10:13pm Tuesday 19 September 2017

Blocking a gene reduces fat

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The gene in question codes for the apoC-III protein. “Our study suggests that the proteine apoC-III plays a key role in the management of triglycerides. Triglycerides, like cholesterol, are lipids. They come from fats carried by our food or produced by our bodies. Depending on the cause, the accumulation of triglycerides in blood is associated with an increased risk of cardiovascular and pancreatic illnesses, and other complications,” explained Dr. Daniel Gaudet, first author of the study. “Our conclusions are promising in terms of the prevention of the risk associated with the accumulation of fat in blood.” The research was published today in the New England Journal of Medicine.

Although rare forms of genetic triglyceride accumulation exist, for which there are few effective treatments, hypertriglyceridemia is the one most often associated with frequent health issues, such as obesity or diabetes. Last December, the same research team demonstrated blocking the expression of the gene that encodes apoC-III led to major relief of triglyceridemia in patients suffering a rare and extreme form of hypertriglyceridemia, which in turn opened the door for the identification of unexpected mechanisms that govern blood fat.

Both studies were published in the New England Journal of Medicine and are the result of a broad collaboration between researchers at the ECOGENE-21 Clinical and Translational Research Center–linked to the Centre de médecine génique communautaire and the University of Montreal’s Department of Medecine in Saguenay, Que.–and ISIS Pharmaceuticals, a Carlsbad, Calif., based company specialised in the development of medications that interfere specifically with the expression of targeted genes.

The results demonstrate apoC-III’s important contribution to the complex mechanisms by which our bodies manage blood fat. “Decoding mechanisms opens the door to precise, individual interventions for the prevention of residual risk associated with the various causes of severe hypertriglyceridemia,” Dr. Gaudet said. “The results of these studies enable the acceleration of research targeting better understanding and control of the risk trajectory associated with various forms of severe hypertriglyceridemia.”

Media contact:
William Raillant-Clark
International Press Attaché
University of Montreal (officially Université de Montréal)
Tel: 514-343-7593 

About these studies

References

Daniel Gaudet, M.D., Ph.D., Veronica J. Alexander, Ph.D., Brenda F. Baker, Ph.D.,

Diane Brisson, Ph.D., Karine Tremblay, Ph.D., Walter Singleton, M.D., Richard S. Geary, Ph.D., Steven G. Hughes, M.B., B.S., Nicholas J. Viney, B.Sc., Mark J. Graham, M.S., Rosanne M. Crooke, Ph.D., Joseph L. Witztum, M.D., John D. Brunzell, M.D., and John J.P. Kastelein, M.D., Ph.D. published “Antisense Inhibition of Apolipoprotein C-III in Patients with Hypertriglyceridemia” in the New England Journal of Medicine on July 29, 2015.

Daniel Gaudet, M.D., Ph.D., Diane Brisson, Ph.D., Karine Tremblay, Ph.D., Veronica J. Alexander, Ph.D., Walter Singleton, M.D., Steven G. Hughes, M.B., B.S., Richard S. Geary, Ph.D., Brenda F. Baker, Ph.D., Mark J. Graham, M.S., Rosanne M. Crooke, Ph.D., and Joseph L. Witztum, M.D., published “Targeting APOC3 in the familial chylomicronemia syndrome” in the New England Journal of Medicine on December 4, 2014.

About the researchers

Dr Daniel Gaudet, PhD, Diane Brisson, PhD, and Karine Tremblay, PhD, are affiliated with the University of Montreal’s Department of Medicine and Centre de médecine génique communautaire, and the ECOGENE-21 Clinical and Translational Research Centre in Chicoutimi, Quebec.

 

Note:

 

The University of Montreal is officially known as Université de Montréal.


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