Evidence map›Paper›PMID 35128849›Full record

ReviewKorean circulation journal2022

Stem Cell and Exosome Therapy in Pulmonary Hypertension.

Seyeon Oh, Ji-Hye Jung, Kyung-Jin Ahn, Albert Youngwoo Jang, Kyunghee Byun, Phillip C Yang, Wook-Jin Chung

Open access · hybridAbstract readReview
In one paragraph

Review in Korean circulation journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

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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 2 countries.

Seyeon Oh *Gachon Cardiovascular Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0002-3565-7139
Ji-Hye Jung *Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID https://orcid.org/0000-0002-2422-3941
Kyung-Jin Ahn *Gachon Cardiovascular Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0002-6286-3157
Albert Youngwoo JangGachon Cardiovascular Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0002-8802-268X
Kyunghee ByunGachon Cardiovascular Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0001-8678-8932
Phillip C YangDivision of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID https://orcid.org/0000-0002-6274-895X
Wook-Jin ChungGachon Cardiovascular Research Institute, Gachon University, Incheon, Korea.ORCID https://orcid.org/0000-0002-9767-7098
Gachon University · KRCardiovascular Institute of the South · USPalo Alto University · US

Funding

Gil Medical Center, Gachon University FRD2020-11Korea Disease Control and Prevention Agency 2018-ER6304-00Korea Disease Control and Prevention Agency 2018-ER6304-01Korea Disease Control and Prevention Agency 2018-ER6304-02Korea Disease Control and Prevention Agency 2021-ER0902-00Korea Disease Control and Prevention Agency 2021-ER0902-01Korea Medical Device Development Fund 9991006834Korea Medical Device Development Fund 9991007387Korea Medical Device Development Fund KMDF_PR_20200901_0164Korea Medical Device Development Fund KMDF_PR_20200901_0170Research and Development for Regional Industry BT190153
6 · The paper itself

Abstract

Pulmonary hypertension is a rare and progressive illness with a devastating prognosis. Promising research efforts have advanced the understanding and recognition of the pathobiology of pulmonary hypertension. Despite remarkable achievements in terms of improving the survival rate, reducing disease progression, and enhancing quality of life, pulmonary arterial hypertension (PAH) is not completely curable. Therefore, an effective treatment strategy is still needed. Recently, many studies of the underlying molecular mechanisms and technological developments have led to new approaches and paradigms for PAH treatment. Management based on stem cells and related paracrine effects, epigenetic drugs and gene therapies has yielded prospective results for PAH treatment in preclinical research. Further trials are ongoing to optimize these important insights into clinical circumstances.

Indexed as

ExosomesPulmonary arterial hypertensionRight heart failureStem cells

Identifiers

PMID35128849
PMCPMC8819574
OpenAlexW4206972919

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.