Multi-omics Analyses on Etiology and Early Detection of Stomach Cancer Precursor Lesions
Condition(s) studied
Investigational drug(s) / intervention(s)
Metabolomic profiling: Metabolomic profiling using serum samples was performed based on Nightingale Blood Biomarker Analysis platform; Proteomic profiling will be performed by both Scanning SWATH and OLINK® Explore 384 Oncology panel.
Study summary
The overall aim is to utilize multi-omics approach to identify novel etiopathogenesis and early detection biomarkers for stomach cancer precursor lesions. To achieve this aim, first the investigators will use stored serum samples to perform metabolomics profiling among 12,599 twin subjects, among whom 1034 were deemed to have chronic atrophic gastritis based on measured pepsinogen I and II levels. Logistic regression will be used to search for metabolites related to the risk of chronic atrophic gastritis. Second, the investigators will further measure serum proteome by using two quantitatively precise proteomics assays, among the above-mentioned twin subjects. Identified protein biomarkers will be combined with metabolomics biomarkers to create a prediction model for chronic atrophic gastritis. The results will hopefully improve our understanding of the etiological factors and provide promising early detection biomarkers for stomach cancer precursor lesions.
Eligibility
Primary outcome measure(s)
- Chronic atrophic gastritis — 1 Sep. 2020 to 31 Dec. 2021
Corpus-dominant chronic atrophic gastritis was characterized by a PGI/PGII ratio of less than 3.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Karolinska Institutet | Solna | Stockholm County |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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