Evidence map›Paper›PMID 23764957›Full record

ArticleJournal of genetic counseling2014

Longitudinal interviews of couples diagnosed with diminished ovarian reserve undergoing fragile X premutation testing.

Lisa M Pastore, Logan B Karns, Karen Ventura, Myra L Clark, Richard H Steeves, Nancy Callanan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of genetic counseling, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 3 institutions in 1 country.

Lisa M PastoreOB/GYN Department, School of Medicine, University of Virginia, Charlottesville, VA, USA, lpastore@virginia.edu.
Logan B Karns
Karen Ventura
Myra L Clark
Richard H Steeves
Nancy Callanan
University of Virginia · USCharlottesville Medical Research · USUniversity of North Carolina at Greensboro · US

Funding

FMR1 CGG Repeats in Primary Ovarian Insufficiency Women vs. 2 Comparison GroupsR01HD068440 · NICHD · UNIVERSITY OF VIRGINIA · PI TIMKO, MICHAEL PAUL · 2011 to 2013
$984k
Fragile X Premutation Tests: Qualitative Study of Infertile Carriers/PartnersR21HD057485 · NICHD · UNIVERSITY OF VIRGINIA · PI PASTORE, LISA M · 2008 to 2009
$312k
Fragile X Premutations Among Women Diagnosed with Diminished Ovarian ReserveR03HD052768 · NICHD · UNIVERSITY OF VIRGINIA · PI PASTORE, LISA M · 2007 to 2008
$162k
NICHD NIH HHS R01 HD068440NICHD NIH HHS R01HD068440NICHD NIH HHS R03 HD052768NICHD NIH HHS R03HD052768NICHD NIH HHS R21 HD057485NICHD NIH HHS R21HD057485
6 · The paper itself

Abstract

About 10 % of infertile/subfertile women are diagnosed with diminished ovarian reserve (DOR), of which < 5 % will become pregnant spontaneously. Fragile X (FMR1) genetic testing may provide a reason for her early ovarian aging and/or have reproductive implications. Seven women with DOR (genetic study subset) and the male partners of six of these women were separately interviewed about the experience of being asked to undergo this unanticipated genetic test. Three interviews were conducted (before, within 1 week after, and 3 months after learning the test results). None of the participants carried the FMR1 premutation (largest FMR1 allele 27-50 CGG repeats). For women, their pregnancy-seeking journey was long and exhausting. Women understood the reproductive implications of carrying the FMR1 premutation, and hoped for a negative result. Being offered a genetic test caused women to pause and re-think their future reproductive plans. Husbands viewed the infertility journey as filled with unknowns, of which the genetic test results would be one more puzzle piece. The expense of fertility testing/treatment was mentioned by both spouses, though more notably by husbands. The introduction of a possible genetic cause of infertility, with additional potential health consequences for future biological children, caused women to re-think their quest for pregnancy. In contrast, the genetic test was viewed as an additional source of information for their husbands as opposed to raising concern regarding potential reproductive ramifications.

Indexed as

MutationAdultFemaleFragile X SyndromeHumansInterviews as TopicLongitudinal Studies

Identifiers

PMID23764957
PMCPMC3800506
OpenAlexW2057997130

What OpenQuestion holds

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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.