Ciliary Beat Frequency and Pattern: An Accessible Tool for the Screening of Primary Ciliary Dyskinesia
<b>Background/Objectives</b>: Primary ciliary dyskinesia (PCD) is a rare inherited disorder caused by dysfunction of motile cilia, leading to chronic respiratory disease. Diagnosis is challenging due to heterogeneous and non-specific clinical manifestations and the absence of a single definitive diagnostic test. Current diagnostic strategies rely on a combination of functional, ultrastructural, and genetic analyses. The objective of this study was to evaluate whether ciliary beat frequency (CBF), combined with ciliary beat pattern (CBP) assessment using digital high-speed video microscopy (DHSV), could serve as an effective first-line screening tool to identify patients requiring further diagnostic investigations. <b>Methods</b>: This single-center retrospective study included 65 patients (52 children and 13 adults) with clinical suspicion of PCD. Ciliary beat analysis was performed on nasal or bronchial samples using DHSV and Sisson-Ammons Video Analysis software. CBF and CBP were assessed and compared between patients with confirmed PCD and those in whom PCD was excluded based on transmission electron microscopy (TEM) and/or molecular genetic analysis. <b>Results</b>: Fifteen patients were diagnosed with PCD. Mean CBF was significantly lower in the PCD group compared with the non-PCD group (3.3 Hz vs. 8.1 Hz; <i>p</i> < 0.001). A CBF cut-off value of 5.25 Hz yielded a sensitivity of 78.6% and a specificity of 95.7%. Three patients with PCD had CBF values above this threshold; however, two of them exhibited abnormal CBP. Sample type, patient age, and the presence of airway pathogens did not significantly influence CBF measurements. <b>Conclusions</b>: CBF and CBP analysis using DHSV represents a useful first-line screening tool within a multifaceted diagnostic approach for PCD, allowing rapid identification of patients who should undergo further confirmatory testing.
Authors
- Julie Mazenq (ORCID: https://orcid.org/0000-0002-8257-7107)
- Karine Baumstarck (ORCID: https://orcid.org/0000-0003-3602-6766)
- M. Boucekine
- Nadine Dufeu
- A. Pagin (ORCID: https://orcid.org/0000-0001-5350-9263)
- Patrice Roll (ORCID: https://orcid.org/0000-0002-0045-5641)
- J Dubus
- Diane Frankel (ORCID: https://orcid.org/0000-0003-3321-6951)
- Élise Kaspi (ORCID: https://orcid.org/0000-0003-0458-5109)
- Rana Mitri-Frangieh
- Justin Michel (ORCID: https://orcid.org/0000-0002-5275-909X)
- T. Radulesco
Institutions
- Centre National de la Recherche Scientifique (FR)
- Ceres (US)
- Inserm (FR)
- Aix-Marseille Université (FR)
- Centre Hospitalier Universitaire de Lille (FR)
- Assistance Publique Hôpitaux de Marseille (FR)
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
- Hôpital de la Conception (FR)
- Hôpital Nord (FR)
- Hôpital Intercommunal de Créteil (FR)
Publication Details
- Journal
- Diagnostics
- Published
- 2026-02-27
- DOI
- https://doi.org/10.3390/diagnostics16050704
- Primary Topic
- Cystic Fibrosis Research Advances
- Type
- article
- Field-Weighted Citation Impact
- 0.00