Evidence map›Paper›PMID 31637345›Full record

ArticleJournal of the Endocrine Society2019

The -839(A/C) Polymorphism in the

Karen E Hansen, Michael G Johnson, Tonia C Carter, John Mayer, Nicholas S Keuler, Robert D Blank

Open access · goldAbstract read
In one paragraph

Article in Journal of the Endocrine Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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 4 institutions in 1 country.

Karen E HansenDepartment of Medicine, University of Wisconsin, Madison, Wisconsin.ORCID 0000-0003-4338-6073
Michael G JohnsonDepartment of Medicine, University of Wisconsin, Madison, Wisconsin.
Tonia C CarterCenter for Human Genetics, Marshfield Clinic Research Institute, Marshfield, Wisconsin.
John MayerOffice of Research Computing and Analytics, Marshfield Clinic Research Institute, Marshfield, Wisconsin.
Nicholas S KeulerDepartment of Statistics, University of Wisconsin, Madison, Wisconsin.
Robert D BlankDivision of Endocrinology, Metabolism and Clinical Nutrition, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0003-2950-1944
University of Wisconsin–Madison · USCenter for Human Genetics · USMarshfield Clinic · USMedical College of Wisconsin · US

Funding

University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
NCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1 TR002373
6 · The paper itself

Abstract

contextWe previously found that variation in a quantitative trait locus, including the gene-encoding endothelin-converting enzyme 1 (

objectiveWe hypothesized that single nucleotide polymorphisms (SNPs) within the human

designWe genotyped DNA for the

settingA community medical center.

participantsPostmenopausal women (3564) with ≥1 dual-energy X-ray absorptiometry scan ≥60 years of age.

main outcome measuresBMD, osteoporosis, and clinical fractures.

resultsIn multivariate models controlling for age, weight, healthcare duration, and tobacco, the CC genotype reduced the odds of lifetime fracture (OR 0.33, 95% CI 0.12, 0.87) and fracture ≥50 years of age (OR 0.31, 95% CI 0.11, 0.87), whereas the AC genotype increased odds of osteoporosis (OR 1.34, 95% CI 1.02 1.78) relative to the AA genotype. However, when controlling the false-discovery rate, findings were no longer significant. We found no consistent relationship between the ECE1 b -338(G/T) and study outcomes.

conclusionsThe CC genotype was associated with fewer fractures, whereas the AC genotype was associated with osteoporosis. Our small sample size and few minorities are study limitations. Findings should be tested in another cohort to confirm a link between the

Indexed as

DNA, endothelin-converting enzyme 1fracturesosteoporosispostmenopausal women

Identifiers

PMID31637345
PMCPMC6795020
OpenAlexW2958111016

What OpenQuestion 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 OpenQuestion graph.