Pulmonary oxygen uptake and muscle deoxygenation kinetics during heavy intensity cycling exercise in patients with emphysema and idiopathic pulmonary fibrosis. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- Pulmonary oxygen uptake and muscle deoxygenation kinetics during heavy intensity cycling exercise in patients with emphysema and idiopathic pulmonary fibrosis. Issue 1 (December 2017)
- Main Title:
- Pulmonary oxygen uptake and muscle deoxygenation kinetics during heavy intensity cycling exercise in patients with emphysema and idiopathic pulmonary fibrosis
- Authors:
- McNarry, Melitta
Harrison, Nicholas
Withers, Tom
Chinnappa, Narendra
Lewis, Michael - Abstract:
- Abstract Background Little is known about the mechanistic basis for the exercise intolerance characteristic of patients with respiratory disease; a lack of clearly defined, distinct patient groups limits interpretation of many studies. The purpose of this pilot study was to investigate the pulmonary oxygen uptake ( V . $$ \overset{.}{V} $$ O2 ) response, and its potential determinants, in patients with emphysema and idiopathic pulmonary fibrosis (IPF). Methods Following a ramp incremental test for the determination of peak V . $$ \overset{.}{V} $$ O2 and the gas exchange threshold, six emphysema (66 ± 7 years; FEV1, 36 ± 16%), five IPF (65 ± 12 years; FEV1, 82 ± 11%) and ten healthy control participants (63 ± 6 years) completed three repeat, heavy-intensity exercise transitions on a cycle ergometer. Throughout each transition, pulmonary gas exchange, heart rate and muscle deoxygenation ([HHb], patients only) were assessed continuously and subsequently modelled using a mono-exponential with ( V . $$ \overset{.}{V} $$ O2, [HHb]) or without (HR) a time delay. Results The V . $$ \overset{.}{V} $$ O2 phase II time-constant (τ) did not differ between IPF and emphysema, with both groups significantly slower than healthy controls (Emphysema, 65 ± 11; IPF, 69 ± 7; Control, 31 ± 7 s;P < 0.05). The HR τ was slower in emphysema relative to IPF, with both groups significantly slower than controls (Emphysema, 87 ± 19; IPF, 119 ± 20; Control, 58 ± 11 s;P < 0.05). In contrast, neither theAbstract Background Little is known about the mechanistic basis for the exercise intolerance characteristic of patients with respiratory disease; a lack of clearly defined, distinct patient groups limits interpretation of many studies. The purpose of this pilot study was to investigate the pulmonary oxygen uptake ( V . $$ \overset{.}{V} $$ O2 ) response, and its potential determinants, in patients with emphysema and idiopathic pulmonary fibrosis (IPF). Methods Following a ramp incremental test for the determination of peak V . $$ \overset{.}{V} $$ O2 and the gas exchange threshold, six emphysema (66 ± 7 years; FEV1, 36 ± 16%), five IPF (65 ± 12 years; FEV1, 82 ± 11%) and ten healthy control participants (63 ± 6 years) completed three repeat, heavy-intensity exercise transitions on a cycle ergometer. Throughout each transition, pulmonary gas exchange, heart rate and muscle deoxygenation ([HHb], patients only) were assessed continuously and subsequently modelled using a mono-exponential with ( V . $$ \overset{.}{V} $$ O2, [HHb]) or without (HR) a time delay. Results The V . $$ \overset{.}{V} $$ O2 phase II time-constant (τ) did not differ between IPF and emphysema, with both groups significantly slower than healthy controls (Emphysema, 65 ± 11; IPF, 69 ± 7; Control, 31 ± 7 s;P < 0.05). The HR τ was slower in emphysema relative to IPF, with both groups significantly slower than controls (Emphysema, 87 ± 19; IPF, 119 ± 20; Control, 58 ± 11 s;P < 0.05). In contrast, neither the [HHb] τ nor [HHb]:O2 ratio differed between patient groups. Conclusions The slower V . $$ \overset{.}{V} $$ O2 kinetics in emphysema and IPF may reflect poorer matching of O2 delivery-to-utilisation. Our findings extend our understanding of the exercise dysfunction in patients with respiratory disease and may help to inform the development of appropriately targeted rehabilitation strategies. … (more)
- Is Part Of:
- BMC pulmonary medicine. Volume 17:Issue 1(2017)
- Journal:
- BMC pulmonary medicine
- Issue:
- Volume 17:Issue 1(2017)
- Issue Display:
- Volume 17, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 17
- Issue:
- 1
- Issue Sort Value:
- 2017-0017-0001-0000
- Page Start:
- 1
- Page End:
- 10
- Publication Date:
- 2017-12
- Subjects:
- Respiratory disease -- V.$$ \overset{.}{V} $$ O2 kinetics -- NIRS -- Cycle
Lungs -- Diseases -- Periodicals
616.24005 - Journal URLs:
- http://www.biomedcentral.com/bmcpulmmed/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=64 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12890-017-0364-z ↗
- Languages:
- English
- ISSNs:
- 1471-2466
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10002.xml