Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus.

Down syndrome consensus criteria & indicators encephalopathy regression

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2022
Historique:
received: 10 05 2022
accepted: 24 06 2022
entrez: 1 8 2022
pubmed: 2 8 2022
medline: 2 8 2022
Statut: epublish

Résumé

To develop standardization for nomenclature, diagnostic work up and diagnostic criteria for cases of neurocognitive regression in Down syndrome. There are no consensus criteria for the evaluation or diagnosis of neurocognitive regression in persons with Down syndrome. As such, previously published data on this condition is relegated to smaller case series with heterogenous data sets. Lack of standardized assessment tools has slowed research in this clinical area. The authors performed a two-round traditional Delphi method survey of an international group of clinicians with experience in treating Down syndrome to develop a standardized approach to clinical care and research in this area. Thirty-eight potential panelists who had either previously published on neurocognitive regression in Down syndrome or were involved in national or international working groups on this condition were invited to participate. In total, 27 panelists (71%) represented nine medical specialties and six different countries reached agreement on preliminary standards in this disease area. Moderators developed a proposed nomenclature, diagnostic work up and diagnostic criteria based on previously published reports of regression in persons with Down syndrome. During the first round of survey, agreement on nomenclature for the condition was reached with 78% of panelists agreeing to use the term Down Syndrome Regression Disorder (DSRD). Agreement on diagnostic work up and diagnostic criteria was not reach on the first round due to low agreement amongst panelists with regards to the need for neurodiagnostic testing. Following incorporation of panelist feedback, diagnostic criteria were agreed upon (96% agreement on neuroimaging, 100% agreement on bloodwork, 88% agreement on lumbar puncture, 100% agreement on urine studies, and 96% agreement on "other" studies) as were diagnostic criteria (96% agreement). The authors present international consensus agreement on the nomenclature, diagnostic work up, and diagnostic criteria for DSRD, providing an initial practical framework that can advance both research and clinical practices for this condition.

Sections du résumé

Objective UNASSIGNED
To develop standardization for nomenclature, diagnostic work up and diagnostic criteria for cases of neurocognitive regression in Down syndrome.
Background UNASSIGNED
There are no consensus criteria for the evaluation or diagnosis of neurocognitive regression in persons with Down syndrome. As such, previously published data on this condition is relegated to smaller case series with heterogenous data sets. Lack of standardized assessment tools has slowed research in this clinical area.
Methods UNASSIGNED
The authors performed a two-round traditional Delphi method survey of an international group of clinicians with experience in treating Down syndrome to develop a standardized approach to clinical care and research in this area. Thirty-eight potential panelists who had either previously published on neurocognitive regression in Down syndrome or were involved in national or international working groups on this condition were invited to participate. In total, 27 panelists (71%) represented nine medical specialties and six different countries reached agreement on preliminary standards in this disease area. Moderators developed a proposed nomenclature, diagnostic work up and diagnostic criteria based on previously published reports of regression in persons with Down syndrome.
Results UNASSIGNED
During the first round of survey, agreement on nomenclature for the condition was reached with 78% of panelists agreeing to use the term Down Syndrome Regression Disorder (DSRD). Agreement on diagnostic work up and diagnostic criteria was not reach on the first round due to low agreement amongst panelists with regards to the need for neurodiagnostic testing. Following incorporation of panelist feedback, diagnostic criteria were agreed upon (96% agreement on neuroimaging, 100% agreement on bloodwork, 88% agreement on lumbar puncture, 100% agreement on urine studies, and 96% agreement on "other" studies) as were diagnostic criteria (96% agreement).
Conclusions UNASSIGNED
The authors present international consensus agreement on the nomenclature, diagnostic work up, and diagnostic criteria for DSRD, providing an initial practical framework that can advance both research and clinical practices for this condition.

Identifiants

pubmed: 35911905
doi: 10.3389/fneur.2022.940175
pmc: PMC9335003
doi:

Types de publication

Journal Article

Langues

eng

Pagination

940175

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR002381
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002378
Pays : United States

Informations de copyright

Copyright © 2022 Santoro, Patel, Kammeyer, Filipink, Gombolay, Cardinale, Real de Asua, Zaman, Santoro, Marzouk, Khoshnood, Vogel, Tanna, Pagarkar, Dhanani, Ortega, Partridge, Stanley, Sanders, Christy, Sannar, Brown, McCormick, Van Mater, Franklin, Worley, Quinn, Capone, Chicoine, Skotko and Rafii.

Déclaration de conflit d'intérêts

JDS receives research support from the National Institutes of Health, the Race to Erase MS Foundation, and the Thrasher Society. He also serves as a consultant to UCB on myelin oligodendrocyte glycoprotein antibody spectrum disorders. GG receives part-time salary support from the Centers for Disease Control and Prevention for acute flaccid myelitis disease surveillance. DA is supported by the Fondo de Investigaciones Sanitarias (FIS grant PI19/00634, from the Ministerio de Economía y Competitividad (Instituto de Salud Carlos III) and co-funded by The European Regional Development Fund (ERDF) “A way to make Europe” and the. Fondation Jérôme Lejeune (grant no. 2021a-2069). The Adult Down Syndrome Outpatient unit at Hospital Universitario de La Princesa is grateful to Licenciado don Jesús Coronado Hinojosa for his financial support of the research endeavors of our unit. BS occasionally consults on the topic of Down syndrome through Gerson Lehrman Group. He receives remuneration from Down syndrome nonprofit organizations for speaking engagements and associated travel expenses. BS receives annual royalties from Woodbine House, Inc., for the publication of his book, Fasten Your Seatbelt: A Crash Course on Down Syndrome for Brothers and Sisters. Within the past 2 years, he has received research funding from F. Hoffmann-La Roche, Inc., and LuMind Research Down Syndrome Foundation to conduct clinical trials for people with Down syndrome. BS is occasionally asked to serve as an expert witness for legal cases where Down syndrome is discussed. He serves in a nonpaid capacity on the Honorary Board of Directors for the Massachusetts Down Syndrome Congress and the Professional Advisory Committee for the National Center for Prenatal and Postnatal Down Syndrome Resources. BS has a sister with Down syndrome. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jonathan D Santoro (JD)

Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.
Department of Neurology, Keck School of Medicine at USC, Los Angeles, CA, United States.

Lina Patel (L)

Department of Psychiatry, University of Colorado School of Medicine, Denver, CO, United States.

Ryan Kammeyer (R)

Department of Neurology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Robyn A Filipink (RA)

Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.

Grace Y Gombolay (GY)

Department of Pediatrics, Division of Neurology, Emory University and Children's Healthcare of Atlanta, Atlanta, GA, United States.

Kathleen M Cardinale (KM)

Department of Neurology, Yale University School of Medicine, New Haven, CT, United States.

Diego Real de Asua (D)

Adult Down Syndrome Outpatient Clinic, Department of Internal Medicine, Fundación de Investigación Biomédica, Hospital Universitario de La Princesa, Madrid, Spain.

Shahid Zaman (S)

Cambridge Intellectual & Developmental Disabilities Research Group, Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom.

Stephanie L Santoro (SL)

Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.

Sammer M Marzouk (SM)

Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.

Mellad Khoshnood (M)

Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, CA, United States.

Benjamin N Vogel (BN)

Department of Neurology, Keck School of Medicine at USC, Los Angeles, CA, United States.

Runi Tanna (R)

Department of Neurology, Keck School of Medicine at USC, Los Angeles, CA, United States.

Dania Pagarkar (D)

Department of Neurology, Keck School of Medicine at USC, Los Angeles, CA, United States.

Sofia Dhanani (S)

Department of Neurology, Keck School of Medicine at USC, Los Angeles, CA, United States.

Maria Del Carmen Ortega (MDC)

Department of Psychiatry, Clinica Universidad de Navarra, Madrid, Spain.

Rebecca Partridge (R)

Virginia Mason Health System, Issaquah, WA, United States.

Maria A Stanley (MA)

Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.

Jessica S Sanders (JS)

Sie Center for Down Syndrome at the University of Colorado, Aurora, CO, United States.

Alison Christy (A)

Providence Health System, Portland, OR, United States.

Elise M Sannar (EM)

Department of Psychiatry, University of Colorado School of Medicine, Denver, CO, United States.
Division of Psychiatry and Behavioral Sciences, Children's Hospital Colorado, Aurora, CO, United States.

Ruth Brown (R)

Department of Psychology, Virginia Commonwealth University, Richmond, VA, United States.

Andrew A McCormick (AA)

Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.

Heather Van Mater (H)

Division of Rheumatology, Department of Pediatrics, Duke University, Durham, NC, United States.

Cathy Franklin (C)

Queensland Center for Intellectual and Developmental Disability, Mater Research Institute, The University of Queensland, South Brisbane, QLD, Australia.

Gordon Worley (G)

Division of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University School of Medicine, Durham, NC, United States.

Eileen A Quinn (EA)

Department of Pediatrics, University of Toledo College of Medicine and Life Sciences, Toledo, OH, United States.

George T Capone (GT)

Department of Pediatrics, Kennedy Krieger Institute, Baltimore, MD, United States.
Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.

Brian Chicoine (B)

Advocate Medical Group Adult Down Syndrome Center, Park Ridge, IL, United States.

Brian G Skotko (BG)

Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.
Department of Pediatrics, Harvard Medical School, Boston, MA, United States.

Michael S Rafii (MS)

Department of Neurology, Keck School of Medicine at USC, Los Angeles, CA, United States.
Department of Neurology, Alzheimer's Therapeutic Research Institute (ATRI), Keck School of Medicine at the University of Southern California, San Diego, CA, United States.

Classifications MeSH