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通过细胞培养方法评估原发性纤毛运动障碍患者的纤毛功能和纤毛拍频。

Evaluation of ciliary functions and ciliary beat frequency via cell culture method in patients with primary ciliary dyskinesia.

机构信息

Departments of 1Pediatric Pulmonology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Department of Histology and Embryology, Bezmi Alem University Faculty of Medicine İstanbul, Turkey.

出版信息

Turk J Pediatr. 2022;64(4):612-618. doi: 10.24953/turkjped.2020.3361.

Abstract

BACKGROUND

Cell culture increases both diagnostic specificity and sensitivity of primary ciliary dyskinesia (PCD) and the most important reason to use cell culture for definitive diagnosis in PCD is to exclude secondary ciliary defects. Here we aimed to evaluate the cilia functions and cilia ultrastructural abnormalities after ciliogenesis of cell culture in patients with definitive diagnosis of PCD. We also aimed to compare high speed videomicroscopy (HSVM) results of patients before and after ciliogenesis and to compare them with electron microscopy, genetic and immunofluorescence results in patients with positive diagnosis of PCD.

METHODS

This study was conducted as a cross-sectional study in patients with PCD. HSVM, transmission electron microscopy (TEM) and immunofluorescence staining results of the nasal biopsy samples taken from patients with the definitive diagnosis of PCD were evaluated and HSVM findings before and after cell culture were described.

RESULTS

Ciliogenesis and regrowth in the cell culture occurred in the nasal biopsy sample of eight patients with PCD. The mean age of the patients was 15.5±4.2 years (8.5-18 years). Mean beat frequency was found to be 7.54±1.01 hz (6.53-9.45 hz) before cell culture, and 7.36±0.86 hz (6.02-7.99 hz) after cell culture in the nasal biopsy of patients. There was no significant difference in the beat frequency of PCD patients before and after cell culture. Ciliary function analysis showed the similar beating pattern before and after cell culture in patients with PCD.

CONCLUSIONS

This study showed us that there was no difference between cilia beat frequency and beat pattern before and after cell culture in patients with definitive diagnosis of PCD and repeated HSVM would be a useful diagnostic approach in patients who have no possibility to reach other diagnostic methods.

摘要

背景

细胞培养提高了原发性纤毛运动障碍(PCD)的诊断特异性和敏感性,将细胞培养用于 PCD 明确诊断的最重要原因是排除继发性纤毛缺陷。在这里,我们旨在评估经细胞培养后纤毛发生的患者的纤毛功能和超微结构异常。我们还旨在比较患者纤毛发生前后高速视频显微镜(HSVM)的结果,并将其与电子显微镜、遗传和免疫荧光结果进行比较,以明确诊断为 PCD 的患者。

方法

本研究是在 PCD 患者中进行的一项横断面研究。评估了经明确诊断为 PCD 的患者鼻活检样本的 HSVM、透射电子显微镜(TEM)和免疫荧光染色结果,并描述了细胞培养前后的 HSVM 发现。

结果

纤毛发生和细胞培养后在 8 例 PCD 患者的鼻活检样本中发生。患者的平均年龄为 15.5±4.2 岁(8.5-18 岁)。在细胞培养前,患者鼻活检的平均拍频为 7.54±1.01 hz(6.53-9.45 hz),细胞培养后为 7.36±0.86 hz(6.02-7.99 hz)。细胞培养前后 PCD 患者的拍频无显著差异。纤毛功能分析显示 PCD 患者细胞培养前后的拍打模式相似。

结论

本研究表明,明确诊断为 PCD 的患者细胞培养前后纤毛拍频和拍打模式无差异,重复 HSVM 是一种有用的诊断方法,适用于无法采用其他诊断方法的患者。

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