Research trends and hotspots of myositis ossificans: a bibliometric analysis from 1993 to 2022

Author:

Lai Bowen1,Jiang Heng1,Gao Yuan1,Zhou Xuhui1ORCID

Affiliation:

1. Department of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China

Abstract

Myositis ossificans (MO) is characterized by benign heterotopic ossificans in soft tissues like muscles, which can be classified into nonhereditary MO and fibrodysplasia ossificans progressiva (FOP). Although MO has been studied for decades, no research reviewed and analyzed the features of publications in this field quantitatively and qualitatively. Using bibliometrics tools (bibliometrix R package, VOSviewer, and CiteSpace), we conducted a bibliometric analysis of 1280 articles regarding MO in the Web of Science Core Collection database from 1993 to 2022. The annual number of publications and related research areas in the MO field increased gradually in the past 20 years. The USA contributed the most percentage (42.58%) of articles. The University of Pennsylvania (UPenn) and the Journal Bone published the most articles among all institutions and journals. Kaplan FS and Shore EM from UPenn were the top two scholars who made the largest contributions to this field. Keyword analysis showed that research hotspots changed from traumatic MO and clinical management of MO to the genetic etiology, pathogenesis, and treatment of FOP. This study can provide new insights into the research trends of MO and helps researchers grasp and determine future study directions more easily.

Publisher

Bioscientifica

Reference32 articles.

1. Myositis ossificans;Walczak,2015

2. Cellular and morphological aspects of fibrodysplasia ossificans progressiva. Lessons of formation, repair, and bone bioengineering;Martelli,2014

3. Fibrodysplasia ossificans progressiva;Kaplan,2008

4. Dysregulation of local stem/progenitor cells as a common cellular mechanism for heterotopic ossification;Kan,2009

5. A recurrent;Shore,2006

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