Evidence map›Paper›PMID 29961584›Full record

ArticleJournal of biomechanics2018

Effects of reproduction on sexual dimorphisms in rat bone mechanics.

Chantal M J de Bakker, Hongbo Zhao, Wei-Ju Tseng, Yihan Li, Allison R Altman-Singles, Yang Liu, Laurel Leavitt, X Sherry Liu

Abstract read
In one paragraph

Article in Journal of biomechanics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. TGFβ Regulation of Perilacunar/Canalicular Remodeling Is Sexually Dimorphic.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  8. Review
  9. Article
  10. 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

8 authors at 1 institution in 2 countries.

Chantal M J de BakkerMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States. Electronic address: chantald@seas.upenn.edu.
Hongbo ZhaoMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States; Key Laboratory of Biorheological Science and Technology, Ministry of Education and Bioengineering College, Chongqing University, Chongqing, China. Electronic address: zhhongbo@pennmedicine.upenn.edu.
Wei-Ju TsengMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States. Electronic address: weits@pennmedicine.upenn.edu.
Yihan LiMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States. Electronic address: yihanl@seas.upenn.edu.
Allison R Altman-SinglesMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States; Pennsylvania State University, Berks Campus, Reading, PA, United States. Electronic address: ara5093@psu.edu.
Yang LiuMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States; Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China. Electronic address: liuyang2@upenn.edu.
Laurel LeavittMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States. Electronic address: leavittl@seas.upenn.edu.
X Sherry LiuMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States. Electronic address: xiaoweil@pennmedicine.upenn.edu.
University of Pennsylvania · US

Funding

Overall: Resource-based Center for Musculoskeletal Disorders Research (Overall Application)P30AR069619 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LOUIS J SOSLOWSKY · 2016 to 2026
$9.1M
Effects of reproduction and lactation on postmenopausal bone health.R01AR071718 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LIU, XIAOWEI SHERRY · 2017 to 2021
$1.8M
The effect of parathyroid hormone on modeling-based bone formationK01AR066743 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LIU, XIAOWEI SHERRY · 2015 to 2018
$511k
Bone structure and strength recovery and the role of PTHrP post lactationR03AR065145 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LIU, XIAOWEI SHERRY · 2014 to 2016
$240k
NIAMS NIH HHS K01 AR066743NIAMS NIH HHS P30 AR069619NIAMS NIH HHS R01 AR071718NIAMS NIH HHS R03 AR065145
6 · The paper itself

Abstract

Osteoporosis most commonly affects postmenopausal women. Although men are also affected, women over 65 are 6 times more likely to develop osteoporosis than men of the same age. This is largely due to accelerated bone remodeling after menopause; however, the peak bone mass attained during young adulthood also plays an important role in osteoporosis risk. Multiple studies have demonstrated sexual dimorphisms in peak bone mass, and additionally, the female skeleton is significantly altered during pregnancy/lactation. Although clinical studies suggest that a reproductive history does not increase the risk of developing postmenopausal osteoporosis, reproduction has been shown to induce long-lasting alterations in maternal bone structure and mechanics, and the effects of pregnancy and lactation on maternal peak bone quality are not well understood. This study compared the structural and mechanical properties of male, virgin female, and post-reproductive female rat bone at multiple skeletal sites and at three different ages. We found that virgin females had a larger quantity of trabecular bone with greater trabecular number and more plate-like morphology, and, relative to their body weight, had a greater cortical bone size and greater bone strength than males. Post-reproductive females had altered trabecular microarchitecture relative to virgins, which was highly similar to that of male rats, and showed similar cortical bone size and bone mechanics to virgin females. This suggests that, to compensate for future reproductive bone losses, females may start off with more trabecular bone than is mechanically necessary, which may explain the paradox that reproduction induces long-lasting changes in maternal bone without increasing postmenopausal fracture risk.

Indexed as

Mechanical PhenomenaSex CharacteristicsAnimalsBiomechanical PhenomenaBone and BonesBone DensityBone RemodelingFemaleMalePregnancyRatsReproductionBone mechanical propertiesBone microarchitectureLactationPubertyReproductionSexual dimorphism

Identifiers

PMID29961584
PMCPMC6481170
OpenAlexW2810914421

What OpenQuestion 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 OpenQuestion graph.