Ignite Creation Date:
2024-05-05 @ 11:11 PM
Last Modification Date:
2024-10-26 @ 10:30 AM
Study NCT ID:
NCT01276678
Status:
UNKNOWN
Last Update Posted:
2013-11-06
First Post:
2011-01-11
Brief Title:
Multi-Analyte Genetic and Thrombogenic Markers of Atherosclerosis
Sponsor:
LifeBridge Health
Organization:
LifeBridge Health
Study Overview
Official Title:
Multi-Analyte Genetic and Thrombogenic Markers of Atherosclerosis The MAGMA STUDY
Status:
UNKNOWN
Status Verified Date:
2013-11
Last Known Status:
RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MAGMA
Brief Summary:
About 13 million people in the United States have coronary artery disease CAD It is the leading cause of death in both men and women
Coronary artery disease CAD occurs when the blood vessels that supply blood to the heart muscle the coronary arteries become hardened and narrowed The arteries harden and narrow due to buildup of fatty and calcified material called plaque on their inner walls The buildup of plaque is also called atherosclerosis This is a process which starts early in life but can be influenced by multiple factors
Several factors increase the risk of developing atherosclerosis They include high blood pressure smoking diabetes high cholesterol and being related to someone who had a heart attack or a stroke The more risk factors you have the greater the chance that you have severe atherosclerosis Some of the risk factors cannot be modified like age and family history of early heart disease The influenceable factors include high blood pressure high blood cholesterol high blood sugar cigarette smoking overweight or obesity and lack of physical activity
Nevertheless there are patients without any above mentioned risk factors who develop atherosclerosis In addition to that there are also patients with several risk factors who do not develop severe coronary artery disease
According to research studies high blood levels of some substances in the blood biochemical markers as well as some genes in the DNA of our cells may be associated with an increased risk of developing CAD and faster progression of the disease
The purpose of this study is to find a correlation between certain blood markers and growth of the plaques regardless of the presence of the classic risk factors for atherosclerosis If we prove our hypothesis we will be one step closer to predicting the extent of atherosclerosis by performing certain blood tests
Coronary artery disease CAD occurs when the blood vessels that supply blood to the heart muscle the coronary arteries become hardened and narrowed The arteries harden and narrow due to buildup of fatty and calcified material called plaque on their inner walls The buildup of plaque is also called atherosclerosis This is a process which starts early in life but can be influenced by multiple factors
Several factors increase the risk of developing atherosclerosis They include high blood pressure smoking diabetes high cholesterol and being related to someone who had a heart attack or a stroke The more risk factors you have the greater the chance that you have severe atherosclerosis Some of the risk factors cannot be modified like age and family history of early heart disease The influenceable factors include high blood pressure high blood cholesterol high blood sugar cigarette smoking overweight or obesity and lack of physical activity
Nevertheless there are patients without any above mentioned risk factors who develop atherosclerosis In addition to that there are also patients with several risk factors who do not develop severe coronary artery disease
According to research studies high blood levels of some substances in the blood biochemical markers as well as some genes in the DNA of our cells may be associated with an increased risk of developing CAD and faster progression of the disease
The purpose of this study is to find a correlation between certain blood markers and growth of the plaques regardless of the presence of the classic risk factors for atherosclerosis If we prove our hypothesis we will be one step closer to predicting the extent of atherosclerosis by performing certain blood tests
Detailed Description:
Cardiovascular diseases CVD primarily coronary artery disease are the leading cause of death and disability in the United States and Europe The cost of cardiovascular disease in the United States in 2009 is estimated to be 4753 billion according to the American Heart Association and the National Heart Lung and Blood Institute Although there have been significant accomplishments in reducing cardiovascular events over the past decade too many people still die of heart and vascular diseases Therefore the improvement of risk stratification of CVD by identification of new biomarkers has been extensively investigated in both primary and secondary clinical settings in the past decade A substantial number of biomarkers representing various stages of atherogenesis and impaired cardiac function have been evaluated against modifiable traditional risk factors such as cholesterol blood pressure smoking status and diabetes However little is known about the true extent that these identified multi-analyte genetic and thrombogenic markers contribute to the presence and degree of atherosclerosis
Patients with severe stenosis of coronary arteries may have a different profile of biochemical and genetic markers than patients with clear coronary vessels Therefore more research is required to improve the predictability and specificity of these known and novel factors before physicians fully implement these tests into their routine clinical practice
At present physicians rely on conventional cardiovascular risk factors to try to identify at-risk patients A number of risk factors stem from genetic or biologic conditions such as gender age ethnicity and family history of heart disease While many risk factors cannot be changed risk factors such as high cholesterol high blood pressure obesity tobacco smoking stress physical inactivity can be modified One of the most significant risk factor for the development of CVD is diabetes mellitus whereby both heredity and lifestyle play a major role Nevertheless there are patients without these known classical risk factors who develop severe CVD Conversely there are patients with these classical risk factors without relevant coronary artery disease The CVD Risk Factor Paradox may be explained by a combination of biological environmental and genetic factors that are under investigation
Animal and human studies have established the role of cholesterol in the development and progression of atherosclerosis Epidemiological studies directly implicated LDL-C to the development of atherosclerosis and CVD Furthermore LDL-C level appears to be directly related to the development and recurrence of CVD While LDL-C is the primary lipid marker for assessing risk evidence has demonstrated the important role of other lipoproteins components in atherogenesis These include lipoprotein a LDL pattern density HDL subtypes VLDL and intermediate-density lipoprotein A substantial body of evidence has also demonstrated Lp-PLA2 as a cardiovascular risk marker in both primary and secondary prevention that provides new information over and above new traditional risk factors Most recently oxidized low-density lipoprotein oxLDL β2-glycoprotein I β2GPI complexes have been implicated in atherogenesis More accurate and expanded depiction of the lipid profile compared to the standard lipid profile may identify important emerging risk factors and secondary targets of therapy for cardiovascular disease
It is also been established that heightened plaque metabolism together with increased blood vulnerability characterized by hypercoagulability heightened platelet reactivity and inflammation are important processes responsible for plaque rupture and subsequent occlusive ischemic events occurrence during ACS Recent developments in catheter-based near-infrared spectroscopy may help to identify vulnerable plaques by characterizing chemical components However information regarding blood vulnerability based on a specific biomarker profile is lacking
Multiple lines of evidence suggest the critical role of platelets in the development of atherosclerosis and thrombosis By expressing adhesion molecules platelets facilitate the diapedesis of leukocytes into the vascular wall during atherosclerotic development Additionally P-selectin and CD40L trigger release of RANTES from platelets and subsequently augment monocyte recruitment and secretion of inflammatory cytokines from monocytes Previous studies have demonstrated the roles of MCP-1 and IL-8 during plaque development and cardiovascular clinical outcomes Gurbel et al demonstrated that incremental changes in platelet function demonstrated by increases in GPIIbIIIa expression and increased release of RANTES IL-8 and MCP-1 as clinical disease progressed from the asymptomatic state to stable angina and finally to unstable anginaThese findings further reinforce the critical role of platelets in plaque destabilization
The role of inflammation during atherosclerotic plaque rupture and subsequent development of thrombus generation at the site of plaque rupture by enhancing tissue factor expression and thrombin generation is well recognized Several studies have demonstrated the association of high IL-6 -8 and -18 elevated CD40 ligand CD40L myeloperoxidase tumor necrosis factor and CRP levels with ischemic events
Epidemiological evidence in addition to experimental and clinical data supports the hypothesis that CRP may be a marker as well as an active participant in the development of atherothrombotic complications More interestingly recent in vitro studies suggest that there is a direct role of CRP on endothelial and platelet function In autopsy studies CRP immune reactivity was detected in atherosclerotic arteries but not in normal arteries In addition the levels of CRP in fibrous tissue and atheroma of atherectomy specimens were higher in patients with unstable angina and myocardial infarction compared to patients with stable angina Gurbel et al demonstrated a statistically significant increase in specific inflammation markers importantly CRP IL-8 RANTES and MCP-1 in patients with progressive CAD compared to patients with asymptomatic disease Although serial changes in markers were not studied in the same patient the incremental changes among various markers across the study population clearly suggests the transition between disease states
Linking vulnerable blood characterized by elevated inflammation markers hypercoagulability and highly reactive platelets to the vulnerable patient who is at risk for thrombotic complications has been the subject of much discussion in recent years
Platelet activation and aggregation are the most critical factors in the generation of ischemic events including stent thrombosis and myocardial infarction MI Unlike the routine measurement of blood glucose cholesterol and C-reactive protein performed during the management of patients with atherosclerosis the measurement of platelet function is largely ignored during the management of cardiovascular patients even in those at the highest risk Multiple laboratory and translational research studies performed at our research center as well as others have demonstrated the importance of platelet reactivity as a new emerging risk factor At our center we primarily utilize two methods to determine coagulation and platelet reactivity thrombelastography TEG and platelet aggregation The indications for TEG testing include assessing bleeding of unclear etiology and assessing hypercoagulable states In addition TEG platelet mapping has been utilized to monitor antiplatelet therapy It has been hypothesized that high platelet-fibrin clot strength measured by TEG predicts robust clot formation at the site of plaque rupture In support of this premise Gurbel et al demonstrated that high thrombin-induced platelet-fibrin clot strength and high platelet reactivity has been associated with ischemic events in patients with CVD In fact all of the current data support that uniform measurement of on-treatment platelet reactivity may be a major diagnostic strategy not only in the treatment of patients who have undergone PCI but also in all patients with cardiovascular disease at risk for thrombotic events
Presently the gold standard to diagnose patients with CVD is coronary angiography If significant lesions are detected coronary intervention with angioplasty or coronary artery bypass grafting can be performed to reestablish flow in the blocked coronary arteries Modification of cardiovascular risk factors and pharmacological management is subsequently implemented to prevent recurrent cardiovascular events including myocardial infarction and stent thrombosis The importance of the ADP-P2Y12 receptor interaction and COX-inhibition has been demonstrated by the clinical benefits associated with the addition of clopidogrel to aspirin therapy in patients with acute coronary syndromes and patients treated with stents However the one size fits all antiplatelet management strategy has proven to be flawed due to clopidogrel and aspirin response variability
Incomplete inhibition of platelet thromboxane generation has been associated with an increased risk of cardiovascular events In the CHARISMA study Eikelboom et al demonstrated that urinary concentrations of 11-dehydro thromboxane B2 potentially was a modifiable determinant of stroke myocardial infarction or cardiovascular death in patients at risk for atherothrombotic events In addition variability in clopidogrel response is well established with multiple translational research studies demonstrating a relationship between antiplatelet nonresponsiveness high on-treatment platelet reactivity and the occurrence of ischemic events in percutaneous coronary intervention patients
Recently the loss-of-function CYP2C192 allele has been shown to be associated with decreased activation of clopidogrel and antiplatelet effect and with increased cardiovascular events in patients receiving clopidogrel Individuals with this genotype have reduced protection from thrombotic events as outlined in the FDA black box warning for clopidogrel Despite the black box warning there has been no large scale study performed to personalize antiplatelet treatment of P2Y12 inhibitors with CYP2C19 genotyping primarily because the technology for point-of-care genotyping is not commercially available From a clinical perspective reporting 2C19 test results in a rapid fashion will help guide therapeutic decisions while patients are in the inpatient setting prior to discharge
Large-scale genome-wide association studies using high-density single nucleotide polymorphism genotyping arrays have revealed genetic variants that are robustly associated with CAD and CAD-related traits such as type 2 diabetes and obesity Also evidence has been obtained that multiple rare alleles with fairly strong phenotypic effects may contribute to the genetic heritability of CAD Although the involvement of specific genes and their level of contribution to CAD have not been established by research it is known that CAD often results from the blended effects of multiple genes These so-called polygenic effects mean that the genetics of CAD are extremely complicated with many different genes influencing persons risk In most cases CAD is not inherited in a clearly dominant or recessive manner Instead a person may have mutations in some genes that increase risk and mutations in other genes that decrease risk and their combined effect plays a role in the development of atherosclerosis At present the replication of results in the reported studies is poor probably because of the lack of high-quality environmental data and not counting for the gene-environment interactions
Many patients have undetected coronary artery disease that if accurately identified would lead to more aggressive early treatment strategies including lifestyle modification and targeted pharmacologic therapy A goal of current study is to determine potential biochemical and genetic markers associated with the presence and progression of CVD
The current studies hypothesis is that specific biomarkers and genetic profile will precisely identify with the severity of angiographically-defined coronary lesions independently of the classic risk factors for atherosclerosis The investigators believe that this will enhance the treatment of patients with cardiovascular disease by implementing personalized treatment strategies
3 STUDY DESIGN 31 Outline A total of 1300 subjects 18 years undergoing coronary angiography inpatient cohortor who have undergone coronary angiography within 5 years outpatient cohort not to exceed 50 subjects will be enrolled In addition 300 healthy controls free from any pharmacologic therapy will also be enrolled After giving informed consent a lifestyle questionnaire on topics of diet physical activity history of high blood pressure hyperlipidemia diabetes smoking and family history of early heart disease will be completed A blood approximately 35 ml and urine sample will be obtained prior to angiogram for the inpatient cohort or on the day of enrollment for the outpatient cohort for laboratory assessments The presence and severity of CAD will be determined according to the following three categories category 1 - no disease or minimal stenosis 25 of major branches without need of any medical therapy category 2 - intermediate stenosis 25-75 of major branches andor patient needs only conservative treatment no need for PTCA category 3 - severe stenosis 75 of major branch andor patient needs PTCA or CABG Statistical tools will be used to detect any correlation between the studied markers and the extent of atherosclerotic plaques Subgroup analysis will be performed to detect the similar correlation in certain risk groups like smokers obese subjects diabetes or subjects with hypercholesterolemia Subjects will be contacted once a year for up to 5 years by telephone and information regarding antiplatelet therapy and cardiovascular events death myocardial infarction stent thrombosis stroke revascularization major bleeding will be collected
Patients with severe stenosis of coronary arteries may have a different profile of biochemical and genetic markers than patients with clear coronary vessels Therefore more research is required to improve the predictability and specificity of these known and novel factors before physicians fully implement these tests into their routine clinical practice
At present physicians rely on conventional cardiovascular risk factors to try to identify at-risk patients A number of risk factors stem from genetic or biologic conditions such as gender age ethnicity and family history of heart disease While many risk factors cannot be changed risk factors such as high cholesterol high blood pressure obesity tobacco smoking stress physical inactivity can be modified One of the most significant risk factor for the development of CVD is diabetes mellitus whereby both heredity and lifestyle play a major role Nevertheless there are patients without these known classical risk factors who develop severe CVD Conversely there are patients with these classical risk factors without relevant coronary artery disease The CVD Risk Factor Paradox may be explained by a combination of biological environmental and genetic factors that are under investigation
Animal and human studies have established the role of cholesterol in the development and progression of atherosclerosis Epidemiological studies directly implicated LDL-C to the development of atherosclerosis and CVD Furthermore LDL-C level appears to be directly related to the development and recurrence of CVD While LDL-C is the primary lipid marker for assessing risk evidence has demonstrated the important role of other lipoproteins components in atherogenesis These include lipoprotein a LDL pattern density HDL subtypes VLDL and intermediate-density lipoprotein A substantial body of evidence has also demonstrated Lp-PLA2 as a cardiovascular risk marker in both primary and secondary prevention that provides new information over and above new traditional risk factors Most recently oxidized low-density lipoprotein oxLDL β2-glycoprotein I β2GPI complexes have been implicated in atherogenesis More accurate and expanded depiction of the lipid profile compared to the standard lipid profile may identify important emerging risk factors and secondary targets of therapy for cardiovascular disease
It is also been established that heightened plaque metabolism together with increased blood vulnerability characterized by hypercoagulability heightened platelet reactivity and inflammation are important processes responsible for plaque rupture and subsequent occlusive ischemic events occurrence during ACS Recent developments in catheter-based near-infrared spectroscopy may help to identify vulnerable plaques by characterizing chemical components However information regarding blood vulnerability based on a specific biomarker profile is lacking
Multiple lines of evidence suggest the critical role of platelets in the development of atherosclerosis and thrombosis By expressing adhesion molecules platelets facilitate the diapedesis of leukocytes into the vascular wall during atherosclerotic development Additionally P-selectin and CD40L trigger release of RANTES from platelets and subsequently augment monocyte recruitment and secretion of inflammatory cytokines from monocytes Previous studies have demonstrated the roles of MCP-1 and IL-8 during plaque development and cardiovascular clinical outcomes Gurbel et al demonstrated that incremental changes in platelet function demonstrated by increases in GPIIbIIIa expression and increased release of RANTES IL-8 and MCP-1 as clinical disease progressed from the asymptomatic state to stable angina and finally to unstable anginaThese findings further reinforce the critical role of platelets in plaque destabilization
The role of inflammation during atherosclerotic plaque rupture and subsequent development of thrombus generation at the site of plaque rupture by enhancing tissue factor expression and thrombin generation is well recognized Several studies have demonstrated the association of high IL-6 -8 and -18 elevated CD40 ligand CD40L myeloperoxidase tumor necrosis factor and CRP levels with ischemic events
Epidemiological evidence in addition to experimental and clinical data supports the hypothesis that CRP may be a marker as well as an active participant in the development of atherothrombotic complications More interestingly recent in vitro studies suggest that there is a direct role of CRP on endothelial and platelet function In autopsy studies CRP immune reactivity was detected in atherosclerotic arteries but not in normal arteries In addition the levels of CRP in fibrous tissue and atheroma of atherectomy specimens were higher in patients with unstable angina and myocardial infarction compared to patients with stable angina Gurbel et al demonstrated a statistically significant increase in specific inflammation markers importantly CRP IL-8 RANTES and MCP-1 in patients with progressive CAD compared to patients with asymptomatic disease Although serial changes in markers were not studied in the same patient the incremental changes among various markers across the study population clearly suggests the transition between disease states
Linking vulnerable blood characterized by elevated inflammation markers hypercoagulability and highly reactive platelets to the vulnerable patient who is at risk for thrombotic complications has been the subject of much discussion in recent years
Platelet activation and aggregation are the most critical factors in the generation of ischemic events including stent thrombosis and myocardial infarction MI Unlike the routine measurement of blood glucose cholesterol and C-reactive protein performed during the management of patients with atherosclerosis the measurement of platelet function is largely ignored during the management of cardiovascular patients even in those at the highest risk Multiple laboratory and translational research studies performed at our research center as well as others have demonstrated the importance of platelet reactivity as a new emerging risk factor At our center we primarily utilize two methods to determine coagulation and platelet reactivity thrombelastography TEG and platelet aggregation The indications for TEG testing include assessing bleeding of unclear etiology and assessing hypercoagulable states In addition TEG platelet mapping has been utilized to monitor antiplatelet therapy It has been hypothesized that high platelet-fibrin clot strength measured by TEG predicts robust clot formation at the site of plaque rupture In support of this premise Gurbel et al demonstrated that high thrombin-induced platelet-fibrin clot strength and high platelet reactivity has been associated with ischemic events in patients with CVD In fact all of the current data support that uniform measurement of on-treatment platelet reactivity may be a major diagnostic strategy not only in the treatment of patients who have undergone PCI but also in all patients with cardiovascular disease at risk for thrombotic events
Presently the gold standard to diagnose patients with CVD is coronary angiography If significant lesions are detected coronary intervention with angioplasty or coronary artery bypass grafting can be performed to reestablish flow in the blocked coronary arteries Modification of cardiovascular risk factors and pharmacological management is subsequently implemented to prevent recurrent cardiovascular events including myocardial infarction and stent thrombosis The importance of the ADP-P2Y12 receptor interaction and COX-inhibition has been demonstrated by the clinical benefits associated with the addition of clopidogrel to aspirin therapy in patients with acute coronary syndromes and patients treated with stents However the one size fits all antiplatelet management strategy has proven to be flawed due to clopidogrel and aspirin response variability
Incomplete inhibition of platelet thromboxane generation has been associated with an increased risk of cardiovascular events In the CHARISMA study Eikelboom et al demonstrated that urinary concentrations of 11-dehydro thromboxane B2 potentially was a modifiable determinant of stroke myocardial infarction or cardiovascular death in patients at risk for atherothrombotic events In addition variability in clopidogrel response is well established with multiple translational research studies demonstrating a relationship between antiplatelet nonresponsiveness high on-treatment platelet reactivity and the occurrence of ischemic events in percutaneous coronary intervention patients
Recently the loss-of-function CYP2C192 allele has been shown to be associated with decreased activation of clopidogrel and antiplatelet effect and with increased cardiovascular events in patients receiving clopidogrel Individuals with this genotype have reduced protection from thrombotic events as outlined in the FDA black box warning for clopidogrel Despite the black box warning there has been no large scale study performed to personalize antiplatelet treatment of P2Y12 inhibitors with CYP2C19 genotyping primarily because the technology for point-of-care genotyping is not commercially available From a clinical perspective reporting 2C19 test results in a rapid fashion will help guide therapeutic decisions while patients are in the inpatient setting prior to discharge
Large-scale genome-wide association studies using high-density single nucleotide polymorphism genotyping arrays have revealed genetic variants that are robustly associated with CAD and CAD-related traits such as type 2 diabetes and obesity Also evidence has been obtained that multiple rare alleles with fairly strong phenotypic effects may contribute to the genetic heritability of CAD Although the involvement of specific genes and their level of contribution to CAD have not been established by research it is known that CAD often results from the blended effects of multiple genes These so-called polygenic effects mean that the genetics of CAD are extremely complicated with many different genes influencing persons risk In most cases CAD is not inherited in a clearly dominant or recessive manner Instead a person may have mutations in some genes that increase risk and mutations in other genes that decrease risk and their combined effect plays a role in the development of atherosclerosis At present the replication of results in the reported studies is poor probably because of the lack of high-quality environmental data and not counting for the gene-environment interactions
Many patients have undetected coronary artery disease that if accurately identified would lead to more aggressive early treatment strategies including lifestyle modification and targeted pharmacologic therapy A goal of current study is to determine potential biochemical and genetic markers associated with the presence and progression of CVD
The current studies hypothesis is that specific biomarkers and genetic profile will precisely identify with the severity of angiographically-defined coronary lesions independently of the classic risk factors for atherosclerosis The investigators believe that this will enhance the treatment of patients with cardiovascular disease by implementing personalized treatment strategies
3 STUDY DESIGN 31 Outline A total of 1300 subjects 18 years undergoing coronary angiography inpatient cohortor who have undergone coronary angiography within 5 years outpatient cohort not to exceed 50 subjects will be enrolled In addition 300 healthy controls free from any pharmacologic therapy will also be enrolled After giving informed consent a lifestyle questionnaire on topics of diet physical activity history of high blood pressure hyperlipidemia diabetes smoking and family history of early heart disease will be completed A blood approximately 35 ml and urine sample will be obtained prior to angiogram for the inpatient cohort or on the day of enrollment for the outpatient cohort for laboratory assessments The presence and severity of CAD will be determined according to the following three categories category 1 - no disease or minimal stenosis 25 of major branches without need of any medical therapy category 2 - intermediate stenosis 25-75 of major branches andor patient needs only conservative treatment no need for PTCA category 3 - severe stenosis 75 of major branch andor patient needs PTCA or CABG Statistical tools will be used to detect any correlation between the studied markers and the extent of atherosclerotic plaques Subgroup analysis will be performed to detect the similar correlation in certain risk groups like smokers obese subjects diabetes or subjects with hypercholesterolemia Subjects will be contacted once a year for up to 5 years by telephone and information regarding antiplatelet therapy and cardiovascular events death myocardial infarction stent thrombosis stroke revascularization major bleeding will be collected
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None