Evidence map›Paper›PMID 33351821›Full record

ArticlePloS one2020

Early myocardial damage and microvascular dysfunction in asymptomatic patients with systemic sclerosis: A cardiovascular magnetic resonance study with cold pressor test.

Nicola Galea, Edoardo Rosato, Antonietta Gigante, Cristian Borrazzo, Andrea Fiorelli, Giovanni Barchetti, Amelia Chiara Trombetta, Maria Anna Digiulio, Marco Francone, Carlo Catalano and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-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

16 citing papers in PubMed, 36 citations in OpenAlex.

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  15. Respiratory Motion-Registered Isotropic Whole-Heart TFrontiers in cardiovascular medicine · 2021
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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

11 authors at 2 institutions in 1 country.

Nicola GaleaDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.ORCID 0000-0003-4708-5120
Edoardo RosatoDepartment of Clinical Medicine, Clinical Immunology Unit- Scleroderma Center, Sapienza University of Rome, Rome, Italy.
Antonietta GiganteDepartment of Clinical Medicine, Clinical Immunology Unit- Scleroderma Center, Sapienza University of Rome, Rome, Italy.
Cristian BorrazzoStatistical Unit, Department of Public Health and Infectious Disease, Sapienza University of Rome, Rome, Italy.
Andrea FiorelliDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Giovanni BarchettiDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Amelia Chiara TrombettaDepartment of Clinical Medicine, Clinical Immunology Unit- Scleroderma Center, Sapienza University of Rome, Rome, Italy.
Maria Anna DigiulioDepartment of Clinical Medicine, Clinical Immunology Unit- Scleroderma Center, Sapienza University of Rome, Rome, Italy.
Marco FranconeDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Carlo CatalanoDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Iacopo CarboneDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Sapienza University of Rome · ITOspedale San Pietro Fatebenefratelli · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCardiac involvement in Systemic Sclerosis (SSc) is increasingly recognized as a mayor cause of morbidity and mortality. The aim of present study is to investigate the early stages of cardiac involvement in SSc by Cardiovascular magnetic resonance (CMR), combining the non-invasive detection of myocardial inflammation and fibrosis using T2 and T1 mapping techniques and the assessment of microcirculatory impairment through perfusion response to cold pressor test (CPT).

methods40 SSc patients (30 females, mean age: 42.1 years) without cardiac symptoms and 10 controls underwent CMR at 1.5 T unit. CMR protocol included: native and contrast-enhanced T1 mapping, T2 mapping, T2-weighted, cineMR and late gadolinium enhancement (LGE) imaging. Microvascular function was evaluated by comparing myocardial blood flow (MBF) on perfusion imaging acquired at rest and after CPT. Native myocardial T1 and T2 relaxation times, extracellular volume fraction (ECV), T2 signal intensity ratio, biventricular volumes and LGE were assessed in each patient.

resultsSSc patients had significantly higher mean myocardial T1 (1029±32ms vs. 985±18ms, p<0.01), ECV (30.1±4.3% vs. 26.7±2.4%, p<0.05) and T2 (50.1±2.8ms vs. 47±1.5ms, p<0.01) values compared with controls. No significant differences were found between absolute MBF values at rest and after CPT; whereas lower MBF variation after CPT was observed in SSc patients (+33 ± 14% vs. +44 ± 12%, p<0.01). MBF variation had inverse correlation with native T1 values (r: -0.32, p<0.05), but not with ECV.

conclusionsMyocardial involvement in SSc at preclinical stage increases native T1, T2 and ECV values, reflecting inflammation and fibrosis, and reduces vasodilatory response to CPT, as expression of microvascular dysfunction.

Indexed as

AdultAsymptomatic DiseasesCase-Control StudiesContrast MediaFemaleFibrosisHumansMagnetic Resonance ImagingMagnetic Resonance Imaging, CineMaleMicrocirculationMiddle AgedMyocarditisMyocardiumMyocytes, CardiacProspective StudiesContrast Media

Identifiers

PMID33351821
PMCPMC7755221
OpenAlexW3114937128

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.