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Kanu Chatterjee Receives 2009 HFSA Lifetime Achievement Award ...

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Heart Failure Society News December <strong>2009</strong><br />

Highlights from the 13th Annual Scientific Meeting<br />

Opening Session – Personalized Medicine: The Dawn of a New Era<br />

The Opening Plenary session presented<br />

three different perspectives on the<br />

application of genetic information and<br />

testing to better understand complex<br />

human disease and personalize<br />

medicine. David A. Schwartz (Denver,<br />

CO), an expert on pulmonary disease,<br />

addressed the role of the epigenome<br />

in the development of disease. One<br />

important aspect of personalized<br />

medicine is how the environment is<br />

altering biology and therefore affecting<br />

the risk of developing disease. Schwartz<br />

explained that the field of epigenetics<br />

concerns the mechanisms that control<br />

gene regulation and transcription. These<br />

epigenetic mechanisms can be altered by the<br />

environment or inherited from one generation<br />

to the next. The goal is to measure these<br />

epigenetic marks in patients and use them<br />

to identify individuals who may respond to<br />

certain medications.<br />

Atul J. Butte (Palo Alto, CA) discussed<br />

translational bioinformatics. There are now<br />

approximately 350,000 publicly available<br />

microarrays, a number that should double or<br />

triple each year. This easily-searched data is<br />

leading to a new taxonomy of disease based<br />

on genomics.<br />

David E. Duncan, a journalist, (Berkley,<br />

CA) anchored the session by recounting<br />

his experiences in the “Experimental<br />

Man” project in a talk, “One Man’s Quest<br />

for Personalized Medicine.” The project<br />

involved taking 320 tests, including<br />

genetic and gene expression tests that<br />

required having 2 liters of blood drawn<br />

and undergoing 22 hours of MRI scans.<br />

Baseline testing showed that Duncan was<br />

a healthy 51-year-old male. However,<br />

a battery of genetic tests indicated that<br />

Duncan was at a lifetime risk for several<br />

illnesses or events, including myocardial<br />

infarction and addiction. He learned<br />

he had a greater tolerance for caffeine,<br />

had a greater propensity for risk taking, and<br />

showed a high exposure to DDT. Duncan<br />

said his experiences underscored the need<br />

to standardize and organize the information<br />

better, since different companies showed<br />

different results.<br />

Oliver Smithies, PhD receiving 3rd Distinguished<br />

Lecture in Basic Science<br />

Excellence in Basic Science<br />

Oliver Smithies, PhD, co-recipient of the<br />

2007 Nobel Prize in Physiology or Medicine<br />

for work on gene modifications in mice<br />

through the use of embryonic stem cells,<br />

delivered the 3rd Distinguished Lecture in<br />

Basic Science. Following Smithies’ lecture<br />

were presentations on the current role of<br />

mouse models in cardiovascular research,<br />

current research in cardiac transgenesis, and<br />

the implications of biased signaling by G<br />

protein-coupled receptors for the treatment<br />

of patients with heart failure. The Special<br />

Sunday Session is the kick off for the basic<br />

science component of the annual meeting, and<br />

always features excellent speakers that attract<br />

a large audience.<br />

Insights from Recent Trials and Registries<br />

Key data and new insights from 4 recent<br />

trials and registries of heart failure therapies<br />

were discussed in a session focusing on<br />

implications for patient care. James K.<br />

Kirklin (Birmingham, AL) presented on the<br />

INTERMACS registry; David J. Whellan<br />

(Philadelphia, PA) presented HF-ACTION;<br />

Peter E. Carson (Washington, DC) discussed<br />

the I-PRESERVE trial; and Eric J. Velazquez<br />

(Durham, NC) presented the STICH trial.<br />

INTERMACS is a U.S. national registry for<br />

patients receiving mechanical circulatory<br />

support therapy for advanced heart failure.<br />

Registry data indicates that the strategy is<br />

increasingly to implant a temporary device<br />

before the patient is in cardiogenic shock<br />

and to do it as an elective procedure. Patients<br />

with an isolated LVAD have the best survival.<br />

However, there are still issues with long-term<br />

survival, and destination therapy currently does<br />

not look favorable. There is a clear movement<br />

from pulsatile to axial flow pumps.<br />

Most patients enrolled in ACTION-HF did not<br />

meet the exercise goal, but approximately 30%<br />

achieved or surpassed the target. When the<br />

results were adjusted for baseline prognostic<br />

factors such as EF, atrial fibrillation, and<br />

depression, there was a significant benefit, with<br />

greater exercise resulting in a greater benefit<br />

in terms of the primary end point. The study<br />

clearly demonstrated that exercise training for<br />

heart failure patients is safe.<br />

Approximately 50% of patients with heart<br />

failure have an ejection fraction of at least<br />

45%, but no pharmacological therapies have<br />

been shown to improve outcomes. Irbesartan<br />

did not improve outcomes in patients in<br />

the I-PRESERVE trial. Although mortality<br />

in the study was substantial, the change in<br />

Minnesota Living with Heart Failure scores<br />

was favorable.<br />

One of the objectives of the STICH trial was<br />

to compare surgical ventricular reconstruction<br />

(SVR) in addition to a coronary artery<br />

bypass graft (CABG) procedure to CABG<br />

alone. Results of the randomized study of<br />

1,000 patients found no differences between<br />

the 2 groups in death or cardiovascular<br />

hospitalization.<br />

3

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