Duodenal-Jejunal Bypass Liner (DJBL) Improves Cardiovascular Risk Biomarkers and Predicted 4-Year Risk of Major CV Events in Patients with Type 2 Diabetes and Metabolic Syndrome.


Journal

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

Informations de publication

Date de publication:
04 2020
Historique:
pubmed: 4 1 2020
medline: 15 4 2021
entrez: 4 1 2020
Statut: ppublish

Résumé

The duodenal-jejunal bypass liner (DJBL) represents a novel endoscopic minimally invasive treatment option for obesity-associated type 2 diabetes (T2D), affecting body weight and metabolic control. Until now, the effects of DJBL on cardiovascular risk have never been investigated. Between 2012 and 2017, 71 patients with T2D and metabolic syndrome (MS) were recruited for implantation of DJBL for 9-12 months. Within DJBL treatment and a follow-up period of 6 months, patients were analysed for dynamics of cardiovascular biomarkers. Overall cardiovascular risk was estimated by the ADVANCE Risk Engine at time of implantation, explantation and 6 months after explantation of DJBL. DJBL-induced weight loss and improvements in blood sugar control were accompanied by significant decreases of the cardiovascular biomarkers high-sensitive CRP, lipoprotein-associated phospholipase A2 and small dense lipoprotein fraction LDL-4 (p = 0.001, p < 0.001 and p = 0.04, respectively). Estimated overall cardiovascular risk decreased significantly after DJBL implantation and remained stable within 6 months after explantation. In addition to beneficial effects of DJBL on weight loss, glycaemic control and lipid parameters in patients with MS, this is the first study that could further reveal significant impact on serological cardiovascular biomarkers and estimated CV risk, suggesting putative protective effects of DJBL on CV outcome.

Sections du résumé

BACKGROUND
The duodenal-jejunal bypass liner (DJBL) represents a novel endoscopic minimally invasive treatment option for obesity-associated type 2 diabetes (T2D), affecting body weight and metabolic control. Until now, the effects of DJBL on cardiovascular risk have never been investigated.
METHODS
Between 2012 and 2017, 71 patients with T2D and metabolic syndrome (MS) were recruited for implantation of DJBL for 9-12 months. Within DJBL treatment and a follow-up period of 6 months, patients were analysed for dynamics of cardiovascular biomarkers. Overall cardiovascular risk was estimated by the ADVANCE Risk Engine at time of implantation, explantation and 6 months after explantation of DJBL.
RESULTS
DJBL-induced weight loss and improvements in blood sugar control were accompanied by significant decreases of the cardiovascular biomarkers high-sensitive CRP, lipoprotein-associated phospholipase A2 and small dense lipoprotein fraction LDL-4 (p = 0.001, p < 0.001 and p = 0.04, respectively). Estimated overall cardiovascular risk decreased significantly after DJBL implantation and remained stable within 6 months after explantation.
CONCLUSIONS
In addition to beneficial effects of DJBL on weight loss, glycaemic control and lipid parameters in patients with MS, this is the first study that could further reveal significant impact on serological cardiovascular biomarkers and estimated CV risk, suggesting putative protective effects of DJBL on CV outcome.

Identifiants

pubmed: 31898040
doi: 10.1007/s11695-019-04324-2
pii: 10.1007/s11695-019-04324-2
doi:

Substances chimiques

Biomarkers 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1200-1210

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Auteurs

Natascha Roehlen (N)

Department of Medicine II, Medical Center, Division of Endocrinology and Diabetology, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, 79106, Freiburg im Breisgau, Germany. natascha.roehlen@uniklinik-freiburg.de.

Katharina Laubner (K)

Department of Medicine II, Medical Center, Division of Endocrinology and Diabetology, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, 79106, Freiburg im Breisgau, Germany.

Dominik Bettinger (D)

Department of Medicine II, Faculty of Medicine, Division of Hepatology, Gastroenterology and Gastrointestinal Endoscopy, University Hospital of Freiburg, Freiburg im Breisgau, Germany.

Henning Schwacha (H)

Department of Medicine II, Faculty of Medicine, Division of Hepatology, Gastroenterology and Gastrointestinal Endoscopy, University Hospital of Freiburg, Freiburg im Breisgau, Germany.

Hanna Hilger (H)

Department of Medicine II, Medical Center, Division of Endocrinology and Diabetology, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, 79106, Freiburg im Breisgau, Germany.

Carolin Koenig (C)

Department of Medicine II, Medical Center, Division of Endocrinology and Diabetology, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, 79106, Freiburg im Breisgau, Germany.

Dirk Grueninger (D)

Centre of Laboratory Diagnostics, MVZ Clotten, Freiburg im Breisgau, Germany.

Andreas Krebs (A)

Centre of Laboratory Diagnostics, MVZ Clotten, Freiburg im Breisgau, Germany.

Jochen Seufert (J)

Department of Medicine II, Medical Center, Division of Endocrinology and Diabetology, Faculty of Medicine, University of Freiburg, Hugstetter Straße 55, 79106, Freiburg im Breisgau, Germany.

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