Heart Failure Clinical Trial
Official title:
Identification Of Blood Markers For Asymptomatic Ventricular Dysfunction
The diagnosis of asymptomatic left ventricular dysfunction is difficult in general practice since it requires transthoracic cardiac echocardiography that is generally performed in specialized services. Although blood BNP levels monitoring can be of some help in heart failure diagnosis is is mostly a late biomarker that is secreted upon heart stretch and has many limitations. Therefore the aim of this study is to identify new specific blood biomarkers that would help for asymptomatic left ventricular dysfunction diagnosis in large populations with cardiovascular risk.
Recognition of asymptomatic left ventricular dysfunction (ALVD) and early stages of heart
failure (HF) are a diagnostic challenge for physicians. Patient history and physical
examination may fail to provide a definitive diagnosis; additional testing are required to
aid in diagnosis. More than 20 million people worldwide are estimated to have HF. Despite
recent therapeutic advances, morbidity and mortality after the onset of heart failure remain
high (35 % at 5 years after diagnosis). In addition, the annual cost of heart failure is
estimated to be greater than that of myocardial infarction and all cancers combined.
Consequently, prevention of heart failure through identification and management of risk
factors and preclinical phases of the disease is a priority. Clearly identification of
asymptomatic patients is difficult but would prevent further development of HF by initiation
of early adapted medical and non medical treatment.
We propose to search for markers of ALVD, in patients that have cardiovascular risk factors.
These new biomarkers should be earlier, more specific and more accurate than the one that we
already have such as B-type natriuretic peptide (BNP), which is the most recently,
established. BNP has been clearly associated with HF but is a relatively late stage marker
for HF and is not specific for HF. In addition BNP has been shown to be a poor marker in
obese or diabetic patients. Therefore the need of early specific biomarkers for LVD before
HF is irreversibly initiated is strong.
We propose to compare blood samples from 5 groups of patients carefully defined: 1) without
cardiovascular risk factors ; 2) With cardiovascular risk factors and without ALVD; 3) With
cardiovascular risk factors and with ALVD. 4) chronic heart failure patients ; 5) Acute
heart failure patients. Groups will be matched for risk factors and treatments.
Three distinct approaches will be performed: - A transcriptomics one that will monitor white
blood cell transcriptome ; a proteomic one that will use high throughput SELDI-TOF profiling
and a metabolic profiling one using Nuclear Magnetic Resonance.
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Observational Model: Case Control
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