Evidence map›Paper›PMID 36574149›Full record

ArticleEndocrine2023

Levels of bioavailable, and free forms of 25(OH)D after supplementation with vitamin D

Lívia Marcela Dos Santos, Monique Nakayama Ohe, Sthefanie Giovanna Pallone, Isabela Ohki Nacaguma, Ilda Sizue Kunii, Renata Elen Costa da Silva, Sergio Setsuo Maeda, José Gilberto Henriques Vieira, Marise Lazaretti-Castro

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 37% 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 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Lívia Marcela Dos SantosDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil. endocrinolivia@gmail.com.ORCID 0000-0002-6590-6319
Monique Nakayama OheDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Sthefanie Giovanna PalloneDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Isabela Ohki NacagumaDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Ilda Sizue KuniiDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Renata Elen Costa da SilvaDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Sergio Setsuo MaedaDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
José Gilberto Henriques VieiraDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Marise Lazaretti-CastroDepartment of Medicine, Endocrinology Unit, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
Universidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 25 hydroxyvitamin D [25(OH)D] is the major metabolite for ascertaining vitamin D status, which circulates bound to a specific carrier (vitamin D-binding protein - VDBP). A portion that circulates unbound vary according to the VDBP genotype. This study evaluates the behavior of different forms of 25(OH)D, before and after supplementation with 14,000 IU of vitamin D3, weekly for 12 weeks, in individuals with primary hyperparathyroidism and controls. Fifty-six patients with active primary hyperparathyroidism (PHPT) and 64 paired controls (CTRL), not taking vitamin D3 for the last three months, were enrolled. The genetic isotypes of VDBP were determined to calculate bioavailable and free 25(OH)D. A p < 0.05 was considered significant. There were no statistical differences in free, bioavailable, and total 25(OH)D levels between PHPT and CTRL groups at baseline. The distribution of VDBP haplotypes 1s/1s, 1f/1f, 1s/1f, 2/2, 1s/2, and 1f/2 was similar between groups. After supplementation, all three forms of 25(OH)D proportionally increased within each group, although the percentage increment was lower in the PHPT group (p < 0.05). Total 25(OH)D is better correlated with PTH in the PHPT group than bioavailable and free 25(OH)D (r = -0.41; p < 0.05). The concentrations of total, free, and bioavailable 25(OH)D were similar in both PHPT and CTRL groups, and all forms increased proportionally after supplementation, although this increment percentage was higher in the CTRL group, with a subsequent reduction of PTH and AP. Total 25(OH)D correlated better with PTH than other forms, suggesting no advantages in measuring free or bioavailable 25(OH)D in these situations.

Indexed as

CholecalciferolHyperparathyroidism, PrimaryDietary SupplementsHumansVitamin DVitamin D-Binding Protein25-hydroxyvitamin DCholecalciferolVitamin DVitamin D-Binding ProteinBioavailable 25(OH)Dfree 25(OH)Dprimary hyperparathyroidismvitamin D-binding protein

Identifiers

PMID36574149
OpenAlexW4312211275

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.