Evidence map›Paper›PMID 35216140›Full record

ReviewInternational journal of molecular sciences2022

New Function of Cholesterol Oxidation Products Involved in Osteoporosis Pathogenesis.

Yanting Che, Jingzhi Yang, Fen Tang, Ziheng Wei, Yufan Chao, Na Li, Henghui Li, Si Wu, Xin Dong

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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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 3 institutions in 2 countries.

Yanting CheCollege of Sciences, Shanghai University, Shanghai 200444, China.
Jingzhi YangInstitute of Translational Medicine, Shanghai University, Shanghai 200444, China.
Fen TangSchool of Medicine, Shanghai University, Shanghai 200444, China.
Ziheng WeiDepartment of Orthopedics, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 201620, China.
Yufan ChaoSchool of Medicine, Shanghai University, Shanghai 200444, China.
Na LiSchool of Medicine, Shanghai University, Shanghai 200444, China.
Henghui LiInstitute of Translational Medicine, Shanghai University, Shanghai 200444, China.
Si WuDepartment of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-8050-7167
Xin DongInstitute of Translational Medicine, Shanghai University, Shanghai 200444, China.
Shanghai University · CNShanghai Jiao Tong University · CNStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoporosis (OP) is a systemic bone disease characterized by decreased bone strength, microarchitectural changes in bone tissues, and increased risk of fracture. Its occurrence is closely related to various factors such as aging, genetic factors, living habits, and nutritional deficiencies as well as the disturbance of bone homeostasis. The dysregulation of bone metabolism is regarded as one of the key influencing factors causing OP. Cholesterol oxidation products (COPs) are important compounds in the maintenance of bone metabolic homeostasis by participating in several important biological processes such as the differentiation of mesenchymal stem cells, bone formation in osteoblasts, and bone resorption in osteoclasts. The effects of specific COPs on mesenchymal stem cells are mainly manifested by promoting osteoblast genesis and inhibiting adipocyte genesis. This review aims to elucidate the biological roles of COPs in OP development, starting from the molecular mechanisms of OP, pointing out opportunities and challenges in current research, and providing new ideas and perspectives for further studies of OP pathogenesis.

Indexed as

AnimalsBone and BonesBone ResorptionCholesterolHumansOsteoblastsOsteogenesisOsteoporosisOxidation-ReductionCholesterol20S-hydroxycholesterol (20S-HC)22S-hydroxycholesterol (22S-HC)27-hydroxycholesterol (27-HC)cholesterol oxidation products (COPs)osteoporosis (OP)

Identifiers

PMID35216140
PMCPMC8876989
OpenAlexW4213337665

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.