Kluijver Louisa G, Wensink Debby, Wagenmakers Margreet A E M, Huidekoper Hidde H, Witters Peter, Rymen Daisy, Langendonk Janneke G
Department of Internal Medicine, Porphyria Center Rotterdam, Center for Lysosomal and Metabolic Diseases, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Department of Pediatrics, Center for Lysosomal and Metabolic Diseases, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
J Dermatol. 2024 Aug;51(8):1068-1078. doi: 10.1111/1346-8138.17348. Epub 2024 Jun 26.
Erythropoietic protoporphyria (EPP) is an inherited metabolic disease that causes painful phototoxic reactions, starting in childhood. Studies have shown a reduced quality of life (QoL) in adults with EPP, however, data on children with the disease are lacking. Since treatment for EPP is currently not registered for children, knowledge about their QoL is of crucial importance. In this prospective, case-control study, we included children from the Netherlands and Belgium diagnosed with EPP and matched to healthy controls. Previously collected EPP quality of life (EPP-QoL) data from matched adults with EPP were used. QoL scores, utilizing the Pediatric Quality of Life Inventory (PedsQL) and the disease-specific EPP-QoL, were collected. Scores range from 0 to 100, with higher scores indicating a higher QoL. Non-parametric tests were used to compare groups. A total of 15 cases, 13 matched healthy control children, and 15 matched adults with EPP were included. Children with EPP exhibited lower median scores in the PedsQL in both physical (cases: 87.5 (interquartile range [IQR] 77.7-96.1), controls: 99.2 [IQR 94.9-100.0], p = 0.03) and social (cases: 77.5 [IQR 69.4-86.3], controls: 97.5 [IQR 78.8-100.0], p = 0.04) domains compared to healthy children, although these differences were not statistically significant after correcting for multiple testing. The overall median EPP-QoL score for children was similar to adults with EPP (children: 44.4 [IQR 25.0-54.2], adults: 45.8 [IQR 25.7-68.1], p = 0.68). However, within the EPP-QoL subdomain on QoL, children were found to have significantly lower median scores (children: 16.7 [IQR 0.0-33.3], adults: 33.3 [IQR 33.3-62.5], p < 0.01). In conclusion, children with EPP experience a reduced QoL compared to both healthy children and adults with EPP. Ensuring treatment availability for this patient group is crucial for improving their QoL. We advocate the inclusion of children in safety and efficacy studies, to ensure availability of treatment in the future.
红细胞生成性原卟啉病(EPP)是一种遗传性代谢疾病,自儿童期起就会引发疼痛性光毒性反应。研究表明,成年EPP患者的生活质量(QoL)有所下降,然而,关于该疾病儿童患者的数据却很匮乏。由于目前EPP的治疗方法尚未在儿童中注册,了解他们的生活质量至关重要。在这项前瞻性病例对照研究中,我们纳入了来自荷兰和比利时被诊断为EPP的儿童,并与健康对照进行匹配。使用了之前收集的来自匹配的成年EPP患者的EPP生活质量(EPP-QoL)数据。收集了使用儿童生活质量量表(PedsQL)和特定疾病的EPP-QoL的生活质量评分。评分范围为0至100,分数越高表明生活质量越高。使用非参数检验来比较各组。总共纳入了15例病例、13名匹配的健康对照儿童和15名匹配的成年EPP患者。与健康儿童相比,EPP儿童在PedsQL的身体领域(病例:87.5[四分位间距(IQR)77.7 - 96.1],对照:99.2[IQR 94.9 - 100.0],p = 0.03)和社会领域(病例:77.5[IQR 69.4 - 86.3],对照:97.5[IQR 78.8 - 100.0],p = 0.04)的中位数得分较低,尽管在进行多重检验校正后这些差异无统计学意义。儿童EPP-QoL的总体中位数得分与成年EPP患者相似(儿童:44.4[IQR 25.0 - 54.2],成人:45.8[IQR 25.7 - 68.1],p = 0.68)。然而,在EPP-QoL中关于生活质量的子领域内,发现儿童的中位数得分显著更低(儿童:16.7[IQR 0.0 - 33.3],成人:33.3[IQR 33.3 - 62.5],p < 0.01)。总之,与健康儿童和成年EPP患者相比,EPP儿童的生活质量有所下降。确保该患者群体能够获得治疗对于改善他们的生活质量至关重要。我们提倡将儿童纳入安全性和有效性研究,以确保未来治疗的可及性。