TY - JOUR
T1 - Durable metabolic improvements 2 years after duodenal mucosal resurfacing (DMR) in patients with type 2 diabetes (REVITA-1 Study)
AU - van Baar, Annieke C. G.
AU - Devière, Jacques
AU - Hopkins, David
AU - Crenier, Laurent
AU - Holleman, Frits
AU - Galvão Neto, Manoel P.
AU - Becerra, Pablo
AU - Vignolo, Paulina
AU - Rodriguez Grunert, Leonardo
AU - Mingrone, Geltrude
AU - Costamagna, Guido
AU - Nieuwdorp, Max
AU - Guidone, Caterina
AU - Haidry, Rehan J.
AU - Hayee, Bu
AU - Magee, Cormac
AU - Carlos Lopez-Talavera, Juan
AU - White, Kelly
AU - Bhambhani, Vijeta
AU - Cozzi, Emily
AU - Rajagopalan, Harith
AU - J.G.H.M. Bergman, Jacques
N1 - Funding Information: This study was supported by Fractyl Laboratories Inc. A.C.G.V.B., P.B., C.M., and P.V. have nothing to disclose. J.D. has received research support from Fractyl Laboratories Inc for IRB-approved studies. D.H. has received honorarium for consultancy and/or speaker fees from Novo Nordisk, Sanofi, Astra Zeneca, Roche, Sunovion, and Fractyl Laboratories Inc. L.C. has received honorarium for consultancy and/or speaker fees from Abbott, Astra Zeneca, Boehringer-Ingelheim, Eli Lilly, Medtronic, Novo Nordisk, and Sanofi. F.H. has received honorarium for consultancy from Bioton, Astra Zeneca, and Sanofi. M.P.G.N. has received honorarium for consultancy from Fractyl Laboratories Inc, GI Windows, GI Dynamics, and Apollo. He has participating in speaker bureaus for Ethicon, Medtronic, and Olympus. L.R.G. has nothing to disclose. G.M. has received funding/grant support from Novo Nordisk, Fractyl Laboratories Inc, Metacure, Keyron Ltd., and honorarium for consultancy from Johnson & Johnson, Novo Nordisk, and Fractyl Laboratories Inc. G.C. has received research grant support from Boston Scientific and Apollo and is on advisory boards for Cook Medical, Olympus, and Ethicon. M.N is on the scientific advisory board of Caelus health and Kaleido Bioscience. C.G. has nothing to disclose. R.J.H. has received funding/grant support/honorarium for consultancy from Cook Endoscopy, Pentax Europe, Medtronic, C2 Therapeutics, and Fractyl Laboratories Inc to support research infrastructure. BH has nothing to disclose. H.R., J.C.L-T., K.W., V.B., and E.C. are full-time employees of Fractyl Laboratories Inc and may hold Fractyl stock and/or stock options. J.J.G.H.M.B. has received research support from Fractyl Laboratories Inc for IRB-based studies and has received a consultancy fee for a single advisory board meeting for Fractyl Laboratories Inc in September 2019.]. Publisher Copyright: © 2022 The Authors
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Aims: Duodenal mucosal resurfacing (DMR) is an endoscopic procedure developed to improve metabolic parameters and restore insulin sensitivity in patients with diabetes. Here we report long-term DMR safety and efficacy from the REVITA-1 study. Materials and Methods: REVITA-1 was a prospective, single-arm, open-label, multicenter study of DMR feasibility, safety, and efficacy in patients with type 2 diabetes (hemoglobin A1c [HbA1c] of 7.5–10.0% (58–86 mmol/mol)) on oral medication. Safety and glycemic (HbA1c), hepatic (alanine aminotransferase [ALT]), and cardiovascular (HDL, triglyceride [TG]/HDL ratio) efficacy parameters were assessed (P values presented for LS mean change). Results: Mean ± SD HbA1c levels reduced from 8.5 ± 0.7% (69.1 ± 7.1 mmol/mol) at baseline (N = 34) to 7.5 ± 0.8% (58.9 ± 8.8 mmol/mol) at 6 months (P < 0.001); and this reduction was sustained through 24 months post-DMR (7.5 ± 1.1% [59.0 ± 12.3 mmol/mol], P < 0.001) while in greater than 50% of patients, glucose-lowering therapy was reduced or unchanged. ALT decreased from 38.1 ± 21.1 U/L at baseline to 32.5 ± 22.1 U/L at 24 months (P = 0.048). HDL and TG/HDL improved during 24-months of follow-up. No device- or procedure-related serious adverse events, unanticipated device effects, or hypoglycemic events were noted between 12 and 24 months post-DMR. Conclusions: DMR is associated with durable improvements in insulin sensitivity and multiple downstream metabolic parameters through 24 months post-treatment in type 2 diabetes. Clinical trial reg. no. NCT02413567, clinicaltrials.gov.
AB - Aims: Duodenal mucosal resurfacing (DMR) is an endoscopic procedure developed to improve metabolic parameters and restore insulin sensitivity in patients with diabetes. Here we report long-term DMR safety and efficacy from the REVITA-1 study. Materials and Methods: REVITA-1 was a prospective, single-arm, open-label, multicenter study of DMR feasibility, safety, and efficacy in patients with type 2 diabetes (hemoglobin A1c [HbA1c] of 7.5–10.0% (58–86 mmol/mol)) on oral medication. Safety and glycemic (HbA1c), hepatic (alanine aminotransferase [ALT]), and cardiovascular (HDL, triglyceride [TG]/HDL ratio) efficacy parameters were assessed (P values presented for LS mean change). Results: Mean ± SD HbA1c levels reduced from 8.5 ± 0.7% (69.1 ± 7.1 mmol/mol) at baseline (N = 34) to 7.5 ± 0.8% (58.9 ± 8.8 mmol/mol) at 6 months (P < 0.001); and this reduction was sustained through 24 months post-DMR (7.5 ± 1.1% [59.0 ± 12.3 mmol/mol], P < 0.001) while in greater than 50% of patients, glucose-lowering therapy was reduced or unchanged. ALT decreased from 38.1 ± 21.1 U/L at baseline to 32.5 ± 22.1 U/L at 24 months (P = 0.048). HDL and TG/HDL improved during 24-months of follow-up. No device- or procedure-related serious adverse events, unanticipated device effects, or hypoglycemic events were noted between 12 and 24 months post-DMR. Conclusions: DMR is associated with durable improvements in insulin sensitivity and multiple downstream metabolic parameters through 24 months post-treatment in type 2 diabetes. Clinical trial reg. no. NCT02413567, clinicaltrials.gov.
KW - Duodenal mucosal resurfacing
KW - Duodenum
KW - Endoscopic ablation
KW - Type 2 diabetes mellitus
UR - http://www.scopus.com/inward/record.url?scp=85123828918&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.diabres.2022.109194
DO - https://doi.org/10.1016/j.diabres.2022.109194
M3 - Article
C2 - 35032562
SN - 0168-8227
VL - 184
JO - Diabetes Research and Clinical Practice
JF - Diabetes Research and Clinical Practice
M1 - 109194
ER -