Evidence map›Paper›PMID 33984497›Full record

ArticleClinical immunology (Orlando, Fla.)2021

Platelet bound complement split product (PC4d) is a marker of platelet activation and arterial vascular events in Systemic Lupus Erythematosus.

Yevgeniya Gartshteyn, Adam Mor, Daichi Shimbo, Leila Khalili, Teja Kapoor, Laura Geraldino-Pardilla, Roberta V Alexander, John Conklin, Thierry Dervieux, Anca D Askanase

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 12% 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, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Platelets and Thrombotic Antiphospholipid Syndrome.Journal of clinical medicine · 2024
    Review
  4. Review
  5. Article
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  7. Article
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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

10 authors at 2 institutions in 1 country.

Yevgeniya GartshteynDivision of Rheumatology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America. Electronic address: yg2372@cumc.columbia.edu.
Adam MorDivision of Rheumatology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America.
Daichi ShimboCenter for Behavioral Cardiovascular Health, Division of Cardiology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America.
Leila KhaliliDivision of Rheumatology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America.
Teja KapoorDivision of Rheumatology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America.
Laura Geraldino-PardillaDivision of Rheumatology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America.
Roberta V AlexanderExagen Diagnostics Inc, Vista, CA, United States of America.
John ConklinExagen Diagnostics Inc, Vista, CA, United States of America.
Thierry DervieuxPrometheus Biosciences, San Diego, CA, United States of America.
Anca D AskanaseDivision of Rheumatology, Department of Medicine, Columbia University Medical Center, New York, NY, United States of America.
Columbia University Irving Medical Center · USPrometheus Biosciences (United States) · US

Funding

NRSA Training CoreTL1TR001875 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI SPANN, MARISA N, TAYLOR, JACQUELYN Y · 2016 to 2025
$8.9M
Novel mechanisms regulating PD-1 signaling and functionR01AI125640 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Adam Mor · 2016 to 2026
$4.3M
PAG is a novel target in immunotherapyR01AI150597 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MOR, ADAM · 2020 to 2024
$2.7M
(PQ8) Predictive biomarkers for the onset of immune-related adverse events associated with PD-1 blockadeR21CA231277 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MOR, ADAM · 2019 to 2020
$361k
NCATS NIH HHS TL1 TR001875NCI NIH HHS R21 CA231277NIAID NIH HHS R01 AI125640NIAID NIH HHS R01 AI150597
6 · The paper itself

Abstract

Platelet-bound complement activation products (PC4d) are associated with thrombosis in Systemic Lupus Erythematosus (SLE). This study investigated the effect of PC4d on platelet function, as a mechanistic link to arterial thrombosis. In a cohort of 150 SLE patients, 13 events had occurred within five years of enrollment. Patients with arterial events had higher PC4d levels (13.6 [4.4-24.0] vs. 4.0 [2.5-8.3] net MFI), with PC4d 10 being the optimal cutoff for event detection. The association of arterial events with PC4d remained significant after adjusting for antiphospholipid status, smoking, and prednisone use (p = 0.045). PC4d levels correlated with lower platelet counts (r = -0.26, p = 0.002), larger platelet volumes (r = 0.22, p = 0.009) and increased platelet aggregation: the adenosine diphosphate (ADP) concentration to achieve 50% maximal aggregation (EC

Indexed as

Adenosine DiphosphateAutoantibodiesAutoimmunityBiomarkersBlood PlateletsComplement ActivationComplement C4Disease SusceptibilityHumansLupus Erythematosus, SystemicPlatelet ActivationPlatelet AggregationPlatelet CountThrombosisVascular DiseasesAdenosine DiphosphateAutoantibodiesBiomarkersComplement C4Antiphospholipid syndromeAutoimmune diseaseBiomarkerCardiovascular diseaseComplement split productsInflammationPlateletSystemic lupus erythematosusThrombosis

Identifiers

PMID33984497
PMCPMC8252918
OpenAlexW3160466796

What OpenQuestion holds

Textmetadata
LicenceTDM
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.