Evidence map›Paper›PMID 39015788›Full record

ArticleFrontiers in medicine2024

Metabolomics reveals altered metabolites in cirrhotic patients with severe portal hypertension in Tibetan population.

Yanting Ye, Chao Xia, Hong Hu, Shihang Tang, Hui Huan

Abstract read
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Article in Frontiers in medicine, 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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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

5 authors.

Yanting Ye *Lab of Gastroenterology and Hepatology, West China Hospital, Sichuan University, Chengdu, China.
Chao Xia *Department of Radiology, and Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital, Sichuan University, Chengdu, China.
Hong HuDepartment of Gastroenterology, Hospital of Chengdu Office of People's Government of Tibetan Autonomous Region, Chengdu, China.
Shihang TangDepartment of Gastroenterology, Chongqing University Cancer Hospital, Chongqing, China.
Hui HuanDepartment of Gastroenterology, Hospital of Chengdu Office of People's Government of Tibetan Autonomous Region, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Portal hypertension (PHT) presents a challenging issue of liver cirrhosis. This study aims to identify novel biomarkers for severe PHT (SPHT) and explore the pathophysiological mechanisms underlying PHT progression. Methods: Twenty-three Tibetan cirrhotic patients who underwent hepatic venous pressure gradient (HVPG) measurement were included. Eleven patients had an HVPG between 5 mmHg and 15 mmHg (MPHT), while 12 had an HVPG ≥16 mmHg (SPHT). Peripheral sera were analyzed using liquid chromatograph-mass spectrometer for metabolomic assessment. An additional 14 patients were recruited for validation of metabolites. Results: Seven hundred forty-five metabolites were detected and significant differences in metabolomics between MPHT and SPHT patients were observed. Employing a threshold of Conclusion: Pisumionoside and N-DG are identified as promising biomarkers for SPHT. The progression of PHT may be associated with disturbances in lipid, linoleic acid, and amino acid metabolisms, as well as alterations in the citrate cycle.

Indexed as

biomarkersliver cirrhosismetabolomicsportal hypertensionTibetan

Identifiers

PMID39015788
PMCPMC11250582

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