Evidence map›Paper›PMID 30681142›Full record

ArticleThe Journal of physiology2019

Unmasking of oestrogen-dependent changes in left ventricular structure and function in aged female rats: a potential model for pre-heart failure with preserved ejection fraction.

Moises Bustamante, Alejandra Garate-Carrillo, Bruce R Ito, Ricardo Garcia, Nancy Carson, Guillermo Ceballos, Israel Ramirez-Sanchez, Jeffrey Omens, Francisco Villarreal

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Mechanisms and implications of sex differences in cardiac aging.The journal of cardiovascular aging · 2022
    Article
  7. Review
  8. Article
  9. Sex related differences in the pathogenesis of organ fibrosis.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
  10. Article
  11. The role of inflammation in driving left ventricular remodeling in a pre-HFpEF model.Experimental biology and medicine (Maywood, N.J.) · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Moises BustamanteDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Alejandra Garate-CarrilloDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Bruce R ItoDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Ricardo GarciaDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Nancy CarsonBristol-Myers Squibb, New York, NY, USA.ORCID 0000-0002-6090-244X
Guillermo CeballosSeccion de Estudios de Posgrado e Investigacion, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico, DF.ORCID 0000-0003-2155-3934
Israel Ramirez-SanchezDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Jeffrey OmensDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.ORCID 0000-0002-6851-0977
Francisco VillarrealDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA, USA.ORCID 0000-0002-3251-4909
University of California San Diego · USBristol-Myers Squibb (Germany) · DEInstituto Politécnico Nacional · MXUC San Diego Health System · US

Funding

Epicatechin and derivatives to preserve muscle structure function in diabetesR01DK098717 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HENRY, ROBERT ROY, VILLARREAL, FRANCISCO J · 2014 to 2017
$1.4M
Epicatechin treatment for sarcopeniaR21AG047326 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLARREAL, FRANCISCO J · 2015 to 2015
$233k
BLRD VA I01 BX003230NIA NIH HHS R21 AG047326NIDDK NIH HHS R01 DK098717
6 · The paper itself

Abstract

key pointsHeart failure with preserved ejection fraction (HFpEF) is seen more frequently in older women; risk factors include age, hypertension and excess weight. No female animal models of early stage remodelling (pre-HFpEF) have examined the effects that the convergence of such factors have on cardiac structure and function. In this study, we demonstrate that ageing can lead to the development of mild chamber remodelling, diffuse fibrosis and loss of diastolic function. The loss of oestrogens further aggravates such changes by leading to a notable drop in cardiac output (while preserving normal ejection fraction) in the presence of diffuse fibrosis that is more predominant in endocardium and is accompanied by papillary fibrosis. Excess weight did not markedly aggravate such findings. This animal model recapitulates many of the features recognized in older, female HFpEF patients and thus, may serve to examine the effects of candidate therapeutic agents. ABSTRACT: Two-thirds of patients with heart failure with preserved ejection fraction (HFpEF) are older women, and risk factors include hypertension and excess weight/obesity. Pathophysiological factors that drive early disease development (before heart failure ensues) remain obscure and female animal models are lacking. The study evaluated the intersecting roles of ageing, oestrogen depletion and excess weight on altering cardiac structure/function. Female, 18-month-old, Fischer F344 rats were divided into an aged group, aged + ovariectomy (OVX) and aged + ovariectomy + 10% fructose (OVF) in drinking water (n = 8-16/group) to induce weight gain. Left ventricular (LV) structure/function was monitored by echocardiography. At 22 months of age, animals were anaesthetized and catheter-based haemodynamics evaluated, followed by histological measures of chamber morphometry and collagen density. All aged animals developed hypertension. OVF animals increased body weight. Echocardiography only detected mild chamber remodelling with ageing while intraventricular pressure-volume loop analysis showed significant (P < 0.05) decreases vs. ageing in stroke volume (13% OVX and 15% for OVF), stroke work (34% and 52%) and cardiac output (29% and 27%), and increases in relaxation time (10% OVX) with preserved ejection fraction. Histology indicated papillary and interstitial fibrosis with ageing, which was higher in the endocardium of OVX and OVF groups. With ageing, ovariectomy leads to the loss of diastolic and global LV function while preserving ejection fraction. This model recapitulates many cardiovascular features present in HFpEF patients and may help understand the roles that ageing and oestrogen depletion play in early (pre-HFpEF) disease development.

Indexed as

AgingAnimalsCollagenEchocardiographyEstrogensFemaleFibrosisHeart DiseasesHeart VentriclesHemodynamicsOvariectomyRatsRats, Inbred F344Ventricular FunctionVentricular RemodelingCollagenEstrogensestrogensfibrosisfructoseheart failureHFpEFsenile

Identifiers

PMID30681142
PMCPMC6442018
OpenAlexW2917147675

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.