患有骨骼发育不良的矮身材儿童的生活质量:使用矮身材青少年生活质量问卷进行的横断面研究。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Yasunari Kamiya, Masaki Matsushita, Kenichi Mishima, Kenta Sawamura, Hiroshi Kitoh
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引用次数: 0

摘要

骨骼发育不良(包括软骨发育不全(ACH)和成骨不全(OI))患者会表现出各种身材矮小的症状,从而影响其生活质量(QoL)的各个方面。关于骨骼发育不良成人患者的 QoL 已有报道,但关于儿童 QoL 的研究仍然有限。矮身材青少年 QoL(QoLISSY)是专为矮身材儿童和青少年开发的 QoL 调查工具。我们对患有各种骨骼发育不良并伴有身材矮小的儿童进行了 QoLISSY 评分评估,并对 ACH、OI 和其他发育不良儿童的 QoLISSY 评分进行了比较。研究人员分别向患有各种骨骼发育不良的儿童及其家长发放了 40 份和 72 份问卷,并分别回收了 24 份和 54 份有效问卷。ACH、OI和其他骨骼发育不良患者在年龄、性别和身高方面没有明显差异。ACH 组家长的社交、情感和 QoL 总分明显低于 OI 组。一项子分析表明,在所有组别中,身高标准偏差评分与 QoLISSY 评分均无相关性,但 OI 父母的信念评分除外。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of Life in Short Stature Children With Skeletal Dysplasia: A Cross Sectional Study Using the Quality of Life in Short Stature Youth Questionnaire.

Patients with skeletal dysplasia, including achondroplasia (ACH) and osteogenesis imperfecta (OI), exhibit a variety of short stature, which affect various aspects of their quality of life (QoL). The QoL of adult patients with skeletal dysplasia have been reported; however, research on QoL in children remains limited. The QoL in Short Stature Youth (QoLISSY) is a QoL survey tool developed specifically for short stature children and adolescent. We assessed the QoLISSY scores in children with various skeletal dysplasias presenting with short stature and compared the scores among ACH, OI, and other dysplasias. Forty and 72 questionnaires were sent to the children with various skeletal dysplasias and their parents, respectively, and 24 and 54 valid questionnaires, respectively, were collected. There were no significant differences in age, sex, or height between the patients with ACH, OI, and other skeletal dysplasias. Parents' social, emotional, and total QoL scores were significantly lower in the ACH group than in the OI group. A sub-analysis revealed that the height standard deviation score did not correlate with the QoLISSY scores in all groups except for the belief score of OI parents.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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