Skip to main content
Top
Published in: Trials 1/2015

Open Access 01-12-2015 | Study protocol

The acute effect of beta-guanidinopropionic acid versus creatine or placebo in healthy men (ABC Trial): study protocol for a randomized controlled trial

Authors: Fares A Karamat, Deborah L Horjus, Yentl C Haan, Lisa van der Woude, Inge Oudman, Gert A van Montfrans, Joseph F Clark, Lizzy M Brewster

Published in: Trials | Issue 1/2015

Login to get access

Abstract

Background

Despite adequate treatment, up to 30% of treated antihypertensive patients with primary, uncomplicated hypertension remain uncontrolled. We proposed that high intracellular activity of the ATP regenerating enzyme creatine kinase (CK) increases pressor responses and hypertension risk. In line with this, we found that plasma CK activity after rest, a surrogate measure of tissue activity, is the main predictor of blood pressure levels and failure of antihypertensive therapy in the general population. In addition, the creatine analog and competitive oral creatine kinase inhibitor beta-guanidinopropionic acid effectively and safely reduced blood pressure in the spontaneously hypertensive rat. However, to our knowledge there are no human data on the safety of oral supplementation with this substance. Therefore, we will assess the tolerability of beta-guanidinopropionic acid in men, compared to creatine and placebo.

Methods/Design

This is a randomized, active and placebo controlled, triple blind, double dummy, single center clinical intervention trial in 24 healthy male volunteers, 18 to 50 years old, recruited in the Netherlands. The intervention consists of one week of daily oral administration of beta-guanidinopropionic acid 100 mg, creatine 5 gram, or placebo. The primary outcome is the tolerability of beta-guanidinopropionic acid as a descriptive measure, in an intent-to-treat analysis. Other outcomes include the placebo-adjusted differences with baseline in biochemical and hemodynamic parameters, including plasma markers of muscle tissue damage, urine sodium excretion, resting sitting systolic and diastolic brachial blood pressure, supine systolic and diastolic central blood pressure, pulse wave velocity and augmentation index, heart rate, cardiac contractility, cardiac output, and total peripheral resistance.

Discussion

There is an unfulfilled need for new conservative options to treat resistant hypertension. This study will provide first-in-men data on creatine kinase inhibition as a potential new class of antihypertensive drugs.

Trial registration

The Netherlands National Trial Register Trialregister.nl (identifier NTR 4444), registered 9 March 2014.
Literature
1.
go back to reference Gu Q, Dillon CF, Burt VL, Gillum RF. Association of hypertension treatment and control with all-cause and cardiovascular disease mortality among US adults with hypertension. Am J Hypertens. 2010;23:38–45.CrossRefPubMed Gu Q, Dillon CF, Burt VL, Gillum RF. Association of hypertension treatment and control with all-cause and cardiovascular disease mortality among US adults with hypertension. Am J Hypertens. 2010;23:38–45.CrossRefPubMed
2.
go back to reference Calhoun DA, Jones D, Textor S, Goff DC, Murphy TP, Toto RD, et al. American Heart Association Professional Education Committee. Resistant hypertension: diagnosis, evaluation, and treatment: a scientific statement from the American Heart Association Professional Education Committee of the Council for High Blood Pressure Research. Circulation. 2008;117:e510–26.CrossRefPubMed Calhoun DA, Jones D, Textor S, Goff DC, Murphy TP, Toto RD, et al. American Heart Association Professional Education Committee. Resistant hypertension: diagnosis, evaluation, and treatment: a scientific statement from the American Heart Association Professional Education Committee of the Council for High Blood Pressure Research. Circulation. 2008;117:e510–26.CrossRefPubMed
3.
go back to reference Brewster LM, Van Montfrans GA, Kleijnen J. Systematic review: antihypertensive drug therapy in black patients. Ann Intern Med. 2004;141:614–27.CrossRefPubMed Brewster LM, Van Montfrans GA, Kleijnen J. Systematic review: antihypertensive drug therapy in black patients. Ann Intern Med. 2004;141:614–27.CrossRefPubMed
4.
go back to reference Laurent S, Schlaich M, Esler M. New drugs, procedures, and devices for hypertension. Lancet. 2012;380:591–600.CrossRefPubMed Laurent S, Schlaich M, Esler M. New drugs, procedures, and devices for hypertension. Lancet. 2012;380:591–600.CrossRefPubMed
5.
go back to reference Oudman I, Kewalbansing P, Valkengoed I, Zwinderman A, Clark JF, Van Montfrans GA, et al. Creatine kinase is associated with failure of hypertension treatment. J Hypertens. 2013;31:1025–31.CrossRefPubMed Oudman I, Kewalbansing P, Valkengoed I, Zwinderman A, Clark JF, Van Montfrans GA, et al. Creatine kinase is associated with failure of hypertension treatment. J Hypertens. 2013;31:1025–31.CrossRefPubMed
6.
go back to reference Brewster LM, Mairuhu G, Bindraban NR, Koopmans RP, Clark JF, Van Montfrans GA. Creatine kinase activity is associated with blood pressure. Circulation. 2006;114:2034–9.CrossRefPubMed Brewster LM, Mairuhu G, Bindraban NR, Koopmans RP, Clark JF, Van Montfrans GA. Creatine kinase activity is associated with blood pressure. Circulation. 2006;114:2034–9.CrossRefPubMed
7.
go back to reference Hittel DS, Hathout Y, Hoffman EP, Houmard JA. Proteome analysis of skeletal muscle from obese and morbidly obese women. Diabetes. 2005;54:1283–8.CrossRefPubMed Hittel DS, Hathout Y, Hoffman EP, Houmard JA. Proteome analysis of skeletal muscle from obese and morbidly obese women. Diabetes. 2005;54:1283–8.CrossRefPubMed
8.
go back to reference Brewster LM, Clark JF, Van Montfrans GA. Is greater tissue activity of creatine kinase the genetic factor increasing hypertension risk in black people of sub-Saharan African descent? J Hypertens. 2000;18:1537–44.CrossRefPubMed Brewster LM, Clark JF, Van Montfrans GA. Is greater tissue activity of creatine kinase the genetic factor increasing hypertension risk in black people of sub-Saharan African descent? J Hypertens. 2000;18:1537–44.CrossRefPubMed
9.
go back to reference Seccia TM, Atlante A, Vulpis V, Marra E, Passarella S, Pirrelli A. Mitochondrial energy metabolism in the left ventricular tissue of spontaneously hypertensive rats: abnormalities in both adeninenucleotide and phosphate translocators and enzyme adenylate-kinase and creatine-phosphokinase activities. Clin Exp Hypertens. 1998;20:345–38.CrossRefPubMed Seccia TM, Atlante A, Vulpis V, Marra E, Passarella S, Pirrelli A. Mitochondrial energy metabolism in the left ventricular tissue of spontaneously hypertensive rats: abnormalities in both adeninenucleotide and phosphate translocators and enzyme adenylate-kinase and creatine-phosphokinase activities. Clin Exp Hypertens. 1998;20:345–38.CrossRefPubMed
10.
go back to reference Jin X, Xia L, Wang LS, Shi JZ, Zheng Y, Chen WL, et al. Differential protein expression in hypertrophic heart with and without hypertension in spontaneously hypertensive rats. Proteomics. 2006;6:1948–56.CrossRefPubMed Jin X, Xia L, Wang LS, Shi JZ, Zheng Y, Chen WL, et al. Differential protein expression in hypertrophic heart with and without hypertension in spontaneously hypertensive rats. Proteomics. 2006;6:1948–56.CrossRefPubMed
11.
go back to reference Brewster LM, Van Bree S, Reijneveld JC, Notermans NC, Verschuren WM, Clark JF, et al. Hypertension risk in idiopathic hyperCKemia. J Neurol. 2008;255:11–5.CrossRefPubMed Brewster LM, Van Bree S, Reijneveld JC, Notermans NC, Verschuren WM, Clark JF, et al. Hypertension risk in idiopathic hyperCKemia. J Neurol. 2008;255:11–5.CrossRefPubMed
12.
go back to reference Brewster LM, Taherzadeh Z, Volger S, Clark JF, Rolf T, Wolf H, et al. Ethnic differences in resistance artery contractility of normotensive pregnant women. Am J Physiol Heart Circ Physiol. 2010;299:H431–6.CrossRefPubMed Brewster LM, Taherzadeh Z, Volger S, Clark JF, Rolf T, Wolf H, et al. Ethnic differences in resistance artery contractility of normotensive pregnant women. Am J Physiol Heart Circ Physiol. 2010;299:H431–6.CrossRefPubMed
13.
go back to reference Karamat FA, Oudman I, Ris-Stalpers C, Afink GB, Keijser R, Clark JF, et al. Resistance Artery Creatine Kinase mRNA and Blood Pressure in Humans. Hypertension. 2014;63:68–73.CrossRefPubMed Karamat FA, Oudman I, Ris-Stalpers C, Afink GB, Keijser R, Clark JF, et al. Resistance Artery Creatine Kinase mRNA and Blood Pressure in Humans. Hypertension. 2014;63:68–73.CrossRefPubMed
14.
go back to reference Brewster LM, Seedat YK. Why do hypertensive patients of African ancestry respond better to calcium blockers and diuretics than to ACE inhibitors and β-adrenergic blockers? A systematic review. BMC Med. 2013;11:141.CrossRefPubMedPubMedCentral Brewster LM, Seedat YK. Why do hypertensive patients of African ancestry respond better to calcium blockers and diuretics than to ACE inhibitors and β-adrenergic blockers? A systematic review. BMC Med. 2013;11:141.CrossRefPubMedPubMedCentral
15.
go back to reference Oudman I, Karamat FA, Spijkers LJA, Clark JF, Van Kuilenburg ABP, Leen R, et al. CK inhibition with a competitive CK inhibitor reduced blood pressure in an animal model of hypertension [abstract]. J Hypertens. 2013;31:e138.CrossRef Oudman I, Karamat FA, Spijkers LJA, Clark JF, Van Kuilenburg ABP, Leen R, et al. CK inhibition with a competitive CK inhibitor reduced blood pressure in an animal model of hypertension [abstract]. J Hypertens. 2013;31:e138.CrossRef
16.
go back to reference Oudman I, Clark JF, Brewster LM. The effect of the creatine analogue beta-guanidinopropionic acid on energy metabolism: a systematic review. PLoS One. 2013;8:e52879.CrossRefPubMedPubMedCentral Oudman I, Clark JF, Brewster LM. The effect of the creatine analogue beta-guanidinopropionic acid on energy metabolism: a systematic review. PLoS One. 2013;8:e52879.CrossRefPubMedPubMedCentral
17.
go back to reference Tachikawa M, Hosoya K. Transport characteristics of guanidine compounds at the blood-brain barrier and blood-cerebrospinal fluid barrier: relevance to neural disorders. Fluids Barriers CNS. 2011;8:13.CrossRefPubMedPubMedCentral Tachikawa M, Hosoya K. Transport characteristics of guanidine compounds at the blood-brain barrier and blood-cerebrospinal fluid barrier: relevance to neural disorders. Fluids Barriers CNS. 2011;8:13.CrossRefPubMedPubMedCentral
18.
go back to reference Boehm EA, Radda GK, Tomlin H, Clark JF. The utilisation of creatine and its analogues by cytosolic and mitochondrial creatine kinase. Biochim Biophys Acta. 1996;1274:119–28.CrossRefPubMed Boehm EA, Radda GK, Tomlin H, Clark JF. The utilisation of creatine and its analogues by cytosolic and mitochondrial creatine kinase. Biochim Biophys Acta. 1996;1274:119–28.CrossRefPubMed
19.
go back to reference Taes YEC, Marescau B, De Vriese A, De Deyn PP, Schepers E, Vanholder R, et al. Guanidino compounds after creatine supplementation in renal failure patients and their relation to inflammatory status. Nephrol Dial Transplant. 2008;23:1330–5.CrossRefPubMed Taes YEC, Marescau B, De Vriese A, De Deyn PP, Schepers E, Vanholder R, et al. Guanidino compounds after creatine supplementation in renal failure patients and their relation to inflammatory status. Nephrol Dial Transplant. 2008;23:1330–5.CrossRefPubMed
20.
go back to reference Gurreri G, Ghiggeri G, Salvidio G, Garibotto G, Robaudo C, Deferrari G. Effects of hemodialysis on guanidinopropionic acid metabolism. Nephron. 1986;42:295–7.CrossRefPubMed Gurreri G, Ghiggeri G, Salvidio G, Garibotto G, Robaudo C, Deferrari G. Effects of hemodialysis on guanidinopropionic acid metabolism. Nephron. 1986;42:295–7.CrossRefPubMed
21.
go back to reference Marescau B, Deshmukh DR, Kockx M, Possemiers I, Qureshi IA, Wiechert P, et al. Guanidino compounds in serum, urine, liver, kidney, and brain of man and some ureotelic animals. Metabolism. 1992;41:526–32.CrossRefPubMed Marescau B, Deshmukh DR, Kockx M, Possemiers I, Qureshi IA, Wiechert P, et al. Guanidino compounds in serum, urine, liver, kidney, and brain of man and some ureotelic animals. Metabolism. 1992;41:526–32.CrossRefPubMed
22.
go back to reference Meyer RA. Linear dependence of muscle phosphocreatine kinetics on total creatine content. Am J Physiol. 1989;257:C1149–57.PubMed Meyer RA. Linear dependence of muscle phosphocreatine kinetics on total creatine content. Am J Physiol. 1989;257:C1149–57.PubMed
23.
go back to reference Chevli R, Fitch CD. Beta-guanidinopropionate and phosphorylated beta-guanidinopropionate as substrates for creatine kinase. Biochem Med. 1979;21:162–7.CrossRefPubMed Chevli R, Fitch CD. Beta-guanidinopropionate and phosphorylated beta-guanidinopropionate as substrates for creatine kinase. Biochem Med. 1979;21:162–7.CrossRefPubMed
26.
go back to reference Kolodsick K, Ramstad T. Determination of trace cyanide in 3-guanidinopropionic acid by stripping preconcentration/isolation followed by flow-injection analysis with amperometric detection at silver. Anal Chim Acta. 1995;313:75–82.CrossRef Kolodsick K, Ramstad T. Determination of trace cyanide in 3-guanidinopropionic acid by stripping preconcentration/isolation followed by flow-injection analysis with amperometric detection at silver. Anal Chim Acta. 1995;313:75–82.CrossRef
27.
go back to reference European Food Safety Authority. Opinion of the Scientific Panel on Contaminants in the Food chain on a request from the European Commission on ethyl carbamate and hydrocyanic acid in food and beverages. EFSA J. 2007;551:1–44. European Food Safety Authority. Opinion of the Scientific Panel on Contaminants in the Food chain on a request from the European Commission on ethyl carbamate and hydrocyanic acid in food and beverages. EFSA J. 2007;551:1–44.
30.
go back to reference Meglasson MD, Wilson JM, Yu JH, Robinson DD, Wyse BM, de Souza CJ. Antihyperglycemic action of guanidinoalkanoic acids: 3-guanidinopropionic acid ameliorates hyperglycemia in diabetic KKAy and C57BL6Job/ob mice and increases glucose disappearance in rhesus monkeys. J Pharmacol Exp Ther. 1993;266:1454–62.PubMed Meglasson MD, Wilson JM, Yu JH, Robinson DD, Wyse BM, de Souza CJ. Antihyperglycemic action of guanidinoalkanoic acids: 3-guanidinopropionic acid ameliorates hyperglycemia in diabetic KKAy and C57BL6Job/ob mice and increases glucose disappearance in rhesus monkeys. J Pharmacol Exp Ther. 1993;266:1454–62.PubMed
31.
go back to reference Brosnan JT, Da Silva RP, Brosnan ME. The metabolic burden of creatine synthesis. Amino Acids. 2011;40:1325–31.CrossRefPubMed Brosnan JT, Da Silva RP, Brosnan ME. The metabolic burden of creatine synthesis. Amino Acids. 2011;40:1325–31.CrossRefPubMed
32.
go back to reference Harris RC, Almada AL, Harris DB, Dunnett M, Hespel P. The creatine content of Creatine Serum and the change in the plasma concentration with ingestion of a single dose. J Sports Sci. 2004;22:851–7.CrossRefPubMed Harris RC, Almada AL, Harris DB, Dunnett M, Hespel P. The creatine content of Creatine Serum and the change in the plasma concentration with ingestion of a single dose. J Sports Sci. 2004;22:851–7.CrossRefPubMed
33.
go back to reference Chan A-W, Tetzlaff JM, Gøtzsche PC, Altman DG, Mann H, Berlin J, et al. SPIRIT 2013 Explanation and Elaboration: Guidance for protocols of clinical trials. BMJ. 2013;346:e7586.CrossRefPubMedPubMedCentral Chan A-W, Tetzlaff JM, Gøtzsche PC, Altman DG, Mann H, Berlin J, et al. SPIRIT 2013 Explanation and Elaboration: Guidance for protocols of clinical trials. BMJ. 2013;346:e7586.CrossRefPubMedPubMedCentral
34.
go back to reference Hoffmann T, Glasziou P, Boutron I, Milne R, Perera R, Moher D, et al. Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide. BMJ. 2014;348:g1687.CrossRefPubMed Hoffmann T, Glasziou P, Boutron I, Milne R, Perera R, Moher D, et al. Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide. BMJ. 2014;348:g1687.CrossRefPubMed
35.
go back to reference Horjus DL, Nieuwland R, Boateng KB, Schaap MC, van Montfrans GA, Clark JF, et al. Creatine kinase inhibits ADP-induced platelet aggregation. Sci Rep. 2014;4:6551. doi: 10.1038/srep06551.CrossRefPubMedPubMedCentral Horjus DL, Nieuwland R, Boateng KB, Schaap MC, van Montfrans GA, Clark JF, et al. Creatine kinase inhibits ADP-induced platelet aggregation. Sci Rep. 2014;4:6551. doi: 10.1038/srep06551.CrossRefPubMedPubMedCentral
37.
go back to reference National Cancer Institute. Common Terminology Criteria for Adverse Events v4.0. NCI, NIH, DHHS. May 29, 2009. NIH publication # 09-7473. National Cancer Institute. Common Terminology Criteria for Adverse Events v4.0. NCI, NIH, DHHS. May 29, 2009. NIH publication # 09-7473.
38.
go back to reference Naranjo CA, Busto U, Sellers EM. A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther. 1981;30:239–45.CrossRefPubMed Naranjo CA, Busto U, Sellers EM. A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther. 1981;30:239–45.CrossRefPubMed
Metadata
Title
The acute effect of beta-guanidinopropionic acid versus creatine or placebo in healthy men (ABC Trial): study protocol for a randomized controlled trial
Authors
Fares A Karamat
Deborah L Horjus
Yentl C Haan
Lisa van der Woude
Inge Oudman
Gert A van Montfrans
Joseph F Clark
Lizzy M Brewster
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Trials / Issue 1/2015
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-015-0581-9

Other articles of this Issue 1/2015

Trials 1/2015 Go to the issue