Coronary Calcification Clinical Trial
Official title:
Effects of Fhytomenadione on Coronary Artery Calcification of Hemodialysis Patients. Randomized Clinical Trial
NCT number | NCT04247087 |
Other study ID # | 1 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 7, 2017 |
Est. completion date | January 2, 2020 |
Verified date | January 2020 |
Source | Instituto Mexicano del Seguro Social |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Until 2013 the reported incidence of chronic kidney disease varied widely between countries,
reporting the highest prevalence Taiwan, the region of Jalisco in Mexico and United States,
with 458, 421 and 363 individuals per million inhabitants respectively. Mexico has around
52,000 patients in replacement therapies, of which 80% of patients are treated in the
Instituto Mexicano del Seguro Social (IMSS).
In each stage of renal disease the principal cause of mortality is cardiovascular disease.
The risk of cardiovascular mortality is greater than the general population. Arterial
calcification, a marker of atherosclerosis and cardiovascular mortality predictor is common
in chronic kidney disease. The presence of arterial calcification leads to an increase in
arterial stiffness and to a decrease in coronary perfusion resulting in cardiac hypertrophy
and myocardial ischemia.
The presence of traditional cardiovascular risk factors like diabetes, hypertension,
hyperlipidemia and old age cannot fully explain the high prevalence of atherosclerosis and
arterial calcification in chronic kidney disease. Another specific factors related to chronic
kidney disease, like hyperphosphatemia, high calcium concentration in dialysis solutions, use
of high doses of vitamin D for the management of hyperparathyroidism has been shown to
positively influence development of arterial calcification. Invitro studies show that in
presence of hyperphosphatemia smooth muscle cells are transformed into osteoblast-like cells
that can express proteins that regulate mineralization. Two of this proteins, the matrix Gla
protein (MGP) and osteocalcin (OC) are regulators of tissue mineralization in arterial walls
and bones respectively. Vitamin K is required as cofactor in the gamma-carboxylation process
of several extracellular matrix proteins, converting inactive carboxylated proteins to
carboxylated active proteins. Prothrombin and coagulation factors 7,9 y 10 require vitamin K2
for its carboxylation process, while osteocalcin and the matrix Gal protein require vitamin
K1. Matrix Gla protein is a calcification inhibitor that plays an important role in the
prevention of arterial calcification. For carboxylation and correct function of the MGP is
necessary an enzymatic cofactor, vitamin K; this is corroborated in the fact that the
antagonism of vitamin K with warfarin antagonizes the carboxylation of MGP and produces rapid
arterial calcification.
There are currently no studies evaluating vitamin K in the prevention of vascular
calcification in patients with chronic kidney disease, therefore, the role of vitamin K in
the patient with kidney disease needs to be clarified with randomized controlled studies, in
which the target will be this population of patients at high risk. The aim of this study is
evaluate the effect of phytomenadione on coronary artery calcification of patients on
hemodialysis compared to placebo, our research hypothesis is that phytomenadione slows the
progression and favors the regression of coronary arterial calcification in patients on
hemodialysis compared to placebo, evaluating the coronary calcium score by coronary
tomography. As secondary objectives was determine changes in the baseline coronary calcium
score and at 12 months of use of phytomenadione and presence of cardiovascular events like
acute myocardial infarction, unstable angina and death of cardiac cause. The intervention
group received phytomenadione 10 mg (1 vial in the venous line of the extracorporeal
hemodialysis circuit) post hemodialysis 3 times a week for 12 months and the control group 1
vial of placebo solution (solution for injection in the venous line of the extracorporeal
hemodialysis circuit) post hemodialysis 3 times a week for 12 months. The follow-up of the
patients was for 12 months, at the end of the follow-up, a coronary control tomography was
performed by the Radiology Department to assess the final calcium score. Relative risk
measurement (RR), absolute risk reduction (ARR) and number to be treated (NTT) were
performed.
Status | Completed |
Enrollment | 60 |
Est. completion date | January 2, 2020 |
Est. primary completion date | September 27, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Patients with chronic kidney disease in hemodialysis - Patients who have 6 months or more on hemodialysis - Patients over 18 years - Patients that meet the tomographic criterion of a coronary calcium score of 10 Agatston units. Exclusion Criteria: - Patients in previous or current treatment with phytomenadione - Coronary stent patients - Patients with arrhythmias and requiring oral anticoagulation with warfarin or acenocoumarin - Pregnant patients - Patients who undergo renal transplantation during the follow-up period - Patients who change the modality to peritoneal dialysis during the follow-up period - Patients who are known allergy to vitamin K |
Country | Name | City | State |
---|---|---|---|
Mexico | Hospital de Alta Especialidad No. 1 Bajío, Boulevard Adolfo López Mateos esquina Insurgentes S/N, colonia Los Paraísos | Leon | Guanajuato |
Lead Sponsor | Collaborator |
---|---|
Instituto Mexicano del Seguro Social | Marco Antonio Ocampo Apolonio, Rodolfo Guardado Mendoza, Texar Alfonso Pereyra Nobara |
Mexico,
Block GA, Raggi P, Bellasi A, Kooienga L, Spiegel DM. Mortality effect of coronary calcification and phosphate binder choice in incident hemodialysis patients. Kidney Int. 2007 Mar;71(5):438-41. Epub 2007 Jan 3. — View Citation
Foley RN, Parfrey PS, Sarnak MJ. Clinical epidemiology of cardiovascular disease in chronic renal disease. Am J Kidney Dis. 1998 Nov;32(5 Suppl 3):S112-9. Review. — View Citation
Geleijnse JM, Vermeer C, Grobbee DE, Schurgers LJ, Knapen MH, van der Meer IM, Hofman A, Witteman JC. Dietary intake of menaquinone is associated with a reduced risk of coronary heart disease: the Rotterdam Study. J Nutr. 2004 Nov;134(11):3100-5. — View Citation
Goodman WG, Goldin J, Kuizon BD, Yoon C, Gales B, Sider D, Wang Y, Chung J, Emerick A, Greaser L, Elashoff RM, Salusky IB. Coronary-artery calcification in young adults with end-stage renal disease who are undergoing dialysis. N Engl J Med. 2000 May 18;342(20):1478-83. — View Citation
Kurnatowska I, Grzelak P, Masajtis-Zagajewska A, Kaczmarska M, Stefanczyk L, Vermeer C, Maresz K, Nowicki M. Effect of vitamin K2 on progression of atherosclerosis and vascular calcification in nondialyzed patients with chronic kidney disease stages 3-5. — View Citation
Longenecker JC, Coresh J, Powe NR, Levey AS, Fink NE, Martin A, Klag MJ. Traditional cardiovascular disease risk factors in dialysis patients compared with the general population: the CHOICE Study. J Am Soc Nephrol. 2002 Jul;13(7):1918-27. — View Citation
National Kidney Foundation. K/DOQI clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification. Am J Kidney Dis. 2002 Feb;39(2 Suppl 1):S1-266. — View Citation
Oikonomaki T, Papasotiriou M, Ntrinias T, Kalogeropoulou C, Zabakis P, Kalavrizioti D, Papadakis I, Goumenos DS, Papachristou E. The effect of vitamin K2 supplementation on vascular calcification in haemodialysis patients: a 1-year follow-up randomized tr — View Citation
Pilkey RM, Morton AR, Boffa MB, Noordhof C, Day AG, Su Y, Miller LM, Koschinsky ML, Booth SL. Subclinical vitamin K deficiency in hemodialysis patients. Am J Kidney Dis. 2007 Mar;49(3):432-9. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | coronary calcium score | Within the population of hemodialysis patients, patients who met the inclusion criteria were sought, once the participation in the study was accepted and an informed consent was signed, a coronary tomography was performed and interpreted by Radiology staff, who had no knowledge about the study groups or their intervention. Those patients who fulfilled the coronary calcification tomographic criterion defined as coronary calcium score of 10 Agatston units were randomized to receive the intervention or the placebo. At the end of the 12 month follow-up, a coronary tomography was performed again to quantify the final Agatston score | 12 months | |
Secondary | cardiovascular events | determine presence of cardiovascular events like acute myocardial infarction, unstable angina and death of cardiac cause during follow-up. The presence of events will be determined according to the clinical record in the patient's file | 12 months |
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