Evidence map›Paper›PMID 38570516›Full record

ArticleScientific reports2024

Aerobic exercise attenuates dysautonomia, cardiac diastolic dysfunctions, and hemodynamic overload in female mice with atherosclerosis.

Bruno Nascimento-Carvalho, Bruno Durante da Silva, Maikon Barbosa da Silva, Adriano Dos-Santos, Thayna Fabiana Ribeiro, Danielle da Silva Dias, Leandro Eziquiel de Souza, Marina Rascio Henriques Dutra, Sergio Catanozi, Elia G Caldini and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

14 authors at 4 institutions in 1 country.

Bruno Nascimento-CarvalhoUnidade de Hipertensao, Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo (InCor-HCFMUSP), São Paulo, SP, Brazil.ORCID 0000-0002-0283-7432
Bruno Durante da SilvaUnidade de Hipertensao, Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo (InCor-HCFMUSP), São Paulo, SP, Brazil.
Maikon Barbosa da SilvaUnidade de Hipertensao, Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo (InCor-HCFMUSP), São Paulo, SP, Brazil.
Adriano Dos-SantosHuman Movement Lab, São Judas Tadeu University (USJT), São Paulo, SP, Brazil.
Thayna Fabiana RibeiroHuman Movement Lab, São Judas Tadeu University (USJT), São Paulo, SP, Brazil.
Danielle da Silva DiasUnidade de Hipertensao, Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo (InCor-HCFMUSP), São Paulo, SP, Brazil.
Leandro Eziquiel de SouzaUnidade de Hipertensao, Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo (InCor-HCFMUSP), São Paulo, SP, Brazil.
Marina Rascio Henriques DutraLaboratório de Fisiologia Translacional, Universidade Nove de Julho (Uninove), São Paulo, SP, Brazil.
Sergio CatanoziLaboratorio de Lipides (LIM-10), Hospital das Clinicas (HCFMUSP), Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Elia G CaldiniDepartamento de Patologia, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Kátia De AngelisLaboratório de Fisiologia Translacional, Universidade Nove de Julho (Uninove), São Paulo, SP, Brazil.
Katia Bilhar ScapiniHuman Movement Lab, São Judas Tadeu University (USJT), São Paulo, SP, Brazil.
Iris Callado SanchesHuman Movement Lab, São Judas Tadeu University (USJT), São Paulo, SP, Brazil.
Maria Claudia IrigoyenUnidade de Hipertensao, Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo (InCor-HCFMUSP), São Paulo, SP, Brazil. hipirigoyen@gmail.com.ORCID 0000-0003-2097-3662
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversidade São Judas Tadeu · BRUniversidade Nove de Julho · BRUniversidade de São Paulo · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) 001MCCI was supported by the National Council for Scientific and Technological Development (427892/2018-0 and 312962/2020-7) and São Paulo Research Foundation (FAPESP, 2018/19006-2) 2018/19006-2MCCI was supported by the National Council for Scientific and Technological Development (427892/2018-0 and 312962/2020-7) and São Paulo Research Foundation (FAPESP, 2018/19006-2) 312962/2020-7MCCI was supported by the National Council for Scientific and Technological Development (427892/2018-0 and 312962/2020-7) and São Paulo Research Foundation (FAPESP, 2018/19006-2) 427892/2018-0This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior-Brasil (CAPES)-Finance Code 001 001
6 · The paper itself

Abstract

Cardiovascular risk increases during the aging process in women with atherosclerosis and exercise training is a strategy for management of cardiac risks in at-risk populations. Therefore, the aims of this study were to evaluate: (1) the influence of the aging process on cardiac function, hemodynamics, cardiovascular autonomic modulation, and baroreflex sensitivity in females with atherosclerosis at the onset of reproductive senescence; and (2) the impact of exercise training on age-related dysfunctions in this model. Eighteen Apolipoprotein-E knockout female mice were divided equally into young (Y), middle-aged (MA), and trained middle-aged (MAT). Echocardiographic exams were performed to verify cardiac morphology and function. Cannulation for direct recording of blood pressure and heart rate, and analysis of cardiovascular autonomic modulation, baroreflex sensitivity were performed. The MA had lower cardiac diastolic function (E'/A' ratio), and higher aortic thickness, heart rate and mean arterial pressure, lower heart rate variability and baroreflex sensitivity compared with Y. There were no differences between Y and MAT in these parameters. Positive correlation coefficients were found between aortic wall thickness with hemodynamics data. The aging process causes a series of deleterious effects such as hemodynamic overload and dysautonomia in female with atherosclerosis. Exercise training was effective in mitigating aged-related dysfunctions.

Indexed as

AtherosclerosisAutonomic Nervous System DiseasesCardiovascular SystemAgedAnimalsBlood PressureFemaleHeartHeart RateHemodynamicsHumansMiceMiddle Aged

Identifiers

PMID38570516
PMCPMC10991254
OpenAlexW4393856467

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.