Evidence map›Paper›PMID 38477760›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2024

RNA-based bone histomorphometry: method and its application to explaining postpubertal bone gain in a G610C mouse model of osteogenesis imperfecta.

Elena Makareeva, Megan Sousa, Tristan Kent, Luis F de Castro, Michael T Collins, Sergey Leikin

Open access · hybridAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
  3. New lens on congenital mild bone fragility: a novel Col1a1 knockout mouse model for osteogenesis imperfecta type 1.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
    Article
  4. 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

6 authors at 1 institution in 1 country.

Elena MakareevaEunice Kennedy Shriver National institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States.
Megan SousaEunice Kennedy Shriver National institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States.
Tristan KentNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, United States.
Luis F de CastroNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0003-3194-9780
Michael T CollinsNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, United States.
Sergey LeikinEunice Kennedy Shriver National institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0001-7095-0739
National Institutes of Health · US

Funding

Collagen-related diseases ZIAHD000256 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI LEIKIN, SERGEY · 2009 to 2025
$19.7M
NIDCR NIH HHSNIH HHS
6 · The paper itself

Abstract

Bone histomorphometry is a well-established approach to assessing skeletal pathology, providing a standard evaluation of the cellular components, architecture, mineralization, and growth of bone tissue. However, it depends in part on the subjective interpretation of cellular morphology by an expert, which introduces bias. In addition, diseases like osteogenesis imperfecta (OI) and fibrous dysplasia are accompanied by changes in the morphology and function of skeletal tissue and cells, hindering consistent evaluation of some morphometric parameters and interpretation of the results. For instance, traditional histomorphometry combined with collagen turnover markers suggested that reduced bone formation in classical OI is accompanied by increased bone resorption. In contrast, the well-documented postpubertal reduction in fractures would be easier to explain by reduced bone resorption after puberty, highlighting the need for less ambiguous measurements. Here we propose an approach to histomorphometry based on in situ mRNA hybridization, which uses Col1a1 as osteoblast and Ctsk as osteoclast markers. This approach can be fully automated and eliminates subjective identification of bone surface cells. We validate these markers based on the expression of Bglap, Ibsp, and Acp5. Comparison with traditional histological and tartrate-resistant acid phosphatase staining of the same sections suggests that mRNA-based analysis is more reliable. Unlike inconclusive traditional histomorphometry of mice with α2(I)-Gly610 to Cys substitution in the collagen triple helix, mRNA-based measurements reveal reduced osteoclastogenesis in 11-wk-old animals consistent with the postpubertal catch-up osteogenesis observed by microCT. We optimize the technique for cryosections of mineralized bone and sections of paraffin-embedded decalcified tissue, simplifying and broadening its applications. We illustrate the application of the mRNA-based approach to human samples using the example of a McCune-Albright syndrome patient. By eliminating confounding effects of altered cellular morphology and the need for subjective morphological evaluation, this approach may provide a more reproducible and accessible evaluation of bone pathology.

Indexed as

Bone and BonesCollagen Type IDisease Models, AnimalOsteogenesis ImperfectaAnimalsBiomarkersCollagen Type I, alpha 1 ChainMiceOsteoblastsOsteoclastsOsteogenesisPubertyRNA, MessengerBiomarkersCollagen Type ICollagen Type I, alpha 1 ChainRNA, Messengerbone histomorphometrymRNA hybridizationosteoblastsosteoclastsosteogenesis imperfecta

Identifiers

PMID38477760
PMCPMC11207954
OpenAlexW4390600715

What OpenQuestion holds

Textmetadata
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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.