Evidence map›Paper›PMID 25773047›Full record

ArticleJournal of bone and mineral metabolism2016

Bone matrix calcification during embryonic and postembryonic rat calvarial development assessed by SEM-EDX spectroscopy, XRD, and FTIR spectroscopy.

Akiko Henmi, Hiroshi Okata, Takahisa Anada, Mariko Yoshinari, Yasuto Mikami, Osamu Suzuki, Yasuyuki Sasano

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of bone and mineral metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Multiscale Characterization of Embryonic Long Bone Mineralization in Mice.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  10. Article
  11. Article
  12. 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

7 authors at 1 institution in 1 country.

Akiko HenmiDivision of Craniofacial Development and Regeneration, Tohoku University Graduate School of Dentistry, Sendai, 980-8575, Japan.
Hiroshi OkataDivision of Periodontology and Endodontology, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Takahisa AnadaDivision of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Mariko YoshinariDivision of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Yasuto MikamiDivision of Craniofacial Development and Regeneration, Tohoku University Graduate School of Dentistry, Sendai, 980-8575, Japan.
Osamu SuzukiDivision of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry, Sendai, Japan.
Yasuyuki SasanoDivision of Craniofacial Development and Regeneration, Tohoku University Graduate School of Dentistry, Sendai, 980-8575, Japan. sasano@anat.dent.tohoku.ac.jp.
Tohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone mineral is constituted of biological hydroxyapatite crystals. In developing bone, the mineral crystal matures and the Ca/P ratio increases. However, how an increase in the Ca/P ratio is involved in maturation of the crystal is not known. The relationships among organic components and mineral changes are also unclear. The study was designed to investigate the process of calcification during rat calvarial bone development. Calcification was evaluated by analyzing the atomic distribution and concentration of Ca, P, and C with scanning electron microscopy (SEM)-energy-dispersive X-ray (EDX) spectroscopy and changes in the crystal structure with X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. Histological analysis showed that rat calvarial bone formation started around embryonic day 16. The areas of Ca and P expanded, matching the region of the developing bone matrix, whereas the area of C became localized around bone. X-ray diffraction and FTIR analysis showed that the amorphous-like structure of the minerals at embryonic day 16 gradually transformed into poorly crystalline hydroxyapatite, whereas the proportion of mineral to protein increased until postnatal week 6. FTIR analysis also showed that crystallization of hydroxyapatite started around embryonic day 20, by which time SEM-EDX spectroscopy showed that the Ca/P ratio had increased and the C/Ca and C/P ratios had decreased significantly. The study suggests that the Ca/P molar ratio increases and the proportion of organic components such as proteins of the bone matrix decreases during the early stage of calcification, whereas crystal maturation continues throughout embryonic and postembryonic bone development.

Indexed as

AnimalsBone MatrixCalcification, PhysiologicDurapatiteMaleMicroscopy, Electron, ScanningRatsSkullSpectroscopy, Fourier Transform InfraredX-Ray DiffractionDurapatiteAmorphous calcium phosphateBone developmentCalcificationHydroxyapatiteOrganic components

Identifiers

PMID25773047
OpenAlexW2152691067

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.