Cardio-pulmonary responses and gas exchange during exercise in adults with homozygous sickle-cell disease (sickle-cell anaemia)

ABSTRACT

Cardio-pulmonary responses and gas exchange during progressive exercise, the ventilatory response to hypercapnia and anthropometric indices were measured in twenty-two Jamiacan adults with homozygous sickle-cell disease. Their anthropometric indices and exercise performances were compared with those observed in healthy but sedentary adults in the Caribbean. The patients had long lower limbs for their height; their body fat, proportion of lean body mass as muscle and vital capacity reduced. Haemoglobin concentration ranged from 4 to 10g/100ml. Heart rate and ventilation were normal at rest. During exercise in the male patients haemoglobin concentrations below about 8g/100ml were associated with an increased demand for anaerobic metabolism. This resulted in excessive lac ticacidaemia and increased ventilation at standard oxygen uptake (hyperpnoea). The ventilation-tidal volume relationship was normal. When allowance was made for differences in body muscle, anaemia did not appear to affect the heart-rate response to exercise. Hyperventilation with respect to carbon dioxide output, increased alveolar-arterial oxygen-tension gradients and abnormal deadspace ventilation during exercise indicated a pulmonary perfusion disturbance with mixed venous shunting. The most likely basis for this disorder was considered to be the sickling phenomenon. Arterial hypoxaemia produced by the pulmonary shunt probably accounted for some of the exercise hyperpnoea, partly by increasing the chemoreceptor drive and partly by encouraging lacticacidaemia. Reduced arterial carbon dioxide tensions and bicarbonate concentrations had lowered the threshold and increased the sensitivity of the ventilatory response to carbon dioxide as measured by rebreathing. Increased chemosensitivity was not thought to have contributed towards the exercise hyperpnoea since arterial carbon dioxide tensions were below the threshold value for ventilatory drive. Exertional dyspnoea in sickle-cell disease was attributed to the combination of hyperpnoea and reduced maximum breathing capacity (MBC) owing to small lung volumes. The fraction of (MBC) used at standard work was therfore abnormally large, and the increased ventilatory effort produced a sensation of breathlessness in some patients (Summary)