Chilvers Mark A, Rutman Andrew, O'Callaghan Christopher
Department of Child Health, University of Leicester School of Medicine, Robert Kilpatrick Clinical Sciences Building, Leicester Royal Infirmary, Leicester LE2 7LX, United Kingdom.
J Allergy Clin Immunol. 2003 Sep;112(3):518-24. doi: 10.1016/s0091-6749(03)01799-8.
The main symptoms of primary ciliary dyskinesia (PCD) are nasal rhinorrhea or blockage and moist-sounding cough. Diagnosis can be difficult and is based on an abnormal ciliary beat frequency, accompanied by specific abnormalities of the ciliary axoneme. It is unknown whether determining ciliary beat pattern related to specific ultrastructural ciliary defects might help in the diagnosis of PCD.
We sought to determine ciliary beat pattern and beat frequency (CBF) associated with the 5 common ultrastructural defects responsible for PCD.
Nasal brushings were performed on 56 children with PCD. Ciliary movement was recorded using digital high-speed video imaging to assess beat frequency and pattern. Electron microscopy was performed.
In patients with an isolated outer dynein arm or with an outer and inner dynein arm defect, 55% and 80% of cilia were immotile, respectively. Cilia that moved were only flickering. Mean CBF (+/- 95% CI) was 2.3 Hz (+/- 1.2) and 0.8 Hz(+/- 0.8), respectively. Cilia with an isolated inner dynein arm or a radial spoke defect had similar beat patterns. Cilia appeared stiff, had a reduced amplitude, and failed to bend along their length. Immotile cilia were present in 10% of cilia with an inner dynein arm defect and in 30% of radial spoke defects. Mean CBF was 9.3 Hz (+/- 2.6) and 6.0 Hz (+/- 3.1), respectively. The ciliary transposition defect produced a large circular beat pattern (mean CBF, 10.7 Hz [+/- 1.1]). No cilia were immotile.
Different ultrastructural defects responsible for PCD result in predictable beat patterns. Recognition of these might help in the diagnostic evaluation of patients suspected of having PCD.
原发性纤毛运动障碍(PCD)的主要症状是鼻溢液或鼻塞以及湿性咳嗽。诊断可能较为困难,其依据是纤毛摆动频率异常,并伴有纤毛轴丝的特定异常。目前尚不清楚确定与特定超微结构纤毛缺陷相关的纤毛摆动模式是否有助于PCD的诊断。
我们试图确定与导致PCD的5种常见超微结构缺陷相关的纤毛摆动模式和摆动频率(CBF)。
对56例PCD患儿进行鼻拭子检查。使用数字高速视频成像记录纤毛运动,以评估摆动频率和模式。进行电子显微镜检查。
在孤立性外动力蛋白臂缺陷或外动力蛋白臂与内动力蛋白臂均有缺陷的患者中,分别有55%和80%的纤毛无运动能力。有运动能力的纤毛仅呈闪烁状。平均CBF(±95%CI)分别为2.3Hz(±1.2)和0.8Hz(±0.8)。孤立性内动力蛋白臂缺陷或辐条缺陷的纤毛具有相似的摆动模式。纤毛显得僵硬,振幅减小,且无法沿其长度弯曲。在10%的内动力蛋白臂缺陷纤毛和30%的辐条缺陷纤毛中存在无运动能力的纤毛。平均CBF分别为9.3Hz(±2.6)和6.0Hz(±3.1)。纤毛转位缺陷产生大的圆形摆动模式(平均CBF,10.7Hz[±1.1])。无纤毛无运动能力。
导致PCD的不同超微结构缺陷会产生可预测的摆动模式。识别这些模式可能有助于对疑似PCD患者进行诊断评估。