Effects of different doses of exercise in adjunct to diet-induced weight loss on the AGE-RAGE axis in patients with short standing type 2 diabetes: Secondary analysis of the DOSE-EX multi-arm, parallel-group, randomised trial

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Aims/hypothesis
These secondary analyses aimed to investigate the effects of different volumes of exercise in adjunct to diet-induced weight loss and standard care on advanced glycation end-products (AGEs) and receptor for AGE (RAGE). We hypothesized that exercise in adjunct to a diet-induced weight loss would dose-dependently increase the soluble decoy receptor for AGE (sRAGE) more than diet-induced weight loss and standard care alone. Secondarily, we expected changes in sRAGE to be associated with improved glycaemic control and inversely associated with low-grade inflammation.

Methods
The DOSE-EX study was a 16-week parallel-group, 4-arm, single-centre, assessor-blinded, randomised, controlled trial (NCT03769883). We included persons living with T2D, duration ≤7 years, BMI >27 kg/m2 and <40 kg/m2, without severe diabetic complications. Participants were randomised (1:1:1:1) to either 1) standard care as control (CON), 2) standard care + diet (DCON), 3) standard care + diet + moderate exercise dose (MED) or 4) standard care + diet + high exercise dose (HED). Standard care included algorithm-guided pharmacological treatment. The diet intervention aimed at 25% reduced energy intake. The supervised exercise sessions included two aerobic sessions + one combined (aerobic and resistance training) session per week for the MED group, and four aerobic sessions + two combined sessions per week for the HED group. Primary outcome was the change in sRAGE from baseline to 16-week follow-up. Secondary outcomes encompassed changes in advanced glycation endproducts (AGE), glycaemic control and markers of low-grade inflammation.

Results
A total of 80 participants (CON: n = 20, DCON: n = 19, MED: n = 20, HED: n = 21) were included in this secondary analysis. The mean age was 58.3 years (SD 9.9), 53% males, and median T2D duration was 4.1 years (IQR 2.0–5.5). No change in sRAGE was observed in any of the groups from baseline to follow-up (p > 0.05).

Conclusion/interpretation
A 16-week intervention with either three or six exercise sessions per week in adjunct to diet-induced weight loss did not change the levels of sRAGE in persons living with well-regulated, short standing T2D.
OriginalsprogEngelsk
TidsskriftFree Radical Biology and Medicine
Vol/bind208
Sider (fra-til)52-61
Antal sider10
ISSN0891-5849
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
HEP and ELL received an unrestricted research grant from Boehringer Ingelheim for an unrelated investigator-initiated study. TPA holds stocks in NovoNordisk. None of the other authors declare any activities or relationships that can bias, or be perceived to bias, their work.

Funding Information:
The Centre for Physical Activity Research is supported by TrygFonden (grants ID 101390, ID 20045, and ID 125132) and the study was supported by grants from TrygFonden (grant ID124708) and Svend Andersen Fonden. MPPL was supported by a research grant from the Danish Diabetes Academy, which is funded by the Novo Nordisk Foundation, grant number NNF17SA0031406. CD was supported by the Canadian Institutes of Health Research (MFE-176582).HEP and ELL received an unrestricted research grant from Boehringer Ingelheim for an unrelated investigator-initiated study. TPA holds stocks in NovoNordisk. None of the other authors declare any activities or relationships that can bias, or be perceived to bias, their work.

Funding Information:
The Centre for Physical Activity Research is supported by TrygFonden (grants ID 101390 , ID 20045 , and ID 125132 ) and the study was supported by grants from TrygFonden (grant ID124708 ) and Svend Andersen Fonden . MPPL was supported by a research grant from the Danish Diabetes Academy , which is funded by the Novo Nordisk Foundation , grant number NNF17SA0031406 . CD was supported by the Canadian Institutes of Health Research ( MFE-176582 ).

Publisher Copyright:
© 2023 Elsevier Inc.

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