Evidence map›Paper›PMID 35486477›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2022

Evaluation of early bilateral ovariectomy in mice as a model of left heart disease.

J Ethan Joll, Matthew R Bersi, Jeffry S Nyman, W David Merryman

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Guidelines on the use of sex and gender in cardiovascular research.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  7. Murine Orchiectomy and Ovariectomy to Reduce Sex Hormone Production.Journal of visualized experiments : JoVE · 2023
    Article
  8. The stronger sex, until menopause: understanding the impact of estrogen loss on heart function.American journal of physiology. Heart and circulatory physiology · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

J Ethan JollDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.
Matthew R BersiDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0003-1848-4165
Jeffry S NymanDepartment of Orthopaedic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.ORCID 0000-0001-7403-7605
W David MerrymanDepartment of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0001-9662-1503
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

Mechanobiology of Cardiopulmonary FibrosisR35HL135790 · NHLBI · VANDERBILT UNIVERSITY · PI MERRYMAN, WILLIAM D · 2017 to 2023
$5.5M
Training Program for Innovative Engineering Research in Surgery and InterventionT32EB021937 · NIBIB · VANDERBILT UNIVERSITY · PI Dario J Englot, Michael Ian Miga · 2016 to 2026
$2.3M
Identification of immunotherapeutic targets in cardiovascular diseaseR00HL146951 · NHLBI · WASHINGTON UNIVERSITY · PI BERSI, MATTHEW RYAN · 2020 to 2022
$747k
Identification of immunotherapeutic targets in cardiovascular diseaseK99HL146951 · NHLBI · VANDERBILT UNIVERSITY · PI BERSI, MATTHEW RYAN · 2019 to 2019
$99k
Investigating the Role of Sclerostin in Calcific Aortic Valve DiseaseF31HL151115 · NHLBI · VANDERBILT UNIVERSITY · PI JOLL, JEFFERY E · 2020 to 2022
$96k
Diabetes-Related Changes Affecting Bone QualityI01BX004297 · VA · VETERANS HEALTH ADMINISTRATION · PI NYMAN, JEFFRY STEPHEN · 2019 to 2023
–
BLRD VA I01 BX004297HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) 135790HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) 151115NHLBI NIH HHS F31 HL151115NHLBI NIH HHS K99 HL146951NHLBI NIH HHS R00 HL146951NHLBI NIH HHS R35 HL135790NIBIB NIH HHS T32 EB021937
6 · The paper itself

Abstract

Postmenopausal women tend to have worse cardiovascular outcomes in a manner that is associated with osteoporosis severity. In this study, we performed the first evaluation of the left ventricle and aortic valve phenotype of ovariectomized mice aged on Western diet to 1 yr. Disease was monitored in vivo using echocardiography and dual X-ray absorptiometry imaging and ex vivo using quantitative histological and immunostaining analysis. Mice had decreased bone mineral density in response to ovariectomy and increased fat mass in response to Western diet. Ovariectomized mice had a significantly increased left ventricle mass compared with control animals, absent of fibrosis. There was a slight increase in aortic valve peak velocity but no change in mean pressure gradient across the valve in the ovariectomy group. There was no evidence of leaflet hypertrophy, fibrosis, or calcification. This model of ovariectomy may present a novel method of studying left ventricle hypertrophy in female populations but does not have a phenotype for the study of aortic stenosis. This is particularly useful as it does not require genetic manipulation or drug treatment and more faithfully mimics aging, high-cholesterol diet, and postmenopausal osteoporosis that many female patients experience potentially resulting in a more translatable disease model.

Indexed as

Aortic Valve StenosisOsteoporosisOsteoporosis, PostmenopausalAnimalsAortic ValveCholesterolDisease Models, AnimalFemaleFibrosisHumansHypertrophy, Left VentricularMiceOvariectomyCholesterolfemalehypertrophyovariectomy

Identifiers

PMID35486477
PMCPMC9142153
OpenAlexW4225138495

What Socratic holds

Textmetadata
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.