Evidence map›Paper›PMID 39342093›Full record

ArticleMolecular medicine (Cambridge, Mass.)2024

SOST/Sclerostin impairs the osteogenesis and angiogesis in glucocorticoid-associated osteonecrosis of femoral head.

Junming Huang, Tianle Ma, Chenzhong Wang, Zhe Wang, Xinyuan Wang, Bingxuan Hua, Chang Jiang, Zuoqin Yan

Abstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  4. Bone reports · 2026
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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.

Junming HuangDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China.ORCID 0000-0002-6800-2788
Tianle MaDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China.
Chenzhong WangDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China.
Zhe WangDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China.
Xinyuan WangDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China.
Bingxuan HuaDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China.
Chang JiangDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China. cjiang_fdu@yeah.net.
Zuoqin YanDepartment of Orthopaedics, Zhongshan Hospital, Fudan University, 180 Feng Lin Road, Xuhui District, Shanghai, 200032, China. yan.zuoqin@zs-hospital.sh.cn.

Funding

China Postdoctoral Science Foundation 2023M741520National Natural Science Foundation of China 81871742National Natural Science Foundation of China 82001471National Natural Science Foundation of China 82172413National Natural Science Foundation of China 82300994Natural Science Foundation of Jiangxi Province 20232BAB216034
6 · The paper itself

Abstract

backgroundGlucocorticoid-associated osteonecrosis of the femoral head (GA-ONFH) is a progressive bone disorder which frequently results in femoral head collapse and hip joint dysfunction. Sclerostin (SOST) is principally secreted by osteocytes in bone and plays an important role in bone homeostasis and homeostasis of skeletal integrity. Our previous study reported that short-term use of glucocorticoid increased serum sclerostin levels. Here this study is aimed to identify whether sclerostin played an essential role in the occurrence and development of GA-ONFH.

methodsGlucocorticoid-induced osteonecrosis of femoral head (ARCO stage II) samples were collected and sclerostin staining was conducted. Osteocyte cell line Ocy454, MC3T3-E1 and endothelial cells was used. MC3T3-E1 or endothelial cells were co-cultured with Ocy454 or SOST-silencing Ocy454 in presence of dexamethasone to mimic the crosstalk of various cells in the bone niche. GA-ONFH rat model and SOST knockout model was built to better understand the phenomenon in vivo.

resultsSclerostin was highly concentrated in osteonecrosis patient sample in the necrotic area. Co-culture with osteocytes aggravated the inhibition of dexamethasone on MC3T3-E1 and endothelial cells. Sclerostin derived from osteocytes impaired osteogenesis and angiogenesis via inhibiting the Wnt pathway. In GA-ONFH rat model, SOST knockout ameliorated the incidence of osteonecrosis and improved bone metabolism compared with the wild type group through histological, immunohistochemical and bone metabolic analyses.

conclusionSclerostin contribute to pathologic process of GA-ONFH by impairing osteogenesis and angiogenesis.

Indexed as

Adaptor Proteins, Signal TransducingFemur Head NecrosisGlucocorticoidsOsteocytesOsteogenesisAnimalsCell LineCoculture TechniquesDexamethasoneDisease Models, AnimalEndothelial CellsFemaleGenetic MarkersHumansMaleMiceAdaptor Proteins, Signal TransducingDexamethasoneGenetic MarkersGlucocorticoidsSOST protein, humanSost protein, mouseAngiogenesisOsteocytesOsteogenesisOsteonecrosis of femoral head (ONFH)Sclerostin (SOST)

Identifiers

PMID39342093
PMCPMC11439244

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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.