Evidence map›Paper›PMID 31281179›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

The Impact of Vitamin D on Cognitive Dysfunction in Mice with Systemic Lupus Erythematosus.

Lijun Yan, Ping Wu, Dong-Mei Gao, Jie Hu, Qian Wang, Nan-Fang Chen, Sheng-Quan Tong, Li Rao, Jing Liu

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. 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
0.9field-weighted citation impact, top 26% 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, 16 citations in OpenAlex.

  1. Review
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  5. Review
  6. What is known about the effects of vitamin D in neuropsychiatric lupus?Advances in rheumatology (London, England) · 2024
    Review
  7. Article
  8. Article
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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

9 authors at 1 institution in 1 country.

Lijun YanDepartment of Rheumatology, Tangshan Gongren Hospita, Tangshan, Hebei, China (mainland).
Ping WuDepartment of Rheumatology, Tangshan Gongren Hospital, Tangshan, Hebei, China (mainland).
Dong-Mei GaoDepartment of Rheumatology, Tangshan Gongren Hospital, Tangshan, Hebei, China (mainland).
Jie HuDepartment of Rheumatology, Tangshan Gongren Hospital Group Rehabilitation Hospital, Tangshan, Hebei, China (mainland).
Qian WangDepartment of Rheumatology, Tangshan Gongren Hospital Group Rehabilitation Hospital, Tangshan, Hebei, China (mainland).
Nan-Fang ChenDepartment of Rheumatology, Tangshan Gongren Hospital Group Rehabilitation Hospital, Tangshan, Hebei, China (mainland).
Sheng-Quan TongDepartment of Rheumatology, Tangshan Gongren Hospital, Tangshan, Hebei, China (mainland).
Li RaoDepartment of Rheumatology, Tangshan Gongren Hospital, Tangshan, Hebei, China (mainland).
Jing LiuDepartment of Rheumatology, Tangshan Gongren Hospital, Tangshan, Hebei, China (mainland).
Tangshan Gongren Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

<strong>BACKGROUND</strong> A growing body of evidence suggests that systemic lupus erythematosus (SLE) may result in reversible cognitive dysfunction. Vitamin D is considered important for neurons. The therapeutic effect of vitamin D was evaluated in a rat model of SLE. <strong>MATERIAL AND METHODS</strong> There were 20 male MRL/lpr mice randomly divided into the SLE model group and the vitamin D group, in addition, 10 male C57BL 6J mice were used as the control (CON) group. Vitamin D was administered intraperitoneally (2 μg/kg) for 4 weeks. After 4 weeks of continuing intervention, we tested the cognitive function using the Morris water maze. The expression of vitamin D receptor (VDR), amyloid-ß, caspase-3, and Bcl-2 were detected by western blot analysis. <strong>RESULTS</strong> In the present study, we observed that vitamin D treatment alleviated neurobehavioral deficits in the mice with SLE. At the molecular levels, administration of vitamin D activated the expression of VDR and reduced the number of dead cells in the CA1 region of the hippocampus as well as regulated caspase-3 and Bcl-2 expression. <strong>CONCLUSIONS</strong> In conclusion, our results indicated that vitamin D played a protective role by suppressing inflammatory cytokines, thereby ultimately inhibiting the progression of apoptosis in a mouse model of SLE. Vitamin D may be promising as a protective intervention in SLE with cognitive dysfunction, and more and more experiments are warranted for its clinical testing in the near future.

Indexed as

Amyloid beta-PeptidesAnimalsCaspase 3Cognitive DysfunctionCytokinesHippocampusInflammation MediatorsInterferon-gammaInterleukin-2Lupus Erythematosus, SystemicMaleMice, Inbred C57BLMice, Inbred MRL lprProto-Oncogene Proteins c-bcl-2Time FactorsVitamin DAmyloid beta-PeptidesCaspase 3CytokinesInflammation MediatorsInterferon-gammaInterleukin-2Proto-Oncogene Proteins c-bcl-2Vitamin D

Identifiers

PMID31281179
PMCPMC6607939
OpenAlexW2953836408

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.