Ma Yan-Li, Zhang Wei-Hua, Chen Guo-Hong, Song Li-Fang, Wang Yuan, Yuan Rui-Li, Wang Ying, Cheng Xiu-Yong
Department of Neonatology, The First Affiliated Hospital of Zheng Zhou University, Zhengzhou, China.
Department of Neurology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, China.
Front Pediatr. 2022 Aug 12;10:985878. doi: 10.3389/fped.2022.985878. eCollection 2022.
To explore the potential of walking alone milestone combined reading-frame rule to improve the early diagnosis of Duchenne muscular dystrophy (DMD).
To retrospectively describe the genotype and phenotype of Duchenne and Becker muscular dystrophies (BMD) patients with deletions and duplicates in the dystrophin gene. The sensitivity and specificity of the reading frame rule were calculated and compared to that of the combined reading frame rule and walking alone milestone. The diagnostic coincidence rate of two different methods was analyzed.
One hundred sixty-nine male DMD/BMD patients were enrolled, including 17 cases of BMD and 152 cases of DMD. The diagnostic coincidence rate, diagnostic sensitivity, and specificity of the reading-frame rule for DMD/BMD were 85.2, 86.8, and 70.59%, respectively. The sensitivity and specificity of the reading frame principle combined with the walking alone milestone for DMD/BMD were 96.05 and 70.59%, respectively. The diagnostic coincidence rate increased to 93.49%, significantly different from that predicted by reading- frame rule ( < 0.05).
The reading-frame rule combined with the walking alone milestone significantly improved the early diagnosis rate of DMD.
探讨单独行走里程碑联合读码框规则在改善杜氏肌营养不良症(DMD)早期诊断方面的潜力。
回顾性描述杜氏和贝克肌营养不良症(BMD)患者肌营养不良蛋白基因缺失和重复的基因型和表型。计算读码框规则的敏感性和特异性,并与联合读码框规则和单独行走里程碑的敏感性和特异性进行比较。分析两种不同方法的诊断符合率。
纳入169例男性DMD/BMD患者,其中BMD患者17例,DMD患者152例。DMD/BMD读码框规则的诊断符合率、诊断敏感性和特异性分别为85.2%、86.8%和70.59%。读码框原则联合单独行走里程碑对DMD/BMD的敏感性和特异性分别为96.05%和70.59%。诊断符合率提高到93.49%,与读码框规则预测的结果有显著差异(<0.05)。
读码框规则联合单独行走里程碑显著提高了DMD的早期诊断率。