Evidence map›Paper›PMID 37011995›Full record

ArticleBMJ case reports2023

Scurvy-induced pulmonary arterial hypertension.

Jehad Azar, Mohammed Ayyad, Yasmin Jaber, Laith Azzam Ayasa

Open access · greenAbstract readCase Reports
In one paragraph

Article in BMJ case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. 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

4 authors at 3 institutions in 2 countries.

Jehad AzarPulmonary and Critical Care Department, Cleveland Clinic Foundation, Cleveland, Ohio, USA jehad.azar@gmail.com.ORCID http://orcid.org/0000-0002-5966-152X
Mohammed AyyadInternal Medicine Department, Al Quds University, Abu Dis, State of Palestine.
Yasmin JaberOncology, Georgetown University, Washington, DC, USA.ORCID http://orcid.org/0000-0002-4485-867X
Laith Azzam AyasaInternal Medicine Department, Al Quds University, Abu Dis, State of Palestine.ORCID http://orcid.org/0000-0003-0340-7685
Al-Quds University · PSCleveland Clinic · USGeorgetown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a progressive disease of the pulmonary vasculature that results in precapillary pulmonary hypertension. PAH is caused by a group of clinical conditions involving multiple organ systems. Several cases have been reported in the literature demonstrating an association between vitamin C deficiency and PAH. Low endothelial nitric oxide levels in the pulmonary vasculature, combined with the inappropriate activation of hypoxia-inducible transcription factors, seen in patients with ascorbic acid deficiency, are believed to be the main contributors to the pathogenesis of pulmonary vasculopathy and the exaggerated pulmonary vasoconstrictive response seen in patients with scurvy-induced PAH. Vitamin C supplementation is considered the definitive treatment.

Indexed as

Ascorbic Acid DeficiencyHypertension, PulmonaryPulmonary Arterial HypertensionScurvyFamilial Primary Pulmonary HypertensionHumansMalnutritionMedical managementPulmonary hypertensionRespiratory medicineVitamins and supplements

Identifiers

PMID37011995
PMCPMC10083756
OpenAlexW4362523332

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.