dc.contributor.author
Huang, Yuanshe
dc.contributor.author
Wang, Xiaodong
dc.contributor.author
Yan, Chen
dc.contributor.author
Li, Chen
dc.contributor.author
Zhang, Lidan
dc.contributor.author
Zhang, Lai
dc.contributor.author
Liang, E.
dc.contributor.author
Liu, Tianlei
dc.contributor.author
Mao, Jingxin
dc.date.accessioned
2023-01-16T08:40:18Z
dc.date.available
2023-01-16T08:40:18Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/37598
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-37313
dc.description.abstract
Background:
Whether metformin is related to nonalcoholic fatty liver disease (NAFLD) is controversial. Our aim was to investigate the relationship between metformin and NAFLD that may predict the metformin potential of these lesions and new prevention strategies in NAFLD patients.
Methods:
The meta-analysis was analyzed by Revman 5.3 softwares systematically searched for works published through July 29, 2022. Network pharmacology research based on databases, Cytoscape 3.7.1 software and R software respectively.
Results:
The following variables were associated with metformin in NAFLD patients: decreased of alanine aminotransferase (ALT) level (mean difference [MD] = −10.84, 95% confidence interval [CI] = −21.85 to 0.16, P = .05); decreased of aspartate amino transferase (AST) level (MD = −4.82, 95% CI = −9.33 to −0.30, P = .04); decreased of triglyceride (TG) level (MD = −0.17, 95% CI = −0.26 to −0.08, P = .0002); decreased of total cholesterol (TC) level (MD = −0.29, 95% CI = −0.47 to −0.10, P = .003); decreased of insulin resistance (IR) level (MD = −0.42, 95% CI = −0.82 to −0.02, P = .04). In addition, body mass index (BMI) (MD = −0.65, 95% CI = −1.46 to 0.16, P = .12) had no association with metformin in NAFLD patients. 181 metformin targets and 868 NAFLD disease targets were interaction analyzed, 15 core targets of metformin for the treatment of NAFLD were obtained. The effect of metformin on NAFLD mainly related to cytoplasm and protein binding, NAFLD, hepatitis B, pathway in cancer, toll like receptor signaling pathway and type 2 diabetes mellitus (T2DM). The proteins of hypoxia inducible factor-1 (HIF1A), nuclear factor erythroid 2-related factor (NFE2L2), nitric oxide synthase 3 (NOS3), nuclear receptor subfamily 3 group C member 1 (NR3C1), PI3K catalytic subunit alpha (PIK3CA), and silencing information regulator 2 related enzyme 1 (SIRT1) may the core targets of metformin for the treatment of NAFLD.
Conclusion:
Metformin might be a candidate drug for the treatment of NAFLD which exhibits therapeutic effect on NAFLD patients associated with ALT, AST, TG, TC and IR while was not correlated with BMI. HIF1A, NFE2L2, NOS3, NR3C1, PIK3CA, and SIRT1 might be core targets of metformin for the treatment of NAFLD.
en
dc.format.extent
12 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
candidate drug
en
dc.subject
meta-analysis
en
dc.subject
network pharmacology
en
dc.subject
nonalcoholic fatty liver disease
en
dc.subject
therapeutic effect
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Effect of metformin on nonalcoholic fatty liver based on meta-analysis and network pharmacology
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e31437
dcterms.bibliographicCitation.doi
10.1097/MD.0000000000031437
dcterms.bibliographicCitation.journaltitle
Medicine
dcterms.bibliographicCitation.number
43
dcterms.bibliographicCitation.volume
101
dcterms.bibliographicCitation.url
https://doi.org/10.1097/MD.0000000000031437
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1536-5964
refubium.resourceType.provider
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