Novel blood test-A non-invasive diagnostic option to detect CAD

Written By :  Hina Zahid
Medically Reviewed By :  Dr. Kamal Kant Kohli
Published On 2021-09-30 03:00 GMT   |   Update On 2021-09-30 05:11 GMT

WOBURN, Mass. - A new blood-based RNA Sequencing method to detect Coronary Artery Disease (CAD) powered by SeqLL's tSMS platform has been reported in the September issue of BMC Medical Genomics.The present studies employed RNA sequencing of whole blood to identify an RNA signature in patients with angiographically confirmed CAD.

The new diagnostic plateform may obviate need for invasive procedures like coronary angiography to diagnose CAD in future.

The study, "RNA Sequencing of Blood in Coronary Artery Disease: Involvement of Regulatory T-cell Imbalance", was led by Timothy McCaffery, PhD, Professor of Medicine at the George Washington University (GW) School of Medicine and Health Sciences, with support from a public-private relationship with SeqLL, and support from the St. Laurent Institute and True Bearing Diagnostics, included researchers and physicians from GW as well as Inova Health System (Inova) of Northern Virginia.

Diagnosis of CAD is typically based on coronary angiography, an imaging process used to detect restricted blood flow in the heart's major arteries. Up to 40% of the 1 million cardiac catheterizations performed in the U.S., however, have a "no blockage" test result, despite clinical indications. To improve diagnostic options, Dr. McCaffrey's study used a cutting-edge sequencing method to identify an RNA signature in the whole blood of CAD patients who had received diagnoses via angiographies.

"Using SeqLL's tSMS platform, our team was able to sequence millions of RNA strands per patient at single molecule resolution. This allowed us to reproducibly identify specific RNA transcripts that were altered in patients with coronary disease," Dr. McCaffrey said. He added that "cardiologists were able to collect the blood while the patients underwent angiographic imaging of their arteries."

Between two cohorts, one at GW and one at Inova, Dr. McCaffrey and the research team pinpointed new biomarkers from the identified genes that could lend insight into the cause of CAD. For example, they determined that patients with atherosclerosis had reduced activity of their regulatory T-cells, or suppressor T-cells.

"Accumulating evidence suggests that autoimmunity may play a significant factor in CAD. Based on the gene expression pattern in our studies, it appears as though the patient's immune system becomes stressed, which causes an inappropriate attack on their own arteries," Dr. McCaffrey explained. "This immune connection extends to COVID-19 as well, as patients have experienced heart-related issues following their bouts with the virus. Our results outperformed the conventional clinical prediction model for CAD and using this new method, blood tests for diagnosing CAD could transform health care."

According to the Centers for Disease Control and Prevention, CAD impacts over 18% of adults in the United States age 20 and older and over 665,000 deaths from cardiovascular disease occur annually.

Daniel Jones, SeqLL's CEO, President, & Co-founder, stated, "This publication demonstrates the tSMS platform's ability to produce accurate molecular profiles and generate novel biological insights. This study represents another step toward providing improved, non-invasive diagnostic options to those suffering from coronary artery disease. We at SeqLL strongly support the application of our tSMS platform to the field of cardiovascular health, especially one that impacts so many Americans daily."

https://bmcmedgenomics.biomedcentral.com/articles/10.1186/s12920-021-01062-2


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Article Source : BMC Medical Genomics

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