Evidence map›Paper›PMID 40297859›Full record

ArticleFrontiers in neurology2025

Metabolomic analysis reveals trimethylamine N-oxide as a biomarker for poor outcome of severe spontaneous intracerebral hemorrhage patients receiving surgical treatment.

Xinguo Sun, Kaige Zheng, Shanjun Wang, Yunzhao Chen, Hongen Liu, Xindong Gu, Zitong Wu, Hui Lu, Shuo Wang, Qingyuan Liu and 1 more

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Article in Frontiers in neurology, 2025. 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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5 · Who and what money

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11 authors.

Xinguo Sun *Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.
Kaige Zheng *Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Shanjun Wang *Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.
Yunzhao ChenDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.
Hongen LiuDepartment of Neurosurgery, Binzhou People's Hospital, Binzhou, Shandong, China.
Xindong GuDepartment of Neurosurgery, Binzhou People's Hospital, Binzhou, Shandong, China.
Zitong WuDepartment of Neurosurgery, Binzhou People's Hospital, Binzhou, Shandong, China.
Hui LuDepartment of Neurosurgery, Binzhou People's Hospital, Binzhou, Shandong, China.
Shuo WangDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Qingyuan LiuDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Zengguang WangDepartment of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objectives: Patients suffering from severe spontaneous intracerebral hemorrhage (SSICH) are at high risk of cardiocerebrovascular diseases postoperatively, which hugely affect patients' long-term outcomes. Metabolic features could reflect the pathological change of the cardiocerebrovascular system and might serve as biomarkers for evaluating the risk of poor outcomes in SSICH patients. The current study aimed to find the early-warning biomarkers for poor outcomes in SSICH patients after surgery. Methods: Severe spontaneous intracerebral hemorrhage patients receiving surgical treatment from a referring hospital were prospectively included and formed the primary cohort after propensity score matching. The primary outcome is poor 180 days after hemorrhage (modified Rankin scale ≥4). Metabolomics analysis on 3-, 7-, and 30-day serum and cerebrospinal fluid samples after surgery revealed the dysregulated metabolites of SSICH patients within the primary cohort. Within the validation cohort of SSICH patients receiving surgical treatment from a multicenter, prospective cohort, dysregulated metabolites were validated and evaluated to see whether they could serve as biomarkers for 180-day poor outcomes by area under the curve (AUC). Results: The primary cohort included 20 SSICH patients with good 180-day outcome and 20 with poor outcome. Untargeted metabolomics analysis found 25 co-dysregulated metabolites, including trimethylamine N-oxide (TMAO), among 3-day, 7-day, and 30-day metabolism features between SSICH patients with poor outcome and good outcome after surgery. A good correlation was found in TMAO between serum and cerebrospinal fluid on 3rd day after surgery. Based on the validation cohort of 794 SSICH patients (147 patients had 180-day poor outcome), the targeted metabolomics analysis revealed increasing TMAO on 3rd day after surgery as a risk factor of poor outcomes (odds ratio, 4.7; 95%CI, 3.6-6.2; Conclusion: This study demonstrated increasing serum TMAO level as an early-warning biomarker for 180-day poor outcomes of SSICH patients receiving surgical treatment. Clinical trial registration: Chinese Clinical Trial Registry, ChiCTR1900024406, https://www.chictr.org.cn/showproj.html?proj=40640.

Indexed as

biomarkermetabolomic analysispoor outcomespontaneous intracerebral hemorrhagesurgical treatment

Identifiers

PMID40297859
PMCPMC12034627

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