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Correction of Colonic Microbiota Dysbiosis Using Synbiotics in Patients with Concurrent Obesity and Chronic Kidney Disease: Clinical Evidence, Mechanistic Insights, and Therapeutic Prospects

Charos Abdudjalilovna AbdullayevaMD, Dr. Sci. (Medicine), Tashkent State Medical University, Tashkent, UzbekistanMalika Sanjarovna IslamovaPhD, Tashkent State Medical University, Tashkent, UzbekistanЗакирова Гульноза АлишеровнаDSc, Tashkent State Medical University, Tashkent, UzbekistanGulnoza Pulatovna AkbarovaPhD, Tashkent State Medical University, Tashkent, UzbekistanBuranova Dilfuza DjamalovnaPhD, Tashkent State Medical University, Tashkent, UzbekistanIrisov Djamshid BahodirovichPhD, Tashkent State Medical University, Tashkent, Uzbekistan
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Background: The coexistence of obesity and chronic kidney disease (CKD) is increasingly recognized as a clinically complex syndrome mediated, in part, by profound gut microbiota dysbiosis. Synbiotics—combined preparations of probiotics and prebiotics—represent a rational intervention capable of targeting microbial composition, intestinal barrier integrity, and host immune modulation. Methods: A prospective, randomized, double-blind, placebo-controlled trial was conducted in 120 adult patients (BMI ≥30 kg/m², eGFR 15–59 mL/min/1.73 m²) over 12 weeks. Participants received either a multi-strain synbiotic formulation (Lactobacillus acidophilus NCFM, Bifidobacterium longum BB536, Lactobacillus rhamnosus GG, 10¹⁰ CFU/day + 10 g fructooligosaccharides) or matched placebo. Results: Synbiotic supplementation significantly increased microbiota alpha diversity (Shannon index: +1.23±0.31 vs. −0.04±0.18; p<0.001) and reduced serum indoxyl sulfate by 28.4% (p<0.001), p-cresyl sulfate by 24.1% (p=0.003), and hs-CRP by 31.2% (p<0.001). The rate of eGFR decline was attenuated (−1.2 vs. −3.8 mL/min/1.73 m²; p=0.007). Significant improvements in BMI, HOMA-IR, and SF-36 vitality scores were also recorded. Conclusion: Synbiotic supplementation produces clinically meaningful improvements in gut microbiota composition, uremic toxin burden, systemic inflammation, and renal functional trajectory in obesity-CKD comorbidity, supporting their integration into multimodal management protocols pending confirmation in larger trials.

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