Evidence map›Paper›PMID 35005243›Full record

ArticleJournal of scleroderma and related disorders2021

A Pilot Study of Dimethyl Fumarate in Pulmonary Arterial Hypertension Associated with Systemic Sclerosis.

Kristi Kong, Diane Koontz, Christina Morse, Eileen Roth, Robyn T Domsic, Marc A Simon, Eric Stratton, Connor Buchholz, Kimberly Tobin-Finch, Robert Simms and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of scleroderma and related disorders, 2021. 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
0.9field-weighted citation impact, top 27% 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. Management of pulmonary arterial hypertension in systemic sclerosis: from classical treatments to new horizons.European respiratory review : an official journal of the European Respiratory Society · 2026
    Pooled it
  2. Review
  3. Emerging therapeutic targets in systemic sclerosis.Journal of molecular medicine (Berlin, Germany) · 2024
    Review
  4. New Drugs and Therapies in Pulmonary Arterial Hypertension.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Review
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

14 authors at 5 institutions in 1 country.

Kristi KongDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA.
Diane KoontzDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA.
Christina MorseDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA.
Eileen RothDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA.
Robyn T DomsicDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA.
Marc A SimonDivision of Cardiology, University of Pittsburgh, Pittsburgh, PA.
Eric StrattonDivision of Rheumatology, Arthritis Center, Boston University, Boston, MA.
Connor BuchholzDivision of Rheumatology, Arthritis Center, Boston University, Boston, MA.
Kimberly Tobin-FinchDivision of Rheumatology, Arthritis Center, Boston University, Boston, MA.
Robert SimmsDivision of Rheumatology, Arthritis Center, Boston University, Boston, MA.
M Patricia GeorgeDivision of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, CO.
Paul M HassounDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University, Baltimore, MD.
Harrison FarberDivision of Pulmonary, Critical Care and Sleep Medicine, Tufts Medical Center, Boston, MA.
Robert LafyatisDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA.
University of Pittsburgh · USBoston University · USJohns Hopkins University · USNational Jewish Health · USTufts Medical Center · US

Funding

Dimethyl Fumarate In Systemic Sclerosis-Associated Pulmonary Arterial HypertensionR21AR069285 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAFYATIS, ROBERT A. · 2017 to 2019
$584k
NIAMS NIH HHS R21 AR069285
6 · The paper itself

Abstract

introductionGiven the poor treatment options for pulmonary arterial hypertension associated systemic sclerosis (SSc-PAH) patients, we sought to determine clinical safety and efficacy of Dimethylfumarate (DMF), an Nrf2 agonist, and the effects on biomarkers of oxidative stress on SSc-PAH in an exploratory interventional clinical trial.

objectivesThe primary objectives were to assess the safety and efficacy of treatment with DMF in patients with SSc-PAH.

methodsThis was an investigator-initiated, double-blind, randomized, placebo-controlled trial conducted at two sites in the United States. The primary safety endpoint was the incidence of serious adverse events (SAEs) and all adverse events (AEs) in DMF compared to placebo-treated patients. The primary efficacy endpoint was the change in 6MWD from baseline to the end of treatment at Week 24 in DMF compared to placebo-treated patients.

resultsSix participants were randomized to either placebo (n = 2) or DMF (n = 4). Baseline demographics were similar in both groups. A total of 25 adverse events (AEs) occurred in 6 subjects, with 14 AEs (56.0%) having occurred in DMF-treated subjects. 3 occurrences were identified as nausea AEs, and two participants withdrew due to nausea. One participant in the placebo group was withdrawn after a hospitalization SAE due to worsening of heart failure and shortness of breath secondary to anemia. One participant in each group completed protocol. Subjects in the DMF-treated group showed a non-significant reduced decline in 6MWD (relative mean change of -7.07%) from baseline to Week 24 as compared to placebo-treated subjects (relative mean change of -14.97%).

conclusionPatients treated for SSc-PAH with 2 and 3-drug regimens, as is now typical for these patients, tolerate DMF poorly. Our small samples size did not provide power to suggest efficacy. We suggest that Nrf2 is still a valid therapeutic target for future trials, using better tolerated Nrf2 agonists.

Identifiers

PMID35005243
PMCPMC8741170
OpenAlexW3172359983

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.