Evidence map›Paper›PMID 30806214›Full record

ReviewCritical reviews in immunology2018

Function of Pro-Resolving Lipid Mediator Resolvin E1 in Type 2 Diabetes.

Corneliu Sima, Bruce Paster, Thomas E Van Dyke

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  4. Article
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  6. Review
  7. Review
  8. Article
  9. Modeling human heterogeneity of obesity with diversity outbred mice reveals a fat mass-dependent therapeutic window for resolvin E1.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Resolvin E1 derived from eicosapentaenoic acid prevents hyperinsulinemia and hyperglycemia in a host genetic manner.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  17. 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

3 authors at 1 institution in 1 country.

Corneliu SimaCenter for Clinical and Translational Research, The Forsyth Institute, Cambridge, MA 02142, USA; Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Harvard Medical School, Boston, MA, 02115, USA.
Bruce PasterCenter for Clinical and Translational Research, The Forsyth Institute, Cambridge, MA 02142, USA; Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Harvard Medical School, Boston, MA, 02115, USA.
Thomas E Van DykeCenter for Clinical and Translational Research, The Forsyth Institute, Cambridge, MA 02142, USA; Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Harvard Medical School, Boston, MA, 02115, USA.
Harvard University · US

Funding

Innate immunity and autoantibodies in the pathogenesis of Sjogren's SyndromeR01DE025030 · NIDCR · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI DESHMUKH, UMESH S · 2016 to 2020
$2.2M
Roles for lymphocyte RANKL in periodontal complications of type 2 diabetesR01DE025383 · NIDCR · UNIVERSITY OF KENTUCKY · PI NIKOLAJCZYK, BARBARA, VAN DYKE, THOMAS ELLIOTT · 2016 to 2017
$1.2M
Regulation of Inflammation in T2D-Associated PeriodontitisR00DE024575 · NIDCR · HARVARD MEDICAL SCHOOL · PI SIMA, CORNELIU · 2018 to 2020
$725k
M1/M2 Regulation of Inflammation in T2D-Associated PeriodontitisK99DE024575 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI SIMA, CORNELIU · 2015 to 2016
$244k
NIDCR NIH HHS K99 DE024575NIDCR NIH HHS R00 DE024575NIDCR NIH HHS R01 DE025030NIDCR NIH HHS R01 DE025383
6 · The paper itself

Abstract

Programming of inflammation resolution is governed by a class of specialized pro-resolving lipid mediators (SPMs) that act in concert to modulate epithelial, endothelial, and immune cell function for restoration of homeostasis. The resolution circuits are altered in obesity and associated morbidities, including type 2 diabetes mellitus (T2D), through reduced production and/or action of SPMs, which can be rescued by therapeutic SPM delivery or up-regulation of SPM receptors. Resolvin E1 (RvE1), an eicosapentaenoic acid derivative, has potent pro-resolving and insulin-sensitizing actions mediated by BLT1 and ERV1 receptors in the vasculature and metabolic organs. Nonetheless, the RvE1-mediated increase in protective adipokines such as adiponectin in white adipose tissues, the enhancement of monocyte patrolling function in the vasculature, as well as the macrophage-clearing functions improve metabolic control in obese-prone conditions. RvE1-enhanced resolving function in obesity prevents dysbiosis of the gut microflora and increased gut permeability. These functions suggest that RE1 has therapeutic potential for immunometabolic alterations associated with T2D in patients with reduced inflammation resolving capacity. SPM profiling in individuals at risk for T2D and associated complications will help to advance personalized disease management and precision medicine.

Indexed as

AnimalsDiabetes Mellitus, Type 2Eicosapentaenoic AcidHumansLipids5S,12R,18R-trihydroxy-6Z,8E,10E,14Z,16E-eicosapentaenoic acidEicosapentaenoic AcidLipids

Identifiers

PMID30806214
PMCPMC6392080
OpenAlexW2890994536

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.