Key result
12-week vitamin D prevents arterial stiffness, and baseline lipids improve response prediction by ~100%.
Why the study?
Exercise or vitamin D can reduce arterial stiffness, but the underlying mechanisms of lipid metabolism remain unexplored.
Does a 12-week exercise program with or without vitamin D supplementation improve arterial stiffness in patients with Type 2 diabetes mellitus, and can baseline lipidomic profiles predict this response?
RCT
Placebo-controlled
Does a 12-week exercise program with or without vitamin D supplementation improve arterial stiffness in patients with Type 2 diabetes mellitus, and can baseline lipidomic profiles predict this response?
Baseline plasma lipidomic profiles significantly improve the prediction of arterial stiffness reduction in response to exercise and vitamin D interventions in patients with T2DM compared to traditional risk factors.
Answers are grounded in this paper and cite their sources.
Supports vitamin D to prevent arterial stiffness in T2DM; extends lipidomics for predicting individual response.
BACKGROUND: Exercise or vitamin D intervention can reduce the risk of arterial stiffness; however, the underlying mechanisms of lipid metabolism remain unexplored. To examine the effects of a 12-week moderate and vigorous exercise program (65-80% maximal heart rate, 60 min/time, 2~3 times/week) with or without vitamin D supplementation (1000 IU/day) on the reduction in arterial stiffness and further explore whether the effects of interventions could be associated with the basal lipidome among patients with Type 2 diabetes mellitum (T2DM). METHOD: = 16). Arterial stiffness risk factors (ankle-brachial index (ABI); brachial-ankle pulse wave velocity (baPWV), systolic blood pressure (SBP), and diastolic blood pressure (DBP)) were evaluated before and after the intervention. The plasma lipidome was determined using ultra-performance liquid chromatography coupled with tandem mass spectrometry. Machine learning was applied to establish prediction models for the responsiveness to arterial stiffness. We observed high inter-individual variability in the arterial stiffness risk factors in response to the interventions. We also found that optimally selecting the lipid predictors at baseline, such as SM d44:6, LPE 18:2, and Hex2Cer 29:0, could enhance the predictive power by 100% for arm SBP changes in the exercise group. Basal levels of Cer (33:1) and GM3 (44:4) could enhance the predictive power by 100% for changes in baPWV in the vitamin D group. CONCLUSIONS: A 12-week vitamin D supplementation was beneficial in preventing arterial stiffness. Compared with traditional clinical risk factors, specific lipids at baseline could significantly improve the ability to predict intervention-induced changes in the reduction of arterial stiffness.
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He et al. (2024) conducted an RCT in Type 2 diabetes mellitum. Exercise program with or without vitamin D supplementation vs. Placebo was evaluated on Arterial stiffness risk factors (ABI, baPWV, SBP, DBP) (p=0.03). A 12-week vitamin D supplementation prevented arterial stiffness, and specific baseline lipids improved the prediction of intervention-induced changes in arterial stiffness by 100%.
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