Occurrence of mosaic Down syndrome and prevalence of co‐occurring conditions in Medicaid enrolled adults, 2016–2019

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Hauptverfasser: Eric Rubenstein, Salina Tewolde, Brian G. Skotko, Amy Michals, Juan Fortea
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Veröffentlicht: Wiley 2024
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author Eric Rubenstein
Salina Tewolde
Brian G. Skotko
Amy Michals
Juan Fortea
author_facet Eric Rubenstein
Salina Tewolde
Brian G. Skotko
Amy Michals
Juan Fortea
Eric Rubenstein
Salina Tewolde
Brian G. Skotko
Amy Michals
Juan Fortea
collection Wiley Open Access
contents Occurrence of mosaic Down syndrome and prevalence of co‐occurring conditions in Medicaid enrolled adults, 2016–2019 Eric Rubenstein Salina Tewolde Brian G. Skotko Amy Michals Juan Fortea American Journal of Medical Genetics Part C: Seminars in Medical Genetics Abstract Background Mosaic Down syndrome is a triplication of chromosome 21 in some but not all cells. Little is known about the epidemiology of mosaic Down syndrome. We described prevalence of mosaic Down syndrome and the co‐occurrence of common chronic conditions in 94,533 Medicaid enrolled adults with any Down syndrome enrolled from 2016 to 2019. Methods We identified mosaic Down syndrome using the International Classification of Diseases and Related Health Problems, tenth edition code for mosaic Down syndrome and compared to those with nonmosaic Down syndrome codes. We identified chronic conditions using established algorithms and compared prevalence by mosaicism. Results In total, 1966 (2.08%) had claims for mosaic Down syndrome. Mosaicism did not differ by sex or race/ethnicity with similar age distributions. Individuals with mosaicism were more likely to present with autism (13.9% vs. 9.6%) and attention deficit hyperactivity disorder (17.7% vs. 14.0%) compared to individuals without mosaicism. In total, 22.3% of those with mosaic Down syndrome and 21.5% of those without mosaicism had claims for Alzheimer's dementia (Prevalence difference: 0.8; 95% Confidence interval: −1.0, 2.8). The mosaic group had 1.19 times the hazard of Alzheimer's dementia compared to the nonmosaic group (95% CI: 1.0, 1.3). Discussion Mosaicism may be associated with a higher susceptibility to certain neurodevelopmental and neurodegenerative conditions, including Alzheimer's dementia. Our findings challenge previous assumptions about its protective effects in Down syndrome. Further research is necessary to explore these associations in greater depth. 10.1002/ajmg.c.32097 http://onlinelibrary.wiley.com/termsAndConditions#vor
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spellingShingle Occurrence of mosaic Down syndrome and prevalence of co‐occurring conditions in Medicaid enrolled adults, 2016–2019
Eric Rubenstein
Salina Tewolde
Brian G. Skotko
Amy Michals
Juan Fortea
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Occurrence of mosaic Down syndrome and prevalence of co‐occurring conditions in Medicaid enrolled adults, 2016–2019 Eric Rubenstein Salina Tewolde Brian G. Skotko Amy Michals Juan Fortea American Journal of Medical Genetics Part C: Seminars in Medical Genetics Abstract Background Mosaic Down syndrome is a triplication of chromosome 21 in some but not all cells. Little is known about the epidemiology of mosaic Down syndrome. We described prevalence of mosaic Down syndrome and the co‐occurrence of common chronic conditions in 94,533 Medicaid enrolled adults with any Down syndrome enrolled from 2016 to 2019. Methods We identified mosaic Down syndrome using the International Classification of Diseases and Related Health Problems, tenth edition code for mosaic Down syndrome and compared to those with nonmosaic Down syndrome codes. We identified chronic conditions using established algorithms and compared prevalence by mosaicism. Results In total, 1966 (2.08%) had claims for mosaic Down syndrome. Mosaicism did not differ by sex or race/ethnicity with similar age distributions. Individuals with mosaicism were more likely to present with autism (13.9% vs. 9.6%) and attention deficit hyperactivity disorder (17.7% vs. 14.0%) compared to individuals without mosaicism. In total, 22.3% of those with mosaic Down syndrome and 21.5% of those without mosaicism had claims for Alzheimer's dementia (Prevalence difference: 0.8; 95% Confidence interval: −1.0, 2.8). The mosaic group had 1.19 times the hazard of Alzheimer's dementia compared to the nonmosaic group (95% CI: 1.0, 1.3). Discussion Mosaicism may be associated with a higher susceptibility to certain neurodevelopmental and neurodegenerative conditions, including Alzheimer's dementia. Our findings challenge previous assumptions about its protective effects in Down syndrome. Further research is necessary to explore these associations in greater depth. 10.1002/ajmg.c.32097 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Occurrence of mosaic Down syndrome and prevalence of co‐occurring conditions in Medicaid enrolled adults, 2016–2019
topic American Journal of Medical Genetics Part C: Seminars in Medical Genetics
url https://onlinelibrary.wiley.com/doi/10.1002/ajmg.c.32097