General Information of Disease (ID: DIST4788)

Disease Name Non-alcoholic steatohepatitis
Synonyms nonalcoholic steatohepatitis; NASH - nonalcoholic steatohepatitis; non-alcoholic steatohepatitis; MASH
Disease Class DB92: Non-alcoholic fatty liver disease
Definition
Metabolic dysfunction-associated steatohepatitis (MASH, formerly known as nonalcoholic steatohepatitis or NASH) is a type of fatty liver disease. It often develops due to a metabolic disorder, such as obesity or diabetes, resulting in a toxic buildup of fat in the liver. It is the most severe form of metabolic dysfunction-associated steatotic liver disease (MASLD, formerly known as nonalcoholic fatty liver disease or NAFLD).
Disease Hierarchy
DISDG1NL: Non-alcoholic fatty liver disease
DISXXX35: Hepatitis
DIST4788: Non-alcoholic steatohepatitis
ICD Code
ICD-11
ICD-11: DB92.1
ICD-10
ICD-10: K75.8
ICD-9
ICD-9: 571.8
Expand ICD-11
'DB92.1
Expand ICD-10
'K75.8
Expand ICD-9
571.8
Disease Identifiers
MONDO ID
MONDO_0007027
MESH ID
D065626
UMLS CUI
C3241937
MedGen ID
469032
SNOMED CT ID
442685003

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 26 Clinical Trial Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
A278 DMKXO9V IND submitted Small molecule [1]
GFT-505 DM7ZOAE Phase 3 NA [2]
GS-9674 DM936V7 Phase 3 Small molecular drug [3]
Aldafermin DM5ITEZ Phase 2 Protein [4]
ASP9831 DM2MSGF Phase 2 Small molecular drug [5]
CRV431 DMW04YQ Phase 2 Small molecular drug [6]
EDP-305 DMGJYZ8 Phase 2 Small molecular drug [7]
Efinopegdutide DMAN2V2 Phase 2 Peptide [8]
EYP001 DM5PBLM Phase 2 Small molecular drug [9]
GR-MD-02 DM9QF65 Phase 2 Protein [10]
GSK4532990 DMBUAC6 Phase 2 NA [11]
HU6 DMQ4523 Phase 2 Small molecule [12]
ION839 DMWZT3N Phase 2 Ligand-conjugated antisense [13]
IVA337 DMJV3AX Phase 2 Small molecular drug [14]
LMB763 DMQOXNL Phase 2 Small molecular drug [15]
MET409 DM89QXT Phase 2 Small molecular drug [16]
MK-3655 DMM5SVL Phase 2 Monoclonal antibody [17]
PF-06865571 DMZE3GK Phase 2 Small molecule [18]
AGN-242266 DMVHPOX Phase 1 Small molecular drug [19]
AMG 609 DMVCA06 Phase 1 Small interfering RNA [20]
AZD7503 DM8XJD2 Phase 1 Small molecule [21]
CB4211 DMP2FP3 Phase 1 NA [22]
HPP971 DMZXG7Q Phase 1 Small molecular drug [23]
ION 224 DMD7LHM Phase 1 Antisense oligonucleotide [24]
JNJ-75220795 DM2LQ5Z Phase 1 NA [25]
SAR-548304 DMJAZF4 Phase 1 NA [26]
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⏷ Show the Full List of 26 Drug(s)
This Disease is Treated as An Indication in 6 Investigative Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
AC-3174 DMNUE4H Investigative Small molecular drug [27]
AK-20 DME4JAQ Investigative NA [28]
MitoAscorbate DM8EU8B Investigative NA [28]
MitoLinoleic DMU8LRD Investigative NA [28]
NRL-0301 DMC23G4 Investigative NA [28]
PN-2XXX DMB3E38 Investigative NA [28]
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⏷ Show the Full List of 6 Drug(s)

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 91 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
ADAMTS13 TTUREBK Limited Biomarker [29]
ADAMTS5 TTXSU2Y Limited Genetic Variation [30]
ADRA2A TTWG9A4 Limited Biomarker [31]
FABP4 TTHWMFZ Limited Biomarker [32]
FFAR1 TTB8FUC Limited Biomarker [33]
GCGR TT9O6WS Limited Biomarker [34]
GPBAR1 TTSDVTR Limited Biomarker [35]
GPR119 TT7QNVC Limited Biomarker [36]
LBP TTVQJLY Limited Biomarker [37]
LDLR TTH0DUS Limited Biomarker [38]
LIPA TTS8T1M Limited Altered Expression [39]
MGAM TTXWASR Limited Altered Expression [40]
MLYCD TT9Z4YD Limited Biomarker [41]
NPPC TTRK0B9 Limited Altered Expression [42]
PPARGC1B TTKSQ3W Limited Biomarker [43]
SLC10A2 TTPI1M5 Limited Biomarker [44]
TMBIM6 TT7QSMG Limited Biomarker [45]
ALDH2 TTFLN4T Disputed Biomarker [46]
CAT TTPS279 Disputed Biomarker [46]
PPARD TT2JWF6 Disputed Therapeutic [47]
SIRT1 TTUF2HO Disputed Altered Expression [48]
ACAT1 TTK3C21 moderate Biomarker [49]
ADRB3 TTMXGCW moderate Genetic Variation [50]
BCAT1 TTES57P moderate Biomarker [51]
GIP TT40HS5 moderate Biomarker [52]
LEP TTBJEZ5 moderate Biomarker [53]
MAP3K11 TTETX6Q moderate Biomarker [54]
NPC1L1 TTPD1CN moderate Biomarker [55]
PEMT TT735V2 moderate Genetic Variation [56]
SLC11A2 TT2IS7P moderate Altered Expression [57]
SLCO1A2 TTUGD21 moderate Altered Expression [58]
ABCB4 TTJUXV6 Strong Biomarker [59]
ABCC2 TTFLHJV Strong Biomarker [60]
ADH1A TT5AHZ0 Strong Biomarker [46]
ADIPOQ TTXKA7D Strong Biomarker [61]
AHCY TTE2KUJ Strong Biomarker [62]
AHR TT037IE Strong Biomarker [63]
CD14 TT6I7DC Strong Biomarker [64]
CD36 TTPJMCU Strong Biomarker [65]
CEACAM1 TTA9CK4 Strong Genetic Variation [66]
CFLAR TTJZQYH Strong Biomarker [67]
CHIT1 TTDYX6T Strong Altered Expression [68]
CLCN2 TT30NW6 Strong Altered Expression [69]
CMKLR1 TT4UGZL Strong Biomarker [70]
CPA1 TT3LJ6G Strong Biomarker [71]
CSF2 TTNYZG2 Strong Biomarker [72]
CYP17A1 TTRA5BZ Strong Biomarker [73]
CYP1A2 TTS1DTU Strong Biomarker [74]
EIF2AK1 TTRUJBV Strong Biomarker [47]
F2 TT6L509 Strong Biomarker [75]
FAS TT7LTUJ Strong Biomarker [76]
FGF19 TTGCH11 Strong Biomarker [77]
FGF21 TTQ916P Strong Biomarker [78]
FGR TTPOGS1 Strong Biomarker [79]
FOLR2 TTT54CI Strong Biomarker [80]
GLP1R TTVIMDE Strong Altered Expression [81]
GSTA1 TT4P8DE Strong Biomarker [82]
GSTP1 TT40K12 Strong Biomarker [83]
IL13RA2 TTMPZ7V Strong Biomarker [84]
IL1A TTPM6HI Strong Altered Expression [72]
IL4 TTLGTKB Strong Biomarker [72]
ITPR2 TTK9OV3 Strong Altered Expression [85]
JAK2 TTRMX3V Strong Biomarker [86]
KLB TTARBVH Strong Biomarker [47]
LIF TTGZ5WN Strong Biomarker [72]
MADCAM1 TTBD6I7 Strong Altered Expression [87]
MAP3K5 TTOQCD8 Strong Biomarker [88]
MC4R TTD0CIQ Strong Biomarker [89]
MGAT2 TTJOW1I Strong Biomarker [90]
MMP1 TTMX39J Strong Biomarker [72]
MTTP TTUS1RD Strong Biomarker [91]
NFE2L2 TTA6ZN2 Strong Biomarker [92]
NQO1 TT8XK6L Strong Biomarker [47]
NR1H4 TTS4UGC Strong Biomarker [35]
NR5A2 TTAU3SY Strong Biomarker [93]
PNPLA3 TTEUAEH Strong Genetic Variation [94]
PPARA TTJ584C Strong Altered Expression [95]
PRDX4 TTPBL9I Strong Biomarker [96]
PRKACA TT5U49F Strong Biomarker [60]
PRKCA TTFJ8Q1 Strong Biomarker [60]
PRKCD TT7A1BO Strong Biomarker [60]
PRKCE TT57MT2 Strong Biomarker [60]
RBP4 TT0C8BY Strong Altered Expression [97]
SCARB1 TTRE324 Strong Biomarker [98]
SLC5A2 TTF8JAT Strong Biomarker [99]
SREBF1 TTER0UB Strong Biomarker [100]
STC2 TT4EFTR Strong Biomarker [101]
TICAM1 TT2GQT6 Strong Biomarker [102]
TLR6 TTWRI8V Strong Altered Expression [103]
TM6SF2 TTE1OHM Strong Genetic Variation [104]
TNFRSF1B TT63WSF Strong Biomarker [64]
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⏷ Show the Full List of 91 DTT(s)
This Disease Is Related to 1 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
SLC51A DTMEQ32 Strong Altered Expression [105]
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This Disease Is Related to 11 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
GSTA4 DEH7XYP Limited Genetic Variation [106]
SI DE5EO4Y Limited Altered Expression [40]
ADH1B DEEN9RD Disputed Biomarker [46]
ADH1C DEM1HNL moderate Biomarker [107]
MAT1A DEQ6NC9 moderate Biomarker [49]
ADH4 DEOCWU3 Strong Biomarker [46]
ALDH1A1 DE2JP1Y Strong Biomarker [46]
ALDH1B1 DEXI4UQ Strong Biomarker [46]
GPT DER5HFI Strong Biomarker [108]
GSTM1 DEYZEJA Strong Biomarker [107]
GSTT1 DE3PKUG Strong Biomarker [107]
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⏷ Show the Full List of 11 DME(s)
This Disease Is Related to 72 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
AEBP1 OTBI1RZ6 Limited Biomarker [109]
ARSH OTG0X9UQ Limited Genetic Variation [110]
AWAT1 OT8OTY3E Limited Biomarker [111]
BHLHE23 OTLSVD17 Limited Biomarker [112]
ENHO OT91QASK Limited Biomarker [113]
FBL OTRODIE5 Limited Biomarker [114]
FBXW5 OT5TQK3H Limited Biomarker [115]
FNDC5 OT5CSK9X Limited Genetic Variation [116]
GGTLC1 OTWJKUHQ Limited Altered Expression [117]
GNMT OT0O2OQO Limited Altered Expression [118]
IBTK OTB2GM4G Limited Biomarker [119]
IL20RA OTSIVBVS Limited Biomarker [120]
JCAD OT7G1WJW Limited Biomarker [121]
LPCAT3 OTWI96P4 Limited Biomarker [122]
MOCOS OT0TL3Q5 Limited Genetic Variation [41]
MYOM2 OTD2UOXW Limited Biomarker [123]
NRF1 OTOXWNV8 Limited Biomarker [124]
RTL1 OTOT33IM Limited Biomarker [125]
SETMAR OTE2MIMZ Limited Biomarker [125]
SMCP OTXKY794 Limited Genetic Variation [41]
ST3GAL4 OTNENJZQ Limited Biomarker [126]
STAM OT6X5RR1 Limited Biomarker [127]
STK24 OTGUHOIL Limited Biomarker [123]
SUV39H2 OTU0F4LL Limited Biomarker [128]
PDK4 OTCMHMBZ Disputed Biomarker [129]
ACO1 OT2VUR7L moderate Altered Expression [57]
ELOVL6 OTB26UJJ moderate Biomarker [130]
PSPH OTV1PVAX moderate Biomarker [51]
SHMT1 OTIINA3J moderate Biomarker [51]
ACE OTDF1964 Strong Biomarker [72]
ACSL4 OTI71MUJ Strong Genetic Variation [131]
ALDH4A1 OT25Z6XH Strong Biomarker [46]
ARNT OTMSIEZY Strong Biomarker [132]
ATP5F1B OTLFZUQK Strong Biomarker [133]
B3GAT1 OTXFP98E Strong Biomarker [134]
CISD2 OTVS7S2H Strong Biomarker [135]
CPT1A OTI862QH Strong Biomarker [47]
FOXA3 OTRGT2OT Strong Altered Expression [136]
GABPA OT9YB2SA Strong Biomarker [92]
GPS2 OT065FSS Strong Biomarker [95]
GSDMD OTH39BKI Strong Biomarker [137]
HCFC1 OT0UCK62 Strong Biomarker [138]
HFE OTDD93KB Strong Biomarker [139]
HSPA12A OTFOCDD6 Strong Biomarker [140]
IKBKG OTNWJWSD Strong Biomarker [141]
IL3 OT0CQ35N Strong Biomarker [72]
INTU OTXB13E6 Strong Biomarker [35]
KRT18 OTVLQFIP Strong Biomarker [142]
LAMA1 OTQZMP86 Strong Biomarker [72]
LGALS14 OTOR23GX Strong Altered Expression [69]
LGALS3BP OT9AGQKH Strong Altered Expression [143]
LITAF OTT5JX1F Strong Biomarker [144]
LRPAP1 OT6DVD2Q Strong Biomarker [145]
MT1B OTUA4FFH Strong Genetic Variation [146]
NCOA2 OTMQFPBB Strong Biomarker [79]
NMU OTW9X7BQ Strong Biomarker [147]
OR10A4 OTYYB8SY Strong Genetic Variation [148]
PLPP3 OTSSF7BK Strong Altered Expression [149]
PNPLA2 OTR3ERMR Strong Biomarker [150]
PRF1 OTFVXD7H Strong Biomarker [134]
PRX OT34Z10B Strong Biomarker [151]
RAB5A OTFR2KM4 Strong Altered Expression [149]
RAG2 OTG9UYTW Strong Biomarker [134]
RDX OTNSYUN6 Strong Biomarker [60]
SAMM50 OTRYFYIU Strong Genetic Variation [152]
SART1 OTHMOGO1 Strong Biomarker [153]
SERPINB2 OT72QLZB Strong Biomarker [72]
SLC25A47 OT5NGRWC Strong Altered Expression [154]
SRSF3 OTOFT707 Strong Genetic Variation [155]
TRIB3 OTG5OS7X Strong Biomarker [47]
TRIM69 OTTEGTRD Strong Biomarker [102]
TRPC4AP OTNJ9IFS Strong Altered Expression [156]
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⏷ Show the Full List of 72 DOT(s)

References

1 Clinical pipeline report, company report or official report of Klus Pharma
2 ClinicalTrials.gov (NCT02704403) Phase 3 Study to Evaluate the Efficacy and Safety of Elafibranor Versus Placebo in Patients With Nonalcoholic Steatohepatitis (NASH) (RESOLVE-IT). U.S. National Institutes of Health.
3 ClinicalTrials.gov (NCT03449446) Study to Evaluate the Safety and Efficacy of Selonsertib, Firsocostat, Cilofexor, and Combinations in Participants With Bridging Fibrosis or Compensated Cirrhosis Due to Nonalcoholic Steatohepatitis (NASH) (ATLAS). U.S. National Institutes of Health.
4 ClinicalTrials.gov (NCT04210245) Evaluation of Efficacy, Safety and Tolerability of NGM282 (Aldafermin) in a Phase 2b, Randomized, Double-blind, Placebo-controlled, Multi-center Study in Subjects With Compensated Cirrhosis Due to Nonalcoholic Steatohepatitis (ALPINE 4). U.S.National Institutes of Health.
5 ClinicalTrials.gov (NCT00668070) A Proof-of-principle Study of Oral Treatment of Non-alcoholic Steatohepatitis With a Novel PDE4 Inhibitor ASP9831 (ASTER). U.S. National Institutes of Health.
6 ClinicalTrials.gov (NCT04480710) A Study of CRV431 Dosed Once Daily in NASH Induced F2 and F3 Subjects (AMBITION). U.S. National Institutes of Health.
7 ClinicalTrials.gov (NCT04378010) A Randomized, Double-blind Study to Assess the Safety and Efficacy of EDP-305 in Subjects With Liver-biopsy Proven NASH. U.S. National Institutes of Health.
8 ClinicalTrials.gov (NCT04944992) A Phase 2a, Randomized, Active-Comparator-Controlled, Open-Label Study to Evaluate the Efficacy and Safety of Efinopegdutide (MK-6024) in Individuals With Nonalcoholic Fatty Liver Disease. U.S.National Institutes of Health.
9 ClinicalTrials.gov (NCT03812029) Safety, Tolerability, Pharmacokinetics and Efficacy of EYP001a in Patients With Nonalcoholic Steatohepatitis (NASH). U.S. National Institutes of Health.
10 ClinicalTrials.gov (NCT01899859) Phase 1 Study to Evaluate Safety of GR-MD-02 in Subjects With Non-Alcoholic Steatohepatitis (NASH) and Advanced Fibrosis. U.S. National Institutes of Health.
11 ClinicalTrials.gov (NCT05583344) 17 beta-Hydroxysteroid Dehydrogenase Type 13 Minimization for the Treatment of NASH (HORIZON): A Double-Blind, Placebo-Controlled Phase 2b Study to Evaluate the Efficacy and Safety of GSK4532990 in Adults With Pre-Cirrhotic Nonalcoholic Steatohepatitis. U.S.National Institutes of Health.
12 ClinicalTrials.gov (NCT04874233) A 61-day Randomized, Double Blind, Placebo-controlled Trial to Assess the Safety and Efficacy of Three Doses of HU6 in Subjects With Elevated Liver Fat and High Body Mass Index (28 to 45 kg/m2). U.S.National Institutes of Health.
13 ClinicalTrials.gov (NCT05809934) A Randomised, Double-blind, Placebo-controlled, Multi-centre Phase 2b Study to Evaluate the Efficacy, Safety and Tolerability of AZD2693 in Participants With Non-cirrhotic Non-alcoholic Steatohepatitis (NASH) With Fibrosis Who Are Carriers of the PNPLA3 rs738409 148M Risk Allele. U.S.National Institutes of Health.
14 ClinicalTrials.gov (NCT03008070) Phase 2b Study in NASH to Assess IVA337 (NATIVE). U.S. National Institutes of Health.
15 ClinicalTrials.gov (NCT02913105) Safety, Tolerability, Pharmacokinetics and Efficacy of LMB763 in Patients With NASH. U.S. National Institutes of Health.
16 ClinicalTrials.gov (NCT04702490) Study to Evaluate MET409 Alone or in Combination With Empagliflozin in Patients With Type 2 Diabetes and NASH. U.S. National Institutes of Health.
17 ClinicalTrials.gov (NCT04583423) A Phase 2b Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of MK-3655 in Individuals With Pre-cirrhotic Nonalcoholic Steatohepatitis. U.S.National Institutes of Health.
18 ClinicalTrials.gov (NCT04321031) A PHASE 2, RANDOMIZED, DOUBLE-BLIND, DOUBLE-DUMMY, PLACEBO-CONTROLLED, DOSE-RANGING, DOSE-FINDING, PARALLEL GROUP STUDY TO ASSESS EFFICACY AND SAFETY OF PF-06865571 (DGAT2I) ALONE AND WHEN COADMINISTERED WITH PF-05221304 (ACCI) IN ADULT PARTICIPANTS WITH BIOPSY-CONFIRMED NONALCOHOLIC STEATOHEPATITIS AND FIBROSIS STAGE 2 OR 3. U.S.National Institutes of Health.
19 Clinical pipeline report, company report or official report of AbbVie.
20 ClinicalTrials.gov (NCT04857606) A Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AMG 609 in Subjects With Non-alcoholic Fatty Liver Disease. U.S.National Institutes of Health.
21 ClinicalTrials.gov (NCT05560607) An Open-label, Non-randomized, Multiple-dose Study to Assess the Knockdown of Hepatic HSD17B13 mRNA Expression, Pharmacokinetics, Safety, and Tolerability Following Administration of AZD7503 in Participants With Non-alcoholic Fatty Liver Disease. U.S.National Institutes of Health.
22 Constrained peptides' time to shine. Nat Rev Drug Discov. 2018 Jul 30;17(8):531-533.
23 Clinical pipeline report, company report or official report of vTv Therapeutics.
24 Clinical pipeline report, company report or official report of Ionis Pharmaceuticals.
25 ClinicalTrials.gov (NCT04844450) A Double-Blind, Placebo-Controlled, Randomized, Multipart, Single and Multiple Ascending Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered JNJ-75220795. U.S.National Institutes of Health.
26 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800030689)
27 2005 approvals: Safety first. Nature Reviews Drug Discovery 5, 92-93 (February 2006).
28 The ChEMBL database in 2017. Nucleic Acids Res. 2017 Jan 4;45(D1):D945-D954.
29 ADAMTS13 deficiency promotes microthrombosis in a murine model of diet-induced liver steatosis.Thromb Haemost. 2017 Jan 5;117(1):19-26. doi: 10.1160/TH16-03-0195. Epub 2016 Sep 8.
30 Functional role of ADAMTS5 in adiposity and metabolic health.PLoS One. 2018 Jan 2;13(1):e0190595. doi: 10.1371/journal.pone.0190595. eCollection 2018.
31 Different roles of FAT10, FOXO1, and ADRA2A in hepatocellular carcinoma tumorigenesis in patients with alcoholic steatohepatitis (ASH) vs non-alcoholic steatohepatitis (NASH).Exp Mol Pathol. 2018 Aug;105(1):144-149. doi: 10.1016/j.yexmp.2018.07.005. Epub 2018 Jul 17.
32 Beneficial Effects of Korean Red Ginseng in the Progression of Non-Alcoholic Steatohepatitis via FABP4 Modulation.Am J Chin Med. 2018 Oct 9:1-27. doi: 10.1142/S0192415X18500817. Online ahead of print.
33 RLA8-A New and Highly Effective Quadruple PPAR-// and GPR40 Agonist to Reverse Nonalcoholic Steatohepatitis and Fibrosis.J Pharmacol Exp Ther. 2019 Apr;369(1):67-77. doi: 10.1124/jpet.118.255216. Epub 2019 Feb 11.
34 MEDI0382, a GLP-1/glucagon receptor dual agonist, meets safety and tolerability endpoints in a single-dose, healthy-subject, randomized, Phase 1 study.Br J Clin Pharmacol. 2018 Oct;84(10):2325-2335. doi: 10.1111/bcp.13688. Epub 2018 Aug 7.
35 INT-767 improves histopathological features in a diet-induced ob/ob mouse model of biopsy-confirmed non-alcoholic steatohepatitis.World J Gastroenterol. 2018 Jan 14;24(2):195-210. doi: 10.3748/wjg.v24.i2.195.
36 Co-administration of APD668, a G protein-coupled receptor 119 agonist and linagliptin, a DPPIV inhibitor, prevents progression of steatohepatitis in mice fed on a high trans-fat diet.Biochem Biophys Res Commun. 2018 Jan 8;495(2):1608-1613. doi: 10.1016/j.bbrc.2017.12.004. Epub 2017 Dec 5.
37 Association between endotoxemia and histological features of nonalcoholic fatty liver disease.World J Gastroenterol. 2017 Jan 28;23(4):712-722. doi: 10.3748/wjg.v23.i4.712.
38 Amitriptyline inhibits nonalcoholic steatohepatitis and atherosclerosis induced by high-fat diet and LPS through modulation of sphingolipid metabolism.Am J Physiol Endocrinol Metab. 2020 Feb 1;318(2):E131-E144. doi: 10.1152/ajpendo.00181.2019. Epub 2019 Dec 10.
39 Reduced lysosomal acid lipase activity: A new marker of liver disease severity across the clinical continuum of non-alcoholic fatty liver disease?.World J Gastroenterol. 2019 Aug 14;25(30):4172-4180. doi: 10.3748/wjg.v25.i30.4172.
40 The Phytocomplex from Fucus vesiculosus and Ascophyllum nodosum Controls Postprandial Plasma Glucose Levels: An In Vitro and In Vivo Study in a Mouse Model of NASH.Mar Drugs. 2017 Feb 15;15(2):41. doi: 10.3390/md15020041.
41 Metformin ameliorates activation of hepatic stellate cells and hepatic fibrosis by succinate and GPR91 inhibition.Biochem Biophys Res Commun. 2018 Jan 22;495(4):2649-2656. doi: 10.1016/j.bbrc.2017.12.143. Epub 2017 Dec 24.
42 C-type natriuretic peptide (CNP) in endothelial cells attenuates hepatic fibrosis and inflammation in non-alcoholic steatohepatitis.Life Sci. 2018 Sep 15;209:349-356. doi: 10.1016/j.lfs.2018.08.031. Epub 2018 Aug 13.
43 Metabolic aspects in NAFLD, NASH and hepatocellular carcinoma: the role of PGC1 coactivators.Nat Rev Gastroenterol Hepatol. 2019 Mar;16(3):160-174. doi: 10.1038/s41575-018-0089-3.
44 Apical sodium-dependent bile acid transporter inhibition with volixibat improves metabolic aspects and components of non-alcoholic steatohepatitis in Ldlr-/-.Leiden mice.PLoS One. 2019 Jun 24;14(6):e0218459. doi: 10.1371/journal.pone.0218459. eCollection 2019.
45 Bax inhibitor-1 protects from nonalcoholic steatohepatitis by limiting inositol-requiring enzyme 1 alpha signaling in mice.Hepatology. 2018 Aug;68(2):515-532. doi: 10.1002/hep.29847. Epub 2018 May 18.
46 Alcohol Metabolism in the Progression of Human Nonalcoholic Steatohepatitis.Toxicol Sci. 2018 Aug 1;164(2):428-438. doi: 10.1093/toxsci/kfy106.
47 Hepatic regulation of VLDL receptor by PPAR/ and FGF21 modulates non-alcoholic fatty liver disease.Mol Metab. 2018 Feb;8:117-131. doi: 10.1016/j.molmet.2017.12.008. Epub 2017 Dec 19.
48 Skeletal muscle miR-34a/SIRT1:AMPK axis is activated in experimental and human non-alcoholic steatohepatitis.J Mol Med (Berl). 2019 Aug;97(8):1113-1126. doi: 10.1007/s00109-019-01796-8. Epub 2019 May 28.
49 Methionine adenosyltransferases in liver cancer.World J Gastroenterol. 2019 Aug 21;25(31):4300-4319. doi: 10.3748/wjg.v25.i31.4300.
50 Polymorphisms of interleukin-1 beta and beta 3-adrenergic receptor in Japanese patients with nonalcoholic steatohepatitis.Alcohol Clin Exp Res. 2004 Aug;28(s2):106S-110S. doi: 10.1111/j.1530-0277.2004.tb03226.x.
51 Genome-scale metabolic modelling of hepatocytes reveals serine deficiency in patients with non-alcoholic fatty liver disease.Nat Commun. 2014;5:3083. doi: 10.1038/ncomms4083.
52 Prolonged saturated fat-induced, glucose-dependent insulinotropic polypeptide elevation is associated with adipokine imbalance and liver injury in nonalcoholic steatohepatitis: dysregulated enteroadipocyte axis as a novel feature of fatty liver.Am J Clin Nutr. 2009 Feb;89(2):558-67. doi: 10.3945/ajcn.2008.26720. Epub 2009 Jan 13.
53 New evidence for the therapeutic potential of curcumin to treat nonalcoholic fatty liver disease in humans.PLoS One. 2017 Mar 3;12(3):e0172900. doi: 10.1371/journal.pone.0172900. eCollection 2017.
54 Mixed-lineage kinase 3 pharmacological inhibition attenuates murine nonalcoholic steatohepatitis.JCI Insight. 2017 Aug 3;2(15):e94488. doi: 10.1172/jci.insight.94488. eCollection 2017 Aug 3.
55 Ezetimibe, an NPC1L1 inhibitor, is a potent Nrf2 activator that protects mice from diet-induced nonalcoholic steatohepatitis.Free Radic Biol Med. 2016 Oct;99:520-532. doi: 10.1016/j.freeradbiomed.2016.09.009. Epub 2016 Sep 12.
56 Total liver phosphatidylcholine content associates with non-alcoholic steatohepatitis and glycine N-methyltransferase expression.Liver Int. 2019 Oct;39(10):1895-1905. doi: 10.1111/liv.14174. Epub 2019 Jul 8.
57 Increased duodenal iron absorption through up-regulation of divalent metal transporter 1 from enhancement of iron regulatory protein 1 activity in patients with nonalcoholic steatohepatitis.Hepatology. 2015 Sep;62(3):751-61. doi: 10.1002/hep.27774. Epub 2015 Apr 8.
58 Synergistic interaction between genetics and disease on pravastatin disposition.J Hepatol. 2014 Jul;61(1):139-47. doi: 10.1016/j.jhep.2014.02.021. Epub 2014 Mar 5.
59 Therapeutic effect of bezafibrate against biliary damage: a study of phospholipid secretion via the PPARalpha-MDR3 pathway.Int J Clin Pharmacol Ther. 2010 Jan;48(1):22-8. doi: 10.5414/cpp48022.
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