Evidence map›Paper›PMID 34524933›Full record

ReviewAnnals of the American Thoracic Society2021

Clinical Presentation and Treatment of High-Risk Sarcoidosis.

David M Perlman, Muthya Tejasvini Sudheendra, Yuka Furuya, Chetan Shenoy, Rajat Kalra, Henri Roukoz, Jeremy Markowitz, Lisa A Maier, Maneesh Bhargava

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the American Thoracic Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Observational
  7. Cellular Recycling Gone Wrong: The Role of Dysregulated Autophagy and Hyperactive mTORC1 in the Pathogenesis of Sarcoidosis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2023
    Article
  8. 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

9 authors at 2 institutions in 1 country.

David M PerlmanDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, and.ORCID 0000-0001-7055-0970
Muthya Tejasvini SudheendraDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, and.
Yuka FuruyaDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, and.
Chetan ShenoyCardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota; and.
Rajat KalraCardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota; and.
Henri RoukozCardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota; and.
Jeremy MarkowitzCardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota; and.ORCID 0000-0001-9389-432X
Lisa A MaierDivision of Environmental and Occupational Health Sciences, National Jewish Health, Denver, Colorado.ORCID 0000-0001-6872-1769
Maneesh BhargavaDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine, and.ORCID 0000-0002-1294-6181
University of Minnesota Medical Center · USNational Jewish Health · US

Funding

Cardiac Fibrosis and Risk Prediction in Cancer Treatment-Related CardiotoxicityK23HL132011 · NHLBI · UNIVERSITY OF MINNESOTA · PI SHENOY, CHETAN N · 2016 to 2020
$884k
NHLBI NIH HHS K23 HL132011
6 · The paper itself

Abstract

Sarcoidosis is a multisystem disease of unknown cause with heterogeneous clinical manifestations and variable course. Spontaneous remissions occur in some patients, whereas others have progressive disease impacting survival, organ function, and quality of life. Four high-risk sarcoidosis phenotypes associated with chronic inflammation have recently been identified as high-priority areas for research. These include treatment-refractory pulmonary disease, cardiac sarcoidosis, neurosarcoidosis, and multiorgan sarcoidosis. Significant gaps currently exist in the understanding of these high-risk manifestations of sarcoidosis, including their natural history, diagnostic criteria, biomarkers, and the treatment strategy, such as the ideal agent, optimal dose, and treatment duration. The use of registries with well-phenotyped patients is a critical first step to study high-risk sarcoidosis manifestations systematically. We review the diagnostic and treatment approach to high-risk sarcoidosis manifestations. Appropriately identifying these disease subgroups will help enroll well-phenotyped patients in sarcoidosis registries and clinical trials, a necessary step to narrow existing gaps in understanding of this enigmatic disease.

Indexed as

Central Nervous System DiseasesSarcoidosisHumansLungPhenotypeQuality of Lifecardiac sarcoidosishigh-risk sarcoidosismultiorgan sarcoidosisneurosarcoidosisprogressive pulmonary sarcoidosis

Identifiers

PMID34524933
PMCPMC12039824
OpenAlexW3199904028

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.