Impact of Aerobic Exercise on Oxygenation, Pulmonary Function, and Nasal Nitric Oxide in Primary Ciliary Dyskinesia
- PMID: 40322499
- PMCID: PMC12046229
- DOI: 10.2174/0118743064365386250212050147
Impact of Aerobic Exercise on Oxygenation, Pulmonary Function, and Nasal Nitric Oxide in Primary Ciliary Dyskinesia
Abstract
Background: Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder characterized by impaired mucociliary clearance, resulting in chronic respiratory complications. While exercise benefits respiratory health, its impacts on PCD remain understudied.
Objective: The objective of this study was to assess how moderate aerobic exercise influences FEV1, SpO2, and nNO levels in PCD patients, with a focus on short-term post-exercise changes.
Methods: This is a matched case-control pilot study involving 12 PCD patients homozygous for the RSPH4A (c.921+3_921+6del) mutation and 12 healthy controls (HC). Baseline FEV1, SpO2, and nNO levels were measured before participants underwent a six-minute exercise challenge test (ECT) on a stationary bicycle. Post-exercise measurements included FEV1 at 5, 10, 15, and 20 minutes, nNO after final spirometry, and SpO2 at 5 minutes.
Results: The PCD group experienced a significant increase in SpO2 from 95.5% ± 2.1 to 97.7% ± 1.5 post-exercise (p < 0.05), while the HC group had stable SpO2 levels with a minor increase from 97.9% ± 1.5 to 98.9% ± 1.4 (p = 0.14). No significant changes in FEV1 or nNO levels were observed post-exercise in either group. One HC participant exhibited exercise-induced bronchoconstriction.
Conclusion: Aerobic exercise improves oxygenation in PCD patients without adverse effects on pulmonary function or nNO levels. Further research is necessary due to the small sample size and genetic homogeneity to confirm these findings and evaluate long-term outcomes. Moreover, this pilot study highlights the safety and potential respiratory benefits of aerobic exercise in PCD patients, supporting further investigation into its role in clinical management.
Keywords: Exercise; Nitric Oxide; Oxygen Saturation; Primary Ciliary Dyskinesia; Quality of Life; RSPH4A; Respiratory Physiology.
© 2025 The Author(s). Published by Bentham Open.
Conflict of interest statement
The authors declare no conflict of interest, financial or otherwise.
Figures
Similar articles
-
Nasal Nitric Oxide Levels: Improving the Diagnosis of Primary Ciliary Dyskinesia in Puerto Rico.Adv Respir Med. 2022 Sep 26;90(5):399-406. doi: 10.3390/arm90050050. Adv Respir Med. 2022. PMID: 36285978 Free PMC article.
-
Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar Diseases.J Clin Immunol. 2019 Feb;39(2):216-224. doi: 10.1007/s10875-019-00613-8. Epub 2019 Mar 26. J Clin Immunol. 2019. PMID: 30911954 Free PMC article.
-
Nasal nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and healthy children.Turk J Pediatr. 2019;61(1):20-25. doi: 10.24953/turkjped.2019.01.004. Turk J Pediatr. 2019. PMID: 31559717 Clinical Trial.
-
Role of Nasal Nitric Oxide in Primary Ciliary Dyskinesia and Other Respiratory Conditions in Children.Int J Mol Sci. 2023 Nov 10;24(22):16159. doi: 10.3390/ijms242216159. Int J Mol Sci. 2023. PMID: 38003348 Free PMC article. Review.
-
Progress in Diagnosing Primary Ciliary Dyskinesia: The North American Perspective.Diagnostics (Basel). 2021 Jul 16;11(7):1278. doi: 10.3390/diagnostics11071278. Diagnostics (Basel). 2021. PMID: 34359360 Free PMC article. Review.
References
-
- Hannah W.B., Seifert B.A., Truty R., Zariwala M.A., Ameel K., Zhao Y., Nykamp K., Gaston B. The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: A genetic database analysis. Lancet Respir. Med. 2022;10(5):459–468. doi: 10.1016/S2213-2600(21)00453-7. - DOI - PMC - PubMed
-
- Daniels M.L.A., Leigh M.W., Davis S.D., Armstrong M.C., Carson J.L., Hazucha M., Dell S.D., Eriksson M., Collins F.S., Knowles M.R., Zariwala M.A. Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia. Hum. Mutat. 2013;34(10):1352–1356. doi: 10.1002/humu.22371. - DOI - PMC - PubMed
LinkOut - more resources
Full Text Sources