Evidence map›Paper›PMID 39281778›Full record

ArticleJournal of inflammation research2024

Comprehensive Serum Proteomic and Metabolomic Profiles of Pediatric Patients with Moyamoya Disease Reveal Core Pathways.

Qingbao Guo, Manli Xie, Qian-Nan Wang, Jingjie Li, Simeng Liu, Xiaopeng Wang, Dan Yu, Zhengxing Zou, Gan Gao, Qian Zhang and 7 more

Abstract read
In one paragraph

Article in Journal of inflammation research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Qingbao Guo *Medical School of Chinese PLA, Beijing, People's Republic of China.
Manli Xie *Department of Occupational Diseases, Xi'an Central Hospital, Xi'an, Shanxi, People's Republic of China.
Qian-Nan Wang *Department of Neurosurgery, Eighth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Jingjie LiMedical School of Chinese PLA, Beijing, People's Republic of China.
Simeng LiuMedical School of Chinese PLA, Beijing, People's Republic of China.
Xiaopeng WangMedical School of Chinese PLA, Beijing, People's Republic of China.
Dan YuDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Zhengxing ZouDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Gan GaoMedical School of Chinese PLA, Beijing, People's Republic of China.
Qian ZhangDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Fangbin HaoMedical School of Chinese PLA, Beijing, People's Republic of China.
Jie FengDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Rimiao YangDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Minjie WangMedical School of Chinese PLA, Beijing, People's Republic of China.
Heguan FuDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Xiangyang BaoDepartment of Neurosurgery, Fifth Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.
Lian DuanDepartment of Neurosurgery, First Medical Centre, Chinese PLA General Hospital, Beijing, People's Republic of China.ORCID 0000-0001-7210-056X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Moyamoya disease (MMD) signifies a cerebrovascular disorder with obscure origin and a more rapid and severe progression in children than adults. This investigation aims to uncover age-associated distinctions through proteomic and metabolomic profiling to gain insights into the underlying mechanisms of MMD. Methods: Twelve MMD patients-six children and six adults-along with six healthy controls (HC), participated, each providing a 10 mL blood sample. Serum proteomic and metabolomic analyses were conducted using ultra-performance liquid chromatography and high-resolution mass spectrometry, complemented by bioinformatics to identify differential biomolecules and their interactions. Pathway implications were ascertained using GO and KEGG enrichment analysis. Results: Notable proteomic and metabolomic discrepancies were observed between pediatric and adult MMD subjects. A total of 235 and 216 proteins varied in adult and pediatric cases compared to HCs, with 73 proteins shared. In addition, 129 and 74 anionic, plus 96 and 104 cationic metabolites, were differentially expressed in the pediatric and adult groups, respectively, with 34 anionic and 28 cationic metabolites in common. Age-specific biomolecules further characterized these distinctions. Enrichment analysis pinpointed immunity and inflammation pathways, with vitamin digestion and absorption highlighted as pivotal in pediatric MMD. Conclusion: This study unveils distinct metabolic and proteomic patterns within pediatric and adult MMD patients. The critical role of the vitamin digestion and absorption pathway in the pathogenesis of pediatric MMD offers novel insight into disease mechanisms.

Indexed as

integration analysismetabolomicsmoyamoya diseasepediatric patientsproteomics

Identifiers

PMID39281778
PMCPMC11397188

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