Evidence map›Paper›PMID 40846895›Full record

ReviewNature reviews. Endocrinology2025

The role of bone in whole-body energy metabolism.

Beata Lecka-Czernik, Clifford J Rosen, Nicola Napoli

Abstract readReview
In one paragraph

Review in Nature reviews. Endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Gut microbes · 2026
    Article
  2. Article
  3. Review
  4. Bone organoids and mitochondrial reprogramming.Journal of orthopaedic translation · 2026
    Review
  5. Article
  6. Review
  7. Hematopoietic stem cell transplantation-associated partial lipodystrophy.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2026
    Review
  8. Article
  9. Myeloid-Specific Deletion ofBiomedicines · 2026
    Article
  10. Bone as an endocrine regulator of lipid and energy metabolism.Reviews in endocrine & metabolic disorders · 2026
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Ciliary-Mediated Mechanotransduction in Skeletal Development and Diseases.Results and problems in cell differentiation · 2026
    Review
  17. Review
  18. Article
  19. Article
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.

Beata Lecka-CzernikDepartment of Orthopaedic Surgery, University of Toledo Health Sciences Campus, Toledo, OH, USA. beata.leckaczernik@utoledo.edu.ORCID http://orcid.org/0000-0002-1216-9634
Clifford J RosenMaineHealth Institute for Research, Scarborough, ME, USA.ORCID http://orcid.org/0000-0003-3436-8199
Nicola NapoliClinical Unit of Unit of Metabolic Bone and Thyroid Disorders, Fondazione Policlinico Campus Bio-Medico, Rome, Italy.ORCID http://orcid.org/0000-0002-3091-8205

Funding

PPARG regulates osteocyte bioenergetics and function during agingR01AG071332 · NIA · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI GRIFFIN, PATRICK ROBERT, LECKA-CZERNIK, BEATA ANNA · 2021 to 2025
$3.4M
Mechanism of action of PTH: New signaling components that regulate bone formation and bone marrow fatR01AR073774 · NIAMS · HARVARD MEDICAL SCHOOL · PI BARON, ROLAND E, ROSEN, CLIFFORD JAMES · 2020 to 2024
$2.8M
NIAMS NIH HHS R01 AR073774NIA NIH HHS R01 AG071332
6 · The paper itself

Abstract

The skeleton is one of the largest organs in the body and is integrated with systemic energy metabolism. This integration is mediated in part through the process of skeletal remodelling, which is fundamental for maintenance of bone mass and quality. Remodelling is an energetically expensive process that contributes to energy balance owing to constant substrate flow to the skeleton in the form of glucose, lipids and amino acids, as well as output of hormonal factors regulating peripheral metabolism. Bone remodelling is orchestrated by osteocytes, the most abundant cells in bone. Hence, it stands to reason that osteocytes must also regulate substrate availability and utilization not only for their own function but also for those of other skeletal cells (namely, osteoblasts and osteoclasts). Osteocytes also secrete factors (such as osteokines) that are engaged in complex molecular signalling networks that influence glucose metabolism, insulin sensitivity and energy homeostasis. Importantly, whole-body metabolism and bone homeostasis share similar regulatory mechanisms, including the RANKL and parathyroid hormone signalling pathways. This Review summarizes our current understanding of how the skeleton regulates whole-body energy metabolism and leads to the conclusion that bone might not be the core regulator of systemic energy metabolism but rather acts as an organ that instead regulates these complex processes.

Indexed as

Bone and BonesEnergy MetabolismAnimalsBone RemodelingHomeostasisHumansOsteocytesSignal Transduction

Identifiers

PMID40846895
PMCPMC13460304

What Socratic 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 Socratic graph.