Evidence map›Paper›PMID 19643986›Full record

ArticleBlood2009

Cell adhesion molecule 1: a novel risk factor for venous thrombosis.

Sandra J Hasstedt, Irene D Bezemer, Peter W Callas, Carla Y Vossen, Winifred Trotman, Robert P Hebbel, Christine Demers, Frits R Rosendaal, Edwin G Bovill

Open access · greenAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.4field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Open biology · 2025
    Review
  3. Chemical mapping of the surface interactome of PIEZO1 identifies CADM1 as a modulator of channel inactivation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Article
  5. Review
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  9. The Role of Cell Adhesion Molecule 1 (CADM1) in Cutaneous Malignancies.International journal of molecular sciences · 2020
    Review
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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

9 authors at 5 institutions in 3 countries.

Sandra J HasstedtDepartment of Human Genetics, University of Utah, Salt Lake City, USA.
Irene D Bezemer
Peter W Callas
Carla Y Vossen
Winifred Trotman
Robert P Hebbel
Christine Demers
Frits R Rosendaal
Edwin G Bovill
Leiden University Medical Center · NLUniversity of Vermont · USUniversité Laval · CAUniversity of Minnesota Medical Center · USUniversity of Utah · US

Funding

VENOUS THROMBOEMBOLISM: GENES, RISK, MANAGEMENTP01HL046703 · NHLBI · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI BRUMMEL-ZIEDINS, KATHLEEN E · 1991 to 2011
$19.8M
MODELS FOR THE GENETIC EPIDEMIOLOGY OF CHRONIC DISEASESR01HD017463 · NICHD · UNIVERSITY OF UTAH · PI HASSTEDT, SANDRA J · 1987 to 2009
$1.7M
NHLBI NIH HHS N01 HV048196NHLBI NIH HHS N01-HV-48196NHLBI NIH HHS P01 HL046703NHLBI NIH HHS P01 HL46703NICHD NIH HHS R01 HD017463
6 · The paper itself

Abstract

Protein C (PC) deficiency increases the risk of venous thrombosis (VT) among members of Kindred Vermont II but fails to fully account for the inheritance pattern. A genome scan of the pedigree supported the presence of a prothrombotic gene on chromosome 11q23 (nominal P < .0001), with weaker support on chromosomes 10p12 (P < .0003) and 18p11.2-q11 (P < .0007). Resequencing of 109 genes in the linkage regions identified 5030 variants in a sample of 20 kindred members. Of 16 single nucleotide polymorphisms in 6 genes tested in the larger family set, only single nucleotide polymorphisms in cell adhesion molecule 1 (CADM1) associated with VT. Among the 8 CADM1 single nucleotide polymorphisms genotyped in the complete sample, rs6589488 was most strongly supported (P < .000007), but the association was limited to the PC-deficient subset of the sample (P < .000001). Haplotype analysis narrowed the region containing the causative variant to the coding region of the CADM1 gene. CADM1 gene expression analyzed in blood outgrowth endothelial cells cultured from family members was decreased compared with control subjects, lending phenotypic support to this conclusion. Finally, we have for the first time demonstrated CADM1 in endothelial cells, where it appears to be selectively involved in endothelial cell migration, suggesting a role in endothelial barrier repair.

Indexed as

Protein C DeficiencyAdultCell Adhesion Molecule-1Cell Adhesion MoleculesCells, CulturedChromosome MappingChromosomes, Human, Pair 10Chromosomes, Human, Pair 11Chromosomes, Human, Pair 18Endothelium, VascularFemaleFluorescent Antibody TechniqueGene Expression ProfilingGenetic LinkageGenetic Predisposition to DiseaseGenome, HumanCADM1 protein, humanCell Adhesion Molecule-1Cell Adhesion MoleculesImmunoglobulinsMembrane ProteinsTumor Suppressor Proteins

Identifiers

PMID19643986
PMCPMC2756210
OpenAlexW1989740305

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.