Evidence map›Paper›PMID 38433974›Full record

ArticleResearch and practice in thrombosis and haemostasis2024

A novel factor IXa-specific enzyme-linked immunosorbent assay detects factor IXa in human plasma.

Tina M Misenheimer, Michael R Lasarev, Kraig T Kumfer, John P Sheehan, Bradford S Schwartz

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Tina M MisenheimerMorgridge Institute for Research, Madison, Wisconsin, USA.
Michael R LasarevDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, USA.
Kraig T KumferMorgridge Institute for Research, Madison, Wisconsin, USA.
John P SheehanDepartment of Medicine/Hematology-Oncology, University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin, USA.
Bradford S SchwartzMorgridge Institute for Research, Madison, Wisconsin, USA.
Morgridge Institute for Research · USUniversity of Wisconsin–Madison · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
TFPI, Protein S, and Plasma FIXa in Hormone-Induced HypercoagulabilityR01HL149364 · NHLBI · VERSITI WISCONSIN, INC. · PI MAST, ALAN E, SHEEHAN, JOHN PATRICK · 2021 to 2024
$2.8M
Comprehensive Characterization of Missense Mutants in Factor IXR01HL152066 · NHLBI · UNIVERSITY OF WASHINGTON · PI FOWLER, DOUGLAS M, JOHNSEN, JILL MARIE · 2020 to 2023
$1.8M
In Vivo Regulation of Factor IXa by Protein S in Hemophilia and Systemic HypercoagulabilityR01HL149855 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI SHEEHAN, JOHN PATRICK · 2020 to 2023
$1.5M
NCATS NIH HHS UL1 TR002373NCI NIH HHS P30 CA014520NHLBI NIH HHS R01 HL149364NHLBI NIH HHS R01 HL149855NHLBI NIH HHS R01 HL152066
6 · The paper itself

Abstract

Background: Factor (F)IXa activity has been detected in human plasma and may impact thrombotic risk. Current FIXa activity assays are complex and cumbersome. Objectives: To develop a reproducible enzyme-linked immunosorbent assay (ELISA) using a novel monoclonal antibody that detects total FIXa in human plasma. Methods: A monoclonal antibody was raised against the new N-terminus exposed upon activation of FIX to FIXa by cleavage after R226. This antibody is specific for FIXa protease and does not recognize FIX zymogen or FIXα. The antibody was used to develop a FIXa-specific ELISA capable of quantifying total FIXa (free FIXa and FIXa-antithrombin complex) in human plasma. Total FIXa quantified using the ELISA was compared to that of FIXa-antithrombin quantified using modifications of a previously described ELISA. Results: The FIXa-specific ELISA was reproducible and quantified total FIXa in human plasma. Total FIXa levels correlated with FIXa-antithrombin levels. Conclusion: A monoclonal antibody was developed that specifically detects human FIXa protease. A FIXa-specific ELISA using the new antibody is capable of reproducibly measuring total FIXa in human plasma (both free FIXa and FIXa-antithrombin). This assay should facilitate the evaluation of total FIXa levels in a variety of clinical circumstances.

Indexed as

antithrombincoagulationCOVID-19ELISAfactor IXahumanmonoclonal antibodyproteasezymogen

Identifiers

PMID38433974
PMCPMC10907220
OpenAlexW4391530047

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.