Evidence map›Paper›PMID 41323125›Full record

ArticleThe World Allergy Organization journal2025

A sensitive and specific assay to characterize plasma kallikrein activity in plasma from patients with hereditary angioedema.

Daniel K Lee, Arije Ghannam, Nivetha Murugesan, Denis Vincent, Micaela Dona, Danny M Cohn, Adil Adatia, Michael D Smith, Paul K Audhya, Sally L Hampton and 1 more

Abstract read
In one paragraph

Article in The World Allergy Organization journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

11 authors.

Daniel K LeeKalVista Pharmaceuticals Inc, Framingham, MA, USA.
Arije GhannamKininBio, Grenoble, France.
Nivetha MurugesanKalVista Pharmaceuticals Inc, Framingham, MA, USA.
Denis VincentUniversité de Montpellier, Montpellier, France.
Micaela DonaAllergist, Private Practice, Paris, France.
Danny M CohnAmsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Adil AdatiaUniversity of Alberta, Edmonton, AB, Canada.
Michael D SmithKalVista Pharmaceuticals Inc, Framingham, MA, USA.
Paul K AudhyaKalVista Pharmaceuticals Inc, Framingham, MA, USA.
Sally L HamptonKalVista Pharmaceuticals Limited, Salisbury, United Kingdom.
Edward P FeenerKalVista Pharmaceuticals Inc, Framingham, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Plasma kallikrein (PKa) activity is increased in the plasma of patients with hereditary angioedema (HAE) and has been implicated in other kallikrein-kinin system (KKS)-mediated diseases. Exogenous substrates commonly used in PKa assays can be cleaved by multiple plasma proteases, which reduce assay specificity and sensitivity for PKa. We describe a sensitive and specific assay to detect PKa activity in plasma as a candidate biomarker for HAE. Methods: PKa activity was measured in plasma samples from patients with HAE with decreased C1 inhibitor (C1INH) levels or activity who were not receiving prophylactic medications for HAE (HAE-C1INH; Results: In control plasma, sPKa activity was 0.69 ± 0.07 nmol/min/mL at baseline and 0.88 ± 0.11 nmol/min/mL after 6 h of cold incubation (mean ± SEM, Conclusion: We developed a specific PKa assay that can detect low levels of PKa activity in plasma and can differentiate patients with HAE-C1INH from controls without HAE with high sensitivity and specificity. Using this assay, we demonstrated that sPKa activity is elevated during the intercritical period in patients with HAE-C1INH and in those with HAE-nC1INH compared with controls when measured after 6 h of cold incubation. This sensitive and specific PKa assay could be useful to characterize PKa activity in plasma samples from patients with HAE and could potentially serve as a future candidate biomarker for HAE-nC1INH.

Indexed as

BiomarkerHAEHereditary angioedemaPlasma kallikrein

Identifiers

PMID41323125
PMCPMC12663008

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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.