Evidence map›Paper›PMID 36287415›Full record

ArticleArquivos brasileiros de cardiologia2022

Vascular Aging and Arterial Stiffness.

Adriana Camargo Oliveira, Pedro Miguel Guimarães Marques Cunha, Priscila Valverde de Oliveria Vitorino, Ana Luiza Lima Souza, Gilcimar Divino Deus, Audes Feitosa, Eduardo Costa Duarte Barbosa, Marco Mota Gomes, Paulo Cesar B Veiga Jardim, Weimar Kunz Sebba Barroso

Open access · diamondAbstract read
In one paragraph

Article in Arquivos brasileiros de cardiologia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
9.8field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

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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

10 authors at 6 institutions in 2 countries.

Adriana Camargo OliveiraUniversidade Federal de Goiás , Liga de Hipertensão , Goiânia , GO - Brasil.ORCID 0000-0002-5537-9033
Pedro Miguel Guimarães Marques CunhaUniversidade do Minho Escola de Medicina , Braga , Portugal.
Priscila Valverde de Oliveria VitorinoPontifícia Universidade Católica de Goiás - Escola de Ciências Sociais e da Saúde , Goiânia , GO - Brasil.ORCID 0000-0002-5487-4649
Ana Luiza Lima SouzaUniversidade Federal de Goiás , Liga de Hipertensão , Goiânia , GO - Brasil.
Gilcimar Divino DeusPontifícia Universidade Católica de Goiás - Escola de Ciências Exatas e da Computação , Goiânia , GO - Brasil.
Audes FeitosaUniversidade de Pernambuco , Recife , PE - Brasil.
Eduardo Costa Duarte BarbosaComplexo Hospitalar Santa Casa de Misericórdia de Porto Alegre - Cardiologia, Porto Alegre , RS - Brasil.
Marco Mota GomesCentro Universitario CESMAC - Hospital do Coração , Maceió , AL - Brasil.
Paulo Cesar B Veiga JardimUniversidade Federal de Goiás , Liga de Hipertensão , Goiânia , GO - Brasil.ORCID 0000-0002-5333-013X
Weimar Kunz Sebba BarrosoUniversidade Federal de Goiás , Liga de Hipertensão , Goiânia , GO - Brasil.ORCID 0000-0002-1265-1930
Universidade Federal de Goiás · BRPontifícia Universidade Católica de Goiás · BRCentro Universitário Cesmac · BRSanta Casa Hospital · BRUniversidade Católica de Pernambuco · BRUniversity of Minho · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biological aging occurs as a result of the interaction between genetics, chronological age and external factors. It is the basis for new concepts of vascular aging, whose progression is determined by the difference between biological and chronological age. From the structural point of view, the effects of vascular aging are more evident in the tunica media of large elastic arteries, marked by increased arterial stiffness, lumen dilation and wall thickness. These effects are described in the continuum of cardiovascular aging (proposed by Dzau in 2010), in which the progressive steps of microvasculature lesions of the heart, kidney and brain are initiated from the aging process. The increase of arterial stiffness can be detected by several non-invasive methods. Cardiovascular events have been traditionally described using scores that combine conventional risk factors for atherosclerosis. In the classic cardiovascular continuum (Dzau, 2006), to determine the exact contribution of each risk factor is challenging; however, since arterial stiffness reflects both early and cumulative damage of these cardiovascular risk factors, it is an indicator of the actual damage to the arterial wall. This article provides a general overview of pathophysiological mechanisms, arterial structural changes, and hemodynamic consequences of arterial stiffness; non-invasive methods for the assessment of arterial stiffness and of central blood pressure; the cardiovascular aging continuum, and the application of arterial stiffness in cardiovascular risk stratification.

Indexed as

Cardiovascular DiseasesVascular StiffnessAgingArteriesHumansRisk FactorsTunica Media

Identifiers

PMID36287415
PMCPMC9563886
OpenAlexW4307583650

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.