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

被引:0
作者
Guo, Qingbao [1 ,2 ]
Xie, Manli [3 ]
Wang, Qian-Nan [4 ]
Li, Jingjie [1 ,2 ]
Liu, Simeng [1 ,2 ]
Wang, Xiaopeng [1 ,2 ]
Yu, Dan [5 ]
Zou, Zhengxing [5 ]
Gao, Gan [1 ,2 ]
Zhang, Qian [5 ]
Hao, Fangbin [1 ,2 ]
Feng, Jie [5 ]
Yang, Rimiao [5 ]
Wang, Minjie [1 ,2 ]
Fu, Heguan [5 ]
Bao, Xiangyang [5 ]
Duan, Lian [2 ]
机构
[1] Med Sch Chinese PLA, Beijing, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Neurosurg, Beijing, Peoples R China
[3] Xian Cent Hosp, Dept Occupat Dis, Xian, Shaanxi, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 8, Dept Neurosurg, Beijing, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Neurosurg, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
proteomics; metabolomics; pediatric patients; moyamoya disease; integration analysis; MASS-SPECTROMETRY; INFLAMMATION; INHIBITION;
D O I
10.2147/JIR.S471538
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:6173 / 6192
页数:20
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