4.6 Article

Autologous fecal microbiota transplantation can retain the metabolic achievements of dietary interventions

Journal

EUROPEAN JOURNAL OF INTERNAL MEDICINE
Volume 92, Issue -, Pages 17-23

Publisher

ELSEVIER
DOI: 10.1016/j.ejim.2021.03.038

Keywords

Weight loss; Weight regain; aFMT; Inflammatory markers; Personalized medicine

Funding

  1. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [209933838, SFB1052, SFB-1052/B11]
  2. Rosetrees trust [A2623]
  3. Israel Ministry of Health [87472511]
  4. Israel Ministry of Science and Technology [3-13604]
  5. Israeli Science Foundation [1733/18]
  6. California Walnuts Commission

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The study found that during autologous fecal microbiota transplantation treatment, patients were able to maintain metabolic benefits achieved during the weight loss phase, including stability in weight, blood sugar, and blood lipids.
Background: We recently reported that autologous fecal microbiota transplantation (aFMT), derived from the time of maximal weight-loss and administrated in the regain-phase, might preserve weight loss and glycemic control in moderately obese subjects, and is associated with specific microbiome signatures. Here, we sought to explore the global effect of aFMT on adipokines, inflammatory markers and blood cholesterol and on the overall gut microbiome preservation. Methods: In the DIRECT-PLUS weight-loss trial, abdominally obese participants were randomized to three distinct weight-loss diets. Following the expected weight loss phase (0-6 m), 90 participants were randomized to receive their personal frozen fecal microbiota or placebo oral capsules (ten 1 g-capsules over ten sessions-total=100 g) during the expected weight regain phase (8-14 m). Results: Of the 90 participants (age=52 yr; 0-6 m weight loss=-8.3 kg), 95.6% ingested at least 80/100 oral aFMT/placebo capsules over 6 months. Overall, the gut microbiome community structure was associated with plasma levels of leptin, cholesterol and interleukin-6 at baseline and after 6 m, whereas 6 m (weight loss phase) changes in specific microbiome species associated with the dynamic of leptin and inflammatory biomarkers. Following the 8-14 m aFMT administration phase, aFMT maintained decreased levels of leptin (Delta aFMT=-3.54 ng/mL vs. Delta placebo=-0.82 ng/mL;P = 0.04), C-reactive-protein (Delta aFMT=-1.45 mg/L vs.Delta placebo=-0.66 mg/L; P = 0.009), Interleukin-6 (Delta aFMT=-0.03pg/mL vs. Delta placebo=1.11pg/mL;P = 0.03) and total cholesterol (Delta aFMT=2.2 mg/dl vs. Delta placebo=13.1 mg/dl;P = 0.04) achieved in the weight loss phase. Overall, aFMT induced a significant preservatory effect on personal gut microbiome global composition (P = 0.03;Jensen-Shannon distance), as compared to placebo. Conclusions: aFMT treatment in the regain phase might retain weight-loss induced metabolic benefits. These findings may suggest a novel aFMT treatment approach for personal metabolic attainment preservation.

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