Evidence map›Paper›PMID 39687684›Full record

ArticleJournal of the Endocrine Society2024

Phenotypes Associated With Polycystic Ovary Syndrome Risk Variants.

Anna Tidwell, Jia Zhu, Tess Battiola, Corrine K Welt

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

4 authors.

Anna TidwellDivision of Endocrinology, Metabolism and Diabetes, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Jia ZhuDivision of Endocrinology, Boston Children's Hospital, Boston, MA 02115, USA.ORCID https://orcid.org/0000-0002-8782-1818
Tess BattiolaDivision of Endocrinology, Metabolism and Diabetes, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.ORCID https://orcid.org/0009-0006-8002-189X
Corrine K WeltDivision of Endocrinology, Metabolism and Diabetes, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.ORCID https://orcid.org/0000-0002-8219-5504

Funding

Genetic Dissection of the Pathophysiology of Polycystic Ovary SyndromeK08HD110723 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Jia Zhu · 2023 to 2026
$672k
NICHD NIH HHS K08 HD110723
6 · The paper itself

Abstract

Context: Polycystic ovary syndrome (PCOS) affects 10% of women of reproductive age. The genetic architecture of the disease is emerging, but there is little data exploring the effect of genetic risk on clinical presentation. Objective: We hypothesized that genetic risk loci would influence measurable phenotypic traits. Methods: This retrospective cohort study, conducted at an academic medical center, included women of European ancestry with PCOS (n = 404), as diagnosed by the National Institutes of Health criteria, and controls with regular menses and no hyperandrogenism (n = 408). We identified association between genetic risk variants and measured phenotypic traits using linear regression. Results: In a combined analysis of cases and controls, 2 variants in loci containing the genes Conclusion: These results demonstrate that PCOS genetic risk variants may influence hormone levels and ovarian morphology and increase the risk of obesity. Increased genetic risk for PCOS appears to drive traits that underly the classical clinical presentation of PCOS.

Indexed as

androgenscholesterolgenome-wide associationobesityovary

Identifiers

PMID39687684
PMCPMC11646653

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.