Widespread kidney anomalies in children with Down syndrome.


Journal

Pediatric nephrology (Berlin, Germany)
ISSN: 1432-198X
Titre abrégé: Pediatr Nephrol
Pays: Germany
ID NLM: 8708728

Informations de publication

Date de publication:
10 2022
Historique:
received: 13 06 2021
accepted: 27 12 2021
revised: 25 12 2021
pubmed: 5 2 2022
medline: 25 8 2022
entrez: 4 2 2022
Statut: ppublish

Résumé

Rare autopsy studies have described smaller kidneys as well as urinary tract anomalies in Down syndrome. This observation has never been investigated in vivo and little is known about the possible consequences upon kidney function. Here we wish to confirm whether children with Down syndrome have smaller kidneys and to evaluate their kidney function in vivo. This retrospective cohort study enrolled 49 children with Down syndrome, as well as 49 age- and sex-matched controls at the Queen Fabiola Children's University Hospital in Brussels, Belgium. Doppler and kidney ultrasonography, spot urine albumin to creatinine ratio, estimated glomerular filtration rate (eGFR), and anthropometric data were recorded. Kidney size in children with Down syndrome was smaller than age- and sex-matched controls in terms of length (p < 0.001) and volume (p < 0.001). Kidney function based on eGFR was also decreased in Down syndrome compared to historical normal. Twenty-one of the children with Down syndrome (42%) had eGFR < 90 mL/min/1.73 m Children with Down syndrome have significantly smaller kidneys than age-matched controls as well as evidence of decreased kidney function. These findings, in addition to well-noted increased kidney and urologic anomalies, highlight the need for universal anatomical and functional assessment of all individuals with Down syndrome. A higher resolution version of the Graphical abstract is available as Supplementary information.

Sections du résumé

BACKGROUND
Rare autopsy studies have described smaller kidneys as well as urinary tract anomalies in Down syndrome. This observation has never been investigated in vivo and little is known about the possible consequences upon kidney function. Here we wish to confirm whether children with Down syndrome have smaller kidneys and to evaluate their kidney function in vivo.
METHODS
This retrospective cohort study enrolled 49 children with Down syndrome, as well as 49 age- and sex-matched controls at the Queen Fabiola Children's University Hospital in Brussels, Belgium. Doppler and kidney ultrasonography, spot urine albumin to creatinine ratio, estimated glomerular filtration rate (eGFR), and anthropometric data were recorded.
RESULTS
Kidney size in children with Down syndrome was smaller than age- and sex-matched controls in terms of length (p < 0.001) and volume (p < 0.001). Kidney function based on eGFR was also decreased in Down syndrome compared to historical normal. Twenty-one of the children with Down syndrome (42%) had eGFR < 90 mL/min/1.73 m
CONCLUSIONS
Children with Down syndrome have significantly smaller kidneys than age-matched controls as well as evidence of decreased kidney function. These findings, in addition to well-noted increased kidney and urologic anomalies, highlight the need for universal anatomical and functional assessment of all individuals with Down syndrome. A higher resolution version of the Graphical abstract is available as Supplementary information.

Identifiants

pubmed: 35118542
doi: 10.1007/s00467-022-05455-y
pii: 10.1007/s00467-022-05455-y
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2361-2368

Informations de copyright

© 2022. The Author(s), under exclusive licence to International Pediatric Nephrology Association.

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Auteurs

Lavinia Postolache (L)

Department of Ophthalmology, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Afshin Parsa (A)

The Division of Kidney, Urologic, and Hematologic Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA.

Paolo Simoni (P)

Department of Radiology, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Grammatina Boitsios (G)

Department of Radiology, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Khalid Ismaili (K)

Department of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Thierry Schurmans (T)

Department of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Anne Monier (A)

Department of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Georges Casimir (G)

Department of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Adelin Albert (A)

Department of Biostatistics, Liège University Hospital, Liège, Belgium.

Cameron F Parsa (CF)

Department of Ophthalmology, Erasmus Hospital, Université Libre de Bruxelles, 808 Route de Lennik, B-1070, Brussels, Belgium. cfparsa@gmail.com.
Faculty of Medicine, Sorbonne University, Paris, France. cfparsa@gmail.com.

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