468
DOI:10.1007/s00198-018-4801-5
关键词:Health-related quality of life; Osteogenesis imperfecta; Pathogenic; mutations; PedsQL 4.0
摘要:A Summary In this large-sample study, we demonstrated that osteogenesis imperfecta (OI) significantly impaired the quality of life (QoL) in children. Moderate/severe OI patients had worse QoL scores than patients with mild OI. Furthermore, the QoL for OI patients was correlated with the presence of pathogenic gene mutations.; Introduction Osteogenesis imperfecta (OI) is a hereditary disease characterized by multiple fragility fractures and progressive skeletal deformities. No detailed investigations about the quality of life (QoL) have been carried out in a large sample of patients with OI. We evaluated the QoL and its influencing factors in a large and well-characterized OI cohort.; Methods We used a validated questionnaire of PedsQL 4.0 to evaluate the health-related quality of life (HRQoL) of children and adolescents with OI. We compared HRQoL among patients with OI types I, III, and IV. The relationship between HRQoL and pathogenic mutations in candidate OI genes was investigated. We also evaluated the influencing factors of HRQoL in OI patients.; Results A total of 138 children with OI and 138 healthy controls were enrolled in this study. The HRQoL scores of OI patients were 64.4 +/- 30.0, 71.9 +/- 22.2, 75.7 +/- 24.8, 63.7 +/- 24.5, and 68.9 +/- 22.0 in physical, emotional, social, school functioning, and total score, respectively, which were significantly lower than those of healthy children (86.5 +/- 12.7, 83.3 +/- 16.0, 92.1 +/- 11.8, 87.5 +/- 11.8, and 87.3 +/- 10.7, all p<0.01). Moderate and severe OI (type III/IV) patients had poorer HRQoL scores than patients with mild OI (type I). Gene mutations inducing qualitative defects in type I collagen led to worse HRQoL scores than those with quantitative defects in type I collagen, except in emotional functioning. The total HRQoL score was positively correlated with family income, lumbar, and femoral bone mineral density (BMD) Z-scores and negatively correlated with disease severity and fracture frequency.; Conclusion HRQoL was significantly impaired in OI patients, and patients with more severe OI had poorer HRQoL scores. For the first time, we found that children with qualitative defects in type I collagen had poorer HRQoL scores than those with quantitative defects in type I collagen.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85058947140&doi=10.1007%2fs00198-018-4801-5&partnerID=40&md5=cc77a86603ec2b03cad94857199630f9
TOP