NIH Media Availability: Researchers take important step in unlocking what causes congenital heart disease
NHLBI Press Release
Findings from the first large-scale sequencing analysis of congenital heart disease bring us closer to understanding this most common type of birth defect. The analysis found that spontaneous, or de novo, mutations affect a specific biological pathway that is critical to aspects of human development, including the brain and heart. Congenital heart disease can cause infants to be born with structural heart problems, which can be serious or even life-threatening.
Related links:
- NHLBI Bench to Bassinet program website
- NHLBI Story of Success: Congenital heart disease
- Media availability: Bench to bassinet program seeks congenital heart disease treatments
- Children and Clinical Studies website
- Health Topic: Congenital Heart Defects
NIH Media Availability: Researchers take important step in unlocking what causes congenital heart disease
WHAT: Findings from the first large-scale sequencing analysis of congenital heart disease bring us closer to understanding this most common type of birth defect. The analysis found that spontaneous, or de novo, mutations affect a specific biological pathway that is critical to aspects of human development, including the brain and heart. Congenital heart disease can cause infants to be born with structural heart problems, which can be serious or even life-threatening.
The findings, which were published online today in the journal Nature, will inform future research into the causes of congenital heart disease.
This research was conducted through the National Heart, Lung, and Blood Institute- (NHLBI) supported Pediatric Cardiac Genomics Consortium, an international, multi-center collaborative research effort. The NHLBI is part of the National Institutes of Health.
The researchers looked at 362 parent-offspring trios, each of which included a child with congenital heart disease and his or her healthy parents, as well as 264 healthy parent-offspring trios, which served as the control group. The team conducted an analysis using state-of-the-art sequencing and genome mapping techniques and found that the children with congenital heart disease had a greatly increased rate of spontaneous mutations among genes that are highly expressed, or active, in the developing heart. Specifically, the analysis found that about 10 percent of the participant cases were associated with spontaneous mutations that arise during fetal development. Many of these genes were involved in a specific pathway that controls and regulates gene expression, which provides some insight into how the defects arise.
The Pediatric Cardiac Genomics Consortium provided resources to recruit thousands of patients in a small amount of time and used advanced sequencing techniques to identify genes that are implicated in congenital heart disease.
Future research aims to better understand how congenital heart disease develops in order to improve treatment and perhaps eventually prevent congenital heart disease in the early stages of heart formation.
WHO: Jonathan R. Kaltman, M.D., chief of the Heart Development and Structural Diseases Branch in the NHLBI's Division of Cardiovascular Sciences and coauthor of the paper, is available to comment on the findings and implications of this research.
For Dr. Kaltman's complete bio, please visit: http://www.nhlbi.nih.gov/news/spokespeople/kaltman-jonathan.html
For a complete list of the Pediatric Cardiac Genomics Consortium Centers involved in this effort, please visit: http://www.benchtobassinet.net/PCGCcenters.asp
CONTACT: For more information or to schedule an interview, please contact the NHLBI Communications Office at 301-496-4236 or nhlbi_news@nhlbi.nih.gov.
The findings, which were published online today in the journal Nature, will inform future research into the causes of congenital heart disease.
This research was conducted through the National Heart, Lung, and Blood Institute- (NHLBI) supported Pediatric Cardiac Genomics Consortium, an international, multi-center collaborative research effort. The NHLBI is part of the National Institutes of Health.
The researchers looked at 362 parent-offspring trios, each of which included a child with congenital heart disease and his or her healthy parents, as well as 264 healthy parent-offspring trios, which served as the control group. The team conducted an analysis using state-of-the-art sequencing and genome mapping techniques and found that the children with congenital heart disease had a greatly increased rate of spontaneous mutations among genes that are highly expressed, or active, in the developing heart. Specifically, the analysis found that about 10 percent of the participant cases were associated with spontaneous mutations that arise during fetal development. Many of these genes were involved in a specific pathway that controls and regulates gene expression, which provides some insight into how the defects arise.
The Pediatric Cardiac Genomics Consortium provided resources to recruit thousands of patients in a small amount of time and used advanced sequencing techniques to identify genes that are implicated in congenital heart disease.
Future research aims to better understand how congenital heart disease develops in order to improve treatment and perhaps eventually prevent congenital heart disease in the early stages of heart formation.
WHO: Jonathan R. Kaltman, M.D., chief of the Heart Development and Structural Diseases Branch in the NHLBI's Division of Cardiovascular Sciences and coauthor of the paper, is available to comment on the findings and implications of this research.
For Dr. Kaltman's complete bio, please visit: http://www.nhlbi.nih.gov/news/spokespeople/kaltman-jonathan.html
For a complete list of the Pediatric Cardiac Genomics Consortium Centers involved in this effort, please visit: http://www.benchtobassinet.net/PCGCcenters.asp
CONTACT: For more information or to schedule an interview, please contact the NHLBI Communications Office at 301-496-4236 or nhlbi_news@nhlbi.nih.gov.
Jonathan R. Kaltman, M.D., of the National Heart, Lung, and Blood Institute's Division of Cardiovascular Sciences, and Richard Lifton, M.D., Ph.D., chair of the Department of Genetics at Yale University, discuss findings from the first large-scale gene sequencing analysis of congenital heart disease. The findings, which were published online March 12, 2013, in the journal Nature, will inform future research into the causes of congenital heart disease.
Supplemental Information
- NHLBI Bench to Bassinet program website
http://www.benchtobassinet.net/ - NHLBI Story of Success: Congenital heart disease
http://www.nhlbi.nih.gov/news/spotlight/success/congenital-heart-disease.html - Media availability: Bench to bassinet program seeks congenital heart disease treatments http://www.nih.gov/news/health/mar2010/nhlbi-16.htm
- Children and Clinical Studies website
http://www.nhlbi.nih.gov/childrenandclinicalstudies/index.php
.png)
No hay comentarios:
Publicar un comentario