Evidence map›Paper›PMID 37479877›Full record

ArticleMolecular biology reports2023

Study on the association of the microstructure and bone metabolism in the osteoporotic femoral head.

Cheng Wang, Peng Wang, Feng Li, Yang Li, Minwei Zhao, Hui Feng, Haoye Meng, Junyang Li, Peng Shi, Jiang Peng and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

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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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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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

11 authors at 3 institutions in 2 countries.

Cheng Wang *Department of Orthopaedics/Engineering Research Center of Bone and Joint Precision Medicine, Ministry of Education /Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Peng Wang *Institute of Orthopaedics, Beijing Key Laboratory of Regenerative Medicine in Orthopedics/Key Laboratory of Musculoskeletal Trauma & War Injuries PLA/The Fourth Medical Center of the General Hospital of People's Liberation Army, Beijing, 100853, China.
Feng Li *Department of Orthopaedics/Engineering Research Center of Bone and Joint Precision Medicine, Ministry of Education /Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Yang LiDepartment of Orthopaedics/Engineering Research Center of Bone and Joint Precision Medicine, Ministry of Education /Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Minwei ZhaoDepartment of Orthopaedics/Engineering Research Center of Bone and Joint Precision Medicine, Ministry of Education /Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Hui FengDepartment of Orthopaedics/Engineering Research Center of Bone and Joint Precision Medicine, Ministry of Education /Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China.
Haoye MengInstitute of Orthopaedics, Beijing Key Laboratory of Regenerative Medicine in Orthopedics/Key Laboratory of Musculoskeletal Trauma & War Injuries PLA/The Fourth Medical Center of the General Hospital of People's Liberation Army, Beijing, 100853, China.
Junyang LiDepartment of Electronic Engineering, Ocean University of China, Qingdao, China.
Peng ShiCentre for Robotics and Automation, Shenzhen Research Institute of City University of Hong Kong, Shenzhen, China.
Jiang PengInstitute of Orthopaedics, Beijing Key Laboratory of Regenerative Medicine in Orthopedics/Key Laboratory of Musculoskeletal Trauma & War Injuries PLA/The Fourth Medical Center of the General Hospital of People's Liberation Army, Beijing, 100853, China. pengjiang301@126.com.
Hua TianDepartment of Orthopaedics/Engineering Research Center of Bone and Joint Precision Medicine, Ministry of Education /Beijing Key Laboratory of Spinal Disease Research, Peking University Third Hospital, 49 North Garden Road, Haidian District, Beijing, 100191, China. tianhua@bjmu.edu.cn.ORCID http://orcid.org/0000-0001-7139-3372
Peking University · CNCity University of Hong Kong · HKChinese PLA General Hospital · CN

Funding

Bethune Charitable Foundation G-X-2019-1107-8International Science and Technology Cooperation Programme No.BYSYZD2019037National Natural Science Foundation of China 82001481National Natural Science Foundation of China U20A20194
6 · The paper itself

Abstract

backgroundWe compared the bone microstructure and metabolism of the femoral heads in patients with osteoporosis (OP) and non-OP patients to investigate the pathologic mechanism of OP and guide clinical treatment. METHODS AND

resultsFrom January 2020 to June 2021, we obtained femoral head samples from 30 patients undergoing hip replacement due to femoral neck fracture. All patients were women aged approximately 67 to 80 years (mean age, 74 years). According to the dual-energy X-ray results, the femoral head samples were divided into the OP (T< - 2.5) and non-OP (T > - 1.5) groups. Microcomputed tomography scanning, bone metrology analysis, hematoxylin and eosin staining, and Masson's trichrome staining were used to compare the local bone trabecular microstructure changes. Quantitative reverse transcription PCR was performed to identify changes in the osteogenesis-related genes and the osteoclast-related genes in specific regions to reflect osteogenic and osteoclastic activities. Femoral heads with OP showed significant changes in the local bone microstructure. Bone density, bone volume fraction, and the number and thickness of the bone trabeculae decreased. Local bone metabolism was imbalanced in the areas with microstructural changes in femoral heads with OP, with increased osteoclast activity and decreased osteoblast activity.

conclusionsDeterioration of bone microstructure is closely related to abnormal bone metabolism associated with the activity of osteoblasts and osteoclasts in osteoporotic femoral heads. Promoting bone formation by improving local bone metabolism, enhancing osteogenic activity and inhibiting osteoclast activity may be a promising way of preventing local OP and osteoporotic fractures.

Indexed as

Femur HeadOsteoporosisAgedFemaleHumansMaleOsteoclastsOsteogenesisX-Ray MicrotomographyBone metabolismBone microstructureFemoral headOsteoporosis

Identifiers

PMID37479877
PMCPMC10460722
OpenAlexW4385064399

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LicenceCC BY
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Registered trials

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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.