Abstracts
OBJECTIVE: To describe the mechanisms of Exercise-Induced Asthma (EIA) as well as the effect of different kinds of physical training on pulmonary function, anaerobic fitness, and aerobic fitness. We highlighted the importance of a correct diagnostic through exercise testing and, concerning treatment, the utilization of drugs such as beta-adrenergics and anticholinergics. DATA SOURCE: The articles were chosen using the PubMed and Scielo databases, considering the year of publication and giving preference to clinical randomized trials with well-defined inclusion criteria. SUMMARY OF THE FINDINGS: The medication used and the frequent symptoms during and after exercise appear as a limiting factor to the practice of exercises among subjects with EIA. This may result in a sedentary lifestyle. CONCLUSION: Subjects with EIA should be allowed to do exercise if well prescribed.
Asthma; Exercise; Prevention
OBJETIVO: Descrever os mecanismos da asma induzida pelo exercício (AIE), bem como os efeitos de diferentes tipos de treinamento físico na função pulmonar e nas capacidades aeróbia e anaeróbia. Destaca-se a importância de um diagnóstico correto mediante o teste de exercício e, no manejo, o uso de drogas beta-adrenérgicas e anticolinérgicas. FONTE DOS DADOS: Os artigos foram criteriosamente escolhidos utilizando as bases de dados PubMed e Scielo pelo ano de publicação e dando preferência a ensaios clínicos randomizados, com critérios de seleção da amostra bem definidos. SÍNTESE DOS DADOS: Os mecanismos para explicar a AIE permanecem sem conclusão, mas parece haver uma interação fisiológica entre as hipóteses aqui apresentadas. O uso de medicamentos e as freqüentes crises durante o exercício aparecem como fatores limitantes para a prática de exercícios físicos, conduzindo para um estilo de vida sedentário. CONCLUSÃO: Deve-se incentivar a prática de exercícios devidamente prescritos e minimizar as restrições aos sujeitos com AIE.
Asma; Exercício; Prevenção
OBJETIVO: Describir los mecanismos del asma inducido por el ejercicio (AIE), así como los efectos de diferentes tipos de entrenamiento físico sobre la función pulmonar y las capacidades aeróbica y anaeróbica. Se destaca la importancia de un diagnóstico correcto mediante el test de ejercicio y el manejo o uso de drogas beta-adrenérgicas y anticolinérgicas. FUENTES: Los artículos fueron cuidadosamente escogidos utilizando las bases de dados de PubMed y Scielo por el año de publicación, dando preferencia a ensayos clínicos randomizados, con criterios de selección de muestra bien definidos. SÍNTESES DE DATOS: Los mecanismos para explicar la AIE permanecen sin conclusión, pero parece haber una interacción fisiológica entre las hipótesis aquí presentadas. El uso de medicamentos y las frecuentes crisis durante el ejercicio aparecen como factores limitantes para la práctica de ejercicios físicos, conduciendo esto a un estilo de vida sedentario. CONCLUSIÓN: Se debe incentivar la práctica de ejercicios debidamente prescritos y minimizar las restricciones a los individuos con AIE.
Asma; Ejercicio; Prevención
REVIEW ARTICLE
Exercise-induced asthma: current aspects and recommendations*
Asma inducido por el ejercicio: aspectos actuales y recomendaciones
Orlando LaitanoI; Flávia MeyerII
IMestrando em Ciências do Movimento Humano ESEF/UFRGS, Brasil lionello@terra.com.br
IIDoutora em Farmacologia e Fisiologia do Exercício Pediátrico McMaster University, Canadá flaviameyer@uol.com.br
ABSTRACT
OBJECTIVE: To describe the mechanisms of Exercise-Induced Asthma (EIA) as well as the effect of different kinds of physical training on pulmonary function, anaerobic fitness, and aerobic fitness. We highlighted the importance of a correct diagnostic through exercise testing and, concerning treatment, the utilization of drugs such as beta-adrenergics and anticholinergics.
DATA SOURCE: The articles were chosen using the PubMed and Scielo databases, considering the year of publication and giving preference to clinical randomized trials with well-defined inclusion criteria.
SUMMARY OF THE FINGINGS: The medication used and the frequent symptoms during and after exercise appear as a limiting factor to the practice of exercises among subjects with EIA. This may result in a sedentary lifestyle.
CONCLUSION: Subjects with EIA should be allowed to do exercise if well prescribed.
Keywords: Asthma. Exercise. Prevention.
RESUMEN
OBJETIVO: Describir los mecanismos del asma inducido por el ejercicio (AIE), así como los efectos de diferentes tipos de entrenamiento físico sobre la función pulmonar y las capacidades aeróbica y anaeróbica. Se destaca la importancia de un diagnóstico correcto mediante el test de ejercicio y el manejo o uso de drogas beta-adrenérgicas y anticolinérgicas.
FUENTES: Los artículos fueron cuidadosamente escogidos utilizando las bases de dados de PubMed y Scielo por el año de publicación, dando preferencia a ensayos clínicos randomizados, con criterios de selección de muestra bien definidos.
SÍNTESES DE DATOS: Los mecanismos para explicar la AIE permanecen sin conclusión, pero parece haber una interacción fisiológica entre las hipótesis aquí presentadas. El uso de medicamentos y las frecuentes crisis durante el ejercicio aparecen como factores limitantes para la práctica de ejercicios físicos, conduciendo esto a un estilo de vida sedentario.
CONCLUSIÓN: Se debe incentivar la práctica de ejercicios debidamente prescritos y minimizar las restricciones a los individuos con AIE.
Palabras-clave: Asma. Ejercicio. Prevención.
INTRODUCTION
Exercise-induced asthma (EIA) is known as a transitory airways obstruction immediately after vigorous exercise, being one of its main symptoms lack of air; cough and wheeze. It ca be evidenced by the decrease in the expiration volume forced in 1 second (VEF1) and by other spirometric parameters(1). The mechanism of development of this obstruction has not been defined yet; however, several studies(1-5) were conducted in order to clarify the mechanisms of action of EIA.
EIA may be observed in children and adolescents of different physical conditioning backgrounds, from those not engaged in sports to competitive athletes. Physical exercise causes bronchoconstriction in the majority (~70%) of the children and adolescents who present asthma; nevertheless, EIA may occur in those who do not present asthma diagnosis(6). Typically, the crisis begins 2 to 4 minutes after the exercise, with peaks from 5 to 10 minutes, and spontaneously disappears in about 20 to 40 minutes. Sometimes the crisis may be sustained for more than an hour. Late responsiveness may appear from 4 to 10 hours post exercise(7).
The prevalence of EIA reaches 12% in school-aged children and varies in different sports modalities, being 50% in cross-country skiing athletes; 35% in ice hockey; 43% in velocity skaters and 17% in winter and summer Olympic athletes(1). It is interesting to observe that the highest EIA prevalence occurs in those athletes who compete in cold weather.
There are usually two used descriptions: EIA and bronchoconstriction exercise-induced (EIB) EIB is bronchial obstruction (spasm) observed after exercise in individuals who present normal pulmonary function in resting; and EIA is sometimes used to describe the increase of the post-exercise symptoms for asthmatic subjects. However, the two terminologies are interchangeable. In this review we chose to use only the expression exercise-induced asthma.
The aim of this review is to describe the EIA mechanisms as well as the kinds of diagnosis and management; to discuss the impact of different kinds of training in the pulmonary function and in the cardiorespiratory capacity and finally to bring recommendations for safe practice of physical exercises.
MECHANISMS OF ACTION OF EIA
The physiological events which trigger the EIA crisis remain unknown; nevertheless, several studies(2-3,5,8-14) suggest some physiological mechanisms of EIA.
EIA may be explained by two hypotheses(2-3). The osmotic hypothesis considers that dehydration of the airways generated by the insensitive water loss by the respiratory tract stimulated by inhaling of dry air during exercise increases the osmolarity of the periciliary liquids. Such process releases hence chemical mediators (histamine, prostaglandins and leukotrienes) which increase the contraction of the bronchial straight musculature, causing obstruction.
The thermal hypothesis considers that EIA is initiated by the thermal effect in the airways caused by exercise, that is, the cooling of the airways followed by a rewarm-up post exercise which causes a reactive hyperemia of the bronchial vasculature and edema on the airways wall(2-3,13). Such episode suggests that the cooling of the airways(14) would be an important stimulus for EIA. Nonetheless, Zeitoun et al.(5) found that EIA occurred when warm and dry air was inhaled, suggesting that the cooling of the airways would not be the single responsible factor for EIA induction.
An inflammatory response can also be an additional mechanism for the EIA triggering. The presence of inflammatory agents such as macrophages, eosinophils and linfocites in the bronchoalveolar liquid of children with EIA has been confirmed, even in those who present normal pulmonary function in resting(9,15). These response are reinforced by exposition to allergenic (dust, smoke), viral and bacterial agents as well as to exercise.
In an epidemiological study, Burney(8) suggested an association between salt ingestion and asthma, suggesting that asthmatic individuals present a tendency to ingest more salt than non-asthmatic ones. In prospective studies, Gotshall et al.(10) and Mickleborough et al.(11-12) demonstrated that salt increased consumption may represent a risk factor, since salt increases EIA. The mechanism through which salt increases EIA is not completely clear yet. Possibly, a saturation of the ATPase Na+/K+ in the straight musculature of the upper airways occurs, overacting the Ca++ ATPase as regulator of the electrolytes influx-efflux in the straight muscular cell. However, the calcium carried in this ATPase accentuates the contractibility of the straight musculature, causing bronchoconstriction(10-12).
The amount of each of these hypotheses influence in EIA occurrence remains inconclusive. The fact is that they do not act in the triggering of this phenomenon isolated, suggesting thus, that the interaction of these factors is crucial for EIA.
DIAGNOSIS AND MANAGEMENT
The EIA diagnosis is usually initiated from the observation of symptoms such as cough, wheeze, difficulty in breathing and chest pain, after exercise. However, subjects who present these abnormal symptoms may not be able to recognize them as EIA, simply believing they are unfit(1-2). Yet, some studies(16-17) demonstrated a weak correlation between self-observation of symptoms with the presence of EIA. Cabral et al.(18) evaluated the influence of asthma severity over IEA occurrence. 164 children, mean age of 11 years, were evaluated and classified in intermittent asthma; medium-persistent; moderate persistent and severe persistent subgroups according to the Global Initiative for Asthma Classification (GINA)(19). The results demonstrated that the EIA prevalence in children with severe or moderate asthma was significantly higher than in those with intermittent asthma. However, the response to exercise may be absent even in children with severe persistent asthma, suggesting that the exercise response, that is the EIA occurrence, is not consistently related to clinical severity of asthma. Another difficulty found for the EIA diagnosis, especially in children, is the fact that family members do not usually observe them during physical activities practice, either in sports schools or in physical education classes(2).
For the consolidation of EIA diagnosis, an exercise test followed by spirometry in which bronchoconstriction is induced by an exercise protocol is usually performed. Such test has presented higher effectiveness in EIA diagnosis than bronchoconstriction induced by drugs such as methacholine and histamine(18). The tests of provocative concentration using such drugs usually aim the diagnosis of bronchial reactivity, which does not necessarily correspond to EIA diagnosis. The test protocol involves a run/cycle at 80 to 90% intensity of the heart rate (HR) maximal reserve during 6 to 8 minutes(18,20). Yet, for children and adolescents engaged in competitive sports, the exercise test must be similar to the sport gesture the subject practices(2). The spirometry is measured before and after (usually at every 5 minutes until 20 minutes) the test performance. The VEF1 spirometric parameter is the most used for the EIA diagnosis. It is justified for the low intra-subjects variability when compared with other parameters such as the expiratory flow peak(18). Decrease of 15% of the VEF1 after the exercise test may be considered EIA(21). However, 10% decrease of the VEF1 compared with the baseline values may be sufficient for the EIA diagnosis, since the results correspond to the double of the coefficient of the VEF1 variation measured(18). In resting, that is, before the exercises performance, the VEF1 of children and adolescents with EIA usually presents normal values, at around 90% of the predicted values; if the resting VEF1 presents values below 90%, it may be indication of non-diagnosed moderate chronic asthma(1).
The performance of sessions with short exercises intervals has shown to reduce the severity of response. This phenomenon is known as refractory period(1-2,13,22-24) and has been used as a device to reduce EIA effects. Despite an intra-subject variability, such maneuver has good effectiveness in EIA prevention(2). It has not been well-defined either how the refractory period reduces the EIA magnitude. Nonetheless, it is possible that the inflammatory mediators suffer depletion during this period and need time for its resynthesis(13,22) hence, reducing the EIA crisis.
The spirometric evaluation is crucial for the treatment strategy of EIA In resting, if the VEF1 presents values lower than 90%, it is recommended that a daily treatment for persistent chronic asthma begins. When the spirometric values are normal, high intensity pre-exercises warm-ups (80% HR maximal) performance may be sufficient to reduce the magnitude of response to exercise.
The most effective treatment for EIA is the utilization of short-duration beta-adrenergic drugs via inhalation, such as salbutamol and dissodium cromoglycate, for its bronchodilator action(25). In other words, the bronchodilation that such kind of drug induces before exercise would possibly be responsible for the minimization of EIA effects. Another alternative would be a more potent bronchodilator during exercise and the inhibition of the chemical mediators release, which would reduce the bronchoconstriction following the exercise(20,26). However, for athletes the therapy may represent risks of positive tests in anti-doping exams, since the beta-adrenergic drugs are listed as prohibited substances by the International Olympic Committee, according to the World Anti-doping Agency (WADA). This group of drugs must be reported as being of therapeutic use, thus allowing values higher than 1000 ng/dL(27).
The long-term use of beta-adrenergic drugs may cause taquifilaxy(1-2) appearance of progressive reduction of responsiveness after repetitive administration of a drug or physiological active substance reducing the effectiveness of these drugs over EIA. Therefore, the intermittent administration may cause an efficient and safe action in the EIA management(9).
Another group pf drugs for the treatment of EIA are the anticholinergic agents. Among them, the ipratropium bromide, which besides presenting a potential anticholinergic action and reasonable bronchodilator effect, presents weak incidence of side effects(5). However, the efficiency of this drug presents great interindividual variability through airways, especially by the need of an accentuated vagal activity(28-30), which justifies its scarce recommendation as EIA treatment.
EIA AND PHYSICAL EXERCISE
The benefits of physical exercise in EIA have been studied in order to measure the effects of the response to different types of training in physical fitness and in the pulmonary function of subjects with EIA. Ram et al.(31) conducted a meta-analysis including randomized clinic essays and observed that the maximal oxygen uptake increases with physical training, suggesting that the response of individuals with EIA is similar to the one from healthy ones and therefore, an increase in the cardiorespiratory capacity is accessible. Yet, the pulmonary function in resting did not present significant improvement.
In a prospective study, Counil et al.(32) evaluated the response of 16 boys (mean age = 13 years) with EIA to anaerobic and aerobic trainings. The authors concluded that both kinds of training may increase the physical capacity of these subjects, besides presenting good tolerance from their part. It seems that when the bronchial obstruction is relieved, the mechanism of muscular fitness is not different from healthy children. Such episode reinforces the recommendation of physical exercises practice for subjects with EIA.
Asthmatic children are usually insufficiently active; therefore their anaerobic performance may be faulty. The studies in this area are inconsistent. While some show normal anaerobic capacity measured either by the Wingate anaerobic test(33-34) or by the accumulated O2 deficit method(35), others show low anaerobic performance in patients with asthma either through strength-velocity tests(36) or the Wingate anaerobic test(37). Such inconsistencies are hard to be explained; however, they may reflect inter-study differences in the asthma severity; the nutritional status; the degree of maturation and the level of physical activity.
Stanford et al.(38) observed the influence of the menstrual cycle over the pulmonary function of asthmatic athletes. Seven women with regular menstrual cycles of 28 days performed exercise tests to exhaustion, on the fifth day (follicular phase) and on the 21st day (luteal phase). The tests of pulmonary function were conducted before and after the exercise test. A significant decrease was observed in the spirometric parameters VEF1 and in the forced expiratory flow of 25 to 75% of the forced vital capacity (FEF25-75%), on the 21st day of the menstrual cycle. Such evidence suggests that asthmatic athletes may need adjustments in their training and competitions calendar according to their menstrual cycle, due to potential negative effects of the luteal phase in performance.
Silva et al.(39) evaluated the effects of the circadian cycle on day variations in the training responsiveness in asthmatic children who were divided in three groups: morning training (MT); afternoon training (AT) and a group with no training (NT). The circuit training program was performed two weekly times and consisted of a 90-minute session in which the children performed the following activities: 5-minute walk, followed by 10-15 minute run (progressive increase during the program); upper and lower limbs activities (to jump rope; exercises of raising their own bodies; to go up and down a stool); abdominal exercises, bar training; individual and team games; postural exercises and back to normal. Pre and post-intervention evaluations involved 9-minute run test, resting heart rate and abdominal strength. Both groups presented significant improvement when compared with the NT group; however, there was no difference in the training responsiveness when it was performed in the morning or afternoon.
According to the American College of Sports Medicine (ACSM)(40), the standard-principles for exercise prescription type; frequency; intensity and duration may be applied in patients with respiratory diseases, including EIA.
Even if the pulmonary function is not altered due to training, strengthening of the respiratory musculature is expected as a training effect, long-term aiding in the reduction of the pulmonary function decrease after exercise and minimizing sedentarism, obesity and EIA effects(41-42).
CONCLUSION
The EIA mechanisms remain inconclusive; nevertheless, a physiological interaction involving the proposed theories seems to exist for the explanation of this phenomenon. The exercise test is an efficient device for EIA diagnosis if compared with bronchial reactivity tests induced by drugs such as methacholine and histamine. Concerning management, we highlight the importance of maneuvers such as the performance of pre-exercise warm-ups due to the refractory period as well as the utilization of beta-adrenergic substances for EIA prevention.
We also highlight the importance of physical activity practice for children and adolescents with EIA, since even if the exercise does not directly affect the pulmonary function, the reduction in sedentarism level as well as better quality of life derived from it justifies its regular application.
ACKNOWLEDGMENTS
We want to thank the National Committee of Scientific and Technological Development (CNPq) for the financial support and Márcia dos Santos Dornelles for the Portuguese language review.
REFERENCES
Received in 20/10/05.
Final version received in 20/4/06.
Approved in 17/7/06.
All the authors declared there is not any potential conflict of interests regarding this article.
References
- 1. Storms WW. Review of exercise-induced asthma. Med Sci Sports Exerc. 2003; 35(9):1464-70.
- 2. Storms WW. Asthma associated with exercise. Immunol Allergy Clin N Am. 2005;25:31-43.
- 3. Anderson A, Daviskas E. The mechanism of exercise-induced asthma is... J Allergy Clin Immunol. 2000;106(3):453-9.
- 4. Strunk R. Defining asthma in the preschool-aged child. Pediatrics. 2002;109(2 Suppl):357-61.
- 5. Zeitoun M, Wilk B, Matsuzaka A, Knöpfli BH, Wilson B, Bar-Or. Facial cooling enhaces exercise-induced bronchoconstriction in asthmatic children. Med Sci Sports Exerc. 2004;36(5):767-71.
- 6. Löwhagem O, Arvidsson M, Bjärneman P, Jorgensen N. Exercise-induced respiratory symptoms are not always asthma. Respir Med. 1999;93(10):734-8.
- 7. Bar-Or O, Rowland TW. Pediatric exercise medicine: from physiological principles to health care application. 1st ed. Human Kinetics, 2005;139-75.
- 8. Burney PGJ. The causes of asthma Does salt potentiate bronchial activity? J R Soc Med. 1987;80:364-7.
- 9. Serafin WE. Drugs used in the treatment of asthma. In: Hardman JG, Limbird LE, Molinoff PB, Ruddon RW, Gilman AG, editors. The pharmacological basis of therapeutics. New York: McGraw-Hill, 1996;659-82.
- 10. Gotshall RW, Mickleborough TD, Cordain L. Dietary salt restriction improves pulmonary function in exercise-induced asthma. Med Sci Sports Exerc. 2000;11(32): 1815-9.
- 11. Mickleborough TD, Gotshall RW, Kluka EM, et al. Dietary chloride as a possible determinant of the severity of exercise-induced asthma. Eur J Appl Physiol. 2001; 85:450-6.
- 12. Mickleborough TD, Gotshall RW, Rhodes J, Tucker A, Cordain L. Elevating dietary salt exacerbate hyperpnea-induced airway obstruction in guinea pigs. J Appl Physiol. 2001;91:1061-6.
- 13. Rundell KW, Spiering BA, Judelson DA, Wilson MH. Bronchoconstriction during cross-country skiing: is there really a refractory period? Med Sci Sports Exerc. 2003;35(1)18-26.
- 14. Davis MS, Malayer JR, Vandeventer L, Royer CM, McKenzie EC, Williamson KK. Cold weather exercise and airway cytokine expression. J Appl Physiol. 2005;98: 2132-6.
- 15. Hallstrand TS, Moody MW, Aitken ML, Henderson WR. Airway immunopathology of asthma with exercise-induced bronchoconstriction. J Allergy Clin Immunol. 2005 [in press].
- 16. Thole RT, Sallis RE, Rubin AL, Smith GN. Exercise induced brochospasm prevalence in collegiate cross country runners. Med Sci Sports Exerc. 2001;33:1641-6.
- 17. Rundell KW, Im J, Mayers LB, Wilber RL, Szmedra L, Schmitz HR. Self-reported symptoms and exercise induced asthma in the elite athlete. Med Sci Sports Exerc. 2001;33:208-13.
- 18. Cabral ALB, Conceição GM, Fonseca-Guedes CHF, Martins MA. Exercise-induced bronchospasm in children: effects of asthma severity. Am J Respir Crit Care Med. 1999;159:1819-23.
- 19 Global Initiative for Asthma [site na Internet]. [atualizado em 25 de junho de 2005; citado em 2 de julho de 2005]. Disponível em: http://www.ginasthma.com/
- 20. Meyer F, Saute L, Winge A. Asma induzida pelo exercício: aspectos fisiopatológicos e manejo. Jornal de Pediatria. 1987;63(2):79-82.
- 21. Katch VL, Katch FI, McArdle WD. Essentials of exercise physiology. 2nd ed. Lippincott Williams & Wilkins, 2000.
- 22. Stearns DR, McFadden ER, Breslin FJ, Ingram RH. Reanalysis of the refractory period in exertional asthma. J Appl Physiol. 1981;50(3):503-8.
- 23. Mckenzie DC, Mcluckie SL, Stirling DR. The protective effects of continuous and interval exercise in athletes with exercise-induced asthma. Med Sci Sports Exerc. 1994;26:951-6.
- 24. de Bisschop C, Guernad H, Desnot P, Vergeret J. Reduction of exercise-induced asthma in children by short, repeated warm-ups. Br J Sports Med. 1999;33(2): 100-4.
- 25. Price J. Choices of therapy for exercise-induced asthma in children. Allergy. 2001; 66:12-7.
- 26. Boskabady MH, Saadatinejad M. Airway responsiveness to beta-adrenergic agonist (salbutamol) in asthma. J Asthma. 2003;40(8):917-25.
- 27. World Anti-Doping Agency. The 2006 prohibited list: International Standard, 2006; 1-11.
- 28. Knöpfli B, Bar-Or O, Araujo CGS. Effect of ipratropium bromide on EIB in childrens depends on vagal activity. Med Sci Sports Exerc. 2005;37:354-9.
- 29. Boulet LP, Turcotte PH, Tennina S. Comparative efficacy of salbutamol, ipratropium and cromoglycate in the prevention of bronchospasm induced by exercise and hiperosmolar challenges. J Allergy Clin. 1979;64:627-33.
- 30. Spooner ET, Spooner GR, Rowe BH. Mast-cell stabilizing agents to prevent exercise-induced bronchoconstriction. Cochrane Database Syst Rev. 2003;4: CD002307.
- 31. Ram F, Robinson SM, Black PN. Effects of physical training in asthma: a systematic review. Br J Sports Med. 2000;34:162-7.
- 32. Counil FP, Varray A, Matecki S, Beurey A, Marchal P, Voisin M, et al. Training of aerobic and anaerobic fitness in children with asthma. J Pediatr. 2003;84:142-79.
- 33. Boas SR, Danduran MJ, McColley AS. Energy metabolism during anaerobic exercise in children with cyctic fibrosis and asthma. Med Sci Sports Exerc. 1999; 31:1242-9.
- 34. Boas SR, Danduran MJ, Saini SK. Anaerobic exercise testing in children with asthma. J Asthma. 1998;35:481-7.
- 35. Buttifant DC, Carlson JS, Naughton GA. Anaerobic characteristics and performance of pre-pubertal asthmatic and nonasthmatic males. Pediatr Exerc Sci. 1996; 8:268-75.
- 36. Counil FP, Karila C, Varray A, Guillaumont S, Voisin M, Préfaut C. Anaerobic fitness in children with asthma: adaptation to maximal intermittent short exercise. Pediatr Pulmonol. 2001;31:198-204.
- 37. Counil FP, Varray A, Karila C, Hayot M, Voisin M, Préfaut C. Wingate test performance in children with asthma: aerobic or anaerobic limitation? Med Sci Sports Exerc. 1997;29:430-5.
- 38. Stanford KI, Mickleborough TD, Ray S, Lindley MR, Koceja DM, Stager JM. Influence of menstrual cycle on pulmonary function in asthmatic athletes. Eur J Appl Physiol. 2006;96:703-10.
- 39. Silva CS, Torres LAGMM, Rahal A, Terra Filho J, Vianna EO. Comparison of morning and afternoon exercise training for asthmatic children. Braz J Med Biol Res. 2006;39:71-8.
- 40. American College of Sports Medicine. ACSM's guidelines for exercise testing and prescription. 7th ed. Philadelphia: Lippincott Williams & Wilkins, 2005.
- 41. Shaheen OS. Obesity and asthma: cause for concern? Clin Exp Allergy. 1999;29: 291-3.
- 42. Lucas SR, Platts-Mills AE. Physical activity and exercise in asthma: relevance to etiology and treatment. J Allergy Clin Immunol. 2005;115:928.
Publication Dates
-
Publication in this collection
11 Sept 2007 -
Date of issue
Feb 2007
History
-
Reviewed
20 Apr 2006 -
Received
20 Oct 2005 -
Accepted
17 July 2006