Renoprotective Effects of Metabolic Surgery Versus GLP1 Receptor Agonists on Progression of Kidney Impairment in Patients with Established Kidney Disease

Author:

Aminian Ali1,Gasoyan Hamlet2,Zajichek Alexander3,Alavi Mohammad Hesam1,Casacchia Nicholas J.2,Wilson Rickesha1,Feng Xiaoxi1,Corcelles Ricard1,Brethauer Stacy A.4,Schauer Philip R.5,Kroh Matthew1,Rosenthal Raul J.6,Taliercio Jonathan J.7,Poggio Emilio D.7,Nissen Steven E.8,Rothberg Michael B.2

Affiliation:

1. Bariatric and Metabolic Institute, Department of General Surgery, Cleveland Clinic, Cleveland, OH

2. Center for Value-Based Care Research, Department of Internal Medicine and Geriatrics, Primary Care Institute, Cleveland Clinic, Cleveland, OH

3. Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH

4. Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH

5. Metamor Institute, Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA

6. Bariatric and Metabolic Institute, Department of General Surgery, Cleveland Clinic Florida, Weston, FL

7. Department of Kidney Medicine, Glickman Urological and Kidney Institute, Cleveland Clinic, Cleveland, OH

8. Cleveland Clinic Coordinating Center for Clinical Research, Cleveland, OH

Abstract

Objective: To examine the renoprotective effects of metabolic surgery in patients with established chronic kidney disease (CKD). Background: The impact of metabolic surgery compared with glucagon-like peptide-1 receptor agonists (GLP-1RA) in patients with established CKD has not been fully characterized. Methods: Patients with obesity (BMI ≥30 kg/m2), type 2 diabetes (T2DM), and baseline estimated glomerular filtration rate (eGFR) 20-60 mL/min/1.73 m² who underwent metabolic bariatric surgery at a large U.S. health system (2010-2017) were compared with nonsurgical patients who continuously received GLP-1RA. The primary end point was CKD progression, defined as decline of eGFR by ≥50% or to <15 mL/min/1.73 m2, initiation of dialysis, or kidney transplant. The secondary end point was the incident kidney failure (eGFR <15 mL/min/1.73 m2, dialysis, or kidney transplant) or all-cause mortality. Results: 425 patients, including 183 patients in the metabolic surgery group and 242 patients in the GLP-1RA group, with a median follow-up of 5.8 years (IQR, 4.4-7.6) were analyzed. The cumulative incidence of the primary end point at 8-years was 21.7% (95% CI, 12.2-30.6) in the surgical group and 45.1% (95% CI, 27.7-58.4) in the nonsurgical group, with an adjusted hazard ratio of 0.40 (95% CI, 0.21-0.76), P=0.006. The cumulative incidence of the secondary composite end point at 8-years was 24.0% (95% CI, 14.1-33.2) in the surgical group and 43.8% (95% CI, 28.1-56.1) in the nonsurgical group, with an adjusted HR of 0.56 (95% CI, 0.31-0.99), P=0.048. Conclusions: Among patients with T2DM, obesity, and established CKD, metabolic surgery, compared with GLP-1RA, was significantly associated with a 60% lower risk of progression of kidney impairment and a 44% lower risk of kidney failure or death. Metabolic surgery should be considered as a therapeutic option for patients with CKD and obesity.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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