Evidence map›Paper›PMID 30961939›Full record

ArticleRespiratory medicine2019

Use of red cell distribution width in a population at high risk for pulmonary hypertension.

Laura A Petrauskas, Lesley Ann Saketkoo, Thomas Kazecki, Shigeki Saito, Vijay Jaligam, Bennett P deBoisblanc, Matthew R Lammi

Open access · greenAbstract readComparative Study
In one paragraph

Article in Respiratory medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Observational
  10. Review
  11. Article
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

7 authors at 3 institutions in 1 country.

Laura A PetrauskasLouisiana State University Health Sciences Center, School of Medicine, New Orleans, LA, USA.
Lesley Ann SaketkooComprehensive Pulmonary Hypertension Center-University Medical Center, New Orleans, LA, USA; Tulane University School of Medicine, New Orleans Scleroderma and Sarcoidosis Patient Care and Research Center, New Orleans, LA, USA.
Thomas KazeckiLouisiana State University Health Sciences Center, School of Medicine, New Orleans, LA, USA.
Shigeki SaitoComprehensive Pulmonary Hypertension Center-University Medical Center, New Orleans, LA, USA; Tulane University School of Medicine, New Orleans Scleroderma and Sarcoidosis Patient Care and Research Center, New Orleans, LA, USA.
Vijay JaligamLouisiana State University Health Sciences Center, Section of Cardiology, Medical Director of Cardiology-JenCare NOLA, New Orleans, LA, USA.
Bennett P deBoisblancComprehensive Pulmonary Hypertension Center-University Medical Center, New Orleans, LA, USA; Louisiana State University Health Sciences Center, Section of Pulmonary/Critical Care and Allergy/Immunology, New Orleans, LA, USA.
Matthew R LammiComprehensive Pulmonary Hypertension Center-University Medical Center, New Orleans, LA, USA; Louisiana State University Health Sciences Center, Section of Pulmonary/Critical Care and Allergy/Immunology, New Orleans, LA, USA. Electronic address: mlammi@lsuhsc.edu.
Louisiana State University Health Sciences Center New Orleans · USTulane University · USUniversity Medical Center New Orleans · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
NHLBI NIH HHS L30 HL129466NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

backgroundPulmonary hypertension (PH) often presents with non-specific symptoms making early diagnosis difficult. Red cell distribution width (RDW) is a parameter routinely reported on an automated complete blood cell count that has been associated with numerous disease states. The purpose of this study was to further evaluate RDW as a biomarker for PH in at-risk populations.

methodsIn a retrospective, cross-sectional analysis of patients seen at a PH center over 1 year, we examined both patients with PH and patients at risk for but without PH (e.g. systemic sclerosis, [SSc]). We also studied a group of age-and sex-matched, non-diseased controls. Relevant characteristics were compared among the 3 groups using one-way ANOVA. Similar comparisons were made across World Health Organization (WHO) PH groups 1-4.

resultsRDW was highest in the PH patients (n = 181), intermediate in the at-risk for PH patients (n = 52), and lowest in matched controls (n = 100) (15.9 ± 2.8 vs 14.8 ± 2.8 vs 14.2 ± 1.1%, respectively; p < 0.0001). There were no significant differences in RDW across WHO PH groups (p = 0.50). SSc patients with PH had significantly higher RDW values compared to SSc patients without PH (16.0 ± 2.2 vs 14.4 ± 1.9%, respectively; p = 0.03).

conclusionsRDW is significantly higher in PH patients, without regard to disease etiology, when compared to age- and sex-matched non-diseased controls. Importantly, RDW is also higher in PH patients compared to at-risk patients, particularly in the SSc cohort. The ease of obtaining RDW as a biomarker may help detect incident PH at earlier stages among patients who are at high risk for development of PH.

Indexed as

AdultAgedBiomarkersCross-Sectional StudiesErythrocyte IndicesFemaleHumansHypertension, PulmonaryMaleMiddle AgedRetrospective StudiesRisk FactorsScleroderma, SystemicBiomarkersBiomarkerHigh risk pulmonary hypertension populationsPulmonary arterial hypertensionRed cell distribution widthSystemic sclerosis

Identifiers

PMID30961939
PMCPMC6461373
OpenAlexW2920887517

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.