Evidence map›Paper›PMID 31014243›Full record

ArticleBMC medical research methodology2019

Disentangling the roles of maternal and paternal age on birth prevalence of down syndrome and other chromosomal disorders using a Bayesian modeling approach.

James A Thompson

Open access · goldAbstract read
In one paragraph

Article in BMC medical research methodology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  9. Review
  10. Review
  11. Down Syndrome in Brazil: Occurrence and Associated Factors.International journal of environmental research and public health · 2021
    Article
  12. Article
  13. The Effects of Parent Ages on Birth Defects.Acta scientific paediatrics · 2020
    Article
  14. Article
  15. 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

1 author at 1 institution in 1 country.

James A ThompsonCollege of Veterinary Medicine and Biomedical Science, Texas A&M University, College Station, TX, 77843-4475, USA. Jthompson@cvm.tamu.edu.ORCID 0000-0002-3712-1856
Texas A&M University · US

Funding

Estimating and communicating spatial certainty when childhood cancers co-clusterR03CA208021 · NCI · TEXAS A&M UNIVERSITY · PI THOMPSON, JAMES A · 2017 to 2019
$149k
NCI NIH HHS R03 CA208021
6 · The paper itself

Abstract

backgroundMultiple neonatal and pediatric disorders have been linked to older paternal ages. Combining these findings with the evidence that many men are having children at much later ages generates considerable public health concern. The risk of paternal age has been difficult to estimate and interpret because children often have parents whose ages are similar and likely to be confounded. Epidemiologic studies often model the conditional effects of paternal age using regression models that typically treat maternal age as linear, curvilinear or as age-band categories. Each of these approaches has limitations. As an alternative, the current study measures age to the nearest year, and fits a Bayesian model in which each parent's age is given a conditional autoregressive prior (CAR).

methodsData containing approximately 12,000,000 birth records were obtained from the United States Natality database for the years 2014 to 2016. Date were cross-tabulated for maternal ages 15-49 years and for paternal ages 15-65 years. A Bayesian logistic model was implemented using conditional autoregressive priors for both maternal and paternal ages modeled separately and jointly for both Down syndrome and chromosomal disorders other than Down syndrome.

resultsModels with maternal and paternal ages given CAR priors were judged to be better fitting than traditional models. For Down syndrome, the approach attributed a very large risk to advancing maternal age with the effect of advancing paternal age having a very small sparing effect on birth prevalence. Maternal age was also related to the birth prevalence of chromosomal disorders other than Down syndrome while paternal age was not.

conclusionsAdvancing paternal age was not associated with an increase in risk for either Down syndrome or chromosomal disorders other than Down syndrome.

Indexed as

AlgorithmsBayes TheoremMaternal AgePaternal AgeAdolescentAdultAgedChromosome DisordersDown SyndromeFemaleHumansLogistic ModelsMaleMiddle AgedParturitionPregnancyChromosomal disordersConditional auto-regressiveDown syndromeMaternal agePaternal age

Identifiers

PMID31014243
PMCPMC6480500
OpenAlexW2946436350

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.