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      Inorganic nitrate benefits contrast-induced nephropathy after coronary angiography for acute coronary syndromes: the NITRATE-CIN trial

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          Abstract

          Background and Aims

          Contrast-induced nephropathy (CIN), also known as contrast-associated acute kidney injury (CA-AKI) underlies a significant proportion of the morbidity and mortality following coronary angiographic procedures in high-risk patients and remains a significant unmet need. In pre-clinical studies inorganic nitrate, which is chemically reduced in vivo to nitric oxide, is renoprotective but this observation is yet to be translated clinically. In this study, the efficacy of inorganic nitrate in the prevention of CIN in high-risk patients presenting with acute coronary syndromes (ACS) is reported.

          Methods

          NITRATE-CIN is a double-blind, randomized, single-centre, placebo-controlled trial assessing efficacy of inorganic nitrate in CIN prevention in at-risk patients presenting with ACS. Patients were randomized 1:1 to once daily potassium nitrate (12 mmol) or placebo (potassium chloride) capsules for 5 days. The primary endpoint was CIN (KDIGO criteria). Secondary outcomes included kidney function [estimated glomerular filtration rate (eGFR)] at 3 months, rates of procedural myocardial infarction, and major adverse cardiac events (MACE) at 12 months. This study is registered with ClinicalTrials.gov: NCT03627130.

          Results

          Over 3 years, 640 patients were randomized with a median follow-up of 1.0 years, 319 received inorganic nitrate with 321 received placebo. The mean age of trial participants was 71.0 years, with 73.3% male and 75.2% Caucasian; 45.9% had diabetes, 56.0% had chronic kidney disease (eGFR <60 mL/min) and the mean Mehran score of the population was 10. Inorganic nitrate treatment significantly reduced CIN rates (9.1%) vs. placebo (30.5%, P < .001). This difference persisted after adjustment for baseline creatinine and diabetes status (odds ratio 0.21, 95% confidence interval 0.13–0.34). Secondary outcomes were improved with inorganic nitrate, with lower rates of procedural myocardial infarction (2.7% vs. 12.5%, P = .003), improved 3-month renal function (between-group change in eGFR 5.17, 95% CI 2.94–7.39) and reduced 1-year MACE (9.1% vs. 18.1%, P = .001) vs. placebo.

          Conclusions

          In patients at risk of renal injury undergoing coronary angiography for ACS, a short (5 day) course of once-daily inorganic nitrate reduced CIN, improved kidney outcomes at 3 months, and MACE events at 1 year compared to placebo.

          Structured Graphical Abstract

          Structured Graphical Abstract

          NITRATE-CIN was a double-blind randomized controlled trial (RCT) of 640 patients presenting with acute coronary syndrome and undergoing angiography and at increased risk of contrast-induced nephropathy (CIN). Treatment of patients with inorganic nitrate (12 mmol/day capsules on the day of surgery and for 4 days after) significantly reduced the incidence of CIN, improved kidney outcomes at 3 months, and major adverse cardiac events at 1 year compared to placebo. eGFR, estimated glomerular filtration rate.

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          Most cited references43

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          KDIGO Clinical Practice Guidelines for Acute Kidney Injury

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            CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials

            The CONSORT statement is used worldwide to improve the reporting of randomised controlled trials. Kenneth Schulz and colleagues describe the latest version, CONSORT 2010, which updates the reporting guideline based on new methodological evidence and accumulating experience
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              The gut microbiome in atherosclerotic cardiovascular disease

              The gut microbiota has been linked to cardiovascular diseases. However, the composition and functional capacity of the gut microbiome in relation to cardiovascular diseases have not been systematically examined. Here, we perform a metagenome-wide association study on stools from 218 individuals with atherosclerotic cardiovascular disease (ACVD) and 187 healthy controls. The ACVD gut microbiome deviates from the healthy status by increased abundance of Enterobacteriaceae and Streptococcus spp. and, functionally, in the potential for metabolism or transport of several molecules important for cardiovascular health. Although drug treatment represents a confounding factor, ACVD status, and not current drug use, is the major distinguishing feature in this cohort. We identify common themes by comparison with gut microbiome data associated with other cardiometabolic diseases (obesity and type 2 diabetes), with liver cirrhosis, and rheumatoid arthritis. Our data represent a comprehensive resource for further investigations on the role of the gut microbiome in promoting or preventing ACVD as well as other related diseases.
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                Author and article information

                Contributors
                Journal
                Eur Heart J
                Eur Heart J
                eurheartj
                European Heart Journal
                Oxford University Press (UK )
                0195-668X
                1522-9645
                07 May 2024
                21 March 2024
                21 March 2024
                : 45
                : 18 , Focus Issue on Ischaemic Heart Disease
                : 1647-1658
                Affiliations
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                Barts Cardiovascular Clinical Trials Unit, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Cardiovascular Clinical Trials Unit, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ, UK
                Barts Cardiovascular Clinical Trials Unit, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ, UK
                Barts Cardiovascular Clinical Trials Unit, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ, UK
                Barts Cardiovascular Clinical Trials Unit, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ, UK
                Department of Pharmacy, Barts Heart Centre , Barts Health NHS Trust, London, UK
                Department of Pharmacy, Barts Heart Centre , Barts Health NHS Trust, London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Department of Nephrology , Barts Health NHS Trust, London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Interventional Group, Barts Heart Centre, Barts Health NHS Trust , London, UK
                William Harvey Research Institute, Barts & The London Faculty of Medicine & Dentistry, Queen Mary University of London , Charterhouse Square, London EC1 M 6BQ, UK
                Barts Cardiovascular Clinical Trials Unit, Queen Mary University of London , Charterhouse Square, London EC1M 6BQ, UK
                Author notes
                Corresponding author. Email: a.ahluwalia@ 123456qmul.ac.uk

                Daniel A. Jones and Anne-Marie Beirne Equal first authors.

                Author information
                https://orcid.org/0000-0003-1441-0417
                https://orcid.org/0000-0003-4268-5055
                https://orcid.org/0000-0001-7941-9653
                https://orcid.org/0000-0001-7626-6399
                Article
                ehae100
                10.1093/eurheartj/ehae100
                11089333
                38513060
                630f59c0-acbd-4add-970d-e07d77eafbd0
                © The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 July 2023
                : 18 January 2024
                : 05 February 2024
                Page count
                Pages: 12
                Funding
                Funded by: Heart Research UK, DOI 10.13039/501100000327;
                Funded by: Translational Research;
                Award ID: RG2667
                Funded by: The Barts Charity Cardiovascular Programme;
                Award ID: MRG00913
                Funded by: NIHR, DOI 10.13039/501100000272;
                Funded by: Thomas Godec and Kamran Khan;
                Funded by: Barts Charity Cardiovascular Programme;
                Award ID: MRG00913.
                Categories
                Clinical Research
                AcademicSubjects/MED00200
                Eurheartj/39
                Eurheartj/41
                Eurheartj/15
                Eurheartj/17

                Cardiovascular Medicine
                nitrate,nitric oxide: contrast induced nephropathy,acute coronary syndrome,angiography,renoprotection

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