Evidence map›Paper›PMID 27512386›Full record

ArticleFrontiers in endocrinology2016

Changes in Skeletal Integrity and Marrow Adiposity during High-Fat Diet and after Weight Loss.

Erica L Scheller, Basma Khoury, Kayla L Moller, Natalie K Y Wee, Shaima Khandaker, Kenneth M Kozloff, Simin H Abrishami, Brian F Zamarron, Kanakadurga Singer

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing 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

80 citing papers in PubMed.

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  13. Role of Body Fat and Metabolic Rate in Site-Specific Fracture Risk: A 20-Year Taiwanese Cohort Study.Medical science monitor : international medical journal of experimental and clinical research · 2025
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20 more citing papers are in PubMed but not listed here.

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

9 authors.

Erica L SchellerDivision of Bone and Mineral Diseases, Department of Medicine, Washington University, St. Louis, MO, USA; Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
Basma KhouryDepartment of Orthopaedic Surgery, University of Michigan , Ann Arbor, MI , USA.
Kayla L MollerDivision of Bone and Mineral Diseases, Department of Medicine, Washington University , St. Louis, MO , USA.
Natalie K Y WeeOsteoporosis and Bone Biology Division, Garvan Institute of Medical Research, Darlinghurst , Sydney, NSW , Australia.
Shaima KhandakerDepartment of Molecular and Integrative Physiology, University of Michigan , Ann Arbor, MI , USA.
Kenneth M KozloffDepartment of Orthopaedic Surgery, University of Michigan , Ann Arbor, MI , USA.
Simin H AbrishamiDivision of Pediatric Endocrinology, Department of Pediatrics and Communicable Diseases, University of Michigan Medical School , Ann Arbor, MI , USA.
Brian F ZamarronGraduate Program in Immunology, University of Michigan , Ann Arbor, MI , USA.
Kanakadurga SingerDivision of Pediatric Endocrinology, Department of Pediatrics and Communicable Diseases, University of Michigan Medical School , Ann Arbor, MI , USA.

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILLIAM H HERMAN · 2013 to 2026
$24.3M
University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
Training in Basic and Translational Digestive SciencesT32DK094775 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JOHN Y KAO, LINDA C. SAMUELSON · 2012 to 2026
$3.6M
Neural regulation of skeletal biology and periodontal disease progression in typeR00DE024178 · NIDCR · WASHINGTON UNIVERSITY · PI SCHELLER, ERICA LYNN · 2016 to 2018
$735k
Mechanisms of hematopoietic stem cell activation in obesityK08DK101755 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SINGER, KANAKADURGA · 2015 to 2018
$644k
Neural regulation of skeletal biology and periodontal disease progression in typeK99DE024178 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHELLER, ERICA LYNN · 2014 to 2015
$203k
NIDCR NIH HHS K99 DE024178NIDCR NIH HHS R00 DE024178NIDDK NIH HHS K08 DK101755NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK034933NIDDK NIH HHS T32 DK094775
6 · The paper itself

Abstract

The prevalence of obesity has continued to rise over the past three decades leading to significant increases in obesity-related medical care costs from metabolic and non-metabolic sequelae. It is now clear that expansion of body fat leads to an increase in inflammation with systemic effects on metabolism. In mouse models of diet-induced obesity, there is also an expansion of bone marrow adipocytes. However, the persistence of these changes after weight loss has not been well described. The objective of this study was to investigate the impact of high-fat diet (HFD) and subsequent weight loss on skeletal parameters in C57Bl6/J mice. Male mice were given a normal chow diet (ND) or 60% HFD at 6 weeks of age for 12, 16, or 20 weeks. A third group of mice was put on HFD for 12 weeks and then on ND for 8 weeks to mimic weight loss. After these dietary challenges, the tibia and femur were removed and analyzed by micro computed-tomography for bone morphology. Decalcification followed by osmium staining was used to assess bone marrow adiposity, and mechanical testing was performed to assess bone strength. After 12, 16, or 20 weeks of HFD, mice had significant weight gain relative to controls. Body mass returned to normal after weight loss. Marrow adipose tissue (MAT) volume in the tibia increased after 16 weeks of HFD and persisted in the 20-week HFD group. Weight loss prevented HFD-induced MAT expansion. Trabecular bone volume fraction, mineral content, and number were decreased after 12, 16, or 20 weeks of HFD, relative to ND controls, with only partial recovery after weight loss. Mechanical testing demonstrated decreased fracture resistance after 20 weeks of HFD. Loss of mechanical integrity did not recover after weight loss. Our study demonstrates that HFD causes long-term, persistent changes in bone quality, despite prevention of marrow adipose tissue accumulation, as demonstrated through changes in bone morphology and mechanical strength in a mouse model of diet-induced obesity and weight loss.

Indexed as

bonefracturehigh-fat dietleptinmarrow adipose tissuemarrow fatobesityweight loss

Identifiers

PMID27512386
PMCPMC4961699

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Registered trials

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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.