Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf

Background<p>Septic liver injury (SLI) is a life-threatening complication of sepsis with limited therapeutic options. The clinical efficacy and safety of Dachaihu Decoction (DCHD) in SLI remain to be elucidated.</p>Methods and Design<p>A prospective, single-center, single-blind, ra...

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Hlavní autor: Zhen Yang (107412) (author)
Další autoři: Xingyu Kao (22679228) (author), Tianwei Zhu (22679231) (author), Junna Lei (22679234) (author), Na Huang (416556) (author), Jingli Chen (600614) (author), Mingfeng He (3164595) (author), Qi Tang (351973) (author), Zhangrong Liang (22679237) (author)
Vydáno: 2025
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author Zhen Yang (107412)
author2 Xingyu Kao (22679228)
Tianwei Zhu (22679231)
Junna Lei (22679234)
Na Huang (416556)
Jingli Chen (600614)
Mingfeng He (3164595)
Qi Tang (351973)
Zhangrong Liang (22679237)
author2_role author
author
author
author
author
author
author
author
author_facet Zhen Yang (107412)
Xingyu Kao (22679228)
Tianwei Zhu (22679231)
Junna Lei (22679234)
Na Huang (416556)
Jingli Chen (600614)
Mingfeng He (3164595)
Qi Tang (351973)
Zhangrong Liang (22679237)
author_role author
dc.creator.none.fl_str_mv Zhen Yang (107412)
Xingyu Kao (22679228)
Tianwei Zhu (22679231)
Junna Lei (22679234)
Na Huang (416556)
Jingli Chen (600614)
Mingfeng He (3164595)
Qi Tang (351973)
Zhangrong Liang (22679237)
dc.date.none.fl_str_mv 2025-11-25T06:24:20Z
dc.identifier.none.fl_str_mv 10.3389/fphar.2025.1671732.s002
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/Supplementary_file_1_Clinical_efficacy_and_metabolomics_profiling_of_dachaihu_decoction_for_patients_with_septic_liver_injury_a_randomized_controlled_trial_pdf/30703979
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Pharmacology
septic liver injury
dachaihu decoction
randomized controlled trial
traditional Chinese medicine
metabolomics
bile acid metabolism
dc.title.none.fl_str_mv Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description Background<p>Septic liver injury (SLI) is a life-threatening complication of sepsis with limited therapeutic options. The clinical efficacy and safety of Dachaihu Decoction (DCHD) in SLI remain to be elucidated.</p>Methods and Design<p>A prospective, single-center, single-blind, randomized, and placebo-controlled clinical trial was conducted. Patients in the DCHD group received DCHD twice a day for five consecutive days on the basis of sepsis bundle, while patients in the placebo group were administered a placebo at the same dosage. Primary outcomes included: (1) liver function indices: alanine transaminase (ALT), aspartate transaminase (AST) and total bilirubin (TBil); (2) Sequential Organ Failure Assessment (SOFA) and Acute Physiology and Chronic Health Evaluation II (APACHE II) scores; (3) 28-day all-cause mortality. Secondary outcomes included the evaluation of several clinical parameters: (1) infection indicators; (2) coagulation indicators; (3) gastrointestinal function indicator; (4) metabolic and respiratory function indicators. Subsequently, we employed Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) to characterize the serum metabolomics profiling of two groups of patients.</p>Results<p>DCHD significantly reduced TBil (−22.50 (interquartile range, IQR, −37.20, −8.10) vs. −3.30 (−17.16, 12.40), p < 0.001), SOFA score (−2.46 ± 2.84 vs. −1.11 ± 2.71, p = 0.047), APACHE II score (−5 (IQR, −5, −2) vs. −2 (−5, 2), p = 0.034), and Oxygenation Index (OI) (29.71 ± 74.76 vs. −15.16 ± 108.51, p = 0.048). However, no statistically significant difference in 28-day all-cause mortality was found between the DCHD and the placebo groups (7 (20.0%) vs. 9 (25.7%), p = 0.569). Additionally, our study demonstrates that DCHD ameliorates systemic infection, coagulation function, gastrointestinal function, and metabolic function in patients to a certain extent, and no severe side effects were reported. Metabolomics analysis reveals that Wogonin, Wogonoside, Cholic acid, and Glycocholic acid are representative differential metabolites, and bile acid metabolism may be the core metabolic pathway.</p>Conclusion<p>As an adjunctive therapy, DCHD demonstrates safety and efficacy in the treatment of SLI, particularly cholestatic hepatic dysfunction, which may be intimately linked to its modulation of bile acid metabolism.</p>Clinical Trial Registration<p>http://itmctr.ccebtcm.org.cn, identifier ITMCTR2025000095.</p>
eu_rights_str_mv openAccess
id Manara_8fdbda95bebdc712269d11a05d8fb3b1
identifier_str_mv 10.3389/fphar.2025.1671732.s002
network_acronym_str Manara
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oai_identifier_str oai:figshare.com:article/30703979
publishDate 2025
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spelling Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdfZhen Yang (107412)Xingyu Kao (22679228)Tianwei Zhu (22679231)Junna Lei (22679234)Na Huang (416556)Jingli Chen (600614)Mingfeng He (3164595)Qi Tang (351973)Zhangrong Liang (22679237)Pharmacologyseptic liver injurydachaihu decoctionrandomized controlled trialtraditional Chinese medicinemetabolomicsbile acid metabolismBackground<p>Septic liver injury (SLI) is a life-threatening complication of sepsis with limited therapeutic options. The clinical efficacy and safety of Dachaihu Decoction (DCHD) in SLI remain to be elucidated.</p>Methods and Design<p>A prospective, single-center, single-blind, randomized, and placebo-controlled clinical trial was conducted. Patients in the DCHD group received DCHD twice a day for five consecutive days on the basis of sepsis bundle, while patients in the placebo group were administered a placebo at the same dosage. Primary outcomes included: (1) liver function indices: alanine transaminase (ALT), aspartate transaminase (AST) and total bilirubin (TBil); (2) Sequential Organ Failure Assessment (SOFA) and Acute Physiology and Chronic Health Evaluation II (APACHE II) scores; (3) 28-day all-cause mortality. Secondary outcomes included the evaluation of several clinical parameters: (1) infection indicators; (2) coagulation indicators; (3) gastrointestinal function indicator; (4) metabolic and respiratory function indicators. Subsequently, we employed Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) to characterize the serum metabolomics profiling of two groups of patients.</p>Results<p>DCHD significantly reduced TBil (−22.50 (interquartile range, IQR, −37.20, −8.10) vs. −3.30 (−17.16, 12.40), p < 0.001), SOFA score (−2.46 ± 2.84 vs. −1.11 ± 2.71, p = 0.047), APACHE II score (−5 (IQR, −5, −2) vs. −2 (−5, 2), p = 0.034), and Oxygenation Index (OI) (29.71 ± 74.76 vs. −15.16 ± 108.51, p = 0.048). However, no statistically significant difference in 28-day all-cause mortality was found between the DCHD and the placebo groups (7 (20.0%) vs. 9 (25.7%), p = 0.569). Additionally, our study demonstrates that DCHD ameliorates systemic infection, coagulation function, gastrointestinal function, and metabolic function in patients to a certain extent, and no severe side effects were reported. Metabolomics analysis reveals that Wogonin, Wogonoside, Cholic acid, and Glycocholic acid are representative differential metabolites, and bile acid metabolism may be the core metabolic pathway.</p>Conclusion<p>As an adjunctive therapy, DCHD demonstrates safety and efficacy in the treatment of SLI, particularly cholestatic hepatic dysfunction, which may be intimately linked to its modulation of bile acid metabolism.</p>Clinical Trial Registration<p>http://itmctr.ccebtcm.org.cn, identifier ITMCTR2025000095.</p>2025-11-25T06:24:20ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.3389/fphar.2025.1671732.s002https://figshare.com/articles/dataset/Supplementary_file_1_Clinical_efficacy_and_metabolomics_profiling_of_dachaihu_decoction_for_patients_with_septic_liver_injury_a_randomized_controlled_trial_pdf/30703979CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/307039792025-11-25T06:24:20Z
spellingShingle Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
Zhen Yang (107412)
Pharmacology
septic liver injury
dachaihu decoction
randomized controlled trial
traditional Chinese medicine
metabolomics
bile acid metabolism
status_str publishedVersion
title Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
title_full Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
title_fullStr Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
title_full_unstemmed Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
title_short Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
title_sort Supplementary file 1_Clinical efficacy and metabolomics profiling of dachaihu decoction for patients with septic liver injury: a randomized controlled trial.pdf
topic Pharmacology
septic liver injury
dachaihu decoction
randomized controlled trial
traditional Chinese medicine
metabolomics
bile acid metabolism