Key result
Older males with Type 2 diabetes did not exhibit abnormal pulmonary oxygen uptake kinetics during submaximal cycling compared to healthy controls (43 vs. 41 s), despite a lower Vo(2max).
Why the study?
Do older Type 2 diabetic males exhibit abnormal pulmonary oxygen uptake and muscle oxygen utilization dynamics during submaximal cycling exercise compared to healthy controls?
Cross-Sectional (n=24)
Do older Type 2 diabetic males exhibit abnormal pulmonary oxygen uptake and muscle oxygen utilization dynamics during submaximal cycling exercise compared to healthy controls?
Answers are grounded in this paper and cite their sources.
Older men with long-standing Type 2 diabetes maintain normal pulmonary oxygen uptake kinetics during submaximal exercise despite lower maximal oxygen uptake, possibly due to compensatory increases in muscle oxygen extraction.
There are reports of abnormal pulmonary oxygen uptake (Vo(2)) and deoxygenated hemoglobin ([HHb]) kinetics in individuals with Type 2 diabetes (T2D) below 50 yr of age with disease durations of <5 yr. We examined the Vo(2) and muscle [HHb] kinetics in 12 older T2D patients with extended disease durations (age: 65 ± 5 years; disease duration 9.3 ± 3.8 years) and 12 healthy age-matched control participants (CON; age: 62 ± 6 years). Maximal oxygen uptake (Vo(2max)) was determined via a ramp incremental cycle test and Vo(2) and [HHb] kinetics were determined during subsequent submaximal step exercise. The Vo(2max) was significantly reduced (P < 0.05) in individuals with T2D compared with CON (1.98 ± 0.43 vs. 2.72 ± 0.40 l/min, respectively) but, surprisingly, Vo(2) kinetics was not different in T2D compared with CON (phase II time constant: 43 ± 17 vs. 41 ± 12 s, respectively). The Δ[HHb]/ΔVo(2) was significantly higher in T2D compared with CON (235 ± 99 vs. 135 ± 33 AU·l(-1)·min(-1); P < 0.05). Despite a lower Vo(2max), Vo(2) kinetics is not different in older T2D compared with healthy age-matched control participants. The elevated Δ[HHb]/ΔVo(2) in T2D individuals possibly indicates a compromised muscle blood flow that mandates a greater O(2) extraction during exercise. Longer disease duration may result in adaptations in the O(2) extraction capabilities of individuals with T2D, thereby mitigating the expected age-related slowing of Vo(2) kinetics.
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Wilkerson et al. (2010) conducted a cross-sectional in Type 2 diabetes (n=24). Type 2 diabetes vs. Healthy age-matched controls was evaluated on Vo(2) kinetics (phase II time constant in seconds). Older males with Type 2 diabetes did not exhibit abnormal pulmonary oxygen uptake kinetics during submaximal cycling compared to healthy controls (43 vs. 41 s), despite a lower Vo(2max).
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