The US Alpha-1 Foundation announced its 2016 grant awardees on Monday, May 16 during a reception at the American Thoracic Society (ATS) International Conference in San Francisco. The 14 grant recipients will receive a record total of $1.9 million for their projects. Among the award recipients were two Irish Alpha-1 researchers, Professor Gerry McElvaney and Dr. Emer Reeves, who are both based at the RCSI Smurfit Building in Beaumont Hospital.
Professor McElvaney received funding to study the risk of lung disease caused by a particular type of alpha-1 antitrypsin deficiency (AATD) called SZ AATD. This will be a family based study looking at the risk for COPD in people who are born with 1 copy of the S and 1 copy of the Z variant. Dr. Reeves received funding to look at how platelets behave in people with AATD, and also explore how platelets interact with neutrophils, the important white blood cell which helps to fight off infections.
The Alpha-1 Foundation is committed to finding a cure for alpha-1 antitrypsin deficiency and to improving the lives of people affected by Alpha-1 worldwide. The Alpha-1 Foundation is a not-for-profit organisation founded in 1995 by John Walsh, Sandy Lindsey and Susan Stanley, three individuals diagnosed with Alpha-1 Antitrypsin Deficiency (Alpha-1). To read more visit the US Alpha-1 Foundation website here.
At the same conference, the Irish Alpha One Foundation presented findings from the national AATD targeted detection programme. So far the national screening programme has detected over 500 people with the severe form of the condition (ZZ or SZ) and over 2,000 people who have a milder form of deficiency (MZ). A further group have been found to have rare variants (for example F, Mmalton and Null) which can also cause lung, liver, and skin problems. The conference was an excellent opportunity to meet others working in the field of AATD and share knowledge and experience.
Info Centre
WhatisAlpha-1Antitrypsin?
Alpha-1 antitrypsin is a vital protein produced by the liver to protect the lungs. It provides protection from the harmful effects of infections and inhaled irritants, particularly tobacco smoke. It can be easily measured by a simple blood test.
WhatisAlpha-1AntitrypsinDeficiency?
Alpha-1 antitrypsin deficiency (Alpha-1) is a genetic condition which, after cystic fibrosis, is the commonest genetic disorder in Ireland. It severely affects more than 15,000 people, with another 250,000 carriers also at risk of lung and liver disease on the island of Ireland. It is a proven genetic risk factor for chronic obstructive pulmonary disease (COPD).
HowDoIGetTested?
The Alpha-1 Foundation Ireland provides free testing for Alpha-1 as part of a national screening programme which is funded by the HSE. It is a simple blood test. For more details ring 01-8093871 or email alpha1@rcsi.ie
Irish Alpha-1 Researchers Awarded Funding
The US Alpha-1 Foundation announced its 2016 grant awardees on Monday, May 16 during a reception at the American Thoracic Society (ATS) International Conference in San Francisco. The 14 grant recipients will receive a record total of $1.9 million for their projects. Among the award recipients were two Irish Alpha-1 researchers, Professor Gerry McElvaney and Dr. Emer Reeves, who are both based at the RCSI Smurfit Building in Beaumont Hospital.
Professor McElvaney received funding to study the risk of lung disease caused by a particular type of alpha-1 antitrypsin deficiency (AATD) called SZ AATD. This will be a family based study looking at the risk for COPD in people who are born with 1 copy of the S and 1 copy of the Z variant. Dr. Reeves received funding to look at how platelets behave in people with AATD, and also explore how platelets interact with neutrophils, the important white blood cell which helps to fight off infections.
The Alpha-1 Foundation is committed to finding a cure for alpha-1 antitrypsin deficiency and to improving the lives of people affected by Alpha-1 worldwide. The Alpha-1 Foundation is a not-for-profit organisation founded in 1995 by John Walsh, Sandy Lindsey and Susan Stanley, three individuals diagnosed with Alpha-1 Antitrypsin Deficiency (Alpha-1). To read more visit the US Alpha-1 Foundation website here.
At the same conference, the Irish Alpha One Foundation presented findings from the national AATD targeted detection programme. So far the national screening programme has detected over 500 people with the severe form of the condition (ZZ or SZ) and over 2,000 people who have a milder form of deficiency (MZ). A further group have been found to have rare variants (for example F, Mmalton and Null) which can also cause lung, liver, and skin problems. The conference was an excellent opportunity to meet others working in the field of AATD and share knowledge and experience.
Info Centre
What is Alpha-1 Antitrypsin?
Alpha-1 antitrypsin is a vital protein produced by the liver to protect the lungs. It provides protection from the harmful effects of infections and inhaled irritants, particularly tobacco smoke. It can be easily measured by a simple blood test.
What is Alpha-1 Antitrypsin Deficiency?
Alpha-1 antitrypsin deficiency (Alpha-1) is a genetic condition which, after cystic fibrosis, is the commonest genetic disorder in Ireland. It severely affects more than 15,000 people, with another 250,000 carriers also at risk of lung and liver disease on the island of Ireland. It is a proven genetic risk factor for chronic obstructive pulmonary disease (COPD).
How Do I Get Tested?
The Alpha-1 Foundation Ireland provides free testing for Alpha-1 as part of a national screening programme which is funded by the HSE. It is a simple blood test. For more details ring 01-8093871 or email alpha1@rcsi.ie