Ma Xiaoran, McPherson Bradley, Ma Lian
Division of Speech and Hearing Sciences, University of Hong Kong , Hong Kong , China.
School of Stomatology, Peking University , Beijing , China.
PeerJ. 2016 Aug 25;4:e2383. doi: 10.7717/peerj.2383. eCollection 2016.
Cleft lip and/or palate is a common congenital craniofacial malformation found worldwide. A frequently associated disorder is conductive hearing loss, and this disorder has been thoroughly investigated in children with non-syndromic cleft lip and/or palate (NSCL/P). However, analysis of auditory processing function is rarely reported for this population, although this issue should not be ignored since abnormal auditory cortical structures have been found in populations with cleft disorders. The present study utilized electrophysiological tests to assess the auditory status of a large group of children with NSCL/P, and investigated whether this group had less robust central auditory processing abilities compared to craniofacially normal children.
146 children with NSCL/P who had normal peripheral hearing thresholds, and 60 craniofacially normal children aged from 6 to 15 years, were recruited. Electrophysiological tests, including auditory brainstem response (ABR), P1-N1-P2 complex, and P300 component recording, were conducted.
ABR and N1 wave latencies were significantly prolonged in children with NSCL/P. An atypical developmental trend was found for long latency potentials in children with cleft compared to control group children. Children with unilateral cleft lip and palate showed a greater level of abnormal results compared with other cleft subgroups, whereas the cleft lip subgroup had the most robust responses for all tests.
Children with NSCL/P may have slower than normal neural transmission times between the peripheral auditory nerve and brainstem. Possible delayed development of myelination and synaptogenesis may also influence auditory processing function in this population. Present research outcomes were consistent with previous, smaller sample size, electrophysiological studies on infants and children with cleft lip/palate disorders. In view of the these findings, and reports of educational disadvantage associated with cleft disorders, further research that focuses on the auditory processing abilities of children with cleft lip/palate disorder is warranted.
唇腭裂是一种在全球范围内常见的先天性颅面畸形。一种常见的相关病症是传导性听力损失,并且这种病症已经在非综合征性唇腭裂(NSCL/P)患儿中得到了充分研究。然而,尽管在患有腭裂病症的人群中已发现听觉皮层结构异常,但针对该人群听觉处理功能的分析却鲜有报道。本研究采用电生理测试来评估一大组NSCL/P患儿的听觉状况,并调查该组患儿与颅面部正常儿童相比,其中枢听觉处理能力是否较弱。
招募了146名外周听力阈值正常的NSCL/P患儿以及60名年龄在6至15岁之间的颅面部正常儿童。进行了包括听觉脑干反应(ABR)、P1-N1-P2复合波和P300成分记录在内的电生理测试。
NSCL/P患儿的ABR和N1波潜伏期显著延长。与对照组儿童相比,腭裂患儿的长潜伏期电位呈现出非典型的发育趋势。单侧唇腭裂患儿的异常结果水平高于其他腭裂亚组,而唇裂亚组在所有测试中的反应最为强烈。
NSCL/P患儿的外周听觉神经与脑干之间的神经传导时间可能比正常情况慢。髓鞘形成和突触发生可能的延迟发育也可能影响该人群的听觉处理功能。目前的研究结果与之前针对唇腭裂患儿的样本量较小的电生理研究一致。鉴于这些发现以及与腭裂病症相关的教育劣势报告,有必要进一步开展专注于唇腭裂患儿听觉处理能力的研究。