Evidence map›Paper›PMID 31513751›Full record

ReviewAmerican journal of respiratory and critical care medicine2020

Beyond the Lungs: Systemic Manifestations of Pulmonary Arterial Hypertension.

Nils P Nickel, Ke Yuan, Peter Dorfmuller, Steeve Provencher, Yen-Chun Lai, Sebastien Bonnet, Eric D Austin, Carl D Koch, Alison Morris, Frédéric Perros and 3 more

Open access · greenAbstract readReview
In one paragraph

Review in American journal of respiratory and critical care medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Integrins as Drug Targets in Vascular and Related Diseases.International journal of drug discovery and pharmacology · 2024
    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

13 authors at 7 institutions in 4 countries.

Nils P NickelDivision of Pulmonary and Critical Care Medicine, Stanford University, Stanford, California.
Ke YuanDivision of Pulmonary and Critical Care Medicine, Stanford University, Stanford, California.
Peter DorfmullerDepartment of Pathology, University of Giessen, Giessen, Germany.
Steeve ProvencherCentre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Quebec, Quebec, Canada.
Yen-Chun LaiDivision of Pulmonary and Critical Care Medicine, Indiana University, Bloomington, Indiana.
Sebastien BonnetCentre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Quebec, Quebec, Canada.
Eric D AustinDivision of Pediatric Pulmonary and Critical Care Medicine, Vanderbilt University, Nashville Tennessee.
Carl D KochDivision of Pulmonary and Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0003-2564-207X
Alison MorrisDivision of Pulmonary and Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Frédéric PerrosCentre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec, Quebec, Quebec, Canada.ORCID 0000-0001-7730-2427
David MontaniInserm Université Paris Sud-Centre chirurgical Marie Lannelongue 999, Université Paris Sud-Paris Saclay, Hôpital Marie Lannelongue, Le Plessis Robinson, France; and.ORCID 0000-0002-9358-6922
Roham T ZamanianDivision of Pulmonary and Critical Care Medicine, Stanford University, Stanford, California.
Vinicio A de Jesus PerezDivision of Pulmonary and Critical Care Medicine, Stanford University, Stanford, California.
Stanford University · USInstitut universitaire de cardiologie et de pneumologie de Québec · CAUniversité Paris-Sud · FRUniversity of Pittsburgh · USIndiana University Bloomington · USJustus-Liebig-Universität Gießen · DEVanderbilt University · US

Funding

The Cellular Response to Elafin in PAHP01HL108797 · NHLBI · STANFORD UNIVERSITY · PI RABINOVITCH, MARLENE · 2011 to 2021
$19.7M
The Wnt7a/ROR2 axis in the pathogenesis of pulmonary arterial hypertensionR01HL134776 · NHLBI · STANFORD UNIVERSITY · PI DE JESUS PEREZ, VINICIO A · 2017 to 2025
$5.0M
Endothelial-pericyte interactions in the pathogenesis of pulmonary arterial hypertensionR01HL139664 · NHLBI · STANFORD UNIVERSITY · PI DE JESUS PEREZ, VINICIO A · 2018 to 2025
$4.7M
Critical Role for Microvasculature in Airway TransplantationR01HL095686 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI NICOLLS, MARK ROBERT · 2010 to 2022
$4.7M
Stanford Training Program in Lung BiologyT32HL129970 · NHLBI · STANFORD UNIVERSITY · PI CORNFIELD, DAVID N., NICOLLS, MARK ROBERT · 2016 to 2025
$3.2M
NHLBI NIH HHS P01 HL108797NHLBI NIH HHS R01 HL095686NHLBI NIH HHS R01 HL134776NHLBI NIH HHS R01 HL139664NHLBI NIH HHS T32 HL129970
6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a disease characterized by progressive loss and remodeling of the pulmonary arteries, resulting in right heart failure and death. Until recently, PAH was seen as a disease restricted to the pulmonary circulation. However, there is growing evidence that patients with PAH also exhibit systemic vascular dysfunction, as evidenced by impaired brachial artery flow-mediated dilation, abnormal cerebral blood flow, skeletal myopathy, and intrinsic kidney disease. Although some of these anomalies are partially due to right ventricular insufficiency, recent data support a mechanistic link to the genetic and molecular events behind PAH pathogenesis. This review serves as an introduction to the major systemic findings in PAH and the evidence that supports a common mechanistic link with PAH pathophysiology. In addition, it discusses recent studies describing morphological changes in systemic vessels and the possible role of bronchopulmonary anastomoses in the development of plexogenic arteriopathy. On the basis of available evidence, we propose a paradigm in which metabolic abnormalities, genetic injury, and systemic vascular dysfunction contribute to systemic manifestations in PAH. This concept not only opens exciting research possibilities but also encourages clinicians to consider extrapulmonary manifestations in their management of patients with PAH.

Indexed as

Bronchial ArteriesCerebrovascular CirculationCerebrovascular DisordersCoronary Artery DiseaseEndothelium, VascularHumansKidney DiseasesMuscular DiseasesPulmonary Arterial HypertensionPulmonary ArteryRespiratory MusclesScleroderma, SystemicVasodilationVentricular Dysfunction, Rightcerebrovascular diseasecoronary artery diseasekidney diseasepulmonary hypertensionrespiratory muscle dysfunction

Identifiers

PMID31513751
PMCPMC6961748
OpenAlexW2973127923

What OpenQuestion holds

Textmetadata
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.