Compositional analysis of the associations between 24-h movement behaviours and cardio-metabolic risk factors in overweight and obese adults with pre-diabetes from the PREVIEW study: cross-sectional baseline analysis.


Journal

The international journal of behavioral nutrition and physical activity
ISSN: 1479-5868
Titre abrégé: Int J Behav Nutr Phys Act
Pays: England
ID NLM: 101217089

Informations de publication

Date de publication:
04 03 2020
Historique:
received: 14 10 2019
accepted: 17 02 2020
entrez: 6 3 2020
pubmed: 7 3 2020
medline: 2 9 2020
Statut: epublish

Résumé

Physical activity, sedentary time and sleep have been shown to be associated with cardio-metabolic health. However, these associations are typically studied in isolation or without accounting for the effect of all movement behaviours and the constrained nature of data that comprise a finite whole such as a 24 h day. The aim of this study was to examine the associations between the composition of daily movement behaviours (including sleep, sedentary time (ST), light intensity physical activity (LIPA) and moderate-to-vigorous activity (MVPA)) and cardio-metabolic health, in a cross-sectional analysis of adults with pre-diabetes. Further, we quantified the predicted differences following reallocation of time between behaviours. Accelerometers were used to quantify daily movement behaviours in 1462 adults from eight countries with a body mass index (BMI) ≥25 kg·m Replacing MVPA with any other behaviour around the mean composition was associated with a poorer cardio-metabolic risk profile. Conversely, when MVPA was increased, the relationships with cardiometabolic risk markers was favourable but with smaller predicted changes than when MVPA was replaced. Further, substituting ST with LIPA predicted improvements in cardio-metabolic risk markers, most notably insulin and HOMA-IR. This is the first study to use compositional analysis of the 24 h movement composition in adults with overweight/obesity and pre-diabetes. These findings build on previous literature that suggest replacing ST with LIPA may produce metabolic benefits that contribute to the prevention and management of type 2 diabetes. Furthermore, the asymmetry in the predicted change in risk markers following the reallocation of time to/from MVPA highlights the importance of maintaining existing levels of MVPA. ClinicalTrials.gov (NCT01777893).

Sections du résumé

BACKGROUND
Physical activity, sedentary time and sleep have been shown to be associated with cardio-metabolic health. However, these associations are typically studied in isolation or without accounting for the effect of all movement behaviours and the constrained nature of data that comprise a finite whole such as a 24 h day. The aim of this study was to examine the associations between the composition of daily movement behaviours (including sleep, sedentary time (ST), light intensity physical activity (LIPA) and moderate-to-vigorous activity (MVPA)) and cardio-metabolic health, in a cross-sectional analysis of adults with pre-diabetes. Further, we quantified the predicted differences following reallocation of time between behaviours.
METHODS
Accelerometers were used to quantify daily movement behaviours in 1462 adults from eight countries with a body mass index (BMI) ≥25 kg·m
RESULTS
Replacing MVPA with any other behaviour around the mean composition was associated with a poorer cardio-metabolic risk profile. Conversely, when MVPA was increased, the relationships with cardiometabolic risk markers was favourable but with smaller predicted changes than when MVPA was replaced. Further, substituting ST with LIPA predicted improvements in cardio-metabolic risk markers, most notably insulin and HOMA-IR.
CONCLUSIONS
This is the first study to use compositional analysis of the 24 h movement composition in adults with overweight/obesity and pre-diabetes. These findings build on previous literature that suggest replacing ST with LIPA may produce metabolic benefits that contribute to the prevention and management of type 2 diabetes. Furthermore, the asymmetry in the predicted change in risk markers following the reallocation of time to/from MVPA highlights the importance of maintaining existing levels of MVPA.
TRIAL REGISTRATION
ClinicalTrials.gov (NCT01777893).

Identifiants

pubmed: 32131847
doi: 10.1186/s12966-020-00936-5
pii: 10.1186/s12966-020-00936-5
pmc: PMC7055067
doi:

Substances chimiques

Blood Glucose 0

Banques de données

ClinicalTrials.gov
['NCT01777893']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

29

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Auteurs

Nils Swindell (N)

Engineering East, Swansea University, Fabian Way, Crymlyn Burrows, Skewen, Swansea, Wales, SA1 8EN. n.j.swindell@swansea.ac.uk.

Paul Rees (P)

Engineering East, Swansea University, Fabian Way, Crymlyn Burrows, Skewen, Swansea, Wales, SA1 8EN.

Mikael Fogelholm (M)

University of Helsinki, Helsinki, Finland.

Mathijs Drummen (M)

Maastricht University, Maastricht, Netherlands.

Ian MacDonald (I)

University of Nottingham, Nottingham, UK.

J Alfredo Martinez (JA)

Centre for Nutrition Research, University of Navarra (UNAV), Pamplona, Spain.
CIBERObn, Instituto de Salud Carlos III, Madrid, Spain.
IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.
Program for Precision Nutrition, IMDEA Food Institute, Madrid, Spain.

Santiago Navas-Carretero (S)

Centre for Nutrition Research, University of Navarra (UNAV), Pamplona, Spain.
CIBERObn, Instituto de Salud Carlos III, Madrid, Spain.
IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.

Teodora Handjieva-Darlenska (T)

Medical University of Sofia, Sofia, Bulgaria.

Nadka Boyadjieva (N)

Medical University of Sofia, Sofia, Bulgaria.

Georgi Bogdanov (G)

Medical University of Sofia, Sofia, Bulgaria.

Sally D Poppitt (SD)

Human Nutrition Unit, School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Nicholas Gant (N)

Human Nutrition Unit, School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Marta P Silvestre (MP)

Human Nutrition Unit, School of Biological Sciences, University of Auckland, Auckland, New Zealand.

Jennie Brand-Miller (J)

University of Sydney, Sydney, Australia.

Wolfgang Schlicht (W)

University of Stuttgart, Stuttgart, Germany.

Roslyn Muirhead (R)

University of Sydney, Sydney, Australia.

Shannon Brodie (S)

University of Sydney, Sydney, Australia.

Heikki Tikkanen (H)

University of Eastern Finland, Kuopio, Finland.

Elli Jalo (E)

University of Helsinki, Helsinki, Finland.

Margriet Westerterp-Plantenga (M)

Maastricht University, Maastricht, Netherlands.

Tanja Adam (T)

Maastricht University, Maastricht, Netherlands.

Pia Siig Vestentoft (PS)

University of Copenhagen, Copenhagen, Denmark.

Thomas M Larsen (TM)

University of Copenhagen, Copenhagen, Denmark.

Anne Raben (A)

University of Copenhagen, Copenhagen, Denmark.

Gareth Stratton (G)

Engineering East, Swansea University, Fabian Way, Crymlyn Burrows, Skewen, Swansea, Wales, SA1 8EN.

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Classifications MeSH