Effects of Diet-Modulated Autologous Fecal Microbiota Transplantation on Weight Regain.
Autologous FMT
Diabetes
Obesity
Weight Regain After Diet
Journal
Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
23
02
2020
revised:
10
08
2020
accepted:
20
08
2020
pubmed:
30
8
2020
medline:
29
6
2021
entrez:
30
8
2020
Statut:
ppublish
Résumé
We evaluated the efficacy and safety of diet-modulated autologous fecal microbiota transplantation (aFMT) for treatment of weight regain after the weight-loss phase. In the DIRECT PLUS (Dietary Intervention Randomized Controlled Trial Polyphenols-Unprocessed) weight-loss trial (May 2017 through July 2018), abdominally obese or dyslipidemic participants in Israel were randomly assigned to healthy dietary guidelines, Mediterranean diet, and green-Mediterranean diet weight-loss groups. All groups received free gym membership and physical activity guidelines. Both isocaloric Mediterranean groups consumed 28 g/d walnuts (+440 mg/d polyphenols provided). The green-Mediterranean dieters also consumed green tea (3-4 cups/d) and a Wolffia globosa (Mankai strain, 100 g/d) green shake (+800 mg/d polyphenols provided). After 6 months (weight-loss phase), 90 eligible participants (mean age, 52 years; mean weight loss, 8.3 kg) provided a fecal sample that was processed into aFMT by frozen, opaque, and odorless capsules. The participants were then randomly assigned to groups that received 100 capsules containing their own fecal microbiota or placebo until month 14. The primary outcome was regain of the lost weight over the expected weight-regain phase (months 6-14). Secondary outcomes were gastrointestinal symptoms, waist circumference, glycemic status, and changes in the gut microbiome, as measured by metagenomic sequencing and 16s ribosomal RNA. We validated the results in a parallel in vivo study of mice specifically fed with Mankai compared with control chow diet. Of the 90 participants in the aFMT trial, 96% ingested at least 80 of 100 oral aFMT or placebo frozen capsules during the transplantation period. No aFMT-related adverse events or symptoms were observed. For the primary outcome, although no significant differences in weight regain were observed among the participants in the different lifestyle interventions during months 6-14 (aFMT, 30.4% vs placebo, 40.6%; P = .28), aFMT significantly attenuated weight regain in the green-Mediterranean group (aFMT, 17.1%, vs placebo, 50%; P = .02), but not in the dietary guidelines (P = .57) or Mediterranean diet (P = .64) groups (P for the interaction = .03). Accordingly, aFMT attenuated waist circumference gain (aFMT, 1.89 cm vs placebo, 5.05 cm; P = .01) and insulin rebound (aFMT, -1.46 ± 3.6 μIU/mL vs placebo, 1.64 ± 4.7 μIU/mL; P = .04) in the green-Mediterranean group but not in the dietary guidelines or Mediterranean diet (P for the interaction = .04 and .03, respectively). The green-Mediterranean diet was the only intervention to induce a significant change in microbiome composition during the weight-loss phase, and to prompt preservation of weight-loss-associated specific bacteria and microbial metabolic pathways (mainly microbial sugar transport) after the aFMT. In mice, Mankai-modulated aFMT in the weight-loss phase compared with control diet aFMT, significantly prevented weight regain and resulted in better glucose tolerance during a high-fat diet-induced regain phase (all, P < .05). Autologous FMT, collected during the weight-loss phase and administrated in the regain phase, might preserve weight loss and glycemic control, and is associated with specific microbiome signatures. A high-polyphenols, green plant-based or Mankai diet better optimizes the microbiome for an aFMT procedure. ClinicalTrials.gov number, NCT03020186.
Sections du résumé
BACKGROUND & AIMS
We evaluated the efficacy and safety of diet-modulated autologous fecal microbiota transplantation (aFMT) for treatment of weight regain after the weight-loss phase.
METHODS
In the DIRECT PLUS (Dietary Intervention Randomized Controlled Trial Polyphenols-Unprocessed) weight-loss trial (May 2017 through July 2018), abdominally obese or dyslipidemic participants in Israel were randomly assigned to healthy dietary guidelines, Mediterranean diet, and green-Mediterranean diet weight-loss groups. All groups received free gym membership and physical activity guidelines. Both isocaloric Mediterranean groups consumed 28 g/d walnuts (+440 mg/d polyphenols provided). The green-Mediterranean dieters also consumed green tea (3-4 cups/d) and a Wolffia globosa (Mankai strain, 100 g/d) green shake (+800 mg/d polyphenols provided). After 6 months (weight-loss phase), 90 eligible participants (mean age, 52 years; mean weight loss, 8.3 kg) provided a fecal sample that was processed into aFMT by frozen, opaque, and odorless capsules. The participants were then randomly assigned to groups that received 100 capsules containing their own fecal microbiota or placebo until month 14. The primary outcome was regain of the lost weight over the expected weight-regain phase (months 6-14). Secondary outcomes were gastrointestinal symptoms, waist circumference, glycemic status, and changes in the gut microbiome, as measured by metagenomic sequencing and 16s ribosomal RNA. We validated the results in a parallel in vivo study of mice specifically fed with Mankai compared with control chow diet.
RESULTS
Of the 90 participants in the aFMT trial, 96% ingested at least 80 of 100 oral aFMT or placebo frozen capsules during the transplantation period. No aFMT-related adverse events or symptoms were observed. For the primary outcome, although no significant differences in weight regain were observed among the participants in the different lifestyle interventions during months 6-14 (aFMT, 30.4% vs placebo, 40.6%; P = .28), aFMT significantly attenuated weight regain in the green-Mediterranean group (aFMT, 17.1%, vs placebo, 50%; P = .02), but not in the dietary guidelines (P = .57) or Mediterranean diet (P = .64) groups (P for the interaction = .03). Accordingly, aFMT attenuated waist circumference gain (aFMT, 1.89 cm vs placebo, 5.05 cm; P = .01) and insulin rebound (aFMT, -1.46 ± 3.6 μIU/mL vs placebo, 1.64 ± 4.7 μIU/mL; P = .04) in the green-Mediterranean group but not in the dietary guidelines or Mediterranean diet (P for the interaction = .04 and .03, respectively). The green-Mediterranean diet was the only intervention to induce a significant change in microbiome composition during the weight-loss phase, and to prompt preservation of weight-loss-associated specific bacteria and microbial metabolic pathways (mainly microbial sugar transport) after the aFMT. In mice, Mankai-modulated aFMT in the weight-loss phase compared with control diet aFMT, significantly prevented weight regain and resulted in better glucose tolerance during a high-fat diet-induced regain phase (all, P < .05).
CONCLUSIONS
Autologous FMT, collected during the weight-loss phase and administrated in the regain phase, might preserve weight loss and glycemic control, and is associated with specific microbiome signatures. A high-polyphenols, green plant-based or Mankai diet better optimizes the microbiome for an aFMT procedure. ClinicalTrials.gov number, NCT03020186.
Identifiants
pubmed: 32860791
pii: S0016-5085(20)35111-8
doi: 10.1053/j.gastro.2020.08.041
pmc: PMC7755729
mid: NIHMS1640119
pii:
doi:
Banques de données
ClinicalTrials.gov
['NCT03020186']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
158-173.e10Subventions
Organisme : NIDDK NIH HHS
ID : K99 DK119412
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK046200
Pays : United States
Organisme : NIDDK NIH HHS
ID : R00 DK119412
Pays : United States
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.
Références
Med Sci Sports Exerc. 2000 Sep;32(9 Suppl):S498-504
pubmed: 10993420
N Engl J Med. 2008 Jul 17;359(3):229-41
pubmed: 18635428
PLoS One. 2016 Aug 16;11(8):e0161174
pubmed: 27529553
Cell Metab. 2017 Oct 3;26(4):611-619.e6
pubmed: 28978426
Cell. 2018 Sep 6;174(6):1406-1423.e16
pubmed: 30193113
Circulation. 2010 Jun 1;121(21):2271-83
pubmed: 20479151
PLoS One. 2012;7(7):e41079
pubmed: 22844426
J Nutr. 2019 Jun 1;149(6):1004-1011
pubmed: 30915471
Am J Epidemiol. 2014 Sep 15;180(6):565-73
pubmed: 25143474
Diabetes. 2015 Aug;64(8):2847-58
pubmed: 25845659
Br J Clin Pharmacol. 2017 Jan;83(1):114-128
pubmed: 27100393
Clin Gastroenterol Hepatol. 2020 Apr;18(4):855-863.e2
pubmed: 31301451
N Engl J Med. 2016 Dec 15;375(24):2369-2379
pubmed: 27974040
Science. 2013 Sep 6;341(6150):1241214
pubmed: 24009397
Front Cell Infect Microbiol. 2016 Aug 30;6:95
pubmed: 27625997
Nutr Clin Pract. 2015 Dec;30(6):780-6
pubmed: 26449892
JAMA. 2014 Nov 5;312(17):1772-8
pubmed: 25322359
Eur J Epidemiol. 2017 May;32(5):363-375
pubmed: 28397016
Am J Clin Nutr. 2001 Nov;74(5):579-84
pubmed: 11684524
J Nutr. 2005 Mar;135(3):573-9
pubmed: 15735096
Gastroenterology. 2012 Oct;143(4):913-6.e7
pubmed: 22728514
Gut. 2018 Nov;67(11):1920-1941
pubmed: 30154172
Nature. 2016 Dec 22;540(7634):544-551
pubmed: 27906159
Microbiome. 2017 Feb 1;5(1):14
pubmed: 28143587
BMJ. 2014 Jul 29;349:g4490
pubmed: 25073782
Nat Med. 2017 Jul;23(7):859-868
pubmed: 28628112
N Engl J Med. 2009 Feb 26;360(9):859-73
pubmed: 19246357
Cell. 2015 Nov 19;163(5):1079-1094
pubmed: 26590418
Int J Obes (Lond). 2011 Jun;35(6):785-792
pubmed: 21042325
Epidemiology. 1996 Jan;7(1):81-6
pubmed: 8664406
N Engl J Med. 2019 Nov 21;381(21):2043-2050
pubmed: 31665575
Circulation. 2018 Mar 13;137(11):1143-1157
pubmed: 29142011
Diabetes Care. 2019 Jul;42(7):1162-1169
pubmed: 31076421
J Diabetes. 2017 Mar;9(3):226-236
pubmed: 27787945
Nat Rev Endocrinol. 2019 May;15(5):274-287
pubmed: 30655624