Atrial Fibrillation Clinical Trial
Official title:
Qatar Cardiovascular Biorepository-AF (QCBio-AF) Study
Qatar Cardiovascular Biorepsoitory-AF (QCBio-AF) of plasma and DNA of Qatari patients with atrial fibrillation (AF) is to establish. AF cases will include patients with acute and chronic AF identified in the Heart Hospital (HH) arrhythmia clinics and Emergency Room (ER). Controls will include blood donors who have no history of AF. Such a resource will enable validation of biomarkers to assess AF risk, response to therapy, and prognosis. QCBio-AF will also allow genomic, marker and proteomic studies of AF and response to drug therapy (pharmacogenetics and pharmacoproteomics). This study will accomplish the following specific aims: Aim 1: Establish a DNA and plasma biorepository (QCBio-AF) of 300 Qatari AF cases and Family members to enable investigation of genomic and proteomic biomarkers for early detection and prognostication and to identify new targets for drug development. Aim 2: Annotate the biorepository of with 1) demographic, laboratory, and clinical variables derived from the EMR using electronic phenotyping algorithms, and 2) detailed information regarding history of cardiovascular diseases and risk factors derived from patient surveys. Aim 3: Develop processes to promote use of the biorepository by Qatari investigators by facilitating access to the biorepository for biomarker research, while maintaining the highest ethical standards with emphasis on patient confidentiality and stewardship of the biospecimens. Timeline. Following IRB approval, the intended collection period will be over 12 months where 300 Qatari patients with AF and their immediate families will be recruited. Significance: Although atrial fibrillation (AF) is reaching epidemic proportions in the aging U.S. and European populations, the worldwide burden of AF in non-white populations is unknown. Furthermore, a substantial proportion of AF in the population is not explained by traditional risk factors. There is increasing evidence that susceptibility to AF is not only determined by underlying etiologic risk factors but also ethnicity with AF occurring more frequently in white than in non-white populations. While reasons for this ethnic variability are unknown, studies have shown that both common and rare genetic variants increase susceptibility to AF in an individual in the presence of ethnic-specific risk factors.
Atrial Fibrillation Epidemic and the Need for Improved Therapies: Atrial fibrillation (AF)
has become a disease of global epidemic proportions due to the burgeoning population of
elderly individuals. The global burden of AF was recently estimated at 33.5 million with
progressive increases in incidence, prevalence and AF-related mortality having major
implications for healthcare costs and public health policy. This study also highlighted
regional variation in AF burden between developed versus developing countries. The number of
persons in the U.S. with AF by the year 2050 is projected to exceed 16 million. The
socioeconomic impacts of AF are substantial, as are the consequences of frequent visits to
the emergency room (ER) and hospitalizations, chronic disease management and loss of
productivity. Moreover, managing patients with AF remains challenging. Despite recent
advances in catheter-based and surgical treatments, antiarrhythmic drugs (AADs) remain the
mainstay of treatment for patients with symptomatic AF. However, membrane active drugs are
incompletely and unpredictably effective and can be proarrhythmic. Furthermore, the selection
of an AAD for an individual patient is based not only on efficacy as on minimizing the risk
of adverse effects. The limited success of AADs in maintaining sinus rhythm is related in
part to the heterogeneity of the underlying substrate, poor understanding of the
pathophysiology of AF and our failure to target therapy to underlying mechanisms. Thus, an
overarching goal of this proposal is to create and utilize a clinical and genetic database
for AF to examine the role of novel and established risk factors for AF in diverse ethnic
populations and determine the role of common AF susceptibility loci in two ethnic groups and
examine gene-environment interactions between ethnic specific risk factors and AF.
Genetic Epidemiology of AF, in 1943, first report of familial AF in three brothers with early
onset AF published. Since then many epidemiologic studies have shown that AF is heritable
especially the form of AF that occurs without underlying cardiac or systemic disease -
previously termed lone but is now designated as early onset AF. As the heritability of AF has
been estimated to be 62%, there is a substantial genetic component to the arrhythmia. While
some of loci influencing this estimate may be pleiotropic and related to other risk factors
such as hypertension and diabetes that are also highly heritable, there are also several
discovered and likely many undiscovered genetic risk factors that are primary determinants of
early onset AF. Many genes and several AF loci have now been identified for Mendelian forms
of early onset AF. In 1997, Brugada and colleagues identified the first AF locus on chr10q22;
since then four other loci have been identified, including a new locus on chr5p15 identified
by us that was associated with a prolonged P-wave duration. In addition, linkage analyses
have identified individual mutations in several familial AF kindreds. The first AF gene
(KCNQ1), identified in 2003, encodes a cardiac potassium channel current (IKs). This
discovery was followed by the identification of other potassium and cardiac ion channels
important in the pathophysiology of AF. The first non-ion channel AF gene (natriuretic
peptide precursor A [NPPA]), was identified by linkage analysis and a positional cloning
approach and encodes for atrial natriuretic peptide (ANP).
With the discovery of KCNQ1 as an AF gene, investigators then applied a candidate gene
approach and identified many more rare 'private' genetic variants in other cardiac ion
channel genes in familial AF kindreds. In 2007, Otway and colleagues identified a KCNQ1
mutation (R14C) in one family with familial AF. When the mutation was expressed in a
heterologous expression system, the IKs current amplitude at baseline was unchanged but
demonstrated marked increase compared to wild-type (WT) channels when exposed to hypotonic
solution. Importantly, only those subjects with left atrial (LA) dilatation developed AF.
These findings and Vanderbilt data showing that penetrance of rare AF-associated variants is
modulated by common AF risk alleles at the chr4q25 locus support the concept of a two-hit
genetic model for the development of AF. Mutations in genes encoding connexins, proteins
important in transmitting electrical activity between cardiac myocytes, have also been
identified stemming from early work in mice with null alleles for GJA5, encoding mutations in
several familial AF kindreds. The first AF gene (KCNQ1), identified in 2003, encodes a
cardiac potassium channel current (IKs). This discovery was followed by the identification of
other potassium and cardiac ion channels important in the pathophysiology of AF. The first
non-ion channel AF gene (natriuretic peptide precursor A [NPPA]), was identified by linkage
analysis and a positional cloning approach and encodes for atrial natriuretic peptide (ANP).
Epidemiology of AF in Qatar: The burden of AF in populations of Middle Eastern Arabs remains
unknown. Researchers explored the etiology and pattern of AF in Middle Eastern Arabs and
South Asians living in Qatar using the CCS Registry at HMC26 and showed that, in this
population, AF is more common in those that are older, have a history of HTN, CHF, DM and
valvular heart disease. Furthermore, they showed that the incidence of AF in Middle Eastern
Arab patients was significantly higher than in South Asians (12% vs. 8%) and this was mostly
due to older age, a greater prevalence of HTN, and DM in the Arabs. The Registry was also
used to compare the clinical demographics, and management of AF in Middle Eastern Arab in
Qatar. Over 2800 Arabs and 500 South Asians were admitted for evaluation and management of AF
over the 20-year period. Middle Eastern Arabs with AF were older, and had a greater
prevalence of HTN, DM, chronic renal insufficient and hyperlipidemia. In contrast, South
Asians were more likely to have acute coronary syndromes and a history of valvular heart
disease. Importantly the in-hospital mortality rate was higher in Arabs than South Asians but
the stroke rates were comparable. These studies highlight the differential impact of
traditional risk factors on the development of AF in Middle eastern Arabs.
Identification of probands and families with early-onset AF in Qatar: Two Middle Eastern Arab
families have been identified with early-onset AF. In one family, three family members
besides the proband presented with highly symptomatic AF at age <40 years. In the second
family, six family members have presented with early-onset AF. These findings are very
preliminary evaluations and upon approval of the submitted protocol by the IRB Ethics
Committee, further evaluations of these two families will take place.
Participant recruitment and enrollment: Patients who are over the age of 18 years presenting
with early-onset AF from cardiology clinics, the ER and in-patient services from the HMC
network of hospitals (Hamad General Hospital, Hamad Heart Hospital, Al-Khor Hospital, Cuban
Hospital, and Al-Wakra Hospital). The HMC hospital network provides both outpatient and
in-patient cardiology services for all Qatar residents, and >95% of all cardiac patients in
the country are treated at these hospitals, including patients with acute cardiac conditions,
representing essentially a population-based cohort for identification and selection of AF
patients and a control cohort of non-AF cardiology patients for the genetic studies. These
participants will comprise two broad ethnic groups that have not been adequately studied
previously, defined as: Qatari and other Middle Eastern Arabs. A diagnosis of AF will be
confirmed when an ECG shows AF during the index hospitalization/ER visit showing AF. Patients
with a history of AF only in the setting of cardiac surgery will be excluded from this study.
For this proposal, only family members of Qatari Middle Eastern Arab patient with early onset
(≤60 years of age) AF will be targeted for recruitment. In 2016, over 600 patients with AF
were seen in the Hamad General Hospital ER and over 400 patients were seen by Dr. Nidal Assad
(LPI) in the Arrhythmia Clinic at the Hamad Heart Hospital. Approximately 30% of these
patients presented with early-onset AF. A projected annual growth of over 20% in new patients
with AF will not only increase the likelihood of meeting our target recruitment but will also
significantly improve our chances of identifying large kindreds with familial AF. At the same
network of hospitals during the same time period, It will identify a cohort of cardiology
patients without AF to be followed prospectively and to serve as a comparison group for
genetic analyses. This control cohort will be a representative sample of the population of
cardiology patients who do not have AF, which is already available from another completed
cardiology biorepository. Patients will not be enrolled if major difficulties with follow-up
are anticipated, for example, patients with no valid residency permit or those planning to
leave the country before the next planned follow-up visit.
Subject Population(s) Total number of QCBio-AF participants: 300 Age range of participants:
18 yrs and above Targeted number of males: 150 Targeted number of females: 150 A informed
consent will be indicated to recruit patients who may be eligible for the study.
Participant Identification, Inclusion/Exclusion Criteria, and Recruitment Patients will be
identified through Hamad Medical Corporation (HMC) Heart Hospital (HH) Arrhythmia and General
Cardiology Clinics and the Emergency Department will be approached for inclusion in the
study. A detailed family history and a DNA sample will then be obtained by the principal
investigator or a research coordinator, following written informed consent under a protocol
approved by the Institutional Review Board of HMC. Upon identification of a patient with a
family history of AF, relatives will be contacted by the by the principal investigator or a
research coordinator. Once this is obtained, outside medical records will be requested.
Identify the criteria for inclusion and exclusion and explain the procedures that will be
used to determine eligibility:
Specimen Collection for the main study:
Blood drawing (indicate total amount drawn for research purposes): 25 cc x 1 (one-time only).
Other specimens (describe the type of specimen and frequency of collection): None
Study-specific questionnaires will be conducted at enrollment, and when appropriate and
available, collected at the subjects' six-month and 12-month scheduled clinic visits. The
questionnaires will take approximately take 10 minutes to complete. These are only applicable
to adult patients.
The baseline, 6-month, and 12-month questionnaires and other information from the medical
record will be collected at regularly scheduled clinic visits on study-specific source
documentation to later be transcribed onto SPSS with only the subject's study-specific code
ID/number assigned to the data.
The ECG, ECHO, and Holter monitoring will be performed (or will have already been performed)
as part of the subjects' clinically indicated treatment/management for their AF. Family
members asked to participate in the study who do not have a documented history of AF will not
have the ECG, ECHO, and Holter monitoring performed because it is not clinically indicated.
Family members who are not part of the UIC medical system and have had an ECG, ECHO, and/or
Holter monitoring performed at outside facilities will be asked to provide this information
for research purposes only.
The creation of a Qatar Cardiovascular Biorepsoitory-AF (QCBio-AF): a resource that will
collect and store clinical, demographic, blood and DNA samples from patients and family
members with AF to enable subsequent clinical, molecular, and genetic studies.
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