Rhinology Unit, General and University Hospital, Medical School, Valencia University, Valencia, Spain.
Am J Rhinol Allergy. 2010 May-Jun;24(3):175-80. doi: 10.2500/ajra.2010.24.3448.
Primary ciliary dyskinesia (PCD) is a clinically uniform entity, although cilia motility and structure can vary among patients, making diagnosis difficult. Chronic sinusitis, bronchiectasis, sinus hypoplasia, secretory otitis media, and low fertility are common in PCD patients. The aim of this work was to correlate nasal ciliary activity with clinical and structural abnormalities in PCD. A secondary aim was to evaluate the usefulness of high-resolution digital high-speed video (DHSV) in the diagnosis of PCD.
We analyzed nasal mucociliary transport and cilia ultrastructure by electron microscopy and studied nasal ciliary beat frequency (CBF) and beat pattern using high-resolution DHSV imaging in 34 healthy volunteers, 25 individuals with PCD (including 11 with Kartagener's syndrome [KS]with situs inversus), and 27 with secondary ciliary dyskinesia (SCD).
Nasal mucociliary transport was defective in the PCD and SCD patients. Ciliary immotility was observed in only six KS patients and was correlated with the absence of dynein. We observed a correlation between partial dynein deficiency and an uncoordinated, stiffly vibrating ciliary beat. Cilia activity and structure were normal in the SCD patients.
Nasal mucociliary transport showed a sensitivity of 100% for the diagnosis of PCD but has low specificity. High-resolution DHSV imaging has high sensitivity and specificity for the diagnosis of PCD. Video analysis is probably more useful than the study of mucociliary transport and cilia ultrastructure in screening for PCD. The absence of dynein was correlated with ciliary immotility and was more common in KS patients.
原发性纤毛运动障碍(PCD)是一种临床表现一致的疾病,尽管患者的纤毛运动和结构可能存在差异,导致诊断困难。慢性鼻窦炎、支气管扩张、鼻窦发育不全、分泌性中耳炎和生育力低下是 PCD 患者的常见表现。本研究旨在探讨鼻纤毛活动与 PCD 患者的临床和结构异常的相关性,评估高分辨率数字高速视频(DHSV)在 PCD 诊断中的作用。
我们分析了 34 名健康志愿者、25 名 PCD 患者(包括 11 名伴有 Kartagener 综合征的患者)和 27 名继发性纤毛运动障碍(SCD)患者的鼻黏膜纤毛传输功能和超微结构,通过高分辨率 DHSV 成像测量鼻纤毛摆动频率(CBF)和摆动模式。
PCD 和 SCD 患者的鼻黏膜纤毛传输功能均存在缺陷。仅在 6 名 Kartagener 综合征患者中观察到纤毛不动,且与动力蛋白缺失相关。我们发现部分动力蛋白缺乏与纤毛不协调、僵硬振动的摆动模式相关。SCD 患者的纤毛活动和结构正常。
鼻黏膜纤毛传输对 PCD 的诊断具有 100%的敏感性,但特异性较低。高分辨率 DHSV 成像对 PCD 的诊断具有较高的敏感性和特异性。视频分析可能比黏膜纤毛传输和纤毛超微结构研究更有助于 PCD 的筛查。动力蛋白缺失与纤毛不动相关,且在 Kartagener 综合征患者中更为常见。