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May 8, 2026Frontiers in Endocrinology3 citationsOpen Access

Effect of probiotics derivatives (postbiotics and metabiotics) on glycemic control in individuals with type 2 diabetes: a randomized clinical trial (DELIDiab study)

MSMaryana SavytskaOBO. BakaЕМЕліна Манжалій

Key Points

  • This trial aims to evaluate the short-term safety and effectiveness of Lactobacillus rhamnosus DV lysate in improving glycemic control in individuals with type 2 diabetes.
  • Randomized, double-blind, placebo-controlled clinical trial enrolling 55 participants with type 2 diabetes.
  • Participants received 100 mg of L. rhamnosus DV lysate or placebo twice daily for 3 months, with follow-up for 3 months.
  • Primary endpoints were measured using HbA1c and fasting plasma glucose after treatment.
  • Intervention group showed a significant reduction in HbA1c of –0.63% (95% CI: –0.98 to –0.28, p<0.001).
  • Fasting plasma glucose showed a favorable trend with a reduction of 1.32 mmol/L in the active group compared to an increase of 0.12 mmol/L in the placebo (p=0.086).
  • Significant effects on waist circumference (p=0.021) and insulin sensitivity (%S, p=0.013) were also observed.

Abstract

Introduction Probiotics have demonstrated positive effects on obesity and type 2 diabetes (T2D) in various studies. Postbiotics, specifically nonliving bacterial lysates derived from cell walls and DNA, are increasingly recognized as safe, stable, and effective alternatives for improving host metabolic health. Aim to conduct a randomized, double-blind, placebo-controlled clinical trial (RCT) to assess the short-term safety and effectiveness of the bacterial lysate of Lactobacillus (L.) rhamnosus DV - NRRL B-68023 as an adjunct to standard antidiabetic therapy. Material and methods Fifty-five participants with T2D were enrolled and assigned via computer-generated randomization to receive either 100 mg of L. rhamnosus DV lysate twice daily or a matching placebo. Blinding was ensured through identical masked packaging. The primary efficacy analysis was performed on a per-protocol (PP) population of 42 participants (intervention, n=20; placebo, n=22) who completed the 3-month treatment and 3-month follow-up. Primary endpoints were HbA1c and fasting plasma glucose (FPG). Secondary endpoints included HOMA-2 modeled insulin sensitivity (%S), β-cell function (%B), and anthropometric parameters, evaluated at baseline, 3, and 6 months. The trial was registered at ClinicalTrials.gov (NCT05770076). Results The primary analysis revealed a significant overall treatment effect for HbA1c (p0.001). After 3 months, the intervention group showed a mean HbA1c reduction of –0.63% (95% CI: –0.98 to –0.28), while the placebo group significantly worsened (0.50%; 95% CI: 0.17 to 0.84). For FPG, a favorable between-group trend was observed (p=0.086), with a reduction of 1.32 mmol/L in the active group compared to an increase of 0.12 mmol/L in the placebo group. Exploratory analysis showed significant treatment effects for waist circumference (p = 0.021) and insulin sensitivity (%S, p = 0.013). Although within-group improvements were noted for BMI and β-cell function (%B) in the intervention group (p0.05), between-group differences for these parameters were not statistically significant (p0.05). Conclusions Three-month supplementation with L. rhamnosus DV lysate significantly improves glycemic control (HbA1c) and reduces waist circumference compared to placebo in T2D patients. While positive trends in insulin sensitivity and anthropometrics were observed, further large-scale studies are required to confirm these metabolic benefits and assess long-term sustainability. Clinical Trial Registration https://clinicaltrials.gov/keywords , identifier NCT05770076.

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Cite This Study

Savytska et al. (2026) studied this question.

synapsesocial.com/papers/69fd7d4abfa21ec5bbf05c72https://doi.org/10.3389/fendo.2026.1802045
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