Evidence map›Paper›PMID 34512556›Full record

ReviewFrontiers in endocrinology2021

Endogenous Glucocorticoid Metabolism in Bone: Friend or Foe.

Claire S Martin, Mark S Cooper, Rowan S Hardy

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Structural and Metabolic Changes in Bone.Animals : an open access journal from MDPI · 2022
    Review
  13. Article
  14. Pathophysiology of Mild Hypercortisolism: From the Bench to the Bedside.International journal of molecular sciences · 2022
    Review
  15. Article
  16. 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 2 institutions in 2 countries.

Claire S MartinInstitute of Metabolism and Systems Research, University of Birmingham, Birmingham, United Kingdom.
Mark S CooperAustralian and New Zealand Army Corps (ANZAC) Research Institute, University of Sydney, Sydney, NSW, Australia.
Rowan S HardyArthritis Research United Kingdom (UK) Career Development Fellow, University of Birmingham, Birmingham, United Kingdom.
University of Birmingham · GBUniversity of Sydney · AU

Funding

Medical Research Council MR/P021220/1Versus Arthritis 20843Wellcome Trust 215243/Z/19/Z
6 · The paper itself

Abstract

The role of tissue specific metabolism of endogenous glucocorticoids (GCs) in the pathogenesis of human disease has been a field of intense interest over the last 20 years, fuelling clinical trials of metabolism inhibitors in the treatment of an array of metabolic diseases. Localised pre-receptor metabolism of endogenous and therapeutic GCs by the 11β-hydroxysteroid dehydrogenase (11β-HSD) enzymes (which interconvert endogenous GCs between their inactive and active forms) are increasingly recognised as being critical in mediating both their positive and negative actions on bone homeostasis. In this review we explore the roles of endogenous and therapeutic GC metabolism by the 11β-HSD enzymes in the context of bone metabolism and bone cell function, and consider future strategies aimed at modulating this system in order to manage and treat various bone diseases.

Indexed as

11-beta-Hydroxysteroid DehydrogenasesAnimalsBone and BonesBone DevelopmentBone DiseasesGlucocorticoidsHumans11-beta-Hydroxysteroid DehydrogenasesGlucocorticoids11beta-hydroxysteroid dehydrogenasebonechronic inflammationglucocorticoidosteoblastosteoclastosteoporosis

Identifiers

PMID34512556
PMCPMC8429897
OpenAlexW3198617935

What OpenQuestion 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 OpenQuestion graph.