Literature DB >> 14693576

Myocardial protection using fructose-1,6-diphosphate during coronary artery bypass graft surgery: a randomized, placebo-controlled clinical trial.

Bernhard J Riedel1, Janos Gal, Gillian Ellis, Paul J Marangos, Anthony W Fox, David Royston.   

Abstract

UNLABELLED: In vitro and in vivo studies suggest that fructose-1,6-diphosphate (FDP), an intermediary glycolytic pathway metabolite, ameliorates ischemic tissue injury through increased high-energy phosphate levels and may therefore have cardioprotective properties in patients undergoing coronary artery bypass graft (CABG) surgery. We designed a randomized, placebo-controlled, double-blinded, sequential-cohort, dose-ranging safety study to test 5 FDP dosage regimens in patients (n = 120; 60 FDP, 60 control) undergoing CABG surgery. Of these dosage regimens, 3 produced no benefit, 1 produced improved cardiac function, and 1 required adjustment as a result of metabolic acidosis. This suggests that we achieved the intended effect of a dose-ranging study. The expected response was observed in patients treated with 250 mg/kg FDP IV before surgery and 2.5 mM FDP as a cardioplegic additive (n = 15). These patients had lower serum creatine kinase-MB levels 2, 4, and 6 h after reperfusion (P < 0.05), fewer perioperative myocardial infarctions (P < 0.05), and improved postoperative cardiac function, as evidenced by higher left ventricular stroke work index (LVSWI) 6, 12, and 16 h (P < 0.01) and cardiac index (CI) at 12 and 16 h (P < 0.05) after reperfusion. Overall efficacy of FDP was tested across all regimens that included IV FDP (n = 88; 44 FDP, 44 control) using 2 (FDP versus placebo) x 3 (dose size) factorial analyses. Area-under-curve (AUC) analysis demonstrated a significant increase in CI (AUC-16h, P = 0.013) and LVSWI (AUC-16h, P = 0.003) and reduction in CK-MB levels (AUC-16h, P < 0.05) in FDP-treated patients. The internal consistency of this dataset suggests that FDP may provide myocardial protection in CABG surgery and supports previous laboratory and clinical studies of FDP in ischemic heart disease. IMPLICATIONS: Fructose-1,6-diphosphate (FDP) may increase high-energy phosphate levels under anaerobic conditions and therefore ameliorate ischemic injury. A dose-ranging safety study for FDP was conducted in patients undergoing coronary artery surgery. Preischemic provision of FDP significantly improved cardiac function and reduced perioperative ischemic injury. These myocardial protective effects may improve patient outcome after cardiac surgery.

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Year:  2004        PMID: 14693576     DOI: 10.1213/01.ane.0000094336.97693.90

Source DB:  PubMed          Journal:  Anesth Analg        ISSN: 0003-2999            Impact factor:   5.108


  8 in total

1.  Use of an Escherichia coli recombinant producing thermostable polyphosphate kinase as an ATP regenerator to produce fructose 1,6-diphosphate.

Authors:  Seishi Iwamoto; Kei Motomura; Yasuharu Shinoda; Masaaki Urata; Junichi Kato; Noboru Takiguchi; Hisao Ohtake; Ryuichi Hirota; Akio Kuroda
Journal:  Appl Environ Microbiol       Date:  2007-07-06       Impact factor: 4.792

2.  Metabolomic profiling of the heart during acute ischemic preconditioning reveals a role for SIRT1 in rapid cardioprotective metabolic adaptation.

Authors:  Sergiy M Nadtochiy; William Urciuoli; Jimmy Zhang; Xenia Schafer; Joshua Munger; Paul S Brookes
Journal:  J Mol Cell Cardiol       Date:  2015-09-24       Impact factor: 5.000

3.  Fructose-1, 6-diphosphate (FDP) as a novel antidote for yellow oleander-induced cardiac toxicity: a randomized controlled double blind study.

Authors:  Indika Gawarammana; Fahim Mohamed; Steven J Bowe; Ashoka Rathnathilake; Shantha K Narangoda; Shifa Azher; Andrew H Dawson; Nick A Buckley
Journal:  BMC Emerg Med       Date:  2010-06-29

4.  Fructose-1,6-bisphosphate has anticonvulsant activity in models of acute seizures in adult rats.

Authors:  Xiao-Yuan Lian; Firdous A Khan; Janet L Stringer
Journal:  J Neurosci       Date:  2007-10-31       Impact factor: 6.167

5.  Protection of rat cardiac myocytes by fructose-1,6-bisphosphate and 2,3-butanedione.

Authors:  Thomas J Wheeler; Sufan Chien
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

6.  Fructose 1,6-Bisphosphate as a Protective Agent for Experimental Fat Grafting.

Authors:  Tao Lv; Yunpeng Gu; Jianhai Bi; Ning Kang; Zhigang Yang; Xin Fu; Qian Wang; Li Yan; Xia Liu; Yilin Cao; Ran Xiao
Journal:  Stem Cells Transl Med       Date:  2019-02-18       Impact factor: 6.940

7.  Fructose-1,6-Bisphosphate Protects Hippocampal Rat Slices from NMDA Excitotoxicity.

Authors:  Kamal M Yakoub; Giacomo Lazzarino; Angela M Amorini; Giuseppe Caruso; Concetta Scazzone; Marcello Ciaccio; Barbara Tavazzi; Giuseppe Lazzarino; Antonio Belli; Valentina Di Pietro
Journal:  Int J Mol Sci       Date:  2019-05-07       Impact factor: 5.923

Review 8.  Fructation in vivo: detrimental and protective effects of fructose.

Authors:  H M Semchyshyn
Journal:  Biomed Res Int       Date:  2013-07-24       Impact factor: 3.411

  8 in total

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