Evidence map›Paper›PMID 24914939›Full record

ArticleEndocrinology2014

FGF-21 and skeletal remodeling during and after lactation in C57BL/6J mice.

Sheila Bornstein, Sue A Brown, Phuong T Le, Xunde Wang, Victoria DeMambro, Mark C Horowitz, Ormond MacDougald, Roland Baron, Sutada Lotinun, Gerard Karsenty and 6 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

50 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. FGF-based drug discovery: advances and challenges.Nature reviews. Drug discovery · 2025
    Review
  6. Article
  7. Article
  8. Observational
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. FGF/FGFR signaling in health and disease.Signal transduction and targeted therapy · 2020
    Review
  20. 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

16 authors at 10 institutions in 2 countries.

Sheila BornsteinMaine Medical Center Research Institute (S.B., P.T.L., V.D., C.J.R.), Scarborough, Maine 04074; Division of Endocrinology, University of Virginia (S.A.B.), Charlottesville, Virginia 22904; Division of Pharmacology (X.W., W.W., Y.W.), University of Texas Southwestern, Dallas, Texas 75390; Department of Orthopaedics and Rehabilitation (M.C.H.), Yale University School of Medicine, New Haven, Connecticut 06510; Metabolism, Endocrinology and Diabetes Division (O.M.), University of Michigan, Ann Arbor, Michigan 48105; Harvard Dental School (R.B., S.L.), Boston, Massachusetts 02115; Department of Genetics (G.K., M.F.), Columbia University College of Physicians and Surgeons, New York, New York 10032; Division of Endocrinology (C.S.K.), Memorial University, St. John's, Newfoundland, Canada A1B 3V6; and Division of Endocrinology (D.C.), University of North Carolina Chapel Hill, Chapel Hill, North Carolina 27599.
Sue A Brown
Phuong T Le
Xunde Wang
Victoria DeMambro
Mark C Horowitz
Ormond MacDougald
Roland Baron
Sutada Lotinun
Gerard Karsenty
Wei Wei
Mathieu Ferron
Christopher S Kovacs
David Clemmons
Yihong Wan
Clifford J Rosen
Maine Medical Center Research Institute · USThe University of Texas Southwestern Medical Center · USColumbia University · USHarvard University · USMaine Medical Center · USMemorial University of Newfoundland · CAUniversity of Michigan–Ann Arbor · USUniversity of North Carolina at Chapel Hill · USUniversity of Virginia · USYale University · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILLIAM H HERMAN · 2013 to 2026
$24.3M
Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
Phase III COBRE in Vascular BiologyP30GM103392 · NIGMS · MAINEHEALTH · PI ST. GERMAIN, DONALD L. · 2012 to 2016
$4.7M
Regulation of Cbfal function by TwistR01AR045548 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KARSENTY, GERARD · 1998 to 2012
$4.6M
COBRE in Stem Cell Biology and Regenerative MedicineP20GM103465 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2012 to 2012
$2.0M
Connection of Mineral and Energy Metabolism by the Nuclear Receptor PPAR-gammaR01DK089113 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI WAN, YIHONG · 2011 to 2015
$1.8M
Bone Accrual and Hormones in Response to LactationK23AR051483 · NIAMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BROWN, SUE A · 2004 to 2008
$631k
CIHR 84253NIAMS NIH HHS 5R01AR45548NIAMS NIH HHS K23 AR051483NIAMS NIH HHS K32 AR051483-06NIAMS NIH HHS R01 AR045548NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK089113NIDDK NIH HHS R01DK089113NIDDK NIH HHS R24 DK092759NIGMS NIH HHS P20 GM103465NIGMS NIH HHS P30 GM103392NIGMS NIH HHS P30 GM106391PHS HHS NIDDK R24 092759
6 · The paper itself

Abstract

Lactation is associated with significant alterations in both body composition and bone mass. Systemic and local skeletal factors such as receptor activator of nuclear factor κ-B ligand (RANKL), PTHrP, calcitonin, and estrogen are known to regulate bone remodeling during and after lactation. Fibroblast growth factor 21 (FGF-21) may function as an endocrine factor to regulate body composition changes during lactation by inducing gluconeogenesis and fatty acid oxidation. In this study, we hypothesized that the metabolic changes during lactation were due in part to increased circulating FGF-21, which in turn could accentuate bone loss. We longitudinally characterized body composition in C57BL/6J (B6) mice during (day 7 and day 21 of lactation) and after normal lactation (day 21 postlactation). At day 7 of lactation, areal bone density declined by 10% (P < .001), bone resorption increased (P < .0001), percent fat decreased by 20%, energy expenditure increased (P < .01), and markers of brown-like adipogenesis were suppressed in the inguinal depot and in preformed brown adipose tissue. At day 7 of lactation there was a 2.4-fold increase in serum FGF-21 vs baseline (P < .0001), a 8-fold increase in hepatic FGF-21 mRNA (P < .03), a 2-fold increase in undercarboxylated osteocalcin (Glu13 OCn) (P < .01), and enhanced insulin sensitivity. Recovery of total areal bone density was noted at day 21 of lactation, whereas the femoral trabecular bone volume fraction was still reduced (P < .01). Because FGF-21 levels rose rapidly at day 7 of lactation in B6 lactating mice, we next examined lactating mice with a deletion in the Fgf21 gene. Trabecular and cortical bone masses were maintained throughout lactation in FGF-21(-/-) mice, and pup growth was normal. Compared with lactating control mice, lactating FGF-21(-/-) mice exhibited an increase in bone formation, but no change in bone resorption. In conclusion, in addition to changes in calciotropic hormones, systemic FGF-21 plays a role in skeletal remodeling and changes in body composition during lactation in B6 mice.

Indexed as

Bone RemodelingLactationAnimalsBone and BonesBone DensityBone ResorptionFemaleFibroblast Growth FactorsLiverMaleMiceMice, Inbred C57BLPregnancyfibroblast growth factor 21Fibroblast Growth Factors

Identifiers

PMID24914939
PMCPMC4138567
OpenAlexW2129533800

What OpenQuestion holds

Textmetadata
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.