Soini Venla, Schreiber Gudrun, Wilken Bernd, Hell Anna Kathrin
Paediatric Orthopaedics, Department of Trauma, Orthopaedic and Plastic Surgery, University Medical Center Göttingen, 37075 Göttingen, Germany.
Department of Paediatric Surgery and Paediatric Orthopaedic Surgery, University of Turku and Turku University Hospital, FI-20520 Turku, Finland.
Children (Basel). 2023 Jun 2;10(6):998. doi: 10.3390/children10060998.
Spinal muscular atrophy (SMA) is a rare genetic disorder, with the most common form being 5q SMA. Survival of children with severe SMA is poor, yet major advances have been made in recent years in pharmaceutical treatment, such as gene-therapy, which has improved patient survival. Therefore, clinical problems, such as the development of spinal deformities in these genetically treated SMA children represent an unknown challenge in clinical work. In a retrospective case series, the development of spinal deformities was analyzed in 16 SMA children (9 male, 7 female) treated with onasemnogene abeparvovec in two institutions during the years 2020 to 2022. Ten out of sixteen patients had a significant kyphosis, and nine out of sixteen patients had significant scoliosis, with the mean curvature angles of 24 ± 27° for scoliosis, and 69 ± 15° for kyphosis. Based on these preliminary data, it can be assumed that early-onset kyphosis presents a clinical challenge in gene-therapy-treated SMA children. Larger datasets with longer follow-up times need to be collected in order to verify these preliminary observations.
脊髓性肌萎缩症(SMA)是一种罕见的遗传性疾病,最常见的类型是5q SMA。重度SMA患儿的生存率较低,但近年来在药物治疗方面取得了重大进展,如基因治疗,这提高了患者的生存率。因此,在这些接受基因治疗的SMA患儿中,脊柱畸形的发展等临床问题在临床工作中是一个未知的挑战。在一项回顾性病例系列研究中,分析了2020年至2022年期间在两个机构接受onasemnogene abeparvovec治疗的16例SMA患儿(9例男性,7例女性)脊柱畸形的发展情况。16例患者中有10例有明显的脊柱后凸,16例患者中有9例有明显的脊柱侧凸,脊柱侧凸的平均弯曲角度为24±27°,脊柱后凸为69±15°。基于这些初步数据,可以假设早发性脊柱后凸在接受基因治疗的SMA患儿中是一个临床挑战。需要收集更大的数据集并进行更长时间的随访,以验证这些初步观察结果。