Evidence map›Paper›PMID 28081773›Full record

ReviewMetabolism: clinical and experimental2017

Mechanisms of marrow adiposity and its implications for skeletal health.

Annegreet G Veldhuis-Vlug, Clifford J Rosen

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Metabolism: clinical and experimental, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07056322 (Optimal Meals to Reduce Bone Resorption in Women With Osteopenia), which is not on this map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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.

NCT07056322 naenrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Optimal Meals to Reduce Bone Resorption in Women With Osteopenia

TypeinterventionalSponsorUniversity of AarhusRan2025 to 2026Enrolled13ConditionsOsteopeniaArms200 ml dairy, 100 ml milk, 100 g banana, 100 ml dairy and fibers, Fasting (control)
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Association of proton-density fat fraction with osteoporosis: a systematic review and meta-analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2024
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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

2 authors at 2 institutions in 2 countries.

Annegreet G Veldhuis-VlugDepartment of Endocrinology and Metabolism, Academic Medical Center Amsterdam, The Netherlands. Electronic address: a.g.veldhuis-vlug@amc.uva.nl.
Clifford J RosenMaine Medical Center Research Institute, Scarborough, ME, USA. Electronic address: rosenc@mmc.org.
Academic Medical Center · NLMaine Medical Center Research Institute · US

Funding

Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
PTH resistance and marrow adipogenesisR56DK112374 · NIDDK · HARVARD MEDICAL SCHOOL · PI MANNSTADT, BEATE, ROSEN, CLIFFORD JAMES · 2016 to 2016
$85k
NIDDK NIH HHS R24 DK092759NIDDK NIH HHS R56 DK112374
6 · The paper itself

Abstract

The bone marrow niche is composed of cells from hematopoietic and mesenchymal origin. Both require energy to power differentiation and these processes are intimately connected to systemic metabolic homeostasis. Glycolysis is the preferred substrate for mesenchymal stromal cells in the niche, although fatty acid oxidation and glutaminolysis are important during stage specific differentiation. Autophagy and lipophagy, in part triggered by adenosine monophosphate-activated protein kinase (AMPK), may also play an important but temporal specific role in osteoblast differentiation. Enhanced marrow adiposity is caused by clinical factors that are genetically, environmentally, and hormonally mediated. These determinants mediate a switch from the osteogenic to the adipogenic lineage. Preliminary evidence supports an important role for fuel utilization in those cell fate decisions. Although both the origin and function of the marrow adipocyte remain to be determined, and in some genetic mouse models high marrow adiposity may co-exist with greater bone mass, in humans changes in marrow adiposity are closely linked to adverse changes in skeletal metabolism. This supports an intimate relationship between bone and fat in the marrow. Future studies will likely shed more light on the relationship of cellular as well as whole body metabolism on the ultimate fate of bone marrow stromal cells.

Indexed as

AdipocytesAdiposityAnimalsBone and BonesBone DensityBone MarrowEnergy MetabolismHumansOsteoblastsAdipocyteBone marrow adiposityEnergy utilizationMesenchymal stem cellOsteoblast

Identifiers

PMID28081773
PMCPMC5325679
OpenAlexW2552167083

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.