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Drug-induced liver injury is a leading cause of acute liver failure worldwide and one of the least understood areas in hepatology research. Increasing evidence has shown that drug-induced liver injury is associated with gut microbiota.
Background:
Drug-induced liver injury(DILI) refers to the liver injury induced by all kinds of drugs and is the leading cause of acute liver failure worldwide. China has a large population base and a wide variety of clinical drugs, and it is common for the population to use drugs irregularly. Therefore, the incidence of DILI is increasing year by year. The pathogenesis of DILI is complicated, and there are often multiple mechanisms successively or altogether. As a result of the same effect, it is particularly important to study the pathogenesis of DILI and find its therapeutic target. Increasing evidence shows that DILI is related to the gut microbiota, which provides broader insights and opportunities for understanding and treating this disease.
Aims:
We aim to map the alterations of gut microbiota and serum biochemical markers in patients with DILI, and to investigate the effects and mechanisms of key strains on the development of DILI, providing a theoretical basis and potential targets for its treatment.
Methods:
Patients who meet the inclusion criteria will sign informed consent, their demographic data, clinical labs, serum, and feces will be collected at baseline. Fecal samples will be subject to 16S rRNA amplicon sequencing. Serum samples were taken for metabolomics detection.
Anticipated Results:
Compared to the healthy control group, patients with DILI will suffer from gut microbiota dysbiosis and have more microbes and microbial genes associated with inflammation and injury. The levels of serum biochemical markers are associated with the severity of DILI.
Implications and Future Studies:
Results of altered gut microbiome and serum biochemical markers could provide potential targets for manipulating intestinal microbiota to prevent or treat DILI.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Drug-induced liver injury | history of taking hepatotoxic drugs, liver injury. |
| |
| Healthy control | no liver disease or other disease |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Collect stool and blood samples from patients | Other | Collect stool and blood samples from patients |
|
| Measure | Description | Time Frame |
|---|---|---|
| The changes of gut microbiota in the levels of phylum, genus, and species in two groups | The changes will be detected by genome sequencing | 2 years |
| The different levels of serum aspartate transaminase/alanine transaminase (AST/ALT) in two groups | The changes will be detected by biochemical analyzers | 2 years |
| The different levels of proinflammatory cytokines in two groups | The changes will be determined by ELISA kits | 2 years |
| The changes of lncRNA and miRNA in two groups | The changes will be measured by quantitative polymerase chain reaction (qPCR) | 2 years |
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Inclusion Criteria:
1. The group of DILI:
2. The group of healthy control:
Exclusion Criteria:
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Patients and healthy control will be recruited mainly from the outpatient or inpatient departments of Wuhan Union Hospital.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Huikuan Chu, M.D. | Contact | +8613554105386 | 2012xh0827@hust.edu.cn | |
| Wenkang Gao, Dr. | Contact | +8618838022896 | gwkmed@163.com |
| Name | Affiliation | Role |
|---|---|---|
| Huikuan Chu, M.D. | Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, wuhan | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Union Hospital, Tongji Medical College, Huazhong University of Science and Technology | Recruiting | Wuhan | Hubei | 430022 | China |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 30767680 | Result | Hartmann P, Chu H, Duan Y, Schnabl B. Gut microbiota in liver disease: too much is harmful, nothing at all is not helpful either. Am J Physiol Gastrointest Liver Physiol. 2019 May 1;316(5):G563-G573. doi: 10.1152/ajpgi.00370.2018. Epub 2019 Feb 15. | |
| 32323178 | Result | Wu G, Win S, Than TA, Chen P, Kaplowitz N. Gut Microbiota and Liver Injury (I)-Acute Liver Injury. Adv Exp Med Biol. 2020;1238:23-37. doi: 10.1007/978-981-15-2385-4_3. |
| Label | URL |
|---|---|
| This web provides information of Human Subjects Protection in this study | View source |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP_ICF | Yes | Yes | Yes | Study Protocol, Statistical Analysis Plan, and Informed Consent Form | Jun 29, 2022 | Jul 6, 2022 | Prot_SAP_ICF_000.pdf |
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| ID | Term |
|---|---|
| D056486 | Chemical and Drug Induced Liver Injury |
| ID | Term |
|---|---|
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D064420 | Drug-Related Side Effects and Adverse Reactions |
| D064419 | Chemically-Induced Disorders |
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Retain patient blood and stool and extract DNA for identification of gut microbiota.
| 29524531 | Result | Gong S, Lan T, Zeng L, Luo H, Yang X, Li N, Chen X, Liu Z, Li R, Win S, Liu S, Zhou H, Schnabl B, Jiang Y, Kaplowitz N, Chen P. Gut microbiota mediates diurnal variation of acetaminophen induced acute liver injury in mice. J Hepatol. 2018 Jul;69(1):51-59. doi: 10.1016/j.jhep.2018.02.024. Epub 2018 Mar 8. |
| 33189892 | Result | Schneider KM, Elfers C, Ghallab A, Schneider CV, Galvez EJC, Mohs A, Gui W, Candels LS, Wirtz TH, Zuehlke S, Spiteller M, Myllys M, Roulet A, Ouzerdine A, Lelouvier B, Kilic K, Liao L, Nier A, Latz E, Bergheim I, Thaiss CA, Hengstler JG, Strowig T, Trautwein C. Intestinal Dysbiosis Amplifies Acetaminophen-Induced Acute Liver Injury. Cell Mol Gastroenterol Hepatol. 2021;11(4):909-933. doi: 10.1016/j.jcmgh.2020.11.002. Epub 2020 Nov 12. |
| D011041 | Poisoning |