Evidence map›Paper›PMID 26148065›Full record

ArticlePloS one2015

Specific Inflammatory Stimuli Lead to Distinct Platelet Responses in Mice and Humans.

Lea M Beaulieu, Lauren Clancy, Kahraman Tanriverdi, Emelia J Benjamin, Carolyn D Kramer, Ellen O Weinberg, Xianbao He, Samrawit Mekasha, Eric Mick, Robin R Ingalls and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Article
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  5. mFrontiers in immunology · 2021
    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

12 authors at 4 institutions in 1 country.

Lea M BeaulieuUniversity of Massachusetts Medical School, Department of Medicine, Division of Cardiovascular Medicine, Worcester, MA, United States of America.
Lauren ClancyUniversity of Massachusetts Medical School, Department of Medicine, Division of Cardiovascular Medicine, Worcester, MA, United States of America.
Kahraman TanriverdiUniversity of Massachusetts Medical School, Department of Medicine, Division of Cardiovascular Medicine, Worcester, MA, United States of America.
Emelia J BenjaminNHLBI and Boston Universitys Framingham Heart Institute, Framingham, MA, United States of America; Boston University School of Medicine, Department of Medicine, Cardiology and Preventive Medicine Section, Boston, MA, United States of America.
Carolyn D KramerBoston University School of Medicine, Department of Medicine, Boston, MA, United States of America.
Ellen O WeinbergBoston University School of Medicine, Department of Medicine, Boston, MA, United States of America.
Xianbao HeBoston University School of Medicine, Department of Medicine, Section of Infectious Diseases, Boston, MA, United States of America.
Samrawit MekashaBoston Medical Center, Boston, MA, United States of America.
Eric MickUniversity of Massachusetts Medical School, Department of Quantitative Health Sciences, Worcester, MA, United States of America.
Robin R IngallsBoston University School of Medicine, Department of Medicine, Boston, MA, United States of America; Boston Medical Center, Boston, MA, United States of America.
Caroline A GencoBoston University School of Medicine, Department of Medicine, Boston, MA, United States of America; Boston University School of Medicine, Department of Medicine, Section of Infectious Diseases, Boston, MA, United States of America; Boston University School of Medicine, Department of Microbiology, Boston, MA, United States of America.
Jane E FreedmanUniversity of Massachusetts Medical School, Department of Medicine, Division of Cardiovascular Medicine, Worcester, MA, United States of America.
University of Massachusetts Chan Medical School · USBoston University · USBoston Medical Center · USFramingham Heart Study · US

Funding

Translational Research Skills Development CoreU54HL112311 · NHLBI · UNIVERSITY OF UTAH · PI WEYRICH, ANDREW S, ZIMMERMAN, GUY A. · 2012 to 2016
$12.9M
Role of Innate Immune System in Pathogen Induced Chronic InflammationP01AI078894 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MADICO, GUILLERMO · 2010 to 2014
$7.4M
Framingham: Inflammation, Genes &Cardiovascular DiseaseR01HL076784 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J. · 2004 to 2008
$3.9M
Aging and Inflammation: Longitudinal Markers and Genetics in the Framingham StudyR01AG028321 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J. · 2006 to 2010
$1.8M
INFLAMMATION: CORRELATES AND PROGNOSIS IN FRAMINGHAMR01HL064753 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J. · 2000 to 2003
$1.2M
THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
–
NHLBI NIH HHS 1R01 HL64753NHLBI NIH HHS N01 HC025195NHLBI NIH HHS N01-HC 25195NHLBI NIH HHS P-01-HL085381NHLBI NIH HHS R01 HL076784NHLBI NIH HHS RFA-HL-12-008NHLBI NIH HHS U54 HL112311NIAID NIH HHS P01 AI078894NIA NIH HHS 1 R01 AG028321NIA NIH HHS R01 AG028321RMOD NIH HHS RFA-RM-12-013
6 · The paper itself

Abstract

introductionDiverse and multi-factorial processes contribute to the progression of cardiovascular disease. These processes affect cells involved in the development of this disease in varying ways, ultimately leading to atherothrombosis. The goal of our study was to compare the differential effects of specific stimuli--two bacterial infections and a Western diet--on platelet responses in ApoE-/- mice, specifically examining inflammatory function and gene expression. Results from murine studies were verified using platelets from participants of the Framingham Heart Study (FHS; n = 1819 participants).

methodsBlood and spleen samples were collected at weeks 1 and 9 from ApoE-/- mice infected with Porphyromonas gingivalis or Chlamydia pneumoniae and from mice fed a Western diet for 9 weeks. Transcripts based on data from a Western diet in ApoE-/- mice were measured in platelet samples from FHS using high throughput qRT-PCR.

resultsAt week 1, both bacterial infections increased circulating platelet-neutrophil aggregates. At week 9, these cells individually localized to the spleen, while Western diet resulted in increased platelet-neutrophil aggregates in the spleen only. Microarray analysis of platelet RNA from infected or Western diet-fed mice at week 1 and 9 showed differential profiles. Genes, such as Serpina1a, Ttr, Fgg, Rpl21, and Alb, were uniquely affected by infection and diet. Results were reinforced in platelets obtained from participants of the FHS.

conclusionUsing both human studies and animal models, results demonstrate that variable sources of inflammatory stimuli have the ability to influence the platelet phenotype in distinct ways, indicative of the diverse function of platelets in thrombosis, hemostasis, and immunity.

Indexed as

AnimalsApolipoproteins EAtherosclerosisBlood PlateletsChlamydophila pneumoniaeDiet, WesternDisease Models, AnimalHumansInflammationMaleMiceNeutrophilsPlatelet AggregationPorphyromonas gingivalisThrombosisApolipoproteins E

Identifiers

PMID26148065
PMCPMC4493099
OpenAlexW1925086491

What OpenQuestion holds

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LicenceCC BY
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.