Evidence map›Paper›PMID 30843124›Full record

ArticleMedical & biological engineering & computing2019

The additional impact of type 2 diabetes on baroreflex sensitivity of coronary artery disease patients might be undetectable in presence of deterioration of mechanical vascular properties.

Mariana de Oliveira Gois, Alberto Porta, Rodrigo Polaquini Simões, Vandeni Clarice Kunz, Patricia Driusso, Humberto Sadanobu Hirakawa, Beatrice De Maria, Aparecida Maria Catai

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Article in Medical & biological engineering & computing, 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
0.5field-weighted citation impact, top 33% 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.

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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

8 authors at 4 institutions in 2 countries.

Mariana de Oliveira GoisDepartment of Physical Therapy, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
Alberto PortaDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy. alberto.porta@unimi.it.ORCID http://orcid.org/0000-0002-6720-9824
Rodrigo Polaquini SimõesDepartment of Physical Therapy, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
Vandeni Clarice KunzAdventist University Center of São Paulo, Campus Engenheiro Coelho, São Paulo, Brazil.
Patricia DriussoDepartment of Physical Therapy, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
Humberto Sadanobu HirakawaDepartment of Physical Therapy, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
Beatrice De MariaIRCCS Istituti Clinici Scientifici Maugeri, Milan, Italy.
Aparecida Maria CataiDepartment of Physical Therapy, Federal University of São Carlos, São Carlos, São Paulo, Brazil.
Universidade Federal de São Carlos · BRCentro Universitário Adventista de São Paulo · BRIstituti Clinici Scientifici Maugeri · ITUniversity of Milan · IT

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior CAPES/CSF/PVE- no. 23038.007721/2013-41Coordenação de Aperfeiçoamento de Pessoal de Nível Superior CAPES/PNPD/Brazil, no. 23038.006927/2011-92
6 · The paper itself

Abstract

Both deterioration of the mechanical vascular properties of barosensitive vessels and autonomic derangement lead to modification of baroreflex sensitivity (BRS) in coronary artery disease (CAD) individuals. Type 2 diabetes (T2D) reduces BRS as well even in absence of cardiac autonomic neuropathy. The aim of the study is to clarify whether, assigned the degree of mechanical vascular impairment and without cardiac autonomic neuropathy, the additional autonomic dysfunction imposed in CAD patients by T2D (CAD-T2D) decreases BRS further. We considered CAD (n = 18) and CAD-T2D (n = 19) males featuring similar increases of average carotid intima media thickness (ACIMT) and we compared them to age- and gender-matched healthy (H, n = 19) subjects. BRS was computed from spontaneous beat-to-beat variability of heart period (HP) and systolic arterial pressure (SAP) at supine resting (REST) and during active standing (STAND). BRS was estimated via methods including time domain, spectral, cross-spectral, and model-based techniques. We found that (i) at REST BRS was lower in CAD and CAD-T2D groups than in H subjects but no difference was detected between CAD and CAD-T2D individuals; (ii) STAND induced an additional decrease of BRS visible in all the groups but again BRS estimates of CAD and CAD-T2D patients were alike; (iii) even though with different statistical power, BRS markers reached similar conclusions with the notable exception of the BRS computed via model-based approach that did not detect the BRS decrease during STAND. In presence of a mechanical vascular impairment, indexes estimating BRS from spontaneous HP and SAP fluctuations might be useless to detect the additional derangement of the autonomic control in CAD-T2D without cardiac autonomic neuropathy compared to CAD, thus limiting the applications of cardiovascular variability analysis to typify CAD-T2D individuals. Graphical abstract Graphical representation of the baroreflex sensitivity (BRS) estimated from spontaneous fluctuations of heart period and systolic arterial pressure via transfer function (TF) in low frequency (LF) band (from 0.04 to 0.15 Hz). BRS was reported as a function of the group (i.e., healthy (H), coronary artery disease (CAD) and CAD with type 2 diabetes (CAD-T2D) groups) at REST (black bars) and during STAND (white bars). Values are shown as mean plus standard deviation. The symbol "*" indicates a significant difference between conditions within the same group (i.e., H, CAD, or CAD-T2D) and the symbol "§" indicates a significant difference between groups within the same experimental condition (i.e., REST or STAND). BRS cannot distinguish CAD and CAD-T2D groups both at REST and during STAND, while it is useful to distinguish experimental conditions and separate pathological groups from H subjects.

Indexed as

Carotid Intima-Media ThicknessAgedBaroreflexBlood PressureCarotid ArteriesCase-Control StudiesCoronary Artery DiseaseDiabetes Mellitus, Type 2Heart RateHumansMaleMiddle AgedActive standingArterial pressureAutonomic nervous systemCardiovascular controlCarotid intima media thicknessHeart rate variability

Identifiers

PMID30843124
OpenAlexW2922041874

What OpenQuestion holds

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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.