Evidence map›Paper›PMID 39528064›Full record

ArticleBone2025

Calorie restriction induces mandible bone loss by regulating mitochondrial function.

Linyi Liu, Phuong T Le, Victoria E DeMambro, Tiange Feng, Hanghang Liu, Wangyang Ying, Roland Baron, Clifford J Rosen

Erratum issuedAbstract read
In one paragraph

Article in Bone, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Bone as an endocrine regulator of lipid and energy metabolism.Reviews in endocrine & metabolic disorders · 2026
    Review
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Linyi LiuMaineHealth Institute for Research, Scarborough, ME 04074, USA. Electronic address: Linyi.Liu@mainehealth.org.
Phuong T LeMaineHealth Institute for Research, Scarborough, ME 04074, USA. Electronic address: Phuong.Le@mainehealth.org.
Victoria E DeMambroMaineHealth Institute for Research, Scarborough, ME 04074, USA. Electronic address: victoria.demambro@mainehealth.org.
Tiange FengMaineHealth Institute for Research, Scarborough, ME 04074, USA. Electronic address: Tiange.Feng@mainehealth.org.
Hanghang LiuWest China Hospital of Stomatology, Sichuan University, Sichuan, China.
Wangyang YingSchool of Computing and Augmented Intelligence, Arizona State University, Tempe, AZ 85281, USA. Electronic address: wangyang.ying@asu.edu.
Roland BaronDivision of Bone and Mineral Research, Dept of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, Boston, MA 02115, USA. Electronic address: roland_baron@hsdm.harvard.edu.
Clifford J RosenMaineHealth Institute for Research, Scarborough, ME 04074, USA. Electronic address: Clifford.Rosen@mainehealth.org.

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Robert A Koza · 2017 to 2026
$51.6M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Lucy Liaw · 2017 to 2026
$25.1M
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 AR073774NIGMS NIH HHS P20 GM121301NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

Caloric restriction (CR), commonly used as both a lifestyle choice and medical strategy, has been shown to adversely impact appendicular bone mass. However, its influence on alveolar bone health and the underlying mechanisms remain poorly understood. In this study, 8-week-old C57BL/6 J mice were fed with 30 % CR for 8 weeks. Micro-architecture, histologic parameters, and in vitro trajectories of osteoblast and adipocyte differentiation were examined. To further explore the underlying mechanisms, metabolic cages and in vitro bioenergetics were performed. Our results showed that 8 weeks of CR led to trabecular and cortical bone loss in the mandibles of female mice. CR in female mice decreased bone formation and bone resorption activities but induced adiposity in the mandibles. After CR, the adipogenesis in mesenchymal cells from orofacial bones (OMSCs) was greatly accelerated, whereas osteogenic differentiation was reduced in females. Undifferentiated CR OMSCs showed marked suppression in ATP production rates from mitochondria in female mice. ATP production rates decreased after osteogenesis but were upregulated during adipogenesis in female mice. Conversely, the generation of reactive oxygen species (ROS) was heightened during both osteoblastic and adipogenic differentiation in female CR groups. Collectively, our study indicated that CR could cause significant bone loss in the mandibles of female mice, almost certainly related to a reduced ATP supply and the unregulated generation of ROS.

Indexed as

AdipogenesisCaloric RestrictionMandibleMice, Inbred C57BLMitochondriaOsteogenesisReactive Oxygen SpeciesAdenosine TriphosphateAdipocytesAnimalsBone ResorptionCell DifferentiationFemaleMesenchymal Stem CellsMiceOsteoblastsAdenosine TriphosphateReactive Oxygen SpeciesAlveolar bone lossBone-fat balanceCalorie restrictionEnergy metabolismMesenchymal cells

Identifiers

PMID39528064
PMCPMC11618829

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.