Evidence map›Paper›PMID 34049522›Full record

ArticleBMC musculoskeletal disorders2021

Changes in macrophage and inflammatory cytokine expressions during fracture healing in an ovariectomized mice model.

Lin Chen, Shao Cheng, Kanghui Sun, Jing Wang, Xinhua Liu, Yongjian Zhao, Junjie Yang, Dongfeng Zhao, Chunchun Xue, Yuren Tao and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  17. Animals : an open access journal from MDPI · 2022
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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

16 authors at 3 institutions in 1 country.

Lin Chen *Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Shao Cheng *Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Kanghui Sun *Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Jing WangLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Xinhua LiuExperiment Center for Science and Technology, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.
Yongjian ZhaoLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Junjie YangLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Dongfeng ZhaoLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Chunchun XueLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Yuren TaoLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Shitian ZhaoLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Hao ZhangLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Sheng LuLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Qi ShiLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Yongjun WangLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Bing ShuLonghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China. siren17721101@163.com.
Shanghai University of Traditional Chinese Medicine · CNMinistry of Education of the People's Republic of China · CNLonghua Hospital Shanghai University of Traditional Chinese Medicine · CN

Funding

the National Key R&D Program of China 2018YFC1704302the National Natural Science Foundation of China 81730107the National Natural Science Foundation of China 81804122the National Natural Science Foundation of China 81929004the National Natural Science Foundation of China 81973876the National Natural Science Foundation of China 82004183the Postgraduates' Training Project of Shanghai University of Traditional Chinese Medicine Y2019010the Program for Innovative Research Team, Ministry of Education of China IRT1270the Program for Innovative Research Team, Ministry of Science and Technology of China 2015RA4002The research program of Shanghai Municipal Health Commission 20174Y0192the Shanghai Sailing Program 19YF1445300the Three Year Action Program, Shanghai Municipal Health Commission ZY(2018-2020)-CCCX-3003
6 · The paper itself

Abstract

backgroundMacrophages and inflammatory cytokines play important roles in bone fracture healing. However, the expression patterns of macrophages and inflammatory cytokines during fracture healing under the condition of postmenopausal osteoporosis have not been fully revealed.

methodsTibia transverse fracture was established 12 weeks after ovariectomy or sham operation in 16-week old female mice. Tibias were harvested before fracture or 1, 3, 5, 7, 14, 21, 28 days after fracture for radiological and histological examinations. M1/M2 inflammatory macrophages, osteal macrophages and gene expressions of tumor necrosis factor-α, interleukin-6, interleukin-1β and macrophage conversion related molecules in the fracture haematoma or callus were also detected.

resultsThe processes of fracture healing, especially the phases of endochondral ossification and callus remodeling, were delayed in ovariectomized mice. The expressions of tumor necrosis factor-α and interleukin-6, but not interleukin-1β, in the fracture haematoma or callus were disturbed. Expressions of tumor necrosis factor-α were decreased at 1, 14 and 21 days post-fracture (DPF), and were increased at 3, 5 and 7 DPF. Interleukin-6 expressions at 1, 3 and 21 DPF were significantly increased. We found the decreases in M1 and M2 macrophages at 1 DPF of the initial inflammatory stage. M2 macrophages at 14 DPF of the middle stage and osteal macrophages at 14, 21 and 28 DPF of the middle and late stages of fracture healing were also reduced in ovariectomized mice.

conclusionsThe expressions of macrophages and inflammatory cytokines were impaired in ovariectomized mice, which might contribute partially to poor fracture healing.

Indexed as

Fracture HealingTibial FracturesAnimalsBony CallusCytokinesFemaleHumansMacrophagesMiceCytokinesFracture healingInterleukin-6MacrophageOvariectomyTumor necrosis factor-α

Identifiers

PMID34049522
PMCPMC8164289
OpenAlexW3164733202

What OpenQuestion holds

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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.