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Baseline vitamin D levels linked to semaglutide glycemic and weight outcomes in type 2 diabetes

Baseline vitamin D levels linked to semaglutide glycemic and weight outcomes in type 2 diabetes
Photo by CDC / Unsplash
Key Takeaway
Consider baseline vitamin D status as a potential marker for semaglutide response in type 2 diabetes, noting the observational nature of the evidence.

This was an observational cohort study of 5,384 adults with type 2 diabetes treated with semaglutide at Leumit Health Services. The study compared patients with baseline serum 25-hydroxyvitamin D [25(OH)D] levels ≥25 ng/mL to those with levels <25 ng/mL over a 12-month follow-up period.

Patients with 25(OH)D levels ≥25 ng/mL had greater reductions in HbA1c (β = −0.083 and β = −0.096) compared to those with levels <25 ng/mL. The 95% confidence intervals were (−0.154 to −0.013), p=0.020, and (−0.173 to −0.017), p=0.016. For BMI, greater reductions were also observed (β = −1.02 and β = −1.29), with 95% CIs of (−1.46 to −0.58) and (−1.77 to −0.80); both p<0.001. Absolute numbers for these changes were not reported.

Safety and tolerability data, including adverse events and discontinuations, were not reported. Key limitations include the retrospective design, single health service setting, no randomization, and potential unmeasured confounding. The practice relevance is that baseline vitamin D status may help identify patients with better glycemic and weight loss responses to semaglutide, but the association does not imply causation.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
Semaglutide, a glucagon-like peptide-1 receptor agonist, is an established therapy for type 2 diabetes (T2D), offering robust glycemic control and weight reduction. Vitamin D has been implicated in metabolic regulation, yet its influence on semaglutide-induced outcomes remains unclear. We conducted a retrospective cohort study of 5,384 adults with T2D, enrolled in Leumit Health Services, who initiated semaglutide therapy between February 1, 2019, and December 31, 2022. All patients had documented serum 25-hydroxyvitamin D [25(OH)D] levels prior to treatment initiation. Metabolic outcomes- including glycemic control (HbA1c), body mass index (BMI), and lipid profile- were assessed at 12 months. Associations between baseline 25(OH)D levels and metabolic changes were evaluated using multivariable regression models, adjusted for demographic and clinical covariates. The median baseline 25(OH)D level was 19.3 ng/mL. Compared with patients with 25(OH)D levels 25 ng/mL exhibited greater reductions in HbA1c [β = −0.083, 95% CI (−0.154 to −0.013), p = 0.020; and β = −0.096, 95% CI (−0.173 to −0.017), p = 0.016, respectively] and BMI [β = −1.02, 95% CI (−1.46 to −0.58); and β = −1.29, 95% CI (−1.77 to −0.80); both p  Higher baseline 25(OH)D levels are independently associated with improved glycemic and weight loss responses to semaglutide in individuals with T2D. Prospective trials are warranted to explore whether vitamin D supplementation may potentiate semaglutide’s metabolic effects.
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