Evidence map›Paper›PMID 33210060›Full record

ArticleJBMR plus2020

Obesity Represses CYP2R1, the Vitamin D 25-Hydroxylase, in the Liver and Extrahepatic Tissues.

Mahmoud-Sobhy Elkhwanky, Outi Kummu, Terhi T Piltonen, Johanna Laru, Laure Morin-Papunen, Maija Mutikainen, Pasi Tavi, Jukka Hakkola

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 2 pooled it
5.2field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

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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 2 institutions in 1 country.

Mahmoud-Sobhy ElkhwankyResearch Unit of Biomedicine, Pharmacology and Toxicology University of Oulu Oulu Finland.
Outi KummuResearch Unit of Biomedicine, Pharmacology and Toxicology University of Oulu Oulu Finland.
Terhi T PiltonenDepartment of Obstetrics and Gynecology, PEDEGO Research Unit, Medical Research Center Oulu University Hospital, University of Oulu Oulu Finland.
Johanna LaruDepartment of Obstetrics and Gynecology, PEDEGO Research Unit, Medical Research Center Oulu University Hospital, University of Oulu Oulu Finland.
Laure Morin-PapunenDepartment of Obstetrics and Gynecology, PEDEGO Research Unit, Medical Research Center Oulu University Hospital, University of Oulu Oulu Finland.
Maija MutikainenA.I. Virtanen Institute for Molecular Sciences University of Eastern Finland Kuopio Finland.
Pasi TaviA.I. Virtanen Institute for Molecular Sciences University of Eastern Finland Kuopio Finland.
Jukka HakkolaResearch Unit of Biomedicine, Pharmacology and Toxicology University of Oulu Oulu Finland.ORCID https://orcid.org/0000-0001-5048-4363
Oulu University Hospital · FIUniversity of Eastern Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low plasma level of 25-hydroxyvitamin D (25-OH-D), namely vitamin D deficiency, is associated with obesity and weight loss improves 25-OH-D status. However, the mechanism behind obesity-induced vitamin D deficiency remains unclear. Here, we report that obesity suppresses the expression of cytochrome P450 (CYP) 2R1, the main vitamin D 25-hydroxylase, in both mice and humans. In humans, weight loss induced by gastric bypass surgery increased the expression of CYP2R1 in the s.c. adipose tissue suggesting recovery after the obesity-induced suppression. At the same time, CYP27B1, the vitamin D 1α-hydroxylase, was repressed by the weight loss. In a mouse (C57BL/6N) model of diet-induced obesity, the plasma 25-OH-D was decreased. In accordance, the CYP2R1 expression was strongly repressed in the liver. Moreover, obesity repressed the expression of CYP2R1 in several extrahepatic tissues, the kidney, brown adipose tissue, and testis, but not in the white adipose tissue. Obesity had a similar effect in both male and female mice. In mice, obesity repressed expression of the vitamin D receptor in brown adipose tissue. Obesity also upregulated the expression of the vitamin D receptor and CYP24A1 in the s.c. adipose tissue of a subset of mice; however, no effect was observed in the human s.c. adipose tissue. In summary, we show that obesity affects CYP2R1 expression both in the mouse and human tissues. We suggest that in mouse the CYP2R1 repression in the liver plays an important role in obesity-induced vitamin D deficiency. Currently, it is unclear whether the CYP2R1 downregulation in extrahepatic tissues could contribute to the obesity-induced low plasma 25-OH-D, however, this phenomenon may affect at least the local 25-OH-D concentrations. © 2020 The Authors.

Indexed as

25‐HYDROXYVITAMIN DCYP24A1CYP27B1CYP2R1HIGH‐FAT DIETOBESITYVITAMIN DVITAMIN D RECEPTOR

Identifiers

PMID33210060
PMCPMC7657391
OpenAlexW3044791914

What OpenQuestion 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 OpenQuestion graph.