Why does maximal ventilation decrease with age




















In this review, the authors intend to present the physiological alterations caused by aging such as changes in respiratory system dynamics, gas exchange abnormalities, and changes in exercise capacity and respiratory muscle strength.

Structural changes induce an increase in the anterior and posterior diameters of thoracic cage, causing it to assume a round shape. Increased stiffness and reduced compliance of the thoracic wall is induced by aging-related calcification of the joint cartilage of the thorax and spinal scoliosis caused by osteoporotic changes.

A study that measured the compliance of the thoracic wall in 61 healthy adults ranging from 24 to 75 years old, reported that the thoracic compliance was reduced according to the participants' age. Aging-induced changes in the respiratory system, such as reduction of compliance and of respiratory muscle strength, result in changes in the results of pulmonary function tests. Lung function reaches its peak when individuals are in their early 20s, is maintained for some time, and then decreases normally with aging.

Total lung capacity TLC does not change or slightly reduces during aging, but residual volume RV is increased and vital capacity VC is reduced. These reductions indicate small airway disease based on the flow rate-volume curve. The diffusion capacity for carbon monoxide DLCO also decreases with age by 0. The degree of decreases in women is reported to be lesser than that in men, possibly due to the influence of estrogen, which maintains integrity of the blood vessel.

A study by Stam et al. This decrease in diffusing capacity may likely be caused by aging-induced changes in the alveolar-capillary membrane. However, the minute ventilation is not decreased and there is no occurrence of the carbon dioxide exchange impairment by aging, therefore, the occurrence of respiratory acidosis should be considered as pathological in old ages as well. Decreased muscle strength is a general consequence of aging, and affects the respiratory muscles as well.

All these parameters have been found to be decreased in elderly people. The reduced strength of the diaphragm with aging is associated with muscle atrophy and with decrease of fast fibers that create a higher level of tension. Reduction of diaphragmatic muscle strength increases the respiratory rate in the elderly, which results in fatigue to the diaphragm, and may eventually cause ventilatory failure. Thus, the reduction of respiratory muscle strength due to aging may not be a serious problem in healthy individuals, but if the ventilation demands are increased due to pulmonary disease, it can be a major problem resulting in respiratory failure.

The cross-sectional area of the intercostal muscles is slightly reduced, while that of the expiratory muscles is reduced to a much greater extent, at the age of 50 years or higher. However, the reduction of compliance in the chest wall results in a reduction in the curvature causing a reduction in Pdi max. Reduction in respiratory muscle strength in the elderly has shown to be associated with nutritional status, and BMI has been reported to have a significant correlation with the MIP as well as with the maximal expiratory pressure.

Minute ventilation remains the same between the younger and the older age groups. Although the tidal volume is reduced with age, the minute ventilation is maintained by increasing the respiration rate. However, the ventilator response to hypoxemia or to increased carbon dioxide concentration may be inadequate in the elderly. Although the mechanism is unclear, these changes might have been caused by dysfunction of chemosensory receptors and by structural changes in the lung and thoracic cage.

In a longitudinal study on the effects of aging on lung function at rest and during exercise in healthy older people, McClaran et al. The cough reflex weakens with aging. This change may be attributed to the decrease in cough sensation, increased activation threshold of the vagus and occipital nerves, decreased tension of smooth muscles, and reduction of cognitive capacity.

Such weakening of the cough reflex contributes to the increase in the incidence of aspiratory pneumonia in elderly individuals. Figure 3. Table 2 Static lung volumes. Tidal volume TV Volume of air inspired or expired during quiet breathing Inspiratory reserve volume IRV Maximum volume of air inspired above the tidal volume Expiratory reserve volume ERV Maximum volume of air expired below the tidal volume Residual volume RV Amount of air in the lungs after maximum expiration.

Table 4 Lung function studies. Dyspnea and response to hypoxia and hypercapnia Minute ventilation, a product of volume inhaled per breath and respiratory rate over one minute, is identical in younger and older individuals. Bronchial hyper-responsiveness and age-related pulmonary receptor changes Age had a significant effect on airway reactivity and response to bronchodilator therapy.

Figure 4. Mechanism of action of beta agonist. Muscarinic receptor The data on age-related changes in pulmonary muscarinic receptor in humans is limited. Cysteinyl-Leukotriene CysLT 1 receptor The stimulation of cysteinyl-leukotriene CysLT 1 receptor located on the airway smooth muscles induces bronchoconstriction. Exercise capacity The effect of aging on exercise capacity is highly variable and depends upon individual fitness and regular physical activity.

Table 5 Ventilatory response to hypoxia and hypercapnia. Summary There is marked variation in the effect of aging on lung function. Table 6 Anatomical and physiological changes of respiratory system with aging. Figure 2. Relationship between lung volumes and lung capacities. Table 3 Lung capacities are sum of two or more static lung volumes. Catalytic unit of adenylate cyclase: reduced activity in aged-human lymphocytes.

J Clin Endocr Metab. Longitudinal changes in forced expiratory volume in one second in adults. Am Rev Respir Dis. Aging, late-onset asthma and the beta-adrenoceptor.

Pharm Therapeutics. Impaired bronchodilator response to albuterol in healthy elderly men and women. Reference spirometric values using techniques and equipment that meets ATS recommendations. Loss of response to treatment with leukotriene receptor antagonists but not inhale corticosteroids in patients over 50 years of age. Ann Allergy Asthma Immunol. Changes in FVC during methacholine-induced bronchoconstriction in elderly patients with asthma: bronchial hyper responsiveness and aging.

Distribution of forced expiratory volume in one second and forced vital capacity in healthy, white, adult, never smokers in six U. Spirometry reference values for women and men 65 to 85 years of age. Cardiovascular Health Study. Respiratory muscle strength in the elderly. N Engl J Med. Airspace size in lungs of lifelong non-smokers: effect of age and sex.

The effect of age on methacholine response. J Allergy Clin Immunol. Physiological changes in respiratory function associated with aging. Eur Respir J. Eur Respir J Suppl. How aging affects the normal lung. J Respir Dis. Changes in the normal maximal expiratory flow-volume curve with growth and aging. Attenuation of the ventilatory and heart rate responses to hypoxia and hypercapnea with aging in normal men.

J Clin Invest. Longitudinal effects of aging on lung function at rest and exercise in healthy active fit elderly adults. J Appl Physiol. Immune dysregulation in the aging human lung. Relationship between chest wall and pulmonary compliance with age. Spirometric standards for health non-smoking adults. Effects of aging on ventilatory and occlusion pressure responses to hypoxia and hypercapnia.

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Our service is free and we are here to help you. Lung Capacity and Aging. Section Menu. What Happens? How Is Lung Capacity Measured? Chest, , pp. Fernandez-Bustamante, S. Hashimoto, A. Serpa, P. Moine, M. Vidal Melo, J. Perioperative lung protective ventilation in obese patients. BMC Anesthesiol, 15 , pp. Al Ghobain. The effect of obesity on spirometry tests among healthy non-smoking adults. BMC Pulm Med, 12 , pp. McCallister, E. Adkins, J. Clin Chest Med, 30 , pp. Ochs-Balcom, B. Grant, P.

Muti, C. Sempos, J. Freudenheim, M. Trevisan, et al. Pulmonary function and abdominal adiposity in the general population. Inchaurraga, J. Pulmonary function in morbid obesity: influence of sex and body distribution. J Obes Weight Loss Ther, 6 , pp. Salome, G. King, N. Physiology of obesity and effects on lung function.

Littleton, A. The effects of obesity on lung volumes and oxygenation. Respir Med, , pp. Verbraecken, W. Respiratory mechanics and ventilatory control in overlap syndrome and obesity hypoventilation. Respir Res, 14 , pp. Lafortuna, F. Agosti, R. Galli, C. Busti, S. Lazzer, A. The energetic and cardiovascular response to treadmill walking and cycle ergometer exercise in obese women.

Eur J Appl Physiol, , pp. Das, H. Mondal, M. Study of dynamic lung function parameters in normal, overweight, and thin school boys. J Sci Soc, 44 , pp. Dundas, N. Marlin, J. Jamaludin, I. Mudway, H. Wood, L. Cross, et al. Ethnic and nutritional determinants of respiratory function in East London children. Eur Respir J, 42 , pp. Schwartz, S. Patil, A. Laffan, V. Polotsky, H. Schneider, P. Proc Am Thorac Soc, 5 , pp.

Curr Opin Pulm Med, 16 , pp. Townsend, V. Miller, Y. Sex differences and sex steroids in lung health and disease. Endocr Rev, 33 , pp. Becklake, F. Gender differences in airway behaviour over the human life span. Thorax, 54 , pp. Bellemare, A. Jeanneret, J. Sex differences in thoracic dimensions and configuration. Gender, sex hormones and respiratory disease: a comprehensive guide. Humana Press, ,. Jagia, R. Int J Biomed Res, 5 , pp.

Smith, K. Brown, J. Murphy, C. Does menstrual cycle phase affect lung diffusion capacity during exercise?. Breathe, 12 , pp. Sheel, P. Dominelli, Y. Revisiting dysanapsis: sex-based differences in airways and the mechanics of breathing during exercise. Exp Physiol, , pp. Physiological limits to endurance exercise performance: influence of sex.

J Physiol, , pp. Bouwsema, V. Tedjasaputra, M. Are there sex differences in the capillary blood volume and diffusing capacity response to exercise?. Naitoh, K. Tomita, K. Sakai, A. Yamasaki, Y. Kawasaki, E. The effect of body position on pulmonary function, chest wall motion, and discomfort in young healthy participants.

J Manip Physiol Ther, 37 , pp. Mase, M. Tagami, S. Imura, K. Tomita, M. Monma, M. Nozoe, et al. Regional lung volume differences between the side-lying and semi-prone positions.

Romei, A. Mauro, M. Turconi, N. Bresolin, A. Pedotti, et al. Effects of gender and posture on thoraco-abdominal kinematics during quiet breathing in healthy adults. Ganapathi, S. The estimation of pulmonary functions in various body postures in normal subjects. Int J Adv Med, 2 , pp. Hudson, F. Joulia, A. Butler, R. Fitzpatrick, S. Gandevia, J. Activation of human inspiratory muscles in an upside-down posture.

Jyothi, G. Effect of different postures on peak expiratory flow rate and peak inspiratory flow rate on healthy individuals. Peces-Barba, M. Verbanck, M. Paiva, N. Lower pulmonary diffusing capacity in the prone vs supine posture. J Appl Physiol, 96 , pp. Palermo, G. Cattadori, M. Bussotti, A. Apostolo, M. Contini, P. Lateral decubitus position generates discomfort and worsens lung function in chronic heart failure.



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