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KPV

Lys-Pro-Val, α-MSH (11-13)

Quick Stats
Studies 104
Trials 57
Score 2
2024 pubmed 6 citations

The Efficacy and Safety of Probiotic Combinations Lobun Forte® Versus Renadyl® in Patients With Chronic Kidney Disease: A Comparative, Phase IV, Randomized, Open-Label, Active-Controlled, Parallel Study.

Kalidindi. Raja Karthik RK; Reddy. C Prabhakar CP; Pv. Kishan K; Kompella. Prasad P

Key Findings

  • Both Lobun Forte and Renadyl significantly improved SF‑8 quality‑of‑life scores (~53% increase)
  • Both reduced blood urea nitrogen, serum creatinine, and increased eGFR (≈40% rise)
  • Lobun Forte lowered uric acid and hs‑CRP significantly; Renadyl lowered p‑cresyl sulfate significantly

Practical Outcomes

  • If you have stage 3‑4 chronic kidney disease, taking a high‑dose multi‑strain probiotic (about 45 billion CFU per capsule, twice daily) may help slow disease progression and improve wellbeing. For healthy individuals, the data are less relevant, but it suggests gut‑kidney axis modulation could be a future strategy for kidney support.

Summary

A study compared two probiotic mixes in people with moderate to severe kidney disease and found both improved quality of life, lowered harmful waste products, and boosted kidney function without major side effects. The differences between the two products were small, so either could be useful for kidney patients looking for a gut‑health boost.

Abstract

Chronic kidney disease (CKD) often leads to gut microbiota imbalance, accelerating disease progression and increasing uremic toxins and inflammation. We conducted a randomized clinical trial comparing outcomes between two multi-strain probiotic supplements Lobun Forte&#xae; (Sanzyme P Ltd, Hyderabad, India) containing <i>Streptococcus thermophilus</i>, <i>Lactobacillus acidophilus</i>, <i>Bifidobacterium longum</i>, and <i>Bacillus coagulans</i> and Renadyl<sup>&#xae;</sup> (Kibow Biotech, LLC., Pennsylvania, United States) containing <i>S. thermophilus</i>, <i>L. acidophilus,</i> and <i>B. longum</i>. Sixty patients with stage 3-4 CKD were randomized to receive either Lobun Forte (n=30) or Renadyl (n=30) for six months, with each supplement providing 45 billion CFU/capsule, twice daily. Primary outcomes included quality of life (QoL) (Short-Form 8 (SF-8) score), reductions in uremic toxins (p-cresyl sulfate (PCS), 3-indoxyl sulfate (IS), indole-3-acetic acid (IAA)), blood urea nitrogen (BUN), serum creatinine, and serum uric acid. Secondary outcomes assessed oxidative stress, inflammatory biomarkers, and estimated glomerular filtration rate (eGFR). <i>Results</i>: Both Lobun Forte and Renadyl groups showed significant improvements in QoL, with Lobun Forte achieving a 53.5% improvement (16.43 point increase) and Renadyl a 51.1% improvement (15.27 point increase) in SF-8 scores (p &lt; 0.0001). The&#xa0;levels of IS decreased significantly in both groups (p &lt; 0.0001), with Lobun Forte reducing IS by 29.72% and Renadyl by 24.20%. In terms of other uremic toxins, Lobun Forte showed non-significant (p &gt; 0.05) reductions in mean PCS (7.63%) and IAA (15.57%), whereas Renadyl demonstrated a significant (p = 0.0314) decrease in PCS (20.75%) and a non-significant (p &gt; 0.05) reduction in IAA (12.35%). Both groups showed significant (p &lt; 0.0001) reductions in BUN and serum creatinine levels. Serum uric acid levels showed a significant (p = 0.0448) reduction with Lobun Forte while Renadyl exhibited a non-significant reduction (p = 0.1034). Lobun Forte significantly (p = 0.0359) reduced mean high-sensitivity C-reactive protein (hsCRP) levels, while Renadyl showed a non-significant reduction (p = 0.0876). Both groups had non-significant reductions in interleukin-6 and tumor necrosis factor-alpha levels (p &gt; 0.05). Further, both groups experienced significant (p &lt; 0.0001) increases in mean glutathione levels and nitric oxide levels. Additionally, Renadyl resulted in a significant reduction in mean malondialdehyde, whereas Lobun Forte showed a non-significant reduction. Both probiotics significantly (p &lt; 0.0001) improved eGFR, with Lobun Forte increasing it by 40.4% and Renadyl by 36.9%. Both probiotics were well tolerated, with a favorable safety profile throughout the study. <i>Conclusion</i>: Both Lobun Forte and Renadyl effectively improve the quality of life in patients with stage 3-4 CKD by modulation of uremic toxins, renal parameters, inflammatory biomarkers, oxidative biomarkers, and eGFR. These findings suggest that both probiotics may help delay CKD progression by modulating the gut-kidney axis.

Study Information

Provider

pubmed

Year

2024

Date

2024-08-28T00:00:00.000Z

DOI

10.7759/cureus.67987

Citations

6

References

27