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Sökning: WFRF:(Ahren I. L.)

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1.
  • Jansson, Per-Anders, 1961, et al. (författare)
  • Probiotic treatment using a mix of three Lactobacillus strains for lumbar spine bone loss in postmenopausal women: a randomised, double-blind, placebo-controlled, multicentre trial
  • 2019
  • Ingår i: Lancet Rheumatology. - : Elsevier BV. - 2665-9913. ; 1:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Background Postmenopausal bone loss in the spine is associated with an increased risk of vertebral fractures. Certain probiotic treatment protects rodents from ovariectomy-induced bone loss. The aim of the present study was to determine if treatment with a combination of three bacterial strains protects against the rapid spine bone loss occurring in healthy early postmenopausal women. Methods This randomised, double-blind, placebo-controlled, multicentre trial was done at four study centres in Sweden. Early postmenopausal women were randomly assigned in a 1:1 ratio to receive probiotic treatment consisting of three Lactobacillus strains (Lactobacillus paracasei DSM 13434, Lactobacillus plantarum DSM 15312, and Lactobacillus plantarum DSM 15313; 1 x 10(10 )colony-forming units per capsule) or placebo once daily for 12 months. The primary outcome was the percentage change from baseline in lumbar spine bone mineral density (LS-BMD) at 12 months. The primary analysis was done in all participants with BMD measurements available both at baseline and at 12 months. Analyses of adverse events and safety included all participants who had taken at least one capsule of placebo or Lactobacillus. This trial is registered with ClinicalTrials.gov, NCT02722980, and is completed. Findings Between April 18 and Nov 11,2016,249 participants were randomly assigned to receive probiotic product or placebo, and 234 (94%) completed the analyses required for the primary outcome. Lactobacillus treatment reduced the LS-BMD loss compared with placebo (mean difference 0.71%, 95% CI 0.06 to 1.35). The LS-BMD loss was significant in the placebo group (-0.72%, -1.22 to -0.22), whereas no bone loss was observed in the Lactobacillus-treated group (-0.01%, -0.50 to 0.48). The adverse events were similar between the two groups. Interpretation Probiotic treatment using a mix of three Lactobacillus strains protects against lumbar spine bone loss in healthy postmenopausal women. Copyright (C) 2019 Elsevier Ltd. All rights reserved.
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2.
  • Rask, Carola, 1970, et al. (författare)
  • Differential effect on cell-mediated immunity in human volunteers after intake of different lactobacilli
  • 2013
  • Ingår i: Clinical and Experimental Immunology. - : Oxford University Press (OUP). - 0009-9104 .- 1365-2249. ; 172:2, s. 321-332
  • Tidskriftsartikel (refereegranskat)abstract
    • Probiotics are live microorganisms which have beneficial effects on the host when ingested in adequate amounts. Probiotic bacteria may stimulate immune effector functions in a strain-specific manner. In this blind placebo-controlled trial, we investigated the effects on the immune system following daily intake of six different strains of lactobacilli or the Gram-negative bacterium Pseudomonas lundensis for 2 or 5 weeks. Blood lymphocyte subsets were quantified by fluorescence activated cell sorter and the expression of activation and memory markers was determined. The bacterial strains were also examined for their capacity to adhere to human intestinal cells and to be phagocytosed by human peripheral blood mononuclear cells. Intake of Lactobacillus plantarum strain 299v increased the expression of the activation marker CD25 (P=0·01) on CD8+ T cells and the memory cell marker CD45RO on CD4+ T cells (P=0·03), whereas intake of L. paracasei tended to expand the natural killerT (NKT) cell population (P=0·06). The phagocytic activity of granulocytes was increased following intake of L. plantarum 299v, L. plantarumHEAL, L. paracasei or L. fermentum. In contrast, ingestion of L. rhamnosus decreased the expression of CD25 and CD45RO significantly within the CD4+ cell population. The observed immune effects after in-vivo administration of the probiotic bacteria could not be predicted by either their adherence capacity or the in-vitro-induced cytokine production. The stimulation of CD8+ T cells and NKT cells suggests that intake of probiotic bacteria may enhance the immune defence against, e.g. viral infections or tumours.
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