Evidence map›Paper›PMID 25005732›Full record

ArticleEuropean journal of human genetics : EJHG2015

An unexpected finding: younger fathers have a higher risk for offspring with chromosomal aneuploidies.

Bernhard Steiner, Rahim Masood, Kaspar Rufibach, Dunja Niedrist, Oliver Kundert, Mariluce Riegel, Albert Schinzel

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Crossover Interference, Crossover Maturation, and Human Aneuploidy.BioEssays : news and reviews in molecular, cellular and developmental biology · 2019
    Review
  5. Article
  6. Article
  7. Intracytoplasmic sperm injection: state of the art in humans.Reproduction (Cambridge, England) · 2017
    Review
  8. Parental Age and Risk of Infant Leukaemia: A Pooled Analysis.Paediatric and perinatal epidemiology · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. 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

7 authors.

Bernhard SteinerInstitute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.
Rahim MasoodInstitute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.
Kaspar RufibachBiostatistics Unit, Institute for Social and Preventive Medicine, University of Zurich, Zurich, Switzerland.
Dunja NiedristInstitute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.
Oliver KundertInstitute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.
Mariluce RiegelInstitute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.
Albert SchinzelInstitute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The past decades have seen a remarkable shift in the demographics of childbearing in Western countries. The risk for offspring with chromosomal aneuploidies with advancing maternal age is well known, but most studies failed to demonstrate a paternal age effect. Retrospectively, we analyzed two case data sets containing parental ages from pre- and postnatal cases with trisomies 21, 13 and 18. The reference data set contains the parental ages of the general Swiss population. We dichotomized all couples into two distinct groups. In the first group, the mothers' integral age was as least as the father's age or older. We compared the frequency of cases in nine 5-year intervals of maternal age. In addition, we computed logistic regression models for the binary endpoint aneuploidy yes/no where paternal ages were incorporated as linear or quadratic, as well as smooth functions within a generalized additive model framework. We demonstrated that the proportion of younger fathers is uniformly different between cases and controls of live-born trisomy 21 as well, although not reaching significance, for fetuses over all mother's ages. Logistic regression models with different strategies to incorporate paternal ages confirmed our findings. The negative paternal age effect was also found in pre- and postnatal cases taken together with trisomies 13 and 18. The couples with younger fathers face almost twofold odds for a child with Down syndrome (DS). We estimated odds curves for parental ages. If confirmation of these findings can be achieved, the management of couples at risk needs a major correction of the risk stratification.

Indexed as

AneuploidyPaternal AgeAdolescentAdultChromosome DisordersChromosomes, Human, Pair 13Chromosomes, Human, Pair 18DemographyDown SyndromeFathersFemaleHumansLogistic ModelsMaleMaternal AgeMiddle Aged

Identifiers

PMID25005732
PMCPMC4666566

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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.