Zeng Yin-Ting, Hwu Wuh-Liang, Torng Pao-Chuan, Lee Ni-Chung, Shieh Jeng-Yi, Lu Lu, Chien Yin-Hsiu
Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Physical Medicine and Rehabilitation, National Taiwan University Hospital, Taipei, Taiwan.
Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Eur J Paediatr Neurol. 2017 May;21(3):485-493. doi: 10.1016/j.ejpn.2016.12.004. Epub 2016 Dec 19.
Patients with infantile-onset Pompe disease (IOPD) can be treated by recombinant human acid alpha glucosidase (rhGAA) replacement beginning at birth with excellent survival rates, but they still commonly present with speech disorders. This study investigated the progress of speech disorders in these early-treated patients and ascertained the relationship with treatments.
Speech disorders, including hypernasal resonance, articulation disorders, and speech intelligibility, were scored by speech-language pathologists using auditory perception in seven early-treated patients over a period of 6 years. Statistical analysis of the first and last evaluations of the patients was performed with the Wilcoxon signed-rank test.
A total of 29 speech samples were analyzed. All the patients suffered from hypernasality, articulation disorder, and impairment in speech intelligibility at the age of 3 years. The conditions were stable, and 2 patients developed normal or near normal speech during follow-up. Speech therapy and a high dose of rhGAA appeared to improve articulation in 6 of the 7 patients (86%, p = 0.028) by decreasing the omission of consonants, which consequently increased speech intelligibility (p = 0.041). Severity of hypernasality greatly reduced only in 2 patients (29%, p = 0.131).
Speech disorders were common even in early and successfully treated patients with IOPD; however, aggressive speech therapy and high-dose rhGAA could improve their speech disorders.
婴儿型庞贝病(IOPD)患者可从出生起接受重组人酸性α-葡萄糖苷酶(rhGAA)替代治疗,生存率良好,但仍普遍存在言语障碍。本研究调查了这些早期治疗患者言语障碍的进展情况,并确定其与治疗的关系。
言语语言病理学家通过听觉感知,对7例早期治疗患者在6年时间内的言语障碍进行评分,包括鼻音过重、发音障碍和言语清晰度。对患者的首次和末次评估进行Wilcoxon符号秩检验统计分析。
共分析了29个言语样本。所有患者在3岁时均存在鼻音过重、发音障碍和言语清晰度受损的情况。病情稳定,随访期间有2例患者言语发展正常或接近正常。言语治疗和高剂量rhGAA似乎使7例患者中的6例(86%,p = 0.028)发音得到改善,减少了辅音遗漏,从而提高了言语清晰度(p = 0.041)。仅2例患者(29%,p = 0.131)鼻音过重的严重程度大幅降低。
即使在早期成功治疗的IOPD患者中,言语障碍也很常见;然而,积极的言语治疗和高剂量rhGAA可改善其言语障碍。