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Effect of Dapagliflozin on Metabolomics and Cardiac Mechanics in Chronic Kidney Disease

Primary Purpose

Chronic Kidney Diseases, Heart Failure With Preserved Ejection Fraction, Kidney Diseases

Status
Not yet recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Dapagliflozin 10 MG [Farxiga]
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Diseases focused on measuring kidney, heart failure, kidney diseases

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: >18 years of age eGFR 25-60 ml/min/1,73m2 (eGFR = estimated glomerular filtration rate) On stable doses of diuretics and/or angiotensin converting enzyme inhibitor or angiotensin receptor blocker Evidence of subclinical heart failure with preserved ejection fraction at their pre-exercise echocardiogram (defined as meeting any of the American Society of Echocardiography (ASE) criteria for diastolic dysfunction [septal e'<7 cm/wc, average E/e' ratio>14, left atrial volume index >34 mL/m2, and peak TR velocity >2.8 m/sec] or absolute left ventricular longitudinal strain < 18%) Exclusion Criteria: presence or history of diabetes coronary revascularization within the last 6 months hemodynamically significant valvular disease significant lung disease requiring home oxygen angina (chest pain) non-revascularized myocardial ischemia systolic BP <100 or >180 mmHg pregnancy clinical heart failure symptoms history of systemic disease processes that can cause HFpEF such as amyloidosis or sarcoidosis any musculoskeletal or chronic condition that will interfere with completion of cardiac testing active cancer immunosuppressive therapy baseline or pre-exercise echocardiogram demonstrates a reduced ejection fraction </= 50% currently on sodium glucose cotransporter 2 inhibitor (SGLT2i) therapy Hypersensitivity to a SGLT2i Pre-existing liver disease ALT/AST> 3x normal (ALT = alanine aminotransferase AST = aspartate aminotransferase) history of recurrent urinary tract infections (in the opinion of the investigator) or a urinary tract infection in the last 3 months

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention group

Standard of Care group

Arm Description

Thirty individuals will be randomized to dapagliflozin 10mg to be taken daily for six months.

Thirty individuals will be randomized to standard of care treatment.

Outcomes

Primary Outcome Measures

Left ventricular longitudinal strain (LVLS)
2D-speckle tracking echocardiography
Peak VO2 (oxygen consumption)
Cardiopulmonary exercise stress test
Circulating plasma metabolite concentrations
Plasma

Secondary Outcome Measures

Left Atrial Reservoir Strain (LARS)
2D-STE
Right ventricular free wall strain
2D-STE

Full Information

First Posted
January 31, 2023
Last Updated
June 16, 2023
Sponsor
Northwestern University
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT05719714
Brief Title
Effect of Dapagliflozin on Metabolomics and Cardiac Mechanics in Chronic Kidney Disease
Official Title
Effect of Dapagliflozin on Metabolomics and Cardiac Mechanics in Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
September 2026 (Anticipated)
Study Completion Date
September 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to better understand the effects of a sodium-glucose transport protein 2 inhibitor, dapagliflozin, added on to standard of care on heart and lung function and circulating metabolites (substances created when our bodies break down food, drugs, or its own tissues) in patients with chronic kidney disease.
Detailed Description
This is a 6-month interventional patient-oriented research study of sixty patients with chronic kidney disease (CKD) and evidence of subclinical heart failure with preserved ejection fraction (HFpEF) (estimated glomerular filtration rate [eGFR] 25-60 ml/min/1.73m2, absolute left ventricular longitudinal strain [LVGLS] <18% on 2D-speckle tracking echocardiography or meeting any of the American Society of Echocardiography criteria for diastolic dysfunction: septal e' <7 cm/sec, lateral e'<10 cm/sec, average E/e' ratio>14, left atrial volume index >34 mL/m2, or peak tricuspid regurgitation velocity >2.8 m/sec). Half of the patients will be randomized to receive dapagliflozin for six months as an add-on to standard of care (SOC). Metabolomic testing and cardiac and functional exercise testing will be done at baseline and at six months. The aim of the current study is to investigate whether SGLT2i-induced metabolomic changes are associated with improved cardiac and functional testing ascertained on 2D-speckle tracking echocardiography or cardiopulmonary functional testing at six months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases, Heart Failure With Preserved Ejection Fraction, Kidney Diseases, Heart Failure
Keywords
kidney, heart failure, kidney diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Model Description
30 subjects will be randomized to intervention. 30 subjects will be randomized to standard of care.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Thirty individuals will be randomized to dapagliflozin 10mg to be taken daily for six months.
Arm Title
Standard of Care group
Arm Type
No Intervention
Arm Description
Thirty individuals will be randomized to standard of care treatment.
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin 10 MG [Farxiga]
Intervention Description
10mg (milligram) tablet to be taken orally once daily for 6 months. Manufacturer: Astrazeneca. Study drug will be stored and dispensed by the Interventional Drug Service Pharmacy at Northwestern University.
Primary Outcome Measure Information:
Title
Left ventricular longitudinal strain (LVLS)
Description
2D-speckle tracking echocardiography
Time Frame
6 months
Title
Peak VO2 (oxygen consumption)
Description
Cardiopulmonary exercise stress test
Time Frame
6 months
Title
Circulating plasma metabolite concentrations
Description
Plasma
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Left Atrial Reservoir Strain (LARS)
Description
2D-STE
Time Frame
6 months
Title
Right ventricular free wall strain
Description
2D-STE
Time Frame
6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >18 years of age eGFR 25-60 ml/min/1,73m2 (eGFR = estimated glomerular filtration rate) On stable doses of diuretics and/or angiotensin converting enzyme inhibitor or angiotensin receptor blocker Evidence of subclinical heart failure with preserved ejection fraction at their pre-exercise echocardiogram (defined as meeting any of the American Society of Echocardiography (ASE) criteria for diastolic dysfunction [septal e'<7 cm/wc, average E/e' ratio>14, left atrial volume index >34 mL/m2, and peak TR velocity >2.8 m/sec] or absolute left ventricular longitudinal strain < 18%) Exclusion Criteria: presence or history of diabetes coronary revascularization within the last 6 months hemodynamically significant valvular disease significant lung disease requiring home oxygen angina (chest pain) non-revascularized myocardial ischemia systolic BP <100 or >180 mmHg pregnancy clinical heart failure symptoms history of systemic disease processes that can cause HFpEF such as amyloidosis or sarcoidosis any musculoskeletal or chronic condition that will interfere with completion of cardiac testing active cancer immunosuppressive therapy baseline or pre-exercise echocardiogram demonstrates a reduced ejection fraction </= 50% currently on sodium glucose cotransporter 2 inhibitor (SGLT2i) therapy Hypersensitivity to a SGLT2i Pre-existing liver disease ALT/AST> 3x normal (ALT = alanine aminotransferase AST = aspartate aminotransferase) history of recurrent urinary tract infections (in the opinion of the investigator) or a urinary tract infection in the last 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rupal Mehta, MD
Phone
(312) 503-1536
Email
rupal.mehta@northwestern.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Tamara Isakova, MD
Phone
(312) 503-6921
Email
tamara.isakova@northwestern.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rupal Mehta, MD
Organizational Affiliation
Northwestern Univeristy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60607
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rupal C Mehta, MD
Phone
312-503-1536
Email
rupal.mehta@northwestern.edu
First Name & Middle Initial & Last Name & Degree
Tamara Isakova, MD
Phone
312-926-2000
Email
tamara.isakova@northwestern.edu
First Name & Middle Initial & Last Name & Degree
Rupal Mehta, MD
First Name & Middle Initial & Last Name & Degree
Tamara Isakova, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
29386200
Citation
Benjamin EJ, Virani SS, Callaway CW, Chamberlain AM, Chang AR, Cheng S, Chiuve SE, Cushman M, Delling FN, Deo R, de Ferranti SD, Ferguson JF, Fornage M, Gillespie C, Isasi CR, Jimenez MC, Jordan LC, Judd SE, Lackland D, Lichtman JH, Lisabeth L, Liu S, Longenecker CT, Lutsey PL, Mackey JS, Matchar DB, Matsushita K, Mussolino ME, Nasir K, O'Flaherty M, Palaniappan LP, Pandey A, Pandey DK, Reeves MJ, Ritchey MD, Rodriguez CJ, Roth GA, Rosamond WD, Sampson UKA, Satou GM, Shah SH, Spartano NL, Tirschwell DL, Tsao CW, Voeks JH, Willey JZ, Wilkins JT, Wu JH, Alger HM, Wong SS, Muntner P; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2018 Update: A Report From the American Heart Association. Circulation. 2018 Mar 20;137(12):e67-e492. doi: 10.1161/CIR.0000000000000558. Epub 2018 Jan 31. No abstract available. Erratum In: Circulation. 2018 Mar 20;137(12 ):e493.
Results Reference
background
PubMed Identifier
29477157
Citation
Saran R, Robinson B, Abbott KC, Agodoa LYC, Bhave N, Bragg-Gresham J, Balkrishnan R, Dietrich X, Eckard A, Eggers PW, Gaipov A, Gillen D, Gipson D, Hailpern SM, Hall YN, Han Y, He K, Herman W, Heung M, Hirth RA, Hutton D, Jacobsen SJ, Jin Y, Kalantar-Zadeh K, Kapke A, Kovesdy CP, Lavallee D, Leslie J, McCullough K, Modi Z, Molnar MZ, Montez-Rath M, Moradi H, Morgenstern H, Mukhopadhyay P, Nallamothu B, Nguyen DV, Norris KC, O'Hare AM, Obi Y, Park C, Pearson J, Pisoni R, Potukuchi PK, Rao P, Repeck K, Rhee CM, Schrager J, Schaubel DE, Selewski DT, Shaw SF, Shi JM, Shieu M, Sim JJ, Soohoo M, Steffick D, Streja E, Sumida K, Tamura MK, Tilea A, Tong L, Wang D, Wang M, Woodside KJ, Xin X, Yin M, You AS, Zhou H, Shahinian V. US Renal Data System 2017 Annual Data Report: Epidemiology of Kidney Disease in the United States. Am J Kidney Dis. 2018 Mar;71(3 Suppl 1):A7. doi: 10.1053/j.ajkd.2018.01.002. No abstract available. Erratum In: Am J Kidney Dis. 2018 Apr;71(4):501.
Results Reference
background
PubMed Identifier
21262990
Citation
Heidenreich PA, Trogdon JG, Khavjou OA, Butler J, Dracup K, Ezekowitz MD, Finkelstein EA, Hong Y, Johnston SC, Khera A, Lloyd-Jones DM, Nelson SA, Nichol G, Orenstein D, Wilson PW, Woo YJ; American Heart Association Advocacy Coordinating Committee; Stroke Council; Council on Cardiovascular Radiology and Intervention; Council on Clinical Cardiology; Council on Epidemiology and Prevention; Council on Arteriosclerosis; Thrombosis and Vascular Biology; Council on Cardiopulmonary; Critical Care; Perioperative and Resuscitation; Council on Cardiovascular Nursing; Council on the Kidney in Cardiovascular Disease; Council on Cardiovascular Surgery and Anesthesia, and Interdisciplinary Council on Quality of Care and Outcomes Research. Forecasting the future of cardiovascular disease in the United States: a policy statement from the American Heart Association. Circulation. 2011 Mar 1;123(8):933-44. doi: 10.1161/CIR.0b013e31820a55f5. Epub 2011 Jan 24.
Results Reference
background
PubMed Identifier
18760751
Citation
Ahmed A, Campbell RC. Epidemiology of chronic kidney disease in heart failure. Heart Fail Clin. 2008 Oct;4(4):387-99. doi: 10.1016/j.hfc.2008.03.008.
Results Reference
background
PubMed Identifier
29478868
Citation
House AA. Management of Heart Failure in Advancing CKD: Core Curriculum 2018. Am J Kidney Dis. 2018 Aug;72(2):284-295. doi: 10.1053/j.ajkd.2017.12.006. Epub 2018 Feb 23.
Results Reference
background
PubMed Identifier
25370599
Citation
Ueda T, Kawakami R, Sugawara Y, Okada S, Nishida T, Onoue K, Soeda T, Okayama S, Takeda Y, Watanabe M, Kawata H, Uemura S, Saito Y. Worsening of renal function during 1 year after hospital discharge is a strong and independent predictor of all-cause mortality in acute decompensated heart failure. J Am Heart Assoc. 2014 Nov 4;3(6):e001174. doi: 10.1161/JAHA.114.001174.
Results Reference
background
PubMed Identifier
10716471
Citation
Dries DL, Exner DV, Domanski MJ, Greenberg B, Stevenson LW. The prognostic implications of renal insufficiency in asymptomatic and symptomatic patients with left ventricular systolic dysfunction. J Am Coll Cardiol. 2000 Mar 1;35(3):681-9. doi: 10.1016/s0735-1097(99)00608-7.
Results Reference
background
PubMed Identifier
16461840
Citation
Hillege HL, Nitsch D, Pfeffer MA, Swedberg K, McMurray JJ, Yusuf S, Granger CB, Michelson EL, Ostergren J, Cornel JH, de Zeeuw D, Pocock S, van Veldhuisen DJ; Candesartan in Heart Failure: Assessment of Reduction in Mortality and Morbidity (CHARM) Investigators. Renal function as a predictor of outcome in a broad spectrum of patients with heart failure. Circulation. 2006 Feb 7;113(5):671-8. doi: 10.1161/CIRCULATIONAHA.105.580506.
Results Reference
background
PubMed Identifier
29166232
Citation
Neal B, Perkovic V, Matthews DR. Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes. N Engl J Med. 2017 Nov 23;377(21):2099. doi: 10.1056/NEJMc1712572. No abstract available.
Results Reference
background
PubMed Identifier
26981940
Citation
Zinman B, Lachin JM, Inzucchi SE. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. N Engl J Med. 2016 Mar 17;374(11):1094. doi: 10.1056/NEJMc1600827. No abstract available.
Results Reference
background
PubMed Identifier
34184823
Citation
Herrington WG, Savarese G, Haynes R, Marx N, Mellbin L, Lund LH, Dendale P, Seferovic P, Rosano G, Staplin N, Baigent C, Cosentino F. Cardiac, renal, and metabolic effects of sodium-glucose co-transporter 2 inhibitors: a position paper from the European Society of Cardiology ad-hoc task force on sodium-glucose co-transporter 2 inhibitors. Eur J Heart Fail. 2021 Aug;23(8):1260-1275. doi: 10.1002/ejhf.2286. Epub 2021 Jul 20.
Results Reference
background
PubMed Identifier
30456329
Citation
Verma S, Rawat S, Ho KL, Wagg CS, Zhang L, Teoh H, Dyck JE, Uddin GM, Oudit GY, Mayoux E, Lehrke M, Marx N, Lopaschuk GD. Empagliflozin Increases Cardiac Energy Production in Diabetes: Novel Translational Insights Into the Heart Failure Benefits of SGLT2 Inhibitors. JACC Basic Transl Sci. 2018 Aug 26;3(5):575-587. doi: 10.1016/j.jacbts.2018.07.006. eCollection 2018 Oct.
Results Reference
background
PubMed Identifier
27289124
Citation
Mudaliar S, Alloju S, Henry RR. Can a Shift in Fuel Energetics Explain the Beneficial Cardiorenal Outcomes in the EMPA-REG OUTCOME Study? A Unifying Hypothesis. Diabetes Care. 2016 Jul;39(7):1115-22. doi: 10.2337/dc16-0542.
Results Reference
background
PubMed Identifier
30265814
Citation
Kumar N, Garg A, Bhatt DL, Sabongui S, Gupta N, Chaudhry S, Arena R, Verma S. Empagliflozin improves cardiorespiratory fitness in type 2 diabetes: translational implications. Can J Physiol Pharmacol. 2018 Nov;96(11):1184-1187. doi: 10.1139/cjpp-2018-0359.
Results Reference
background
PubMed Identifier
27679584
Citation
Verma S, Garg A, Yan AT, Gupta AK, Al-Omran M, Sabongui A, Teoh H, Mazer CD, Connelly KA. Effect of Empagliflozin on Left Ventricular Mass and Diastolic Function in Individuals With Diabetes: An Important Clue to the EMPA-REG OUTCOME Trial? Diabetes Care. 2016 Dec;39(12):e212-e213. doi: 10.2337/dc16-1312. Epub 2016 Sep 27. No abstract available.
Results Reference
background
PubMed Identifier
15504931
Citation
Bagby SP. Obesity-initiated metabolic syndrome and the kidney: a recipe for chronic kidney disease? J Am Soc Nephrol. 2004 Nov;15(11):2775-91. doi: 10.1097/01.ASN.0000141965.28037.EE. No abstract available.
Results Reference
background
PubMed Identifier
3361755
Citation
Smogorzewski M, Piskorska G, Borum PR, Massry SG. Chronic renal failure, parathyroid hormone and fatty acids oxidation in skeletal muscle. Kidney Int. 1988 Feb;33(2):555-60. doi: 10.1038/ki.1988.33.
Results Reference
background
PubMed Identifier
26050125
Citation
Rhee EP. Metabolomics and renal disease. Curr Opin Nephrol Hypertens. 2015 Jul;24(4):371-9. doi: 10.1097/MNH.0000000000000136.
Results Reference
background
PubMed Identifier
28262773
Citation
Hocher B, Adamski J. Metabolomics for clinical use and research in chronic kidney disease. Nat Rev Nephrol. 2017 May;13(5):269-284. doi: 10.1038/nrneph.2017.30. Epub 2017 Mar 6.
Results Reference
background
PubMed Identifier
29724883
Citation
Grams ME, Shafi T, Rhee EP. Metabolomics Research in Chronic Kidney Disease. J Am Soc Nephrol. 2018 Jun;29(6):1588-1590. doi: 10.1681/ASN.2018030256. Epub 2018 May 3. No abstract available.
Results Reference
background
PubMed Identifier
27692817
Citation
Kalim S, Rhee EP. An overview of renal metabolomics. Kidney Int. 2017 Jan;91(1):61-69. doi: 10.1016/j.kint.2016.08.021. Epub 2016 Sep 28.
Results Reference
background
PubMed Identifier
30931940
Citation
Chen DQ, Cao G, Chen H, Argyopoulos CP, Yu H, Su W, Chen L, Samuels DC, Zhuang S, Bayliss GP, Zhao S, Yu XY, Vaziri ND, Wang M, Liu D, Mao JR, Ma SX, Zhao J, Zhang Y, Shang YQ, Kang H, Ye F, Cheng XH, Li XR, Zhang L, Meng MX, Guo Y, Zhao YY. Identification of serum metabolites associating with chronic kidney disease progression and anti-fibrotic effect of 5-methoxytryptophan. Nat Commun. 2019 Apr 1;10(1):1476. doi: 10.1038/s41467-019-09329-0.
Results Reference
background
PubMed Identifier
29519950
Citation
Wang F, Sun L, Sun Q, Liang L, Gao X, Li R, Pan A, Li H, Deng Y, Hu FB, Wu J, Zeng R, Lin X. Associations of Plasma Amino Acid and Acylcarnitine Profiles with Incident Reduced Glomerular Filtration Rate. Clin J Am Soc Nephrol. 2018 Apr 6;13(4):560-568. doi: 10.2215/CJN.07650717. Epub 2018 Mar 8.
Results Reference
background
PubMed Identifier
29121091
Citation
Hiltunen TP, Rimpela JM, Mohney RP, Stirdivant SM, Kontula KK. Effects of four different antihypertensive drugs on plasma metabolomic profiles in patients with essential hypertension. PLoS One. 2017 Nov 9;12(11):e0187729. doi: 10.1371/journal.pone.0187729. eCollection 2017.
Results Reference
background
PubMed Identifier
30281132
Citation
Cozzolino M, Mangano M, Stucchi A, Ciceri P, Conte F, Galassi A. Cardiovascular disease in dialysis patients. Nephrol Dial Transplant. 2018 Oct 1;33(suppl_3):iii28-iii34. doi: 10.1093/ndt/gfy174.
Results Reference
background
PubMed Identifier
28379378
Citation
Zewinger S, Kleber ME, Rohrer L, Lehmann M, Triem S, Jennings RT, Petrakis I, Dressel A, Lepper PM, Scharnagl H, Ritsch A, Thorand B, Heier M, Meisinger C, de Las Heras Gala T, Koenig W, Wagenpfeil S, Schwedhelm E, Boger RH, Laufs U, von Eckardstein A, Landmesser U, Luscher TF, Fliser D, Marz W, Meinitzer A, Speer T. Symmetric dimethylarginine, high-density lipoproteins and cardiovascular disease. Eur Heart J. 2017 May 21;38(20):1597-1607. doi: 10.1093/eurheartj/ehx118.
Results Reference
background
PubMed Identifier
29550017
Citation
Potocnjak I, Radulovic B, Degoricija V, Trbusic M, Pregartner G, Berghold A, Meinitzer A, Frank S. Serum concentrations of asymmetric and symmetric dimethylarginine are associated with mortality in acute heart failure patients. Int J Cardiol. 2018 Jun 15;261:109-113. doi: 10.1016/j.ijcard.2018.03.037. Epub 2018 Mar 11.
Results Reference
background
PubMed Identifier
21817129
Citation
Schepers E, Barreto DV, Liabeuf S, Glorieux G, Eloot S, Barreto FC, Massy Z, Vanholder R; European Uremic Toxin Work Group (EUTox). Symmetric dimethylarginine as a proinflammatory agent in chronic kidney disease. Clin J Am Soc Nephrol. 2011 Oct;6(10):2374-83. doi: 10.2215/CJN.01720211. Epub 2011 Aug 4. Erratum In: Clin J Am Soc Nephrol. 2012 May;7(5):874.
Results Reference
background
PubMed Identifier
24218128
Citation
Memon L, Spasojevic-Kalimanovska V, Stanojevic NB, Kotur-Stevuljevic J, Simic-Ogrizovic S, Giga V, Dopsaj V, Jelic-Ivanovic Z, Spasic S. Are levels of NT-proBNP and SDMA useful to determine diastolic dysfunction in chronic kidney disease and renal transplant patients? J Clin Lab Anal. 2013 Nov;27(6):461-70. doi: 10.1002/jcla.21628.
Results Reference
background
PubMed Identifier
27561923
Citation
Daniele G, Xiong J, Solis-Herrera C, Merovci A, Eldor R, Tripathy D, DeFronzo RA, Norton L, Abdul-Ghani M. Dapagliflozin Enhances Fat Oxidation and Ketone Production in Patients With Type 2 Diabetes. Diabetes Care. 2016 Nov;39(11):2036-2041. doi: 10.2337/dc15-2688. Epub 2016 Aug 25.
Results Reference
background
PubMed Identifier
26861783
Citation
Ferrannini E, Baldi S, Frascerra S, Astiarraga B, Heise T, Bizzotto R, Mari A, Pieber TR, Muscelli E. Shift to Fatty Substrate Utilization in Response to Sodium-Glucose Cotransporter 2 Inhibition in Subjects Without Diabetes and Patients With Type 2 Diabetes. Diabetes. 2016 May;65(5):1190-5. doi: 10.2337/db15-1356. Epub 2016 Feb 9.
Results Reference
background
PubMed Identifier
32115853
Citation
Mulder S, Hammarstedt A, Nagaraj SB, Nair V, Ju W, Hedberg J, Greasley PJ, Eriksson JW, Oscarsson J, Heerspink HJL. A metabolomics-based molecular pathway analysis of how the sodium-glucose co-transporter-2 inhibitor dapagliflozin may slow kidney function decline in patients with diabetes. Diabetes Obes Metab. 2020 Jul;22(7):1157-1166. doi: 10.1111/dom.14018. Epub 2020 Mar 25.
Results Reference
background
PubMed Identifier
28874423
Citation
Kappel BA, Lehrke M, Schutt K, Artati A, Adamski J, Lebherz C, Marx N. Effect of Empagliflozin on the Metabolic Signature of Patients With Type 2 Diabetes Mellitus and Cardiovascular Disease. Circulation. 2017 Sep 5;136(10):969-972. doi: 10.1161/CIRCULATIONAHA.117.029166. No abstract available.
Results Reference
background
PubMed Identifier
29526832
Citation
Radholm K, Figtree G, Perkovic V, Solomon SD, Mahaffey KW, de Zeeuw D, Fulcher G, Barrett TD, Shaw W, Desai M, Matthews DR, Neal B. Canagliflozin and Heart Failure in Type 2 Diabetes Mellitus: Results From the CANVAS Program. Circulation. 2018 Jul 31;138(5):458-468. doi: 10.1161/CIRCULATIONAHA.118.034222.
Results Reference
background
PubMed Identifier
29133604
Citation
Mahaffey KW, Neal B, Perkovic V, de Zeeuw D, Fulcher G, Erondu N, Shaw W, Fabbrini E, Sun T, Li Q, Desai M, Matthews DR; CANVAS Program Collaborative Group. Canagliflozin for Primary and Secondary Prevention of Cardiovascular Events: Results From the CANVAS Program (Canagliflozin Cardiovascular Assessment Study). Circulation. 2018 Jan 23;137(4):323-334. doi: 10.1161/CIRCULATIONAHA.117.032038. Epub 2017 Nov 13.
Results Reference
background
PubMed Identifier
25533966
Citation
Zamani P, Rawat D, Shiva-Kumar P, Geraci S, Bhuva R, Konda P, Doulias PT, Ischiropoulos H, Townsend RR, Margulies KB, Cappola TP, Poole DC, Chirinos JA. Effect of inorganic nitrate on exercise capacity in heart failure with preserved ejection fraction. Circulation. 2015 Jan 27;131(4):371-80; discussion 380. doi: 10.1161/CIRCULATIONAHA.114.012957. Epub 2014 Dec 22.
Results Reference
background
PubMed Identifier
29762782
Citation
Chong J, Soufan O, Li C, Caraus I, Li S, Bourque G, Wishart DS, Xia J. MetaboAnalyst 4.0: towards more transparent and integrative metabolomics analysis. Nucleic Acids Res. 2018 Jul 2;46(W1):W486-W494. doi: 10.1093/nar/gky310.
Results Reference
background
Links:
URL
https://cardiab.biomedcentral.com/articles/10.1186/s12933-017-0569-8
Description
Reference #28 in protocol. Symmetric and asymmetric dimethylarginine as risk markers of cardiovascular disease, all-cause mortality and deterioration in kidney function in persons with type 2 diabetes and microalbuminuria.

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Effect of Dapagliflozin on Metabolomics and Cardiac Mechanics in Chronic Kidney Disease

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