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The implications of dysglycaemia on aerobic exercise and ventilatory function in cystic fibrosis

The implications of dysglycaemia on aerobic exercise and ventilatory function in cystic fibrosis
The implications of dysglycaemia on aerobic exercise and ventilatory function in cystic fibrosis

BACKGROUND: The development of cystic fibrosis (CF)-related diabetes (CFRD) in paediatric groups is associated with a reduced aerobic fitness. However, this has yet to be investigated in adults with more severe lung disease.

METHODS: Cardiopulmonary exercise and glycaemic control tests were retrospectively analysed in 46 adults with CF (age: 26.9 y [range: 16.3-66.5 y]; forced expiratory volume in 1s: 65.3% [range: 26.8-105.7%]; 26 males), diagnosed with CFRD (n = 19), impaired glucose tolerance (IGT; n = 8) or normal glucose tolerance (NGT; n = 19).

RESULTS: Maximal oxygen uptake (V˙O2max) was reduced in adults with IGT and CFRD compared to their age- and gender-matched counterparts with NGT (p < 0.05); however, there was no difference when lung function was included as a covariate (all p > 0.05). V˙O2max was greater in adults who experienced post-reactive hypoglycaemia vs. NGT without hypoglycaemia (p < 0.05). The frequency of ventilatory limitation (84%, 63% and 37%, respectively; p < 0.05) but not ventilation-perfusion mismatch (42%, 38% and 16%, respectively; p > 0.05), was greater with CFRD and IGT vs. NGT. There was also no difference in arterial oxygen saturation changes between groups (p > 0.05). Gender and body mass index were significant predictors of V˙O2max (adjusted R2 = 0.37, p < 0.01), but glycaemic control did not explain additional variance (p > 0.05).

CONCLUSIONS: Adults with CF-related dysglycaemia had a reduced V˙O2max compared to age- and gender-matched counterparts, due to a greater degree of CF lung disease in these populations.

Adult, Cardiorespiratory Fitness/physiology, Correlation of Data, Cystic Fibrosis/diagnosis, Diabetes Mellitus/blood, Exercise/physiology, Exercise Test/methods, Female, Forced Expiratory Volume, Glucose Intolerance/diagnosis, Glucose Tolerance Test/methods, Humans, Male, Oxygen Consumption, Respiratory Function Tests/methods, Retrospective Studies, Severity of Illness Index, United Kingdom/epidemiology
1569-1993
427-433
Causer, Adam J
17d4182a-d52f-4b92-89fc-99cec813e98d
Shute, Janis K
a5eef853-50ae-4abf-9e34-1c873601437f
Cummings, Michael H
49e830d1-aa87-4dd0-8258-35c3d5ac9c35
Shepherd, Anthony I
f7073e22-cda6-4816-a4b4-f6246e1aa42e
Wallbanks, Samuel R
153b083d-fb87-45ad-b571-517f738a2c6c
Allenby, Mark I
f04ca0f2-e772-4fc2-925b-9fae103db2f6
Arregui-Fresneda, Irantzu
437ca897-6ae3-4a6a-8908-a1a14d203c76
Bright, Victoria
b9927700-00e1-489f-a671-27fa7d3d2995
Carroll, Mary P
b836d262-6b07-4006-9c81-26653a26588b
Connett, Gary
55d5676c-90d8-46bf-a508-62eded276516
Daniels, Thomas
d635a2fb-96a1-46ec-8cdf-8eb44a4bd0f5
Meredith, Tom
b7f0ef50-7375-4880-8f84-99aa9332238c
Saynor, Zoe L
ffd5d87a-2cfd-4c83-8f3c-4ef0144c8db8
Causer, Adam J
17d4182a-d52f-4b92-89fc-99cec813e98d
Shute, Janis K
a5eef853-50ae-4abf-9e34-1c873601437f
Cummings, Michael H
49e830d1-aa87-4dd0-8258-35c3d5ac9c35
Shepherd, Anthony I
f7073e22-cda6-4816-a4b4-f6246e1aa42e
Wallbanks, Samuel R
153b083d-fb87-45ad-b571-517f738a2c6c
Allenby, Mark I
f04ca0f2-e772-4fc2-925b-9fae103db2f6
Arregui-Fresneda, Irantzu
437ca897-6ae3-4a6a-8908-a1a14d203c76
Bright, Victoria
b9927700-00e1-489f-a671-27fa7d3d2995
Carroll, Mary P
b836d262-6b07-4006-9c81-26653a26588b
Connett, Gary
55d5676c-90d8-46bf-a508-62eded276516
Daniels, Thomas
d635a2fb-96a1-46ec-8cdf-8eb44a4bd0f5
Meredith, Tom
b7f0ef50-7375-4880-8f84-99aa9332238c
Saynor, Zoe L
ffd5d87a-2cfd-4c83-8f3c-4ef0144c8db8

Causer, Adam J, Shute, Janis K, Cummings, Michael H, Shepherd, Anthony I, Wallbanks, Samuel R, Allenby, Mark I, Arregui-Fresneda, Irantzu, Bright, Victoria, Carroll, Mary P, Connett, Gary, Daniels, Thomas, Meredith, Tom and Saynor, Zoe L (2019) The implications of dysglycaemia on aerobic exercise and ventilatory function in cystic fibrosis. Journal of Cystic Fibrosis, 19 (3), 427-433. (doi:10.1016/j.jcf.2019.09.014).

Record type: Article

Abstract

BACKGROUND: The development of cystic fibrosis (CF)-related diabetes (CFRD) in paediatric groups is associated with a reduced aerobic fitness. However, this has yet to be investigated in adults with more severe lung disease.

METHODS: Cardiopulmonary exercise and glycaemic control tests were retrospectively analysed in 46 adults with CF (age: 26.9 y [range: 16.3-66.5 y]; forced expiratory volume in 1s: 65.3% [range: 26.8-105.7%]; 26 males), diagnosed with CFRD (n = 19), impaired glucose tolerance (IGT; n = 8) or normal glucose tolerance (NGT; n = 19).

RESULTS: Maximal oxygen uptake (V˙O2max) was reduced in adults with IGT and CFRD compared to their age- and gender-matched counterparts with NGT (p < 0.05); however, there was no difference when lung function was included as a covariate (all p > 0.05). V˙O2max was greater in adults who experienced post-reactive hypoglycaemia vs. NGT without hypoglycaemia (p < 0.05). The frequency of ventilatory limitation (84%, 63% and 37%, respectively; p < 0.05) but not ventilation-perfusion mismatch (42%, 38% and 16%, respectively; p > 0.05), was greater with CFRD and IGT vs. NGT. There was also no difference in arterial oxygen saturation changes between groups (p > 0.05). Gender and body mass index were significant predictors of V˙O2max (adjusted R2 = 0.37, p < 0.01), but glycaemic control did not explain additional variance (p > 0.05).

CONCLUSIONS: Adults with CF-related dysglycaemia had a reduced V˙O2max compared to age- and gender-matched counterparts, due to a greater degree of CF lung disease in these populations.

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More information

Published date: 2 November 2019
Additional Information: Crown Copyright © 2019. Published by Elsevier B.V. All rights reserved.
Keywords: Adult, Cardiorespiratory Fitness/physiology, Correlation of Data, Cystic Fibrosis/diagnosis, Diabetes Mellitus/blood, Exercise/physiology, Exercise Test/methods, Female, Forced Expiratory Volume, Glucose Intolerance/diagnosis, Glucose Tolerance Test/methods, Humans, Male, Oxygen Consumption, Respiratory Function Tests/methods, Retrospective Studies, Severity of Illness Index, United Kingdom/epidemiology

Identifiers

Local EPrints ID: 488036
URI: http://eprints.soton.ac.uk/id/eprint/488036
ISSN: 1569-1993
PURE UUID: a5947c11-3c66-422d-a368-48519a96f996
ORCID for Gary Connett: ORCID iD orcid.org/0000-0003-1310-3239

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Date deposited: 12 Mar 2024 18:23
Last modified: 18 Mar 2024 03:46

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Contributors

Author: Adam J Causer
Author: Janis K Shute
Author: Michael H Cummings
Author: Anthony I Shepherd
Author: Samuel R Wallbanks
Author: Mark I Allenby
Author: Irantzu Arregui-Fresneda
Author: Victoria Bright
Author: Mary P Carroll
Author: Gary Connett ORCID iD
Author: Thomas Daniels
Author: Tom Meredith
Author: Zoe L Saynor

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