Neuro-Orthopaedic Unit, Department of Orthopaedic Surgery and Traumatology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Department of Neurology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
J Intellect Disabil Res. 2024 Dec;68(12):1331-1343. doi: 10.1111/jir.13193. Epub 2024 Oct 21.
Rett syndrome (RTT), a developmental disorder primarily affecting girls and linked to methyl-CpG binding protein-2 (MECP2) gene mutations, presents musculoskeletal abnormalities with varying prevalence across studies and age groups. Our aim was to delineate the prevalence of orthopaedic conditions in individuals with RTT.
Three databases were searched and independently screened by two reviewers to retrieve observational studies published after 2000 that recruited 10 or more patients diagnosed with RTT and reported the prevalence of any orthopaedic conditions (scoliosis, hip displacement, knee problems or foot deformities). A random-effects meta-analysis was performed to determine the pooled prevalence based on study weight.
Of 867 screened studies, 21 studies involving 9997 girls with RTT (mean age 14.1 years; range, 3-38.5) met the inclusion criteria. The pooled prevalence of scoliosis was 64.5% [95% confidence interval (CI) 55.4-73.6%; I = 99%; P < 0.01], of hip displacement was 29.6% (95% CI 8.9-50.2%; I = 97%; P < 0.01) and of foot deformities was 53% (95% CI 17.5-89.2%; I = 98%; P < 0.01). Knee problems were reported in only one study. Scoliosis prevalence increased in studies with a high percentage of genetic testing and MECP2 positivity [69.1% (95% CI 58.9-79.2%; I = 99%; P < 0.01)], those with a mean age over 13 years [73% (95% CI 59.1-87%; I = 100%; P < 0.01)], and studies combining both variables [80.13% (95% CI 70.8-89.4%; I = 81%; P < 0.01)].
This meta-analysis found that approximately two in three girls with RTT develop scoliosis, one in two exhibit foot deformities and one in three experience hip displacement. These findings enhance our understanding of the prevalence of orthopaedic conditions in RTT, which can guide the establishment of surveillance protocols, clinical guidelines and management strategies tailored to the needs of RTT patients.
雷特综合征(RTT)是一种主要影响女孩的发育障碍疾病,与甲基-CpG 结合蛋白-2(MECP2)基因突变有关,其骨骼肌肉异常在不同研究和年龄组中具有不同的流行率。我们的目的是描述 RTT 患者的骨科疾病患病率。
检索了三个数据库,并由两名审查员独立筛选,以检索 2000 年后招募了 10 名或更多被诊断为 RTT 并报告任何骨科疾病(脊柱侧凸、髋关节移位、膝关节问题或足部畸形)患病率的观察性研究。基于研究权重进行随机效应荟萃分析以确定汇总患病率。
在 867 项筛选研究中,有 21 项研究纳入了 9997 名患有 RTT 的女孩(平均年龄 14.1 岁;范围,3-38.5 岁),符合纳入标准。脊柱侧凸的汇总患病率为 64.5%[95%置信区间(CI)55.4-73.6%;I=99%;P<0.01],髋关节移位的患病率为 29.6%(95%CI 8.9-50.2%;I=97%;P<0.01),足部畸形的患病率为 53%(95%CI 17.5-89.2%;I=98%;P<0.01)。只有一项研究报告了膝关节问题。在高基因检测百分比和 MECP2 阳性率[69.1%(95%CI 58.9-79.2%;I=99%;P<0.01)]、平均年龄超过 13 岁[73%(95%CI 59.1-87%;I=100%;P<0.01)]以及同时结合这两个变量的研究中[80.13%(95%CI 70.8-89.4%;I=81%;P<0.01)],脊柱侧凸的患病率更高。
这项荟萃分析发现,大约三分之二的 RTT 女孩会发展为脊柱侧凸,二分之一会出现足部畸形,三分之一会出现髋关节移位。这些发现提高了我们对 RTT 中骨科疾病患病率的认识,这有助于制定针对 RTT 患者需求的监测方案、临床指南和管理策略。