Evidence map›Paper›PMID 28442421›Full record

ArticleAnaerobe2017

Distinct roles for dietary lipids and Porphyromonas gingivalis infection on atherosclerosis progression and the gut microbiota.

Carolyn D Kramer, Alexandra M Simas, Xianbao He, Robin R Ingalls, Ellen O Weinberg, Caroline Attardo Genco

Abstract read
In one paragraph

Article in Anaerobe, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 21% 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, 40 citations in OpenAlex.

  1. Article
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  4. Periodontal bacteria influence systemic diseases through the gut microbiota.Frontiers in cellular and infection microbiology · 2024
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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

6 authors at 2 institutions in 1 country.

Carolyn D KramerDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, 650 Albany Street, Boston, MA 02118, USA; Department of Integrative Physiology and Pathobiology, Tufts University School of Medicine, 136 Harrison Ave, M & V 701, Boston, MA 02111, USA. Electronic address: carolyn.kramer@tufts.edu.
Alexandra M SimasDepartment of Integrative Physiology and Pathobiology, Tufts University School of Medicine, 136 Harrison Ave, M & V 701, Boston, MA 02111, USA; Graduate Program in Biochemical and Molecular Nutrition, Gerald J. and Dorothy R. Friedman School of Nutrition and Science Policy, Tufts University, Boston, MA 02111, USA. Electronic address: alexandra.simas@tufts.edu.
Xianbao HeDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, 650 Albany Street, Boston, MA 02118, USA; Boston Medical Center, Evans Biomedical Research Center, 650 Albany Street, Boston, MA 02118, USA. Electronic address: xhe@bu.edu.
Robin R IngallsDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, 650 Albany Street, Boston, MA 02118, USA; Boston Medical Center, Evans Biomedical Research Center, 650 Albany Street, Boston, MA 02118, USA. Electronic address: ringalls@bu.edu.
Ellen O WeinbergDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, 650 Albany Street, Boston, MA 02118, USA; Department of Integrative Physiology and Pathobiology, Tufts University School of Medicine, 136 Harrison Ave, M & V 701, Boston, MA 02111, USA. Electronic address: ellen.weinberg@tufts.edu.
Caroline Attardo GencoDepartment of Medicine, Section of Infectious Diseases, Boston University School of Medicine, 650 Albany Street, Boston, MA 02118, USA; Department of Integrative Physiology and Pathobiology, Tufts University School of Medicine, 136 Harrison Ave, M & V 701, Boston, MA 02111, USA; Graduate Program in Immunology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Ave, M & V 701, Boston, MA 02111, USA; Graduate Program in Microbiology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, 136 Harrison Ave, M & V 701, Boston, MA 02111, USA. Electronic address: caroline.genco@tufts.edu.
Boston University · USTufts University · US

Funding

Role of Innate Immune System in Pathogen Induced Chronic InflammationP01AI078894 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GENCO, CAROLINE A · 2010 to 2014
$7.4M
Research Training Program in Nutrition, Obesity and Metabolic DisordersT32DK062032 · NIDDK · TUFTS UNIVERSITY BOSTON · PI GREENBERG, ANDREW S · 2002 to 2016
$2.6M
NIAID NIH HHS P01 AI078894NIDDK NIH HHS T32 DK062032
6 · The paper itself

Abstract

Mounting evidence in humans supports an etiological role for the microbiota in inflammatory atherosclerosis. Atherosclerosis is a progressive disease characterized by accumulation of inflammatory cells and lipids in vascular tissue. While retention of lipoprotein into the sub-endothelial vascular layer is believed to be the initiating stimulus leading to the development of atherosclerosis, activation of multiple pathways related to vascular inflammation and endothelial dysfunction sustain the process by stimulating recruitment of leukocytes and immune cells into the sub-endothelial layer. The Gram-negative oral pathogen Porphyromonas gingivalis has been associated with the development and acceleration of atherosclerosis in humans and these observations have been validated in animal models. It has been proposed that common mechanisms of immune signaling link stimulation by lipids and pathogens to vascular inflammation. Despite the common outcome of P. gingivalis and lipid feeding on atherosclerosis progression, we established that these pro-atherogenic stimuli induced distinct gene signatures in the ApoE

Indexed as

Gastrointestinal MicrobiomeLipid MetabolismAnimalsAtherosclerosisBacterial InfectionsDisease Models, AnimalGastrointestinal TractMaleMice, Inbred C57BLPorphyromonas gingivalisAtherosclerosisGut microbiotaImmunityInflammationLipidsOral microbiota

Identifiers

PMID28442421
PMCPMC5521207
OpenAlexW2606294814

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.