Evidence map›Paper›PMID 18627265›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2008

Calcitonin receptor plays a physiological role to protect against hypercalcemia in mice.

Rachel A Davey, Andrew G Turner, Julie F McManus, W S Maria Chiu, Francisca Tjahyono, Alison J Moore, Gerald J Atkins, Paul H Anderson, Cathy Ma, Vaida Glatt and 6 more

Open access · greenAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact, top 95% 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

29 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Regulation of 1 and 24 hydroxylation of vitamin D metabolites in the proximal tubule.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  6. Article
  7. The Sperm Olfactory Receptor OLFR601 is Dispensable for Mouse Fertilization.Frontiers in cell and developmental biology · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Insight into Evolution and Conservation Patterns of B1-Subfamily Members of GPCR.International journal of peptide research and therapeutics · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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 6 institutions in 2 countries.

Rachel A DaveyDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia. r.davey@unimelb.edu.au
Andrew G Turner
Julie F McManus
W S Maria Chiu
Francisca Tjahyono
Alison J Moore
Gerald J Atkins
Paul H Anderson
Cathy Ma
Vaida Glatt
Helen E MacLean
Cristina Vincent
Mary Bouxsein
Howard A Morris
David M Findlay
Jeffrey D Zajac
Austin Health · AUHanson Institute · AUUniversity of Melbourne · AUBeth Israel Deaconess Medical Center · USHarvard University · USUniversity of Adelaide · AU

Funding

MICROCOMPUTED TOMOGRAPHY DEVICE (SCANCO UCT40): PHYSIOLOGYS10RR017868 · NCRR · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUXSEIN, MARY L · 2004 to 2004
$220k
NCRR NIH HHS S10 RR017868
6 · The paper itself

Abstract

It is well established that calcitonin is a potent inhibitor of bone resorption; however, a physiological role for calcitonin acting through its cognate receptor, the calcitonin receptor (CTR), has not been identified. Data from previous genetically modified animal models have recognized a possible role for calcitonin and the CTR in controlling bone formation; however, interpretation of these data are complicated, in part because of their mixed genetic background. Therefore, to elucidate the physiological role of the CTR in calcium and bone metabolism, we generated a viable global CTR knockout (KO) mouse model using the Cre/loxP system, in which the CTR is globally deleted by >94% but <100%. Global CTRKOs displayed normal serum ultrafiltrable calcium levels and a mild increase in bone formation in males, showing that the CTR plays a modest physiological role in the regulation of bone and calcium homeostasis in the basal state in mice. Furthermore, the peak in serum total calcium after calcitriol [1,25(OH)(2)D(3)]-induced hypercalcemia was substantially greater in global CTRKOs compared with controls. These data provide strong evidence for a biological role of the CTR in regulating calcium homeostasis in states of calcium stress.

Indexed as

Acid PhosphataseActinsAnimalsCalcitoninCalcitriolCalciumFemaleFemurGene DeletionGene TargetingHypercalcemiaIntegrasesIsoenzymesMaleMiceMice, Inbred C57BLAcid PhosphataseActinsCalcitoninCalcitriolCalciumCre recombinaseIntegrasesIsoenzymesReceptors, CalcitoninTartrate-Resistant Acid Phosphatase

Identifiers

PMID18627265
PMCPMC2680171
OpenAlexW1577004313

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.