Evidence map›Paper›PMID 32200572›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2020

The Utility of Plasma Vascular Biomarkers in Systemic Sclerosis: A Prospective Longitudinal Analysis.

Christopher A Mecoli, Ami A Shah, Francesco Boin, Fredrick M Wigley, Laura K Hummers

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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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

5 authors at 2 institutions in 1 country.

Christopher A MecoliJohns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-1429-8392
Ami A ShahJohns Hopkins University School of Medicine, Baltimore, Maryland.
Francesco BoinUniversity of California, San Francisco.
Fredrick M WigleyJohns Hopkins University School of Medicine, Baltimore, Maryland.
Laura K HummersJohns Hopkins University School of Medicine, Baltimore, Maryland.
Johns Hopkins University · USUniversity of California, San Francisco · US

Funding

SCLERODERMA-ASSOCIATED PAHP50HL084946 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HASSOUN, PAUL M. · 2007 to 2011
$20.6M
Sample Processing and Immunoassay Research CoreP30AR070254 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI CLIFTON O BINGHAM, Antony Rosen · 2016 to 2026
$8.9M
Multidisciplinary Rheumatology Training ProgramT32AR048522 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI CLIFTON O BINGHAM, LIVIA A CASCIOLA-ROSEN · 2003 to 2026
$6.4M
Autoantibodies Define Scleroderma Subgroups with Distinct Relationships to CancerR01AR073208 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI LIVIA A CASCIOLA-ROSEN, Ami Aalok Shah · 2018 to 2026
$5.2M
Optimizing the Approach to Identify Cancer-Associated MyositisK23AR075898 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI MECOLI, CHRISTOPHER · 2019 to 2023
$773k
Biomarkers of Vascular Disease in SclerodermaK23AR052742 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI HUMMERS, LAURA K · 2005 to 2009
$614k
NHLBI NIH HHS P50 HL084946NHLBI NIH HHS P50-HL084946-01NIAMS NIH HHS 1K23AR075898-01A1NIAMS NIH HHS 5K23AR52742-5NIAMS NIH HHS K23 AR052742NIAMS NIH HHS K23 AR075898NIAMS NIH HHS P30 AR070254NIAMS NIH HHS P30-AR-070254NIAMS NIH HHS R01 AR-073208NIAMS NIH HHS R01 AR073208NIAMS NIH HHS T32 AR048522NIAMS NIH HHS T32AR048522
6 · The paper itself

Abstract

objectiveIn cross-sectional studies, pulmonary hypertension (PH) and ischemic digital lesions are 2 scleroderma vascular outcomes associated with abnormalities in biomarkers of angiogenesis. The clinical usefulness of these biomarkers is unknown, in part due to lack of data on longitudinal measurement. This prospective longitudinal study was undertaken to evaluate vascular biomarker measurements in patients with systemic sclerosis (SSc) over time.

methodsWe conducted a prospective cohort study of 300 patients with SSc who were followed up for at least a 5-year period and lacked evidence of PH and/or active ischemic digital lesions at enrollment. Levels of hepatocyte growth factor (HGF), soluble Flt-1 (sFlt-1), soluble endoglin, endostatin, and placental growth factor (PLGF) were obtained at multiple time points and assessed for their ability to predict the development of PH/ischemic digital lesions. Hazard ratios (HRs) with 95% confidence intervals (95% CIs) were calculated.

resultsForty-six patients (15%) developed PH and 69 patients (23%) developed an ischemic digital lesion. In time-to-event analyses, the following 3 biomarkers measured at cohort entry were found to be significantly associated with the development of PH: HGF (HR 1.99 [95% CI 1.24-3.17], P = 0.004), sFlt-1 (HR 3.04 [95% CI 1.29-7.14], P = 0.011), and PLGF (HR 2.74 [95% CI 1.32-5.69], P = 0.007). As time approaching PH diagnosis decreased, there was no corresponding increase in any biomarker level. Upon converting each continuous vascular biomarker into a binary variable, a dose-response relationship was observed for the number of elevated biomarkers at cohort entry and the risk of developing PH. With each additional elevated biomarker at cohort entry, there was a 78% increase in the risk of developing PH (HR 1.78 [95% CI 1.2-2.6], P = 0.004).

conclusionThese data suggest that molecules involved in angiogenesis reflect vascular perturbation, and that elevations in these biomarkers at first encounter can indicate patients who are at risk of PH development.

Indexed as

AdultBiomarkersEndoglinEndostatinsFemaleFingersHeart Disease Risk FactorsHepatocyte Growth FactorHumansHypertension, PulmonaryIschemiaLongitudinal StudiesMaleMiddle AgedNeovascularization, PathologicPlacenta Growth FactorBiomarkersEndoglinEndostatinsENG protein, humanFLT1 protein, humanHepatocyte Growth FactorHGF protein, humanPGF protein, humanPlacenta Growth FactorVascular Endothelial Growth Factor Receptor-1

Identifiers

PMID32200572
PMCPMC8214152
OpenAlexW3012705588

What OpenQuestion holds

Textmetadata
LicenceTDM
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.