Evidence map›Paper›PMID 42359363›Full record

ArticleBioactive materials2026

Restoring cartilage-subchondral bone metabolism with biphasic magnesium microspheres ameliorate early osteoarthritis.

Tao Chen, Weiliang Zhi, Guangcheng Wu, Xiangming He, Hanbo Wang, Ziyue Wang, Xianyi Yang, Xiling Qi, Long Chen, Sixiang Rao and 8 more

Abstract read
In one paragraph

Article in Bioactive materials, 2026. 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
–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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Tao ChenCollege of Basic Medicine (Digital Medical Center) & The Second Affiliated Hospital, Inner Mongolia Medical University, Hohhot, 010059, PR China.
Weiliang ZhiSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Guangcheng WuSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Xiangming HeDepartment of Food and Nutrition, University of Helsinki, Helsinki, 00014, Finland.
Hanbo WangDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, NY, United States.
Ziyue WangSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Xianyi YangSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Xiling QiCollege of Basic Medicine (Digital Medical Center) & The Second Affiliated Hospital, Inner Mongolia Medical University, Hohhot, 010059, PR China.
Long ChenSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Sixiang RaoSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Liming ZhengOrthopedic Department, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310000, PR China.
Jiankun XuMusculoskeletal Research Laboratory, Department of Orthopedics and Traumatology, The Sir Yue-Kong Pao Cancer Centre, Disruptive Innovation Centre for Spatiotemporal Imaging, Li Ka Shing Institute of Health Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, 999077, PR China.
Guangtao ZanDepartment of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong SAR, 999077, PR China.
Wei LiuCollege of Basic Medicine (Digital Medical Center) & The Second Affiliated Hospital, Inner Mongolia Medical University, Hohhot, 010059, PR China.
Yifan LiuSchool of Life Science and Technology & School of Physical Science and Technology, ShanghaiTech University, 393 Huaxia Middle Road, Pudong, Shanghai, 201210, PR China.
Jinwu WangResearch Center of Traditional Chinese Medicine Intelligent Rehabilitation, Ministry of Education, School of Rehabilitation Science, Institute of Rehabilitation Medicine, Shanghai Academy of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, PR China.
Hui WangResearch Center of Traditional Chinese Medicine Intelligent Rehabilitation, Ministry of Education, School of Rehabilitation Science, Institute of Rehabilitation Medicine, Shanghai Academy of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, PR China.
Yifeng ZhangCollege of Basic Medicine (Digital Medical Center) & The Second Affiliated Hospital, Inner Mongolia Medical University, Hohhot, 010059, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spatiotemporal histopathological features of articular cartilage in osteoarthritis (OA) remain inadequately characterized, which impedes the advancement of strategies to halt irreversible joint deterioration. Herein a murine OA model, the initial phase (<10 days post-surgery) is characterized by pronounced mitochondrial dysfunction in chondrocytes and concurrent activation of subchondral osteoclasts. Beyond this period, irreversible cartilage degeneration ensues, marked by chondrocyte apoptosis and subchondral bone sclerosis. We further identified magnesium (Mg) as a key regulator of cellular metabolic balance, capable of reinstating homeostasis in inflamed chondrocytes while modulating osteoclast overactivity. Based on this, we developed dual-concentration Mg-releasing biphasic microspheres that effectively halted early OA progression in vivo. In contrast, delayed administration conferred benefits predominantly limited to the subchondral bone, without achieving cartilage preservation. These results underscore the existence of a critical therapeutic window for metabolic intervention in OA, wherein Mg-based biomaterials exert protective effects exclusively during the early disease stage. Thus, this study offers a new strategic perspective for the clinical management of OA.

Indexed as

ChondrocytesMagnesiumMetabolismOsteoarthritisOsteoclasts

Identifiers

PMID42359363
PMCPMC13292249

What OpenQuestion holds

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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.