Clinical OMICs - Issue 7 - (Page 13)
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Determination of an individual's
risk for severe arrhythmias before a
life-threatening event occurs remains
a significant medical challenge.
last year that it now offers clinicians linked to long-QT syndrome, a rare
genetic testing through the school's inherited arrhythmia that lengthens
Genomics
and
the time between
Pathology Services
heartbeats, potenFor patients whose signs and
(GPS) to aid in diagtially causing heart
symptoms may be consistent
nosing and treatpalpitations or carwith a number of disease
ing heart disorders
diac arrest. These
that could lead
genes can identify
processes, genome or exome
to sudden death. sequencing may be quicker and particular subtypes
The test, called
of long QT, distinless expensive.
the Washington
guishing among
University Cardioforms of it that
Gene Set, analyzes genes linked to respond to different therapies to help
arrhythmias and cardiomyopathies, guide treatment decisions.
yielding a report based on patient
Patients with hypertrophic cardioblood samples submitted by their myopathy (HCM), a thickening of the
physicians. The cardiac testing panel heart muscle that can lead to sudden
includes genes linked to eight car- cardiac arrest and other problems,
diac disorders that are characterized also can benefit, according to the GPS,
by arrhythmias or cardiomyopathies. from the CardioGene Set. HCM can
Testing is traditionally offered one cause sudden fatal cardiac arrest in
gene at a time, but the new test can young athletes who have not shown
report on as many as 69 genes.
any prior symptoms of heart probThe testing panel analyzes, for lems. Genetic diagnosis of this condiexample, the sequences of genes tion could lead physicians to advise a
www.clinicalomics.com
patient against physical overexertion,
for example.
Common Clinical Challenge
The determination of the underlying
etiology of symptoms suggestive of
coronary artery disease (CAD), which
is defined as greater than or equal
to 50% stenosis in a major coronary
artery, presents a common clinical
challenge in both primary care and
cardiology clinics, according to physicians. Usual care, they say, in low to
medium risk patients involves a family history, risk factor assessment, and
then stress testing with or without
noninvasive imaging. If positive, this
is often followed by invasive coronary
angiography. Despite extensive adoption of this usual care paradigm, more
than 60% of patients referred for angiography do not have obstructive CAD.
CardioDx, a Palo Alto-based molecular diagnostics company specializ(continued on next page)
July 16, 2014 Clinical OMICs
13
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Table of Contents for the Digital Edition of Clinical OMICs - Issue 7
Contents
Clinical OMICs - Issue 7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss1
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss12
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss10
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss1
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue15
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue14
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue13
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue12
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue10
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue3
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