Evidence map›Paper›PMID 36895792›Full record

ReviewFrontiers in cell and developmental biology2023

The benefits of adipocyte metabolism in bone health and regeneration.

Lisa-Marie Burkhardt, Christian H Bucher, Julia Löffler, Charlotte Rinne, Georg N Duda, Sven Geissler, Tim J Schulz, Katharina Schmidt-Bleek

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. The importance of B cells for osteogenic homeostasis.Cell communication and signaling : CCS · 2026
    Article
  2. The Intimate Relationship between Adipose Tissue, Fertility, and Bone.Journal of frailty, sarcopenia and falls · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Fracture nonunions.OTA international : the open access journal of orthopaedic trauma · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. 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

8 authors at 4 institutions in 1 country.

Lisa-Marie BurkhardtJulius Wolff Institute, Berlin Institute of Health (BIH) Charité, Berlin, Germany.
Christian H BucherJulius Wolff Institute, Berlin Institute of Health (BIH) Charité, Berlin, Germany.
Julia LöfflerJulius Wolff Institute, Berlin Institute of Health (BIH) Charité, Berlin, Germany.
Charlotte RinneDepartment of Adipocyte Development and Nutrition, German Institute of Human Nutrition, Potsdam-Rehbrücke, Nuthetal, Germany.
Georg N DudaJulius Wolff Institute, Berlin Institute of Health (BIH) Charité, Berlin, Germany.
Sven GeisslerJulius Wolff Institute, Berlin Institute of Health (BIH) Charité, Berlin, Germany.
Tim J SchulzDepartment of Adipocyte Development and Nutrition, German Institute of Human Nutrition, Potsdam-Rehbrücke, Nuthetal, Germany.
Katharina Schmidt-BleekJulius Wolff Institute, Berlin Institute of Health (BIH) Charité, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEGerman Institute of Human Nutrition · DEHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients suffering from musculoskeletal diseases must cope with a diminished quality of life and an increased burden on medical expenses. The interaction of immune cells and mesenchymal stromal cells during bone regeneration is one of the key requirements for the restoration of skeletal integrity. While stromal cells of the osteo-chondral lineage support bone regeneration, an excessive accumulation of cells of the adipogenic lineage is thought to promote low-grade inflammation and impair bone regeneration. Increasing evidence indicates that pro-inflammatory signaling from adipocytes is responsible for various chronic musculoskeletal diseases. This review aims to summarize the features of bone marrow adipocytes by phenotype, function, secretory features, metabolic properties and their impact on bone formation. In detail, the master regulator of adipogenesis and prominent diabetes drug target, peroxisome proliferator-activated receptor γ (PPARG), will be debated as a potential therapeutic approach to enhance bone regeneration. We will explore the possibilities of using clinically established PPARG agonists, the thiazolidinediones (TZDs), as a treatment strategy to guide the induction of a pro-regenerative, metabolically active bone marrow adipose tissue. The impact of this PPARG induced bone marrow adipose tissue type on providing the necessary metabolites to sustain osteogenic-as well as beneficial immune cells during bone fracture healing will be highlighted.

Indexed as

adipocytesbone marrow adipose tissue (BMAT)bone regenerationimmune cellsinflammationmesenchymal stromal cells (MSCs)peroxisome proliferator-activated receptor γ (PPARG) agoniststhiazolidinediones

Identifiers

PMID36895792
PMCPMC9988968
OpenAlexW4321459368

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.