Evidence map›Paper›PMID 37892484›Full record

ReviewNutrients2023

Calcifediol: Mechanisms of Action.

Simone Donati, Gaia Palmini, Cinzia Aurilia, Irene Falsetti, Francesca Marini, Francesca Giusti, Teresa Iantomasi, Maria Luisa Brandi

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Nutrients · 2024
    Article
  7. Role of Calcitriol and Vitamin D Receptor (International journal of molecular sciences · 2024
    Review
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 1 country.

Simone DonatiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.
Gaia PalminiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.ORCID 0000-0002-8376-7404
Cinzia AuriliaDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.
Irene FalsettiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.
Francesca MariniFondazione Italiana Ricerca Sulle Malattie dell'Osso (FIRMO Onlus), 50129 Florence, Italy.ORCID 0000-0002-3678-4922
Francesca GiustiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.ORCID 0000-0002-8576-9606
Teresa IantomasiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.ORCID 0000-0001-7461-330X
Maria Luisa BrandiFondazione Italiana Ricerca Sulle Malattie dell'Osso (FIRMO Onlus), 50129 Florence, Italy.ORCID 0000-0002-8741-0592
University of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to its essential role in calcium and phosphate homeostasis, the secosteroid hormone calcitriol has received growing attention over the last few years. Calcitriol, like other steroid hormones, may function through both genomic and non-genomic mechanisms. In the traditional function, the interaction between the biologically active form of vitamin D and the vitamin D receptor (VDR) affects the transcription of thousands of genes by binding to repeated sequences present in their promoter region, named vitamin D-responsive elements (VDREs). Non-transcriptional effects, on the other hand, occur quickly and are unaffected by inhibitors of transcription and protein synthesis. Recently, calcifediol, the immediate precursor metabolite of calcitriol, has also been shown to bind to the VDR with weaker affinity than calcitriol, thus exerting gene-regulatory properties. Moreover, calcifediol may also trigger rapid non-genomic responses through its interaction with specific membrane vitamin D receptors. Membrane-associated VDR (mVDR) and protein disulfide isomerase family A member 3 (Pdia3) are the best-studied candidates for mediating these rapid responses to vitamin D metabolites. This paper provides an overview of the calcifediol-related mechanisms of action, which may help to better understand the vitamin D endocrine system and to identify new therapeutic targets that could be important for treating diseases closely associated with vitamin D deficiency.

Indexed as

CalcifediolCalcitriolGene Expression RegulationHomeostasisReceptors, CalcitriolVitamin DCalcifediolCalcitriolReceptors, CalcitriolVitamin Dcalcifediolcalcitriolgenomic actionsmembrane-associated rapid response to steroidnon-genomic actionsvitamin Dvitamin D deficiencyvitamin D receptor

Identifiers

PMID37892484
PMCPMC10610216
OpenAlexW4387707569

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.