Litcius/Paper detail

Opportunities, barriers, and recommendations in Down syndrome research

James A. Hendrix, Angelika Amon, Leonard Abbeduto, Stamatis Agiovlasitis, Tarek Alsaied, Heather A. Anderson, Lisa J. Bain, Nicole Baumer, Anita Bhattacharyya, Dusan Bogunovic, Kelly N. Botteron, George T. Capone, Priya Chandan, Isabelle Chase, Brian Chicoine, Cécile Cieuta‐Walti, Lara R. DeRuisseau, Sophie Durand, Anna J. Esbensen, Juan Fortea, Sandra Giménez, Ann‐Charlotte Granholm, Laura J. Mattie, Elizabeth Head, Hampus Hillerstrom, Lisa M. Jacola, Matthew P. Janicki, Joan Jasien, Angela R. Kamer, Raymond D. Kent, Bernard Khor, Jeanne B. Lawrence, Catherine Lemonnier, Amy Feldman Lewanda, William C. Mobley, Paul E. Moore, Linda Nelson, Nicolas M. Oreskovic, Ricardo S. Osorio, David Patterson, Sonja A. Rasmussen, Roger H. Reeves, Nancy Roizen, Stephanie L. Santoro, Stephanie L. Sherman, Nasreen Talib, Ignacio E. Tapia, Kyle M. Walsh, Steven F. Warren, A. Nicole White, G. William Wong, John S. Yi

2021Translational Science of Rare Diseases99 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Recent advances in medical care have increased life expectancy and improved the quality of life for people with Down syndrome (DS). These advances are the result of both pre-clinical and clinical research but much about DS is still poorly understood. In 2020, the NIH announced their plan to update their DS research plan and requested input from the scientific and advocacy community. OBJECTIVE: The National Down Syndrome Society (NDSS) and the LuMind IDSC Foundation worked together with scientific and medical experts to develop recommendations for the NIH research plan. METHODS: NDSS and LuMind IDSC assembled over 50 experts across multiple disciplines and organized them in eleven working groups focused on specific issues for people with DS. RESULTS: This review article summarizes the research gaps and recommendations that have the potential to improve the health and quality of life for people with DS within the next decade. CONCLUSIONS: This review highlights many of the scientific gaps that exist in DS research. Based on these gaps, a multidisciplinary group of DS experts has made recommendations to advance DS research. This paper may also aid policymakers and the DS community to build a comprehensive national DS research strategy.

Topics & Concepts

Multidisciplinary approachLife expectancyPlan (archaeology)Political scienceMedical educationHealth careMedical researchPublic relationsMedicineEngineering ethicsPsychologyEngineeringEnvironmental healthGeographyPathologyPopulationLawArchaeologyDown syndrome and intellectual disability researchDisability Rights and RepresentationDisability Education and Employment
Opportunities, barriers, and recommendations in Down syndrome research | Litcius