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. 1997 Oct-Dec;32(4):309–314.

Effects of Viral Upper Respiratory Illness on Running Gait

Thomas G Weidner 1,2, Gale Gehlsen 1,2, Gregory B Dwyer 1,2, Terry Schurr 1,2
PMCID: PMC1320346  PMID: 16558464

Abstract

Objective:

To determine the kinematic changes that may occur during running with a cold of known etiology and to assess the impact of select accompanying upper respiratory illness symptoms.

Design and Setting:

In this nonrandomized study, subjects with colds and subjects without colds were videotaped while exercising on a treadmill. Three weeks later, the trials were repeated.

Subjects:

Eighteen young adults (5 females, 13 males; mean age = 20.4± 2.4 yr) with naturally acquired moderate to severe (total symptom score) colds were screened and selected for inclusion in the illness group (ILL). A control group (CRL) of 20 subjects (2 females, 18 males) was also examined. Virologic confirmation of specific viral infections, unprecedented in this line of research, revealed that 12 of the 18 subjects in the ILL group (67%) were infected with human rhinoviruses. None of the subjects had a fever.

Measurements:

All subjects exercised on a treadmill for 5 minutes at a heart rate of approximately 85% of their age-predicted maximum. Both groups were videotaped kinematically during two running trials 3 weeks apart. All subjects in the ILL group displayed upper respiratory illness symptoms for the first running trial and were asymptomatic by the second.

Results:

We identified significant differences in mean changes between the ILL and CRL group stride lengths (p <.01), stride frequencies (p <.05), and ankle maximum angle displacement (p <.01). Mean changes in stride length (p <.03) and in stride frequency (p <.04) were larger for ILL subjects who felt feverish.

Conclusions:

Alterations in running gait during a rhinovirus-caused upper respiratory illness, and possibly increases in injury incidence, may be associated with feeling feverish. Gait alterations may increase injury incidence or decrease athletic performance, or both.

Keywords: kinematics, stride length, stride frequency, human rhinovirus

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ardawi M. S., Newsholme E. A. Metabolism in lymphocytes and its importance in the immune response. Essays Biochem. 1985;21:1–44. [PubMed] [Google Scholar]
  2. Aström E., Friman G., Pilström L. Effects of viral and mycoplasma infections on ultrastructure and enzyme activities in human skeletal muscle. Acta Pathol Microbiol Scand A. 1976 Mar;84(2):113–122. doi: 10.1111/j.1699-0463.1976.tb00080.x. [DOI] [PubMed] [Google Scholar]
  3. Blair H. T., Greenberg S. B., Stevens P. M., Bilunos P. A., Couch R. B. Effects of rhinovirus infection of pulmonary function of healthy human volunteers. Am Rev Respir Dis. 1976 Jul;114(1):95–102. doi: 10.1164/arrd.1976.114.1.95. [DOI] [PubMed] [Google Scholar]
  4. Dick E. C., Blumer C. R., Evans A. S. Epidemiology of infections with rhinovirus types 43 and 55 in a group of university of Wisconsin student families. Am J Epidemiol. 1967 Sep;86(2):386–400. doi: 10.1093/oxfordjournals.aje.a120749. [DOI] [PubMed] [Google Scholar]
  5. Fitzgerald L. Exercise and the immune system. Immunol Today. 1988 Nov;9(11):337–339. doi: 10.1016/0167-5699(88)91332-1. [DOI] [PubMed] [Google Scholar]
  6. Hamparian V. V., Colonno R. J., Cooney M. K., Dick E. C., Gwaltney J. M., Jr, Hughes J. H., Jordan W. S., Jr, Kapikian A. Z., Mogabgab W. J., Monto A. A collaborative report: rhinoviruses--extension of the numbering system from 89 to 100. Virology. 1987 Jul;159(1):191–192. doi: 10.1016/0042-6822(87)90367-9. [DOI] [PubMed] [Google Scholar]
  7. Hanley D. F. Medical care of the US Olympic Team. JAMA. 1976 Jul 12;236(2):147–148. [PubMed] [Google Scholar]
  8. Larson H. E., Reed S. E., Tyrrell D. A. Isolation of rhinoviruses and coronaviruses from 38 colds in adults. J Med Virol. 1980;5(3):221–229. doi: 10.1002/jmv.1890050306. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Little J. W., Hall W. J., Douglas R. G., Jr, Hyde R. W., Speers D. M. Amantadine effect on peripheral airways abnormalities in influenza. A study in 15 students with natural influenza A infection. Ann Intern Med. 1976 Aug;85(2):177–182. doi: 10.7326/0003-4819-85-2-177. [DOI] [PubMed] [Google Scholar]
  10. Meschievitz C. K., Schultz S. B., Dick E. C. A model for obtaining predictable natural transmission of rhinoviruses in human volunteers. J Infect Dis. 1984 Aug;150(2):195–201. doi: 10.1093/infdis/150.2.195. [DOI] [PubMed] [Google Scholar]
  11. Minor T. E., Baker J. W., Dick E. C., DeMeo A. N., Ouellette J. J., Cohen M., Reed C. E. Greater frequency of viral respiratory infections in asthmatic children as compared with their nonasthmatic siblings. J Pediatr. 1974 Oct;85(4):472–477. doi: 10.1016/S0022-3476(74)80447-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Minor T. E., Dick E. C., DeMeo A. N., Ouellette J. J., Cohen M., Reed C. E. Viruses as precipitants of asthmatic attacks in children. JAMA. 1974 Jan 21;227(3):292–298. [PubMed] [Google Scholar]
  13. O'Connor S. A., Jones D. P., Collins J. V., Heath R. B., Campbell M. J., Leighton M. H. Changes in pulmonary function after naturally acquired respiratory infection in normal persons. Am Rev Respir Dis. 1979 Nov;120(5):1087–1093. doi: 10.1164/arrd.1979.120.5.1087. [DOI] [PubMed] [Google Scholar]
  14. Roberts J. A. Viral illnesses and sports performance. Sports Med. 1986 Jul-Aug;3(4):298–303. doi: 10.2165/00007256-198603040-00006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Weidner T. G. Reporting behaviors and activity levels of intercollegiate athletes with an URI. Med Sci Sports Exerc. 1994 Jan;26(1):22–26. [PubMed] [Google Scholar]

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