Health-related quality of life in French pediatric patients with X-linked hypophosphatemia: real-world data from the International XLH Registry.

IF 2.4 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2025-08-30 eCollection Date: 2025-10-01 DOI:10.1093/jbmrpl/ziaf142
Agnès Linglart, Cyril Amouroux, Iva Gueorguieva, Jerome Harambat, Jean-Pierre Salles, Diana-Alexandra Ertl, Kerry Sandilands, Angela Rylands, Angela Williams, Haruka Ishii, Annabel Bowden, James W Varni, Justine Bacchetta
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Abstract

X-linked hypophosphatemia (XLH) is a phosphate-wasting disorder caused by increased fibroblast growth factor 23 (FGF23); it leads to skeletal deformities, muscle weakness, and pain. In a pediatric phase 3 trial, the FGF23 inhibitor burosumab improved rickets severity and bone biochemistry. The current study characterizes health-related quality of life (HRQL) in children with XLH using real-world data collected at centers in France for the International XLH Registry from April 2017 to January 2024. Age-appropriate versions of the Pediatric Quality of Life Inventory were completed. Data from the first completion after registry entry were analyzed. Variation in scores by demographic, medical history, and treatment history variables was assessed using bivariate analysis. The data were collected from 96 children (59% female; mean age 8.1 [SD 4.4] yr); 82% were taking burosumab. Mean total, summary, and domain scores were similar in different age groups. Mean total score (74.2 [SD 14.1]), Psychosocial Health Summary (72.0 [16.8]), and Physical Health Summary (78.3 [12.3]) scores were lowest in patients aged 5-7 yr and highest in patients aged 13-17 yr (81.0 [13.3], 79.8 [14.1], and 83.1 [15.2]). The mean Psychosocial Health Summary score was lower than the Physical Health Summary score for all patients combined (77.8 [13.9] vs 81.7 [14.3]). Better total scores were associated with not currently taking phosphate/vitamin D analogs, better Psychosocial Health Summary scores with higher serum phosphate and not taking phosphate/vitamin D analogs, and better Physical Health Summary scores with lower serum PTH and currently taking burosumab. Patients with XLH who were taking burosumab at the time of PedsQL completion had better total and summary scores than children with other chronic musculoskeletal disorders. Children aged 5-7 yr had worse HRQL than a healthy Dutch sample. Overall, better HRQL was associated with higher serum phosphate levels and burosumab treatment.

法国儿童x连锁低磷血症患者的健康相关生活质量:来自国际XLH登记处的真实世界数据
x连锁低磷血症(XLH)是一种由成纤维细胞生长因子23 (FGF23)升高引起的磷酸盐消耗紊乱;它会导致骨骼畸形、肌肉无力和疼痛。在一项儿科3期试验中,FGF23抑制剂burrosumab改善了佝偻病的严重程度和骨生化。目前的研究使用2017年4月至2024年1月在法国的国际XLH注册中心收集的真实世界数据,对XLH儿童的健康相关生活质量(HRQL)进行了表征。完成了与年龄相适应的儿童生活质量量表。对登记后首次完成的数据进行分析。采用双变量分析评估人口统计学、病史和治疗史变量对得分的影响。数据来自96名儿童(59%为女性,平均年龄8.1 [SD 4.4]岁);82%的患者服用了布罗单抗。不同年龄组的平均总得分、总得分和领域得分相似。5-7岁患者的平均总分(74.2 [SD 14.1])、心理社会健康总结(72.0[16.8])和身体健康总结(78.3[12.3])得分最低,13-17岁患者的得分最高(81.0[13.3]、79.8[14.1]和83.1[15.2])。所有患者的平均心理社会健康总结评分低于生理健康总结评分(77.8 [13.9]vs 81.7[14.3])。较高的总分与目前未服用磷酸盐/维生素D类似物相关,较高的血清磷酸盐和未服用磷酸盐/维生素D类似物的患者有较好的心理社会健康总结评分,较低的血清PTH和目前正在服用布罗单抗的患者有较好的身体健康总结评分。在PedsQL完成时服用布罗单抗的XLH患者比患有其他慢性肌肉骨骼疾病的儿童有更好的总得分和总结得分。5-7岁儿童的HRQL比健康的荷兰样本更差。总体而言,较好的HRQL与较高的血清磷酸盐水平和布罗单抗治疗相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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