Tandem mass spectrometry in screening for inborn errors of metabolism: comprehensive bibliometric analysis.

IF 2 3区 医学 Q2 PEDIATRICS Frontiers in Pediatrics Pub Date : 2025-02-20 eCollection Date: 2025-01-01 DOI:10.3389/fped.2025.1463294
Victoria Kononets, Gulmira Zharmakhanova, Saule Balmagambetova, Lyazzat Syrlybayeva, Gulshara Berdesheva, Zhanna Zhussupova, Aidana Tautanova, Yergen Kurmambayev
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Abstract

Tandem mass spectrometry (MS/MS) for detection of inborn errors of metabolism (IEM) is recognized as an ethical, safe, simple, and reliable screening test. Presented bibliometric analysis aims to describe the network structure of the scientific community in the study area at the level of countries, institutions, authors, papers, keywords, and sources; scientific productivity, directions, and collaboration efforts in a considered period (1991-2024, May). Using the PRISMA method, we conducted a systematic search for articles reporting using MS/MS to screen for inherited metabolic disorders and inborn errors of metabolism collected from the Web of Science Core Collection (WoSCC). A total of 677 articles out of 826, by 3,714 authors, published in 245 journals, with 21,193 citations in 11,295 citing articles, with an average citation of 31.3 per article, and an H-index of 69 were retrieved from the WoSCC. The research status of MS/MS in IEM screening was identified. The most relevant current research directions and future areas of interest were revealed: "selective screening for IEM," "new treatments for IEM," "new disorders considered for MS/MS testing," "ethical issues associated with newborn screening," "new technologies that may be used for newborn screening," and "use of a combination of MS/MS and gene sequencing".

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串联质谱法筛查先天性代谢错误:综合文献计量学分析。
串联质谱(MS/MS)检测先天性代谢错误(IEM)被认为是一种道德、安全、简单、可靠的筛查试验。文献计量分析旨在从国家、机构、作者、论文、关键词和来源等层面描述研究领域的科学界网络结构;研究期间(1991-2024年5月)的科学生产力、方向和合作努力。采用PRISMA方法,我们系统检索了Web of Science Core Collection (WoSCC)中报道使用MS/MS筛查遗传代谢疾病和先天性代谢错误的文章。共检索到3714位作者在245个期刊上发表的826篇论文中的677篇,被引用11295篇,被引用21193次,平均被引用31.3次/篇,h指数为69。明确了质谱联用技术在IEM筛选中的研究现状。揭示了当前最相关的研究方向和未来的兴趣领域:“选择性筛选IEM”,“IEM的新治疗方法”,“考虑MS/MS检测的新疾病”,“与新生儿筛查相关的伦理问题”,“可能用于新生儿筛查的新技术”,以及“使用MS/MS和基因测序的组合”。
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来源期刊
Frontiers in Pediatrics
Frontiers in Pediatrics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
3.60
自引率
7.70%
发文量
2132
审稿时长
14 weeks
期刊介绍: Frontiers in Pediatrics (Impact Factor 2.33) publishes rigorously peer-reviewed research broadly across the field, from basic to clinical research that meets ongoing challenges in pediatric patient care and child health. Field Chief Editors Arjan Te Pas at Leiden University and Michael L. Moritz at the Children''s Hospital of Pittsburgh are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Pediatrics also features Research Topics, Frontiers special theme-focused issues managed by Guest Associate Editors, addressing important areas in pediatrics. In this fashion, Frontiers serves as an outlet to publish the broadest aspects of pediatrics in both basic and clinical research, including high-quality reviews, case reports, editorials and commentaries related to all aspects of pediatrics.
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