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SEX DIFFERENCES IN THE HEART
25 April 2007 - University of Bristol

New research has identified a potential key to understanding the sex differences in heart function. This exciting development could minimise fatal heart disturbances in women.

It is widely accepted that men tend to get coronary heart disease at a younger age than women. However, many people are not aware that heart disease is more deadly for women.

Each year, over eight million women worldwide die from heart disease or strokes, the highest cause of death amongst women. In developing countries, half of all deaths of women over 50 are due to heart disease and strokes.

This brand new research by Professor Meyer and Dr Grohe from the University of Bonn, points to the oestrogen receptor (ERalpha) as having a key influence in female heart function. The research shows that if females lack the ERalpha receptor, the electrical property of heart function closely mirrors that of males.

Dr Andy James, lecturer in physiology at Bristol University and convener for the cardiac symposium at the conference comments: "What Professor Meyer and Dr Grohe will show us is that one of the two oestrogen receptors, ER-Alpha, plays an important role in male/female differences in electrical properties of the heart muscle. This could help us understand the gender difference and how we can isolate and potentially minimise the risk to women."

According to the scientists there are also important differences between men and women in their chance of suffering potentially fatal disturbances to the normal heart rhythm (arrhythmias). Arrhythmias are the result of disruption to the electrical properties of the heart. There are many different forms of arrhythmia and they have different causes.

There are gender differences in a number of different forms of arrhythmia. For example, women are three times more likely than men of suffering a form of arrhythmia associated with unwanted drug side-effects that can also arise from inheritance of faulty genes.

This difference between men and women in heart beat irregularity is associated with sex differences in the QT intervals (intervals between signals within each heart beat) measured by electrocardiograph. It is well established that testosterone in males plays a key role in this gender difference.

Dr James continues: "This is a departure from the currently well publicised but controversial suggestion that oestrogen protects women against heart disease. It is also suggests that the view that sex differences in risk of heart rhythm disturbance is all down to testosterone may be overly simplistic.

The Future: 'His and Hers' Heart Drugs?
Dr James added: "With a more thorough understanding of sex difference in the maintenance of normal heart rhythm, we will be able to develop gender-specific therapies. We will be able to capitalise on the new understanding of the sex hormone function in the heart by producing medication that matches the different requirements currently faced by men and women."

http://www.bris.ac.uk

About: University of Bristol
The University College of Bristol opened in 1876, after six years of discussions and controversy, in a bid to bring university culture to the provinces. It was the first college in the country to admit men and women on an equal footing.

The University’s Research and Enterprise Development (RED) division was launched in 2000 to stimulate and support an entrepreneurial culture and encourage the growth of technology-based business.

2003 saw the completion of the Dorothy Hodgkin building, named after the University’s fifth Chancellor. The £18 million building is dedicated to research in neuroendocrinology. 2003 also saw the opening of the University’s £5 million Centre for Sport, Exercise and Health.

Work on a new, state-of-the-art engineering building is due to be completed in early 2004. The £20 million BLADE project (Bristol Laboratory for Advanced Dynamics Engineering) will bring together the Engineering Faculty’s six departments to establish Europe’s most advanced dynamics engineering research facilities.


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