Adults with both Down Syndrome and congenital heart defects, also known as congenital heart disease (CHD), are showing remarkable resilience despite facing significant medical challenges, according to a new MUSC study in Pediatric Cardiology. The study found that adults ages 18 to 45 with both conditions are just as likely to work, volunteer and experience the same quality of life as those with Down Syndrome alone.
The study was conducted through the Pediatric Heart Network, a consortium of leading children’s hospitals that includes the MUSC Shawn Jenkins Children’s Hospital. The network conducts research in children and adults living with CHD. Andrew Atz, M.D., professor and chairman of Pediatrics at MUSC, is the senior author on the study and a principal investigator for the Pediatric Heart Network.
Understanding Down syndrome and CHD
Down syndrome is a genetic condition caused by an extra copy of chromosome 21. This extra chromosome affects how the body and brain develop. Down syndrome is the most common genetic cause of intellectual disability in the U.S.
Congenital heart disease is a serious health issue that affects nearly half of people with Down syndrome. It occurs when there is a defect in how the heart or blood vessels are formed at birth.
For many families, it’s hard to know what life will look like for children with both conditions.
“I think people want to know, ‘When my child grows up, will they live a normal life? Will they have a good life, a happy, a productive life?’” said Stephanie Gaydos, M.D., associate professor of Pediatrics and lead researcher on the study. “I think those are things that really matter a lot to people.”
To answer those questions, Gaydos designed her study to take a deeper look. She aimed to find out if adults living with a dual diagnosis of Down syndrome and CHD had greater difficulties with their day-to-day lives than those with a diagnosis of Down Syndrome alone. Gaydos, Atz and their team also looked at other important health issues that occur more commonly in people with CHD or people with Down syndrome, like mental health problems or neurologic disorders such as seizures and/or stroke, which can affect quality of life and employment abilities.
The study included 287 adults with Down syndrome, 104 of whom also had CHD, and their caregivers. Participants were invited to complete a comprehensive online questionnaire that assessed medical history, employment/volunteer experience, quality of life, mental health and caregiver burden. Researchers then compared the results between participants with and without CHD. The questionnaire was created and administered using REDCap, a secure, web-based software platform developed at Vanderbilt University to support data capture for research studies, with the help of the REDCap team at the South Carolina Clinical & Translational Research Institute.
Good news for patients and their families
Gaydos and her team were heartened by the study’s findings.
“Is community engagement or quality of life worse in adulthood if you also have congenital heart disease?” Gaydos asked. “In our sample, we didn’t find that to be the case, which is fantastic.”
The researchers found that having both Down syndrome and CHD doesn’t hold people back from participatingin their communities. Adults with the dual diagnosis are statistically just as likely to hold jobs as those with only Down syndrome and reported more volunteer participation – despite having more neurologic problems. This information sheds light on how these health issues translate into adult-life functioning and also challenges long-held assumptions to offer a hopeful outlook for families and care providers.
Adults with Down syndrome and CHD showed nearly identical employment rates as those without CHD, at 61% and 60%, respectively. Rates of volunteerism were even more striking – 32% of participants with Down syndrome and CHD volunteered in their communities, compared with 19% of participants with just Down syndrome.
Laying the groundwork for future research
For Gaydos and Atz, this research is just the beginning. They see this work as a foundation for building a deeper understanding of life with these conditions and tailoring medical care to support long-term success more fully.
"We think it's a really optimistic finding for patients and their families, for children who are born with both of these health issues,” said Gaydos. “Having a heart defect from birth plus Down syndrome doesn't necessarily mean that you'll be at lower odds for having a productive role in the community in adulthood."
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About the Medical University of South Carolina
Founded in 1824 in Charleston, MUSC is the state’s only comprehensive academic health system, with a mission to preserve and optimize human life in South Carolina through education, research and patient care. Each year, MUSC educates over 3,300 students in six colleges and trains more than 1,060 residents and fellows across its health system. MUSC leads the state in federal, National Institutes of Health and other research funding. For information on our academic programs, visit musc.edu.
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About the South Carolina Clinical & Translational Research Institute
The South Carolina Clinical & Translational Research (SCTR) Institute is the catalyst for changing the culture of biomedical research, facilitating the sharing of resources and expertise and streamlining research-related processes to bring about large-scale change in the clinical and translational research efforts in South Carolina. Our vision is to improve health outcomes and quality of life for the population through discoveries translated into evidence-based practice. To learn more, visit https://research.musc.edu/resources/sctr
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