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The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes
The aim of this study was to investigate the associations of accelerometer-assessed sedentary time and breaks in sedentary time with 24-h events and duration of hypoglycaemia (<3.9 mmol/l), euglycaemia (3.9–7.8 mmol/l), hyperglycaemia (>7.8 mmol/l) and above target glucose (>9 mmol/l). Thir...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134430/ https://www.ncbi.nlm.nih.gov/pubmed/30214853 http://dx.doi.org/10.1016/j.pmedr.2018.09.002 |
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author | Paing, Aye C. McMillan, Kathryn A. Kirk, Alison F. Collier, Andrew Hewitt, Allan Chastin, Sebastien F.M. |
author_facet | Paing, Aye C. McMillan, Kathryn A. Kirk, Alison F. Collier, Andrew Hewitt, Allan Chastin, Sebastien F.M. |
author_sort | Paing, Aye C. |
collection | PubMed |
description | The aim of this study was to investigate the associations of accelerometer-assessed sedentary time and breaks in sedentary time with 24-h events and duration of hypoglycaemia (<3.9 mmol/l), euglycaemia (3.9–7.8 mmol/l), hyperglycaemia (>7.8 mmol/l) and above target glucose (>9 mmol/l). Thirty-seven participants with type 2 diabetes (age, 62.8 ± 10.5 years; body mass index, 29.6 ± 6.8 kg/m(2)) in Glasgow, United Kingdom were enrolled between February 2016 and February 2017. Participants wore an activity monitor (activPAL3) recording the time and pattern of sedentary behaviour and a continuous glucose monitoring (CGM, Abbott FreeStyle Libre) for up to 14 days. Linear regression analyses were used to investigate the associations. Participants spent 3.7%, 64.7%, 32.1% and 19.2% of recording h/day in hypoglycaemia, euglycaemia, hyperglycaemia and above target, respectively. There was a negative association between sedentary time and time in euglycaemia (β = −0.44, 95% CI −0.86; −0.03, p = 0.04). There was a trend towards a positive association between sedentary time and time in hyperglycaemia (β = 0.36, 95% CI −0.05; 0.78, p = 0.08). Breaks in sedentary time was associated with higher time in euglycaemia (β = 0.38, 95% CI 0.00; 0.75, p = 0.04). To conclude, in individuals with type 2 diabetes, more time spent in unbroken and continuous sedentary behaviour was associated with poorer glucose control. Conversely, interrupting sedentary time with frequent breaks appears to improve glycaemic control. Therefore, this should be considered as a simple adjunct therapy to improve clinical outcomes in type 2 diabetes. |
format | Online Article Text |
id | pubmed-6134430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61344302018-09-13 The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes Paing, Aye C. McMillan, Kathryn A. Kirk, Alison F. Collier, Andrew Hewitt, Allan Chastin, Sebastien F.M. Prev Med Rep Regular Article The aim of this study was to investigate the associations of accelerometer-assessed sedentary time and breaks in sedentary time with 24-h events and duration of hypoglycaemia (<3.9 mmol/l), euglycaemia (3.9–7.8 mmol/l), hyperglycaemia (>7.8 mmol/l) and above target glucose (>9 mmol/l). Thirty-seven participants with type 2 diabetes (age, 62.8 ± 10.5 years; body mass index, 29.6 ± 6.8 kg/m(2)) in Glasgow, United Kingdom were enrolled between February 2016 and February 2017. Participants wore an activity monitor (activPAL3) recording the time and pattern of sedentary behaviour and a continuous glucose monitoring (CGM, Abbott FreeStyle Libre) for up to 14 days. Linear regression analyses were used to investigate the associations. Participants spent 3.7%, 64.7%, 32.1% and 19.2% of recording h/day in hypoglycaemia, euglycaemia, hyperglycaemia and above target, respectively. There was a negative association between sedentary time and time in euglycaemia (β = −0.44, 95% CI −0.86; −0.03, p = 0.04). There was a trend towards a positive association between sedentary time and time in hyperglycaemia (β = 0.36, 95% CI −0.05; 0.78, p = 0.08). Breaks in sedentary time was associated with higher time in euglycaemia (β = 0.38, 95% CI 0.00; 0.75, p = 0.04). To conclude, in individuals with type 2 diabetes, more time spent in unbroken and continuous sedentary behaviour was associated with poorer glucose control. Conversely, interrupting sedentary time with frequent breaks appears to improve glycaemic control. Therefore, this should be considered as a simple adjunct therapy to improve clinical outcomes in type 2 diabetes. Elsevier 2018-09-05 /pmc/articles/PMC6134430/ /pubmed/30214853 http://dx.doi.org/10.1016/j.pmedr.2018.09.002 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Paing, Aye C. McMillan, Kathryn A. Kirk, Alison F. Collier, Andrew Hewitt, Allan Chastin, Sebastien F.M. The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
title | The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
title_full | The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
title_fullStr | The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
title_full_unstemmed | The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
title_short | The associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
title_sort | associations of sedentary time and breaks in sedentary time with 24-hour glycaemic control in type 2 diabetes |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134430/ https://www.ncbi.nlm.nih.gov/pubmed/30214853 http://dx.doi.org/10.1016/j.pmedr.2018.09.002 |
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