Exercise responses in patients with an enzyme deficiency in the mitochondrial respiratory chain

Responses to exercise were obtained in six patients with a biochemically diagnosed enzyme deficiency at the level of NADH-CoQ reductase. The responses were compared with those of a control group, consisting of fourteen patients with inexplicable dyspnoea or muscle pain during exercise, for which no firm diagnosis could be established and of which the exercise responses were in the normal range. Metabolic, ventilatory and cardiological variables such as oxygen uptake (VO2), minute ventilation (VE), respiratory exchange ratio (R), heart rate (HR) and difference in blood lactate or base-excess (BE) between rest and maximal workload were measured during cycle ergometry from samples obtained in the last minutes of four minute periods, in which the load increased stepwise by 30 W per four minutes. The threshold of lactate metabolism (Tlact) was assumed to be equal to the threshold determined both by the VO2 at which the VE versus VO2 response started to deviate from a straight line and the ventilatory equivalent for oxygen (VE/VO2) showed a minimum (Tvent), Tvent was estimated from the mean of these values, obtained by linear and parabolic regression analysis respectively. In the patient group, mean values for symptom limited maximal VO2 (VO2,max,sl; % of VO2,max,ref), Tvent (% of VO2,max,ref) and R at maximal workload were 43, 17 and 1.23 against 85, 47 and 1.06 for the same variables in the control group, respectively. The differences were highly significant (p less than 0.001; p less than 0.005 for mean R difference). Mean maximal HR and mean change in blood lactate or BE were not significantly different in the two groups.(ABSTRACT TRUNCATED AT 250 WORDS)

This article has been cited by other articles:

				J. E. Hansen, R. Casaburi, M. S. Riley, D. P. Nicholls, K. Wasserman, K. R. Flaherty, M. M. Blaivas, J. Wald, M. Rubenfire, F. J. Martinez, et al. Mitochondrial disorders and exertional intolerance: Controversy continues Am. J. Respir. Crit. Care Med., July 1, 2002; 166(1): 118 - 120. [Full Text] [PDF]

				A. S. Clay, M. Behnia, and K. K. Brown Mitochondrial Disease : A Pulmonary and Critical-Care Medicine Perspective Chest, August 1, 2001; 120(2): 634 - 648. [Abstract] [Full Text] [PDF]

				F. Monzani, N. Caraccio, G. Siciliano, L. Manca, L. Murri, and E. Ferrannini Clinical and Biochemical Features of Muscle Dysfunction in Subclinical Hypothyroidism J. Clin. Endocrinol. Metab., October 1, 1997; 82(10): 3315 - 3318. [Abstract] [Full Text] [PDF]