Evidence map›Paper›PMID 35118542›Full record

ArticlePediatric nephrology (Berlin, Germany)2022

Widespread kidney anomalies in children with Down syndrome.

Lavinia Postolache, Afshin Parsa, Paolo Simoni, Grammatina Boitsios, Khalid Ismaili, Thierry Schurmans, Anne Monier, Georges Casimir, Adelin Albert, Cameron F Parsa

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  3. Rethinking Creatinine in Children With Down Syndrome.Acta paediatrica (Oslo, Norway : 1992) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Lavinia PostolacheDepartment of Ophthalmology, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Afshin ParsaThe Division of Kidney, Urologic, and Hematologic Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA.
Paolo SimoniDepartment of Radiology, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Grammatina BoitsiosDepartment of Radiology, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Khalid IsmailiDepartment of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Thierry SchurmansDepartment of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Anne MonierDepartment of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Georges CasimirDepartment of Pediatrics, Queen Fabiola Children's University Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Adelin AlbertDepartment of Biostatistics, Liège University Hospital, Liège, Belgium.
Cameron F ParsaDepartment of Ophthalmology, Erasmus Hospital, Université Libre de Bruxelles, 808 Route de Lennik, B-1070, Brussels, Belgium. cfparsa@gmail.com.
Queen Fabiola Children's University Hospital · BEUniversité Libre de Bruxelles · BEErasmus Hospital · BENational Institute of Diabetes and Digestive and Kidney Diseases · USUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRare 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.

methodsThis 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.

resultsKidney 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

conclusionsChildren 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.

Indexed as

Down SyndromeUrinary TractChildGlomerular Filtration RateHumansKidneyRetrospective StudiesCAKUTDown syndromeKidney anomaliesKidney sizeTrisomy 21

Identifiers

PMID35118542
OpenAlexW4210328248

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.