Bricmont Noemie, Bonhiver Romane, Benchimol Lionel, Louis Bruno, Papon Jean-François, Monseur Justine, Donneau Anne-Françoise, Moermans Catherine, Schleich Florence, Calmès Doriane, Poirrier Anne-Lise, Louis Renaud, Seghaye Marie-Christine, Kempeneers Céline
Pneumology Laboratory, I3 Group, GIGA Research Center, University of Liège, 4000 Liège, Belgium.
Division of Respirology, Department of Pediatrics, University Hospital Liège, 4000 Liège, Belgium.
Diagnostics (Basel). 2023 Sep 18;13(18):2974. doi: 10.3390/diagnostics13182974.
Primary ciliary dyskinesia is a heterogeneous, inherited motile ciliopathy in which respiratory cilia beat abnormally, and some ultrastructural ciliary defects and specific genetic mutations have been associated with particular ciliary beating alterations. Ciliary beating can be evaluated using digital high-speed videomicroscopy (DHSV). However, normal reference values, essential to assess ciliary beating in patients referred for a PCD diagnostic, vary between centres, as minor variations in protocols might influence ciliary beating. Consequently, establishment of normal values is essential for each PCD diagnostic centre. We aimed to evaluate whether delay after sampling, and temperature for conservation of respiratory ciliated samples, might modify assessments of ciliary beating. In total, 37 healthy nasal brushing samples of respiratory ciliated epithelia were collected. Video sequences were recorded at 37 °C immediately using DHSV. Then, the samples were divided and conserved at 4 °C or at room temperature (RT). Ciliated beating edges were then recorded at 37 °C, at 3 h and at 9 h post sampling. In six samples, recordings were continued up to 72 h after sampling. Ciliary beating was assessed manually by ciliary beat frequency (CBF) and ciliary beat pattern (CBP). A semi-automatic software was used for quantitative analysis. Both CBF and CBP evaluated manually and by a semi-automated method were stable 9 h after sampling. CBF was higher when evaluated using samples stored at RT than at 4 °C. CBP and the semi-automated evaluation of ciliary beating were not affected by storage temperature. When establishing normal references values, ciliary beating can be evaluated at 37 °C up to 9 h after nasal brushing, but the storage temperature modifies ciliary beating and needs to be controlled.
原发性纤毛运动障碍是一种异质性遗传性运动性纤毛病,其中呼吸道纤毛跳动异常,一些超微结构的纤毛缺陷和特定基因突变与特定的纤毛跳动改变有关。纤毛跳动可使用数字高速视频显微镜(DHSV)进行评估。然而,对于进行原发性纤毛运动障碍(PCD)诊断的患者,评估纤毛跳动所必需的正常参考值在不同中心之间存在差异,因为检测方案的微小差异可能会影响纤毛跳动。因此,为每个PCD诊断中心建立正常值至关重要。我们旨在评估采样后的延迟时间以及呼吸道纤毛样本的保存温度是否会改变对纤毛跳动的评估。总共收集了37份健康的呼吸道纤毛上皮鼻刷样本。使用DHSV立即在37°C下记录视频序列。然后,将样本分开并保存在4°C或室温(RT)下。然后在采样后3小时和9小时在37°C下记录纤毛跳动边缘。在6个样本中,记录持续到采样后72小时。通过纤毛跳动频率(CBF)和纤毛跳动模式(CBP)手动评估纤毛跳动。使用半自动软件进行定量分析。手动评估和半自动方法评估的CBF和CBP在采样后9小时均稳定。使用保存在室温下的样本评估时,CBF高于保存在4°C下的样本。CBP和纤毛跳动的半自动评估不受储存温度的影响。在建立正常参考值时,可在鼻刷后9小时内于37°C评估纤毛跳动,但储存温度会改变纤毛跳动情况且需要加以控制。