Gastric ulcer

disease
On this page

Also known as acute gastric ulcer with haemorrhage and obstructionacute gastric ulcer with haemorrhage and perforationacute gastric ulcer with haemorrhage and perforation, with obstructionacute gastric ulcer with haemorrhage and perforation, without mention of obstructionacute gastric ulcer with haemorrhage and with perforation but without obstructionacute gastric ulcer with hemorrhage and obstructionacute gastric ulcer with hemorrhage and perforationacute gastric ulcer with hemorrhage and perforation, with obstructionacute gastric ulcer with hemorrhage and perforation, without mention of obstructionacute gastric ulcer with hemorrhage and with perforation but without obstructionacute gastric ulcer with hemorrhage, with obstructionacute gastric ulcer with hemorrhage, with perforation and with obstructionacute gastric ulcer with perforationacute gastric ulcer with perforation and obstructionacute gastric ulcer with perforation, with obstructionacute gastric ulcer without haemorrhage and without perforationacute gastric ulcer without hemorrhage and without perforationacute gastric ulcer without hemorrhage, without perforation and without obstructionacute gastric ulcer without mention of haemorrhage or perforation, without mention of obstructionacute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction

Summary

Gastric ulcer (MONDO:0001126) is a disease with 56 GWAS associations across 34 studies and 81 clinical trials. Top therapeutic interventions include vonoprazan, lansoprazole, and rabeprazole. A subtype of peptic ulcer disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • GWAS associations: 56
  • Clinical trials: 81

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namegastric ulcer
Mondo IDMONDO:0001126
EFOEFO:0009454
MeSHD013276
DOIDDOID:10808
ICD-10-CMK25
ICD-111437411258
NCITC3388
SNOMED CT397825006
UMLSC0038358
MedGen21330
Anatomy (UBERON)UBERON:0000945
Is cancer (heuristic)no

Also known as: acute gastric ulcer with haemorrhage and obstruction · acute gastric ulcer with haemorrhage and perforation · acute gastric ulcer with haemorrhage and perforation, with obstruction · acute gastric ulcer with haemorrhage and perforation, without mention of obstruction · acute gastric ulcer with haemorrhage and with perforation but without obstruction · acute gastric ulcer with hemorrhage and obstruction · acute gastric ulcer with hemorrhage and perforation · acute gastric ulcer with hemorrhage and perforation, with obstruction · acute gastric ulcer with hemorrhage and perforation, without mention of obstruction · acute gastric ulcer with hemorrhage and with perforation but without obstruction · acute gastric ulcer with hemorrhage, with obstruction · acute gastric ulcer with hemorrhage, with perforation and with obstruction · acute gastric ulcer with perforation · acute gastric ulcer with perforation and obstruction · acute gastric ulcer with perforation, with obstruction · acute gastric ulcer without haemorrhage and without perforation · acute gastric ulcer without hemorrhage and without perforation · acute gastric ulcer without hemorrhage, without perforation and without obstruction · acute gastric ulcer without mention of haemorrhage or perforation, without mention of obstruction · acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction (+11 more)

Data availability: 56 GWAS associations (34 studies) · 1 HPO phenotype.

Disease family

This is a subtype of peptic ulcer disease. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › digestive system disorderpeptic ulcer diseasegastric ulcer

Related subtypes (5): gastrojejunal ulcer, active peptic ulcer disease, peptic ulcer perforation, duodenal ulcer, peptic esophagitis

Subtypes (1): gastroduodenitis

Genetics & variants

GWAS landscape

56 GWAS associations across 34 studies. Top hits map to 21 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs22940081e-58JRK, PSCAT0.43
rs346356475e-39JRK, PSCAG0.14
rs1434843041e-38PSCA, JRKT0.14
rs354643793e-25PSCA - LY6KC0.11
rs29763976e-24PSCA - LY6KT0.13
rs1831785504e-13KCNJ5-AS1A2.59
rs1475046192e-12NPEPPSP1 - MRPL45C1.78
rs6813433e-12FUT2?0.91
rs5586851914e-12PPM1AP1 - RPL32P19C2.62
rs760367995e-12IRF4 - EXOC2C3.19
rs5429758916e-12LINC03109, LINC02006C3.02
rs5447679836e-12TMEM244 - L3MBTL3T3.29
rs5529641871e-11LRRK2G2.37
rs746077791e-11MUC5ACG1.82
rs5459349102e-11MRPS33P3 - RPF2P2A1.67
rs1895783452e-11ZNF970P - AK6P2A2.54
rs29202813e-11JRK, PSCA?0.91
rs5297767543e-11ALK - YPEL5C1.77
rs7674534893e-11MIR4634 - LINC01951G2.38
rs1848293204e-11VAPA - LINC01254A2.87
rs6876211e-10ABO?0.91
rs12055312e-10RNU6-309P - GAPDHP77T0.07
rs178669123e-10PRELID3BP10 - ZNF800G0.15
rs68603286e-10TTC33C0.07
rs5462383999e-10PRKAA1CTCT0.07
rs81146892e-09GNASA0.06
rs60265762e-09GNASG0.16
rs1470486772e-09MUC1?1.18
chr11:176428042e-09A2.68
rs46854053e-09PLCL2T0.06

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90432136Jiang Y2023116,382213,325A cross-disorder study to identify causal relationships, shared genetic variants, and genes across 21 digestive disorders.
GCST90270927He Y202320,972240,675East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease.
GCST90270931He Y202320,972240,675East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease.
GCST90018631Sakaue S202112,650161,227A cross-population atlas of genetic associations for 220 human phenotypes.
GCST90473779UK Biobank Whole-Genome Sequencing Consortium202512,139446,301Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90667756UK Biobank Whole-Genome Sequencing Consortium202512,139446,301Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90651695Liu TY202512,035202,293Diversity and longitudinal records: Genetic architecture of disease associations and polygenic risk in the Taiwanese Han population.
GCST90018851Sakaue S20216,293467,985A cross-population atlas of genetic associations for 220 human phenotypes.
GCST90080197Backman JD20215,549381,689Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084183Backman JD20215,549381,689Exome sequencing and analysis of 454,787 UK Biobank participants.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding4
Tier 2: splice/UTR2
Tier 3: regulatory0
Tier 4: intronic/intergenic41

MAF distribution

BucketVariants
common (>=0.05)25
low_freq (0.01-0.05)0
rare (<0.01)14
unknown8

Functional consequences

ConsequenceCount
intron_variant17
intergenic_variant16
unknown6
missense_variant2
synonymous_variant2
5_prime_UTR_variant1
stop_gained1
frameshift_variant1
3_prime_UTR_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs22940088142680513C>T0.3585_prime_UTR_variantJRK, PSCA1e-58Tier 2: splice/UTR
rs346356478142675472A>G0.377intergenic_variantJRK, PSCA5e-39Tier 4: intronic/intergenic
rs14348430481426789490.366intergenic_variantPSCA, JRK1e-38Tier 4: intronic/intergenic
rs354643798142698205CTT>C,CT,CTTT,CTTTT0.05intergenic_variantPSCA - LY6K3e-25Tier 4: intronic/intergenic
rs29763978142683195G>A,C,T0.496intergenic_variantPSCA - LY6K6e-24Tier 4: intronic/intergenic
rs18317855011128883365A>G0.001intron_variantKCNJ5-AS14e-13Tier 4: intronic/intergenic
rs1475046191738266717C>T0.003intergenic_variantNPEPPSP1 - MRPL452e-12Tier 4: intronic/intergenic
rs6813431948703205C>A,T0.05stop_gainedFUT23e-12Tier 1: coding
rs558685191815864638C>A,T0intergenic_variantPPM1AP1 - RPL32P194e-12Tier 4: intronic/intergenic
rs760367996445634C>T0intergenic_variantIRF4 - EXOC25e-12Tier 4: intronic/intergenic
rs5429758913153420017C>T0intron_variantLINC03109, LINC020066e-12Tier 4: intronic/intergenic
rs5447679836129965131T>C0intergenic_variantTMEM244 - L3MBTL36e-12Tier 4: intronic/intergenic
rs5529641871240325063G>A0intron_variantLRRK21e-11Tier 4: intronic/intergenic
rs74607779111160635G>A,C0.001missense_variantMUC5AC1e-11Tier 1: coding
rs5459349104115240446A>G0.003intergenic_variantMRPS33P3 - RPF2P22e-11Tier 4: intronic/intergenic
rs1895783451238039429A>T0intergenic_variantZNF970P - AK6P22e-11Tier 4: intronic/intergenic
rs29202818142679026C>G,T0.05intergenic_variantJRK, PSCA3e-11Tier 4: intronic/intergenic
rs529776754230115642C>T0.002intron_variantALK - YPEL53e-11Tier 4: intronic/intergenic
rs7674534895174806394G>A0intron_variantMIR4634 - LINC019513e-11Tier 4: intronic/intergenic
rs1848293201810338771A>G0intron_variantVAPA - LINC012544e-11Tier 4: intronic/intergenic
rs6876219133261662G>A,C,T0.05intron_variantABO1e-10Tier 4: intronic/intergenic
rs1205531X109296833G>A,C,T0.367intergenic_variantRNU6-309P - GAPDHP772e-10Tier 4: intronic/intergenic
rs178669127127305741T>G0.098intergenic_variantPRELID3BP10 - ZNF8003e-10Tier 4: intronic/intergenic
rs6860328540729872T>C0.424intron_variantTTC336e-10Tier 4: intronic/intergenic
rs546238399540790526C>CTCT,CTCTT,CTCTTT,CTCTTTT,CTCTTTTT,CTCTTTTTT,CTCTTTTTTT,CTCTTTTTTTT,CTCTTTTTTTTT,CTCTTTTTTTTTT,CTCTTTTTTTTTTT,CTCTTTTTTTTTTTT,CTCTTTTTTTTTTTTT,CTCTTTTTTTTTTTTTT,CTCTTTTTTTTTTTTTTTTT0.387intron_variantPRKAA19e-10Tier 4: intronic/intergenic
rs81146892058901835G>A,C0.407intron_variantGNAS2e-09Tier 4: intronic/intergenic
rs60265762058884112A>C,G,T0.339intron_variantGNAS2e-09Tier 4: intronic/intergenic
rs1470486771155192003C>G,T0.05synonymous_variantMUC12e-09Tier 4: intronic/intergenic
chr11:176428042e-09Tier 4: intronic/intergenic
rs4685405316940191G>A,T0.458intron_variantPLCL23e-09Tier 4: intronic/intergenic

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated for this disease

5 approved, 10 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
FamotidineApproved (phase 4)
LansoprazoleApproved (phase 4)
MisoprostolApproved (phase 4)
NaproxenApproved (phase 4)
OmeprazoleApproved (phase 4)
AmoxicillinPhase 3 (in late-stage trials)
AspirinPhase 3 (in late-stage trials)
Bismuth Subcitrate PotassiumPhase 3 (in late-stage trials)
ClarithromycinPhase 3 (in late-stage trials)
DiclofenacPhase 3 (in late-stage trials)
EsomeprazolePhase 3 (in late-stage trials)
GefarnatePhase 3 (in late-stage trials)
RanitidinePhase 3 (in late-stage trials)
RebamipidePhase 3 (in late-stage trials)
TegoprazanPhase 3 (in late-stage trials)

Clinical trials & evidence

Clinical trials

Clinical trials: 81.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE329
Not specified28
PHASE411
PHASE19
PHASE22
PHASE2/PHASE31
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07312370PHASE4NOT_YET_RECRUITINGEsomeprazole Plus Sucralfate for Post-ESD Ulcer Healing
NCT00125736PHASE4COMPLETEDA Double-blind, Comparative Study in Patients With Gastric Ulcer to Evaluate the Efficacy of Combination Use of E0671 and Rabeprazole Sodium
NCT00233389PHASE4COMPLETEDPost-marketing Clinical Study of Rebamipide in Patients With Gastric Ulcer
NCT00239551PHASE4COMPLETEDEffect of Prevacid on Prostaglandin Levels in Patient With Stress Ulcer
NCT00272467PHASE4COMPLETEDHealing Effects of Rebamipide and Omeprazole in Helicobacter Pylori-positive Gastric Ulcer After Eradication Therapy
NCT00428701PHASE4COMPLETEDAn Open-label, Exploratory Trial to Assess Gastric Acid Control in Critically Ill Subjects Receiving Nexium
NCT00839488PHASE4TERMINATEDComparison of Intravenous Pantoprazole and Famotidine for Stress Ulcer Prophylaxis
NCT01190657PHASE4COMPLETEDEfficacy and Safety of Teprenone in Patients With Acute Gastritis, Acute Gastric Lesion of Chronic Gastritis With Acute Exacerbation or Gastric Ulcer
NCT03609892PHASE4COMPLETEDHelicobacter Rescue Therapy With Berberine Plus Amoxicillin Quadruple Therapy Versus Tetracycline Plus Furazolidone Quadruple Therapy
NCT04885751PHASE4UNKNOWNCompare the Effect of Eupatilin and Rebamipide on the Prevention of Gastroenteropathy
NCT05518929PHASE4COMPLETEDHypoxia During Gastroenterological Endoscope Procedures Sedated With Ciprofol In Overweight Or Obesity Patients
NCT00132171PHASE3COMPLETEDHelicobacter Pylori Eradication With a New Sequential Treatment
NCT00149084PHASE3UNKNOWNTailored Treatment of H. Pylori Infection Based Polymorphisms of CYP2C19 and 23S rRNA of H. Pylori
NCT00153673PHASE3COMPLETEDEffect of Selective COX-2 Inhibition on Ulcer Healing
NCT00197418PHASE2/PHASE3UNKNOWNSecond Line Therapy for the Cure of Helicobacter Pylori (H. Pylori) Infection
NCT00401752PHASE3COMPLETEDEfficacy and Safety Study of Esomeprazole 20mg qd vs Ranitidine 150mg Bid in Patients With an NSAID-induced Gastric Ulcer
NCT00441727PHASE3COMPLETEDStudy of Esomeprazole 20 mg or 40 mg vs Placebo Effectiveness on the Occurrence of Peptic Ulcers in Subjects on Low Dose Acetylsalicylic Acid (LDA)
NCT00527787PHASE3COMPLETEDEvaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers Compared to Non-steroidal Antiinflammatory Drug (NSAID) Naproxen
NCT00527904PHASE3COMPLETEDA 12-month, Phase 3, Open-label, Multi-center Study to Evaluate the Long-term Safety of PN400 (VIMOVO)
NCT00542789PHASE3COMPLETEDComparative Efficacy & Safety Study of Esomeprazole Versus Placebo for the Prevention of Gastric and Duodenal Ulcers With NSAID
NCT00594854PHASE3TERMINATEDEvaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers in High Risk Subjects Compared to Arthrotec
NCT00595517PHASE3COMPLETEDLong Term Study to Investigate the Efficacy & Safety of D961H (Esomeprazole) for the Prevention of NSAIDs-induced Ulcer
NCT00762359PHASE3TERMINATEDA Safety and Efficacy Study of Lansoprazole in Preventing Aspirin-Induced Gastric and Duodenal Ulcers
NCT00787254PHASE3COMPLETEDEfficacy and Safety of Lansoprazole on Gastric and Duodenal Ulcers in Patients Taking Nonsteroidal Anti-Inflammatory Drugs
NCT00960869PHASE3COMPLETEDStudy to Evaluate the Incidence of Gastric Ulcers Following Administration of Either PA32540 or Enteric Coated Aspirin 325 mg in Subjects Who Are at Risk for Developing Aspirin-Associated Ulcers
NCT00961350PHASE3COMPLETEDA Study to Evaluate the Incidence of Gastric Ulcers Following Administration of Either PA32540 or Enteric Coated Aspirin 325 mg in Subjects Who Are at Risk for Developing Aspirin-Associated Ulcers
NCT01129011PHASE3COMPLETEDEvaluating PN 400 (VIMOVO) in Reducing Gastric Ulcers Compared to Non-steroidal Antiinflammatory Drug (NSAID) Naproxen
NCT01150162PHASE3COMPLETEDMucosta in Gastric Ulcer Treatment, Effectiveness and Safety Evaluation
NCT01452711PHASE3COMPLETEDEfficacy of TAK-438 Compared to AG-1749 (Lansoprazole) in the Treatment of Gastric Ulcer
NCT01452750PHASE3COMPLETEDEfficacy and Safety of TAK-438 for the Prevention of Recurrent Gastric or Duodenal Ulcers During Therapy of Non-steroidal Anti-inflammatory Drug (NSAID)
NCT01452763PHASE3COMPLETEDEfficacy and Safety of TAK-438 for the Prevention of Recurrent Gastric or Duodenal Ulcers During Therapy of Low-dose Aspirin
NCT01456247PHASE3COMPLETEDLong-term Extension Study of TAK-438 for the Prevention of Recurrent Gastric or Duodenal Ulcers During Therapy of Low-dose Aspirin
NCT01456260PHASE3COMPLETEDLong-term Extension Study of TAK-438 for the Prevention of Recurrent Gastric or Duodenal Ulcers During Therapy of Non-steroidal Anti-inflammatory Drug (NSAID)
NCT01568385PHASE3COMPLETEDA Unblinded Study of TAK-438 (20 mg) for Prevention of Recurrence of Gastric or Duodenal Ulcer During Long-Term Non-Steroid Anti-Inflammatory Drug (NSAID) Therapy
NCT01568398PHASE3COMPLETEDA Unblinded Study of TAK-438 (20 mg) for Prevention of Recurrence of Gastric or Duodenal Ulcer During Long-Term Low-Dose Aspirin Therapy
NCT02153398PHASE3COMPLETEDA Phase I/III Study of D961H 10 mg and 20 mg in Japanese Paediatric Patients With Gastrointestinal Acid Related Diseases
NCT02761512PHASE3COMPLETEDStudy to Evaluate the Safety and Efficacy of CJ-12420 in Patients With Gastric Ulcer
NCT03050307PHASE3COMPLETEDComparison of TAK-438 (Vonoprazan) to Lansoprazole in the Treatment of Gastric Ulcer Participants With or Without Helicobacter Pylori Infection
NCT03553563PHASE3COMPLETEDA Study of Esomeplazole (D961H) in Japanese Paediatric Patients With Reflux Esophagitis, Gastric Ulcer or Duodenal Ulcer
NCT05448001PHASE3COMPLETEDClinical Trial to Evaluate the Efficacy and Safety of JP-1366 in Patients With Gastric Ulcer

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
VONOPRAZAN424
LANSOPRAZOLE411
RABEPRAZOLE44
BERBERINE43
NAPROXEN43
CLARITHROMYCIN42
ESOMEPRAZOLE42
OMEPRAZOLE42
AMOXICILLIN41
DICLOFENAC41
FURAZOLIDONE41
RANITIDINE41
SUCRALFATE41
TETRACYCLINE41
REBAMIPIDE35
CIPEPOFOL32
GEFARNATE32
LAFUTIDINE31
TEPRENONE31
INTERLEUKIN-1021
IRSOGLADINE MALEATE11
CHEMBL170333605
CHEMBL161825402
CHEMBL408270401
CHEMBL137473801
CHEMBL157216701
CHEMBL313767301
CHEMBL236770601
TNF-ALPHA01
EUPATILIN-11