Evidence map›Paper›PMID 18618017›Full record

ArticleThe Journal of clinical investigation2008

Sex differences in thrombosis in mice are mediated by sex-specific growth hormone secretion patterns.

Joshua H Wong, Jonathan Dukes, Robert E Levy, Brandon Sos, Sara E Mason, Tina S Fong, Ethan J Weiss

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Mouse models to study von Willebrand factor in thrombosis: a scoping review.Research and practice in thrombosis and haemostasis · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Sex-Dependent Occlusive Cardiovascular Disease Effects of Short-Term Thirdhand Smoke Exposure.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The sex and gender dimensions of COVID-19: A narrative review of the potential underlying factors.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2022
    Review
  13. Article
  14. Mouse models of growth hormone deficiency.Reviews in endocrine & metabolic disorders · 2021
    Review
  15. Article
  16. Article
  17. Article
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  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Joshua H WongCardiovascular Research Institute, Department of Medicine, Division of Cardiology, UCSF, San Francisco, California 94143-0124, USA.
Jonathan Dukes
Robert E Levy
Brandon Sos
Sara E Mason
Tina S Fong
Ethan J Weiss
University of California, San Francisco · US

Funding

Thrombin Signaling in Hemostasis and ThrombosisK08HL074922 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WEISS, ETHAN · 2004 to 2007
$487k
NHLBI NIH HHS K08 HL074922NHLBI NIH HHS K08 HL74922-01
6 · The paper itself

Abstract

Sex differences in thrombosis are well described, but their underlying mechanism(s) are not completely understood. Coagulation proteins are synthesized in the liver, and liver gene expression is sex specific and depends on sex differences in growth hormone (GH) secretion--males secrete GH in a pulsatile fashion, while females secrete GH continuously. Accordingly, we tested the hypothesis that sex-specific GH secretion patterns cause sex differences in thrombosis. Male mice were more susceptible to thrombosis than females in the thromboplastin-induced pulmonary embolism model and showed shorter clotting times ex vivo. GH-deficient little (lit) mice were protected from thrombosis, and pulsatile GH given to lit mice restored the male clotting phenotype. Moreover, pulsatile GH administration resulted in a male clotting phenotype in control female mice, while continuous GH caused a female clotting phenotype in control male mice. Expression of the coagulation inhibitors Proc, Serpinc1, Serpind1, and Serpina5 were strongly modulated by sex-specific GH patterns, and GH modulated resistance to activated protein C. These results reveal what we believe to be a novel mechanism whereby sex-specific GH patterns mediate sex differences in thrombosis through coordinated changes in the expression of coagulation inhibitor genes in the liver.

Indexed as

Sex CharacteristicsAnimalsFemaleGrowth HormoneLiverMaleMiceMice, Inbred StrainsMice, Mutant StrainsThrombosisGrowth Hormone

Identifiers

PMID18618017
PMCPMC2447928
OpenAlexW2009614797

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.