Evidence map›Paper›PMID 25765282›Full record

ArticlePublic health genomics2015

Parent and public interest in whole-genome sequencing.

Daniel S Dodson, Aaron J Goldenberg, Matthew M Davis, Dianne C Singer, Beth A Tarini

Abstract read
In one paragraph

Article in Public health genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

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

  1. Pooled it
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  9. Review
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  12. Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment.Genetics in medicine : official journal of the American College of Medical Genetics · 2018
    Article
  13. Marking 15 years of the Genetic and Rare Diseases Information Center.Translational science of rare diseases · 2017
    Article
  14. Article
  15. Article
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  17. What are people willing to pay for whole-genome sequencing information, and who decides what they receive?Genetics in medicine : official journal of the American College of Medical Genetics · 2016
    Article
  18. Article
  19. Article
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

5 authors.

Daniel S DodsonChild Health Evaluation and Research (CHEAR) Unit, University of Michigan, Ann Arbor, Mich., USA.
Aaron J Goldenberg
Matthew M Davis
Dianne C Singer
Beth A Tarini

Funding

Improving Healthcare Delivery for Infants with Positive Newborn Screening ResultsK23HD057994 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TARINI, BETH A · 2009 to 2013
$662k
NICHD NIH HHS K23 HD057994NICHD NIH HHS K23HD057994
6 · The paper itself

Abstract

objectiveThe aim of this study was to assess the baseline interest of the public in whole-genome sequencing (WGS) for oneself, parents' interest in WGS for their youngest children, and factors associated with such interest.

methodsA random sample of adults from a probability-based nationally representative online panel was surveyed. All participants were provided basic information about WGS and then asked about their interest in WGS for themselves. Those participants who were parents were additionally asked about their interest in WGS for their children. The order in which parents were asked about their interest in WGS for themselves and for their child was randomized. The relationship between parent/child characteristics and interest in WGS was examined.

resultsThe overall response rate was 62% (55% among parents). 58.6% of the total population (parents and nonparents) was interested in WGS for themselves. Similarly, 61.8% of the parents were interested in WGS for themselves and 57.8% were interested in WGS for their youngest children. Of note, 84.7% of the parents showed an identical interest level in WGS for themselves and their youngest children. Mothers as a group and parents whose youngest children had ≥2 health conditions had significantly more interest in WGS for themselves and their youngest children, while those with conservative political ideologies had considerably less.

conclusionsWhile US adults have varying interest levels in WGS, parents appear to have similar interests in genome testing for themselves and their youngest children. As WGS technology becomes available in the clinic and private market, clinicians should be prepared to discuss WGS risks and benefits with their patients.

Indexed as

GenomicsPublic OpinionAdultAttitude to HealthChildConsumer BehaviorCross-Sectional StudiesDemographyFemaleGenetic TestingHumansMaleMiddle AgedParentsRisk AssessmentSequence Analysis, DNA

Identifiers

PMID25765282
PMCPMC4406802

What OpenQuestion holds

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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.