Publikasi Scopus 2010 s/d 2022

Widhani A., Djauzi S., Suyatna F.D., Dewi B.E.
57202561455;23495847800;56039633100;24076058600;
Changes in Gut Microbiota and Systemic Inflammation after Synbiotic Supplementation in Patients with Systemic Lupus Erythematosus: A Randomized, Double-Blind, Placebo-Controlled Trial
2022
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11
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Allergy and Clinical Immunology Division, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia; Dr. Cipto Mangunkusumo Hospital, Jakarta, 10430, Indonesia; Doctoral Program in Biomedical Science, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia; Department of Pharmacology and Therapeutics, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia; Department of Microbiology, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia
Widhani, A., Allergy and Clinical Immunology Division, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia, Dr. Cipto Mangunkusumo Hospital, Jakarta, 10430, Indonesia, Doctoral Program in Biomedical Science, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia; Djauzi, S., Allergy and Clinical Immunology Division, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia, Dr. Cipto Mangunkusumo Hospital, Jakarta, 10430, Indonesia; Suyatna, F.D., Department of Pharmacology and Therapeutics, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia; Dewi, B.E., Department of Microbiology, Faculty of Medicine, Universitas Indonesia, Jakarta, 10430, Indonesia
Gut dysbiosis has a role in the pathogenesis of lupus. Synbiotic supplementation may restore the balance of gut microbiota. This study investigated whether synbiotics could improve gut microbiota and systemic inflammation in lupus patients. This randomized, double-blind, placebo-controlled trial was conducted in adult systemic lupus erythematosus (SLE) patients. Subjects were randomized to receive either synbiotics or a placebo. Fecal microbiota, hs-CRP, IL-6, and IL-17 were measured at baseline and after 60 days. Patients who fulfilled the inclusion criteria were randomized into synbiotic (n = 23) and placebo groups (n = 23). In the synbiotic group, hs-CRP was not significantly increased (1.8 [0.9; 4.85] vs. 2.1 [0.9; 4.25] mg/L; pre vs. post; p = 0.23), whereas in the placebo group hs-CRP was increased significantly (1.75 [0.4; 4.45] vs. 3.75 [0.58; 7.05] mg/L; pre vs. post; p = 0.005). In the synbiotic group, IL-6 decreased significantly (8.76 [6.62; 11.39] vs. 6.59 [4.96; 8.01]; pre vs. post; p = 0.02), while there was no significant change in IL-17 level. In the placebo group, there was no significant change in IL-6 and IL-17. Synbiotic supplementation increased the Firmicutes:Bacteroidetes ratio (0.05 ± 0.60 vs. −0.08 ± 0.63, synbiotic vs. placebo p = 0.48) and butyrate metabolism (p = 0.037) and decreased amino sugar and nucleotide sugar metabolism (p = 0.040). There was improvement in the SLE disease activity index 2K (SLEDAI-2K) score in the synbiotic group (14 [9; 16] vs. 8 [2; 12]; pre vs. post; p < 0.001), while no change in the placebo group (9 [8; 18.25] vs. 9 [5.5; 15]; pre vs. post; p = 0.31). Synbiotic supplementation could reduce systemic inflammation and SLE disease activity and alter the composition and functions of gut microbiota. © 2022 by the authors.
inflammation; microbiota; probiotic; synbiotic; systemic lupus erythematosus
alpha tocopherol; azathioprine; butyric acid; C reactive protein; cyclosporine; fructose oligosaccharide; hydroxychloroquine; hydroxymethylglutaryl coenzyme A reductase inhibitor; interleukin 17; interleukin 6; mycophenolic acid; polyunsaturated fatty acid; prednisone; proton pump inhibitor; retinol; RNA 16S; steroid; synbiotic agent; vitamin D; zinc; abdominal pain; adult; alpha diversity; Article; Bacteroidetes; Bifidobacterium bifidum R0071; Bifidobacterium infantis R0033; bloating; body mass; Chao1 index; chronic inflammation; clinical article; colony forming unit; comparative study; constipation; controlled study; diarrhea; diet composition; diet supplementation; DNA extraction; double blind procedure; dysbiosis; dyspnea; energy; enzyme linked immunosorbent assay; feces analysis; fema
Universitas Indonesia
The manuscript preparation and publication were funded by a grant from Universitas Indonesia (NKB-4425/UN2.RST/HKP.05.00/2020).
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20734409
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