Metabolite Profiles Predict Acute Kidney Injury and Mortality in Patients Undergoing Transcatheter Aortic Valve Replacement

Author:

Elmariah Sammy123,Farrell Laurie A.12,Daher Maureen1,Shi Xu12,Keyes Michelle J.12,Cain Carolyn H.1,Pomerantsev Eugene1,Vlahakes Gus J.4,Inglessis Ignacio1,Passeri Jonathan J.1,Palacios Igor F.1,Fox Caroline S.567,Rhee Eugene P.28,Gerszten Robert E.12

Affiliation:

1. Cardiology Division, Massachusetts General Hospital, Harvard Medical School, Boston, MA

2. Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA

3. Harvard Clinical Research Institute, Boston, MA

4. Department of Cardiac Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA

5. Framingham Heart Study of the National Heart, Lung, and Blood Institute and Boston University School of Medicine, Framingham, MA

6. Endocrinology Division, Brigham & Women's Hospital, Boston, MA

7. Division of Intra‐mural Research, National Heart, Lung, and Blood Institute, Bethesda, MD

8. Nephrology Division, Massachusetts General Hospital, Harvard Medical School, Boston, MA

Abstract

Background Acute kidney injury ( AKI ) occurs commonly after transcatheter aortic valve replacement ( TAVR ) and is associated with markedly increased postoperative mortality. We previously identified plasma metabolites predictive of incident chronic kidney disease, but whether metabolite profiles can identify those at risk of AKI is unknown. Methods and Results We performed liquid chromatography–mass spectrometry–based metabolite profiling on plasma from patients undergoing TAVR and subjects from the community‐based Framingham Heart Study (N=2164). AKI was defined by using the Valve Academic Research Consortium‐2 criteria. Of 44 patients (mean age 82±9 years, 52% female) undergoing TAVR , 22 (50%) had chronic kidney disease and 9 (20%) developed AKI . Of 85 metabolites profiled, we detected markedly concordant cross‐sectional metabolic changes associated with chronic kidney disease in the hospital‐based TAVR and Framingham Heart Study cohorts. Baseline levels of 5‐adenosylhomocysteine predicted AKI after TAVR , despite adjustment for baseline glomerular filtration rate (odds ratio per 1‐ SD increase 5.97, 95% CI 1.62–22.0; P =0.007). Of the patients who had AKI , 6 (66.7%) subsequently died, compared with 3 (8.6%) deaths among those patients who did not develop AKI ( P =0.0008) over a median follow‐up of 7.8 months. 5‐adenosylhomocysteine was predictive of all‐cause mortality after TAVR (hazard ratio per 1‐ SD increase 2.96, 95% CI 1.33–6.58; P =0.008), independent of baseline glomerular filtration rate. Conclusions In an elderly population with severe aortic stenosis undergoing TAVR , metabolite profiling improves the prediction of AKI. Given the multifactorial nature of AKI after TAVR , metabolite profiles may identify those patients with reduced renal reserve.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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