Analysis of the Efficacy and the Long-term Metabolic and Nutritional Status of Sleeve Gastrectomy with Transit Bipartition Compared to Roux-en-Y Gastric Bypass in Obese Rats.


Journal

Obesity surgery
ISSN: 1708-0428
Titre abrégé: Obes Surg
Pays: United States
ID NLM: 9106714

Informations de publication

Date de publication:
04 2023
Historique:
received: 18 06 2022
accepted: 19 01 2023
revised: 12 01 2023
medline: 10 4 2023
pubmed: 3 2 2023
entrez: 2 2 2023
Statut: ppublish

Résumé

Sleeve gastrectomy with transit bipartition (SG-TB) could be an attractive alternative to Roux-en-Y gastric bypass (RYGB) on weight loss and improvement of comorbidities in patients with obesity. However, there is little long-term data. Translational research on a rat model could allow long-term projection to assess efficacy and safety of SG-TB. The aim of this research was to evaluate the long-term efficacy and safety of SG-TB compared to RYGB and SHAM in rat model. Ninety-four male obese Wistar rats were distributed into 3 groups: SG-TB (n = 34), RYGB (n = 32), and SHAM (control group, n = 28). The percentage of total weight loss (%TWL), coprocalorimetry, glucose and insulin tolerance test, insulin, GLP-1, PYY, and GIP before and after surgery were assessed. The animals were followed over 6 months (equivalent to 16 years in humans). At 6 months, %TWL was significantly greater(p = 0.025) in the SG-TB group compared to the RYGB group. There was no difference between the groups (p = 0.86) in malabsorption 15 and 120 days postoperatively. Glucose tolerance was significantly improved (p = 0.03) in the SG-TB and RYGB groups compared to the preoperative state. Insulin secretion, at 3 months, was significantly more important in the SG-TB group (p = 0.0003), compared to the RYGB and SHAM groups. GLP-1 secretion was significantly increased in the SG-TB and RYGB groups compared to the preoperative state (p = 0.001) but similar between SG-TB and RYGB animals (p = 0.72). In a rat model, at long term compared to RYGB, SG-TB provides greater and better-maintained weight loss and an increased insulin secretion without impairing nutritional status.

Identifiants

pubmed: 36729363
doi: 10.1007/s11695-023-06477-7
pii: 10.1007/s11695-023-06477-7
doi:

Substances chimiques

Insulin 0
Glucagon-Like Peptide 1 89750-14-1
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1121-1132

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Clement Baratte (C)

Université de Paris Cité, F-75015, Paris, France.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Service de chirurgie digestive, œsogastrique et bariatrique, Centre Spécialisé Obésité (CSO) Ile de France Nord, Hôpital Bichat-Claude Bernard, 16 rue Henri Huchard, 75018, Paris, France.

Alexandra Willemetz (A)

Université de Paris Cité, F-75015, Paris, France.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France.

Lara Ribeiro-Parenti (L)

Université de Paris Cité, F-75015, Paris, France.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Service de chirurgie digestive, œsogastrique et bariatrique, Centre Spécialisé Obésité (CSO) Ile de France Nord, Hôpital Bichat-Claude Bernard, 16 rue Henri Huchard, 75018, Paris, France.

Claire Carette (C)

Université de Paris Cité, F-75015, Paris, France.
Assistance Publique-Hôpitaux de Paris, service de Nutrition, Centre Spécialisé Obésité (CSO) Ile de France Sud, Hôpital Européen Georges Pompidou, 75015, Paris, France.

Simon Msika (S)

Université de Paris Cité, F-75015, Paris, France.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France.
Assistance Publique-Hôpitaux de Paris (AP-HP), Service de chirurgie digestive, œsogastrique et bariatrique, Centre Spécialisé Obésité (CSO) Ile de France Nord, Hôpital Bichat-Claude Bernard, 16 rue Henri Huchard, 75018, Paris, France.

Andre Bado (A)

Université de Paris Cité, F-75015, Paris, France.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France.

Sebastien Czernichow (S)

Université de Paris Cité, F-75015, Paris, France.
Assistance Publique-Hôpitaux de Paris, service de Nutrition, Centre Spécialisé Obésité (CSO) Ile de France Sud, Hôpital Européen Georges Pompidou, 75015, Paris, France.
Inserm, INRAE, Center for Research in Epidemiology and StatisticS (CRESS), F-75004, Paris, France.

Maude Le Gall (M)

Université de Paris Cité, F-75015, Paris, France.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France.

Tigran Poghosyan (T)

Université de Paris Cité, F-75015, Paris, France. tigran.poghosyan@aphp.fr.
INSERM, U1149, Centre de Recherche sur l'Inflammation, 75018, Paris, France. tigran.poghosyan@aphp.fr.
Assistance Publique-Hôpitaux de Paris (AP-HP), Service de chirurgie digestive, œsogastrique et bariatrique, Centre Spécialisé Obésité (CSO) Ile de France Nord, Hôpital Bichat-Claude Bernard, 16 rue Henri Huchard, 75018, Paris, France. tigran.poghosyan@aphp.fr.

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