Evidence map›Paper›PMID 39212714›Full record

ArticleJournal of bone and mineral metabolism2024

Enpp1 mutations promote upregulation of hedgehog signaling in heterotopic ossification with aging.

Zhongyuan He, Zhengya Zhu, Tao Tang, Fuan Wang, Peng Guo, Jianfeng Li, Nguyen Tran Canh Tung, Qian Liang, Shaoyu Liu, ManMan Gao and 2 more

Abstract read
In one paragraph

Article in Journal of bone and mineral metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

12 authors.

Zhongyuan He *Innovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China.ORCID http://orcid.org/0000-0002-6194-0720
Zhengya Zhu *Innovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China.
Tao Tang *Innovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China.
Fuan Wang *Innovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China.
Peng GuoInnovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China.
Jianfeng LiInnovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China.
Nguyen Tran Canh TungDepartment of Orthopaedic Surgery, Faculty of Medicine, University of Toyama, Toyama, 930-0194, Japan.
Qian LiangDepartment of Spine Surgery, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, 518025, China.
Shaoyu LiuGuangdong Provincial Key Laboratory of Orthopedics and Traumatology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510062, China.
ManMan GaoDepartment of Sport Medicine, Inst Translat Med, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, 518025, China. gaomanm@mail2.sysu.edu.cn.
Xizhe LiuGuangdong Provincial Key Laboratory of Orthopedics and Traumatology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510062, China. liuxizhe@mail.sysu.edu.cn.
Zhiyu ZhouInnovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, 517108, China. zhouzhy23@mail.sysu.edu.cn.

Funding

Academic Affairs Office of Sun Yat-sen University 202211583Academic Affairs Office of Sun Yat-sen University 202211589AOCMF Translational approaches for bone constructs CPP, Sun Yat-sen University Clinical Research 5010 Program 2019009foundation of Shenzhen Committee for foundation of Shenzhen Committee for Science and Technology InnovationScience and Technology Innovation JCYJ20190809142211354 GJHZ20180929160004704Medical Science and Technology Research Foundation of Guangdong Province A2022257National Natural Science Foundation of China 31900583National Natural Science Foundation of China 32071351National Natural Science Foundation of China 81772400National Natural Science Foundation of China 82102604Natural Science Foundation of Guangzhou City 201807010031Sanming Project of Medicine in Shenzhen SZSM201911002
6 · The paper itself

Abstract

introductionHeterotopic ossification of the tendon and ligament (HOTL) is a chronic progressive disease that is usually accompanied by thickening and ossification of ligaments and high osteogenic activity of the surrounding ligament tissue. However, the molecular mechanism of maintaining the cellular phenotype of HOTL remains unclear. MATERIALS AND

methodsWe first constructed a model of HOTL, Enpp1

resultsThe results indicate that Enpp1 deficiency led to markedly progressive heterotopic ossification (HO), especially spine, and Achilles tendons, and was associated with progressive degeneration of the knees. The bone mass was decreased in the long bone. Furthermore, fibroblasts from Enpp1

conclusionOur study indicated that with increasing age, mutations in Enpp1 promote ectopic ossification of spinal ligaments and endochondral ossification in tendons and further aggravate knee degeneration by upregulating hedgehog signaling.

Indexed as

AgingHedgehog ProteinsMutationOssification, HeterotopicOsteogenesisPhosphoric Diester HydrolasesPyrophosphatasesSignal TransductionUp-RegulationAnimalsFibroblastsMiceectonucleotide pyrophosphatase phosphodiesterase 1Hedgehog ProteinsPhosphoric Diester HydrolasesPyrophosphatasesEnpp1Hedgehog signalingHOTLOPLL

Identifiers

PMID39212714
PMCPMC11632054

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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.