Evidence map›Paper›PMID 24495335›Full record

ArticleBJOG : an international journal of obstetrics and gynaecology2014

Prevalence and risk of Down syndrome in monozygotic and dizygotic multiple pregnancies in Europe: implications for prenatal screening.

B Boyle, J K Morris, R McConkey, E Garne, M Loane, M C Addor, M Gatt, M Haeusler, A Latos-Bielenska, N Lelong and 4 more

Abstract readComparative Study
In one paragraph

Article in BJOG : an international journal of obstetrics and gynaecology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Observational
  2. ISUOG Practice Guidelines (updated): role of ultrasound in twin pregnancy.Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. EUROCAT: an update on its functions and activities.Journal of community genetics · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Screening and Invasive Testing in Twins.Journal of clinical medicine · 2014
    Review
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

14 authors.

B BoyleEUROCAT Central Registry, Centre for Maternal Fetal and Infant Research, Institute for Nursing and Health Research, University of Ulster, Newtownabbey, UK.
J K Morris
R McConkey
E Garne
M Loane
M C Addor
M Gatt
M Haeusler
A Latos-Bielenska
N Lelong
R McDonnell
C Mullaney
M O'Mahony
H Dolk

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine risk of Down syndrome (DS) in multiple relative to singleton pregnancies, and compare prenatal diagnosis rates and pregnancy outcome.

designPopulation-based prevalence study based on EUROCAT congenital anomaly registries.

settingEight European countries. POPULATION: 14.8 million births 1990-2009; 2.89% multiple births.

methodsDS cases included livebirths, fetal deaths from 20 weeks, and terminations of pregnancy for fetal anomaly (TOPFA). Zygosity is inferred from like/unlike sex for birth denominators, and from concordance for DS cases.

main outcome measuresRelative risk (RR) of DS per fetus/baby from multiple versus singleton pregnancies and per pregnancy in monozygotic/dizygotic versus singleton pregnancies. Proportion of prenatally diagnosed and pregnancy outcome. STATISTICAL ANALYSIS: Poisson and logistic regression stratified for maternal age, country and time.

resultsOverall, the adjusted (adj) RR of DS for fetus/babies from multiple versus singleton pregnancies was 0.58 (95% CI 0.53-0.62), similar for all maternal ages except for mothers over 44, for whom it was considerably lower. In 8.7% of twin pairs affected by DS, both co-twins were diagnosed with the condition. The adjRR of DS for monozygotic versus singleton pregnancies was 0.34 (95% CI 0.25-0.44) and for dizygotic versus singleton pregnancies 1.34 (95% CI 1.23-1.46). DS fetuses from multiple births were less likely to be prenatally diagnosed than singletons (adjOR 0.62 [95% CI 0.50-0.78]) and following diagnosis less likely to be TOPFA (adjOR 0.40 [95% CI 0.27-0.59]).

conclusionsThe risk of DS per fetus/baby is lower in multiple than singleton pregnancies. These estimates can be used for genetic counselling and prenatal screening.

Indexed as

Pregnancy, MultiplePrenatal DiagnosisAdultDown SyndromeEuropeFemaleHumansMaternal AgeMiddle AgedPregnancyPregnancy OutcomePrevalenceRiskRisk AssessmentTwins, DizygoticTwins, MonozygoticConcordanceDown syndromemonozygotic and dizygotic pregnanciesmultiple birthspregnancy outcomestwins

Identifiers

PMID24495335
PMCPMC4234000

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.