Cilia have multiple functions including olfaction. We hypothesised that olfactory function could be impaired in primary ciliary dyskinesia (PCD). Olfaction, nasal nitric oxide (nNO) and sinus CT were assessed in patients with PCD and non-PCD sinus disease, and healthy controls (no CT scan). PCD and non-PCD patients had similar severity of sinus disease. Despite this, defective olfaction was more common in patients with PCD (P<0.0001) and more severe in patients with PCD with major Transmission Electron Microscopy (TEM) abnormalities. Only in classical PCD did olfaction inversely correlate with sinusitis and nNO. We speculate that defective olfaction in PCD is primary in nature.
- nasal nitric oxide
- olfactory dysfunction
- primary ciliary dyskinesia
- sensory cilia
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Contributors MPif, AB and ALB designed the study, analysed all data and wrote the manuscript. MR, AT, MDC, MPir, AC and AM collected the experimental data and contributed to data evaluation. DC collected the radiological data and contributed to data evaluation. FM and GP performed statistical analyses and contributed to data evaluation. DP contributed to interpretation of data and helped to draft the manuscript for important intellectual content. All authors approved the version of the manuscript to be submitted. All authors take responsibility for the integrity of the data and the accuracy of the data analysis.
Funding This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent Obtained.
Ethics approval Hospital Ethical Committee of Pisa.
Provenance and peer review Not commissioned; externally peer reviewed.
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