Evidence map›Paper›PMID 42592556›Full record

ArticleFortune journal of health sciences2026

Pathophysiological Drivers of Mast Cell Activation Syndrome and Implications for Treatment.

Spencer Collins, Tyler Williams, Edgar Sanchez, Devendra K Agrawal

Abstract read
In one paragraph

Article in Fortune journal of health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Spencer CollinsDepartment of Translational Research, College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California 91766 USA.
Tyler WilliamsDepartment of Translational Research, College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California 91766 USA.
Edgar SanchezDepartment of Translational Research, College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California 91766 USA.
Devendra K AgrawalDepartment of Translational Research, College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, California 91766 USA.

Funding

Research Education Program to Promote Diversity in Immunologic and Allergic DiseasesR25AI179582 · NIAID · WESTERN UNIVERSITY OF HEALTH SCIENCES · PI Devendra K. Agrawal · 2025 to 2026
$756k
NIAID NIH HHS R25 AI179582
6 · The paper itself

Abstract

Mast Cell Activation Syndrome (MCAS) is an underrecognized multisystem disorder causing nonspecific and diverse symptoms, making it difficult for clinicians to diagnose and treat. This comprehensive review provides an overview of the signs and symptoms of MCAS while investigating the known pathophysiological signaling pathways and mediators that contribute to mast cell (MC) dysregulation. Unraveling the mechanisms of MC activation is essential for elucidating the underlying disease and exploring techniques to improve quality of life. Immunoglobulin E (IgE)- and non-IgE-mediated pathways are emphasized in addition to the various intracellular signaling like PI3K/Akt/mTOR, RAS/MAPK, and JAK/STAT that play pivotal roles in the amplification of MC activation and dysregulation. After activation of intracellular pathways, MC degranulation releases mediators, notably histamine, tryptase, heparin, leukotrienes, prostaglandins, and cytokines, thus facilitating further aberrant regulation. Finally, with a thorough understanding of these advanced molecular processes, there are numerous opportunities to be able to apply specialized inhibitors and novel therapies for treating MCAS. With antihistamines remaining the most well-established first-line treatment, the goal is to continue strengthening research in the field through education on the immunology of MCAS and to encourage discoveries that improve diagnostic biomarkers and therapeutic strategies.

Indexed as

AcalabrutinibBruton tyrosine kinase inhibitorsCorticosteroidsCromolyn sodiumCyclosporineFcεRIH1/H2 blockersHeparinHistamineIbrutinibIgE-Mediated Immune responseJAK/STATKetotifenKIT(D816V)LeukotrienesMast Cell Activation SyndromeMast CellsMastocytosisMontelukastMultisystemicNon-IgE ActivationOmalizumabProstaglandinsTryptaseZanubrutinib

Identifiers

PMID42592556
PMCPMC13465963

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.