Evidence map›Paper›PMID 34176145›Full record

ArticlePrenatal diagnosis2021

Does non-invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population-based register study.

Maurike de Groot-van der Mooren, Gert de Graaf, Michel E Weijerman, Mariette J V Hoffer, Jeroen Knijnenburg, Anne-Marie M F van der Kevie-Kersemaekers, Angelique J A Kooper, Els Voorhoeve, Birgit Sikkema-Raddatz, Laura J C M van Zutven and 6 more

Abstract read
In one paragraph

Article in Prenatal diagnosis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Observational
  2. Impact of National Screening Programs on Down syndrome prevalence and outcomes.Acta obstetricia et gynecologica Scandinavica · 2026
    Article
  3. Observational
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Maurike de Groot-van der MoorenDepartment of Neonatology, Amsterdam Public Health and Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centres, location VUmc, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-5471-4119
Gert de GraafDutch Down Syndrome Foundation, Meppel, The Netherlands.ORCID https://orcid.org/0000-0002-4990-5711
Michel E WeijermanDepartment of Pediatrics, Alrijne Hospital, Leiderdorp, The Netherlands.
Mariette J V HofferDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Jeroen KnijnenburgDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Anne-Marie M F van der Kevie-KersemaekersDepartment of Clinical Genetics, Amsterdam University Medical Centres, location AMC, Amsterdam, The Netherlands.
Angelique J A KooperDepartment of Clinical Genetics, Amsterdam University Medical Centres, location AMC, Amsterdam, The Netherlands.
Els VoorhoeveDepartment of Clinical Genetics, Amsterdam University Medical Centres, location VUmc, Amsterdam, The Netherlands.
Birgit Sikkema-RaddatzDepartment of Genetics, University Medical Centre Groningen, Groningen, The Netherlands.
Laura J C M van ZutvenDepartment of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.
Malgorzata Ilona SrebniakDepartment of Clinical Genetics, Erasmus Medical Centre, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0003-3429-6156
Karin Huijsdens-van AmsterdamDepartment of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
John J M EngelenDepartment of Clinical Genetics, Research Institute Growth and Development (GROW), Maastricht University Medical Centre, Maastricht, The Netherlands.
Dominique SmeetsDepartment of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
Anton H van KaamDepartment of Neonatology and Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centres, location VUmc, Amsterdam, The Netherlands.
Martina C CornelDepartment of Clinical Genetics and Amsterdam Public Health Research Institute, Amsterdam University Medical Centres, Vrije Universiteit Amsterdam, location VUmc, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate if non-invasive prenatal testing (NIPT) affects livebirth (LB) prevalence of Down syndrome (DS) in the Netherlands.

methodData from clinical genetics laboratories and the Working Party on Prenatal Diagnosis and Therapy (2014-2018) and previous published data (1991-2013) were used to assess trends for DS LB prevalence and reduction percentage (the net decrease in DS LBs resulting from selective termination of pregnancies). Statistics Netherlands provided general population data.

resultsDS LB prevalence increased from 11.6/10,000 in 1991 to 15.9/10,000 in 2002 (regression coefficient 0.246 [95% CI: 0.105-0.388; p = 0.003]). After 2002, LB prevalence decreased to 11.3/10,000 in 2014 and further to 9.9/10,000 in 2018 (regression coefficient 0.234 (95% CI: -0.338 to -0.131; p < 0.001). The reduction percentage increased from 26% in 1991 to 55.2% in 2018 (regression coefficient 0.012 (95% CI: 0.010-0.013; p < 0.001)). There were no trend changes after introducing NIPT as second-tier (2014) and first-tier test (2017).

conclusionsIntroducing NIPT did not change the decreasing trend in DS LB prevalence and increasing trend in reduction percentage. These trends may be caused by a broader development of more prenatal testing that had already started before introducing NIPT.

Indexed as

AdultDown SyndromeFemaleHumansLive BirthNetherlandsNoninvasive Prenatal TestingPregnancyPrevalenceRegistries

Identifiers

PMID34176145
PMCPMC8519113

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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.