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Boston Children's, Brigham and Women's receive $6 million for genome sequencing in newborns

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Boston Children’s, Brigham and Women’s receive $6 million
for genome sequencing in newborns

Randomized trial is first to explore benefits and risks

Boston, MA, Sept. 4, 2013 – Parents of some Boston-area newborns will have a rare opportunity to have their baby’s DNA completely analyzed as part of the first-ever randomized trial to explore the benefits and risks of genome sequencing (reading the entirety of a person’s DNA) in this age group.  The five-year study will assess the baby’s risks of future diseases and how that information affects the baby’s medical care, and the relationship between the parents, baby and baby’s pediatrician.  The study is funded by a $6-million grant from the National Institutes of Health (NIH) to Boston Children’s Hospitaland Brigham and Women’s Hospital (BWH). The study will be led equally by principal investigators Alan H. Beggs, PhDat Boston Children’s Hospital, and Robert C. Green, MD, MPH at Brigham and Women’s Hospital, both faculty at Harvard Medical School.

“This first-of-its-kind study will accelerate the use of genomics in clinical pediatric medicine by creating and safely testing novel methods for integrating sequencing into the care of newborns,” said Green, a medical geneticist in the Division of Genetics at BWH and director of the Genomes2People Research Program.  “We will implement and study a futuristic goal: that genomic information examined shortly after birth can serve as a resource throughout infancy and childhood to inform clinical care and identify appropriate and timely interventions.”

Beginning in early 2014, the study will enroll 480 newborns and their parents in order to compare outcomes that occur when genomic newborn sequencing is added to the conventional newborn screening that babies currently receive.  The volunteers, healthy newborns from Brigham and Women’s Hospital and infants from Boston Children’s Hospital’s Neonatal Intensive Care Unit, will be divided into two groups.  One group will receive conventional state-mandated newborn screening, the other will receive conventional screening and genome sequencing.  Researchers will collect and analyze the genomic sequences, which may include information on potential causes of any birth defects, predispositions to future medical conditions and predictions about responses to certain drugs, and will return that information to parents and pediatricians to evaluate the medical, psychosocial and economic outcomes. 

“These analyses will help illuminate the full spectrum of benefits and risks associated with genome sequencing of newborns,” said Beggs, director of the Manton Center for Orphan Disease Researchand a professor of pediatrics and scientist in the Division of Genetics at Boston Children’s Hospital.

This research project follows the start of a similar NIH-funded study at Brigham and Women’s Hospital, the MedSeq Project, which is the first NIH-funded randomized clinical trial to study the integration of whole genome sequencing into the practice of adult medicine.  The Manton Center at Boston Children’s is a multidisciplinary center for research into the causes and prevention of rare “orphan” diseases that is working with Claritas Genomicsto develop genomic testing to enhance pediatric health. 

Beggs said, “Synergies between the MedSeq Project, the Manton Center, and this newborn sequencing project we are calling the BabySeq Project will help us discover how best to integrate genomic sequencing into medical care to benefit all adults, children and their families.”

In addition to Beggs and Green, the project will be co-led by a multidisciplinary team of investigators in pediatrics, neonatology, genetics, psychology, ethics and newborn screening, including Ingrid Holm, MD, MPH, Peter Park, PhD, Timothy Yu, MD, PhD, Harvey Levy, MD, Pankaj Agrawal, MD, and Susan Waisbren, PhD, at Boston Children’s Hospital; Heidi Rehm, PhD, Richard Parad, MD, MPH; Steve Ringer, MD, PhD, and Lise Johnson, MD at BWH, and Amy McGuire, PhD, JD, at Baylor College of Medicine. 

Contact:
Cyndi Lepore
Boston Children’s Hospital
617-919-3110
cynthia.lepore@childrens.harvard.edu

Boston Children’s Hospitalis home to the world’s largest research enterprise based at a pediatric medical center, where its discoveries have benefited both children and adults since 1869. More than 1,100 scientists, including seven members of the National Academy of Sciences, 13 members of the Institute of Medicine and 14 members of the Howard Hughes Medical Institute comprise Boston Children’s research community. Founded as a 20-bed hospital for children, Boston Children’s today is a 395 bed comprehensive center for pediatric and adolescent health care grounded in the values of excellence in patient care and sensitivity to the complex needs and diversity of children and families. Boston Children’s also is the primary pediatric teaching affiliate of Harvard Medical School. For more information about research and clinical innovation at Boston Children’s, visit: http://vectorblog.org.

The Manton Center for Orphan Disease Researchat Boston Children's Hospital is a multidisciplinary program dedicated to understanding the causes and prevention of "orphan diseases" - genetic syndromes, immune system problems, errors of metabolism, neuromuscular disorders and other little-noticed but scientifically important disease processes.

We are grateful to have been ranked #1 on U.S. News & World Report's list of the best children's hospitals in the nation for the third year in a row, an honor we could not have achieved without the patients and families who inspire us to do our very best for them. Thanks to you, Boston Children's is a place where we can write the greatest children's stories ever told.”
- Sandra L. Fenwick, President and CEO

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