Evidence map›Paper›PMID 37239938›Full record

ReviewInternational journal of molecular sciences2023

NOD-like Receptors-Emerging Links to Obesity and Associated Morbidities.

Sarah Bauer, Lucy Hezinger, Fjolla Rexhepi, Sheela Ramanathan, Thomas A Kufer

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Pattern Recognition by NOD-Like Receptors.Advances in experimental medicine and biology · 2025
    Review
  9. Mechanistic insights from inflammasome structures.Nature reviews. Immunology · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. 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

5 authors at 2 institutions in 2 countries.

Sarah BauerInstitute of Nutritional Medicine, Department of Immunology, University of Hohenheim, 70593 Stuttgart, Germany.
Lucy HezingerInstitute of Nutritional Medicine, Department of Immunology, University of Hohenheim, 70593 Stuttgart, Germany.ORCID 0000-0002-2670-6365
Fjolla RexhepiDepartment of Immunology and Cell Biology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
Sheela RamanathanDepartment of Immunology and Cell Biology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
Thomas A KuferInstitute of Nutritional Medicine, Department of Immunology, University of Hohenheim, 70593 Stuttgart, Germany.ORCID 0000-0003-4563-0412
University of Hohenheim · DEUniversité de Sherbrooke · CA

Funding

CIHR CIHR- 202003PJT-437040
6 · The paper itself

Abstract

Obesity and its associated metabolic morbidities have been and still are on the rise, posing a major challenge to health care systems worldwide. It has become evident over the last decades that a low-grade inflammatory response, primarily proceeding from the adipose tissue (AT), essentially contributes to adiposity-associated comorbidities, most prominently insulin resistance (IR), atherosclerosis and liver diseases. In mouse models, the release of pro-inflammatory cytokines such as TNF-alpha (TNF-α) and interleukin (IL)-1β and the imprinting of immune cells to a pro-inflammatory phenotype in AT play an important role. However, the underlying genetic and molecular determinants are not yet understood in detail. Recent evidence demonstrates that nucleotide-binding and oligomerization domain (NOD)-like receptor (NLR) family proteins, a group of cytosolic pattern recognition receptors (PRR), contribute to the development and control of obesity and obesity-associated inflammatory responses. In this article, we review the current state of research on the role of NLR proteins in obesity and discuss the possible mechanisms leading to and the outcomes of NLR activation in the obesity-associated morbidities IR, type 2 diabetes mellitus (T2DM), atherosclerosis and non-alcoholic fatty liver disease (NAFLD) and discuss emerging ideas about possibilities for NLR-based therapeutic interventions of metabolic diseases.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceAnimalsCarrier ProteinsInflammasomesMiceMorbidityNLR Family, Pyrin Domain-Containing 3 ProteinNLR ProteinsObesityTumor Necrosis Factor-alphaCarrier ProteinsInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNLR ProteinsTumor Necrosis Factor-alphaHFDIL-1βinflammasomeinsulin resistancemicrobiotaNLRC5NLRP12NLRP3NOD1NOD2

Identifiers

PMID37239938
PMCPMC10218625
OpenAlexW4378515487

What Socratic holds

Textmetadata
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 Socratic graph.