TY - JOUR
T1 - Fecal Microbiota Transplantation: a Future Therapeutic Option for Obesity/Diabetes?
AU - Aron-Wisnewsky, Judith
AU - Clément, Karine
AU - Nieuwdorp, Max
N1 - Funding Information:
Funding Information Grant supports in this field were obtained by Ministry of Health and Solidarity (Assistance Publique-Hôpitaux de Paris: to JAW/PHRC-N Drifter, to KC/PHRC Micronaria), by European Union (Metacardis to KC HEALTH-F4-2012-305312, JPI MICRODIET Grant (5290510105) to KC and MN, EU Horizon 2020 grant (LITMUS 777377) to KC and MN) and by LeDucq Foundation consortium grant (17CVD01) to KC and MN. MN is also supported by a ZONMW-VIDI grant 2013 (016.146.327). JAW and KC are part of ICAN (Institute of Cardiometabolism and Nutrition Institute).
Publisher Copyright:
© 2019, Springer Science+Business Media, LLC, part of Springer Nature.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Purpose of Review: The aim of this review is to summarize the current data available on the metabolic effects of fecal microbiota transplantation (FMT) including obesity and glucose metabolism in humans. Recent Findings: Gut microbiota dysbiosis is a frequent characteristic observed in obesity and related metabolic diseases. Pieces of evidence mostly generated in mouse models suggest that rescuing this dysbiosis associates with improved metabolism. In humans, dietary or bariatric surgery interventions are often accompanied by complete or partial restoration of this dysbiosis together with weight reduction and metabolic amelioration. FMT is an interesting option to modify gut microbiota and has been associated with improved clinical outcomes, albeit only used in routine care for Clostridium difficile infection. However, there are only limited data on using FMT in the metabolic context. Summary: FMT from lean donors significantly improves insulin sensitivity in obese subjects with metabolic syndrome. However, there is a wide range of clinical responses. Interestingly in subjects with high microbial gene richness at baseline and when FMT donors that are metabolically compromised are used, no metabolic improvement is seen. Moreover, more studies evaluating the effect of FMT in patients with overt type 2 diabetes are warranted. Furthermore, interventions (in the receiver prior to FMT) aiming to enhance FMT response also need evaluation.
AB - Purpose of Review: The aim of this review is to summarize the current data available on the metabolic effects of fecal microbiota transplantation (FMT) including obesity and glucose metabolism in humans. Recent Findings: Gut microbiota dysbiosis is a frequent characteristic observed in obesity and related metabolic diseases. Pieces of evidence mostly generated in mouse models suggest that rescuing this dysbiosis associates with improved metabolism. In humans, dietary or bariatric surgery interventions are often accompanied by complete or partial restoration of this dysbiosis together with weight reduction and metabolic amelioration. FMT is an interesting option to modify gut microbiota and has been associated with improved clinical outcomes, albeit only used in routine care for Clostridium difficile infection. However, there are only limited data on using FMT in the metabolic context. Summary: FMT from lean donors significantly improves insulin sensitivity in obese subjects with metabolic syndrome. However, there is a wide range of clinical responses. Interestingly in subjects with high microbial gene richness at baseline and when FMT donors that are metabolically compromised are used, no metabolic improvement is seen. Moreover, more studies evaluating the effect of FMT in patients with overt type 2 diabetes are warranted. Furthermore, interventions (in the receiver prior to FMT) aiming to enhance FMT response also need evaluation.
KW - Encapsulated feces
KW - Fecal microbiota transplantation
KW - Microbiota
KW - Obesity
KW - Type 2 diabetes
UR - http://www.scopus.com/inward/record.url?scp=85068063474&partnerID=8YFLogxK
U2 - 10.1007/s11892-019-1180-z
DO - 10.1007/s11892-019-1180-z
M3 - Review article
C2 - 31250122
VL - 19
JO - Current Diabetes Reports
JF - Current Diabetes Reports
SN - 1534-4827
IS - 8
M1 - 51
ER -