Evidence map›Paper›PMID 33319384›Full record

ArticleJournal of genetic counseling2021

A survey of aortic disease biorepository participants' preferences for return of research genetic results.

Jamie Love-Nichols, Wendy R Uhlmann, Patricia Arscott, Cristen Willer, Whitney Hornsby, J Scott Roberts

Open access · bronzeAbstract read
In one paragraph

Article in Journal of genetic counseling, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Views of adults living with sickle cell disease on the theoretical return of secondary genomic findings.Genetics in medicine : official journal of the American College of Medical Genetics · 2024
    Article
  6. Article
  7. 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

6 authors at 2 institutions in 1 country.

Jamie Love-NicholsDepartment of Genetics, Seattle Children's Hospital, Seattle, WA, USA.
Wendy R UhlmannDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
Patricia ArscottDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
Cristen WillerDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
Whitney HornsbyDepartment of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
J Scott RobertsCenter for Bioethics and Social Sciences in Medicine, University of Michigan, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USSeattle Children's Hospital · US

Funding

Using genetic variation to study biology of blood lipids & coronary heart diseaseR01HL127564 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Pradeep Natarajan, Gina Marie Peloso · 2015 to 2026
$7.3M
Using Genetics to Inform Mechanism of Cardiovascular DiseaseR35HL135824 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILLER, CRISTEN J · 2017 to 2022
$5.4M
Integrative analysis to uncover biology of blood lipids & coronary heart diseaseR01HL142023 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILLER, CRISTEN J, ZHOU, XIANG · 2018 to 2019
$859k
NHLBI NIH HHS R01 HL127564NHLBI NIH HHS R01 HL142023NHLBI NIH HHS R35 HL135824
6 · The paper itself

Abstract

There is ongoing debate on whether and what research genetic results to return to study participants. To date, no study in this area has focused on aortopathy populations despite known genes that are clinically actionable. Participants (n = 225, 79% male, mean age = 61 years) with an aortopathy were surveyed to assess preferences for receiving research genetic results. Participants were 'very' or 'extremely likely' to want results for pathogenic variants in aortopathy genes with implications for family members (81%) or that would change medical management (76%). Similarly, participants were 'very' or 'extremely likely' to want actionable secondary findings related to cancer (75%) or other cardiac diseases (70%). Significantly lower interest was observed for non-actionable findings-pathogenic variants in aortopathy genes that would not change medical management (51%) and variants of uncertain significance (38%) (p < .0001). Higher health and genomic literacy were positively associated with interest in actionable findings. Most participants (>63%) were accepting of any means of return; however, a substantial minority (18%-38%) deemed certain technological means unacceptable (e.g., patient portal). Over 90% of participants reported that a range of health professionals, including cardiovascular specialists, genetics specialists, and primary care providers, were acceptable to return results. Participants with aortopathies are highly interested in research genetic results perceived to be medically actionable for themselves or family members. Participants are accepting of a variety of means for returning results. Findings suggest that research participants should be asked what results are preferred at time of informed consent and that genetic counseling may clarify implications of results that are not personally medically actionable.

Indexed as

Aortic DiseasesNeoplasmsFemaleGenetic CounselingGenomicsHumansInfant, NewbornMaleSurveys and Questionnairesaortic diseasebiobankresearch genetic resultsservice delivery modelsvariants of uncertain significance

Identifiers

PMID33319384
PMCPMC8192438
OpenAlexW3111499426

What OpenQuestion holds

Textmetadata
LicenceTDM
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.