Different Metabolites of the Gastric Mucosa between Patients with Current Helicobacter pylori Infection, Past Infection, and No Infection History
( ) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric mucosa according to the status of the infection. Patients who visited the outpatient clinic for a gastroscopy and tests were included. Gas chromatography-time-of-flight mass...
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Published in | Biomedicines Vol. 10; no. 3; p. 556 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Abstract | (
) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric mucosa according to the status of the
infection. Patients who visited the outpatient clinic for a gastroscopy and
tests were included. Gas chromatography-time-of-flight mass spectrometry (GC-TOF-MS) analysis was performed using gastric biopsied specimens from the corpus. Twenty-eight discriminative metabolites were found in the gastric mucosa of 10 patients with current
infection, in 15 with past infection, and in five with no infection history. The relative abundances (RAs) of amino acids and sugars/sugar alcohols were higher in patients with no infection history than in patients with current or past infection. The current infection group showed higher RAs of organic acids and lower RAs of fatty acids and lipids compared with the other groups. The RA of inosine was highest in the past infection group. Based on GC-TOF-MS analysis findings, metabolites differed not only between the infected and non-infected patients, but also between those with and without infection history. Amino acid and sugars/sugar alcohol metabolites decreased in patients with current or past infection, whereas fatty acid and lipid metabolites decreased only during current infection. |
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AbstractList | (
) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric mucosa according to the status of the
infection. Patients who visited the outpatient clinic for a gastroscopy and
tests were included. Gas chromatography-time-of-flight mass spectrometry (GC-TOF-MS) analysis was performed using gastric biopsied specimens from the corpus. Twenty-eight discriminative metabolites were found in the gastric mucosa of 10 patients with current
infection, in 15 with past infection, and in five with no infection history. The relative abundances (RAs) of amino acids and sugars/sugar alcohols were higher in patients with no infection history than in patients with current or past infection. The current infection group showed higher RAs of organic acids and lower RAs of fatty acids and lipids compared with the other groups. The RA of inosine was highest in the past infection group. Based on GC-TOF-MS analysis findings, metabolites differed not only between the infected and non-infected patients, but also between those with and without infection history. Amino acid and sugars/sugar alcohol metabolites decreased in patients with current or past infection, whereas fatty acid and lipid metabolites decreased only during current infection. Helicobacter pylori ( H. pylori ) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric mucosa according to the status of the H. pylori infection. Patients who visited the outpatient clinic for a gastroscopy and H. pylori tests were included. Gas chromatography–time-of-flight mass spectrometry (GC-TOF-MS) analysis was performed using gastric biopsied specimens from the corpus. Twenty-eight discriminative metabolites were found in the gastric mucosa of 10 patients with current H. pylori infection, in 15 with past infection, and in five with no infection history. The relative abundances (RAs) of amino acids and sugars/sugar alcohols were higher in patients with no infection history than in patients with current or past infection. The current infection group showed higher RAs of organic acids and lower RAs of fatty acids and lipids compared with the other groups. The RA of inosine was highest in the past infection group. Based on GC-TOF-MS analysis findings, metabolites differed not only between the infected and non-infected patients, but also between those with and without infection history. Amino acid and sugars/sugar alcohol metabolites decreased in patients with current or past infection, whereas fatty acid and lipid metabolites decreased only during current infection. Helicobacter pylori (H. pylori) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric mucosa according to the status of the H. pylori infection. Patients who visited the outpatient clinic for a gastroscopy and H. pylori tests were included. Gas chromatography–time-of-flight mass spectrometry (GC-TOF-MS) analysis was performed using gastric biopsied specimens from the corpus. Twenty-eight discriminative metabolites were found in the gastric mucosa of 10 patients with current H. pylori infection, in 15 with past infection, and in five with no infection history. The relative abundances (RAs) of amino acids and sugars/sugar alcohols were higher in patients with no infection history than in patients with current or past infection. The current infection group showed higher RAs of organic acids and lower RAs of fatty acids and lipids compared with the other groups. The RA of inosine was highest in the past infection group. Based on GC-TOF-MS analysis findings, metabolites differed not only between the infected and non-infected patients, but also between those with and without infection history. Amino acid and sugars/sugar alcohol metabolites decreased in patients with current or past infection, whereas fatty acid and lipid metabolites decreased only during current infection. |
Author | Son, Su-Young Lee, Sun-Young Lee, Choong-Hwan |
AuthorAffiliation | 1 Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea; syson119@naver.com (S.-Y.S.); chlee123@konkuk.ac.kr (C.-H.L.) 2 Research Institute for Bioactive-Metabolome Network, Konkuk University, Seoul 05029, Korea 3 Department of Internal Medicine, Konkuk University School of Medicine, Seoul 05030, Korea |
AuthorAffiliation_xml | – name: 1 Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea; syson119@naver.com (S.-Y.S.); chlee123@konkuk.ac.kr (C.-H.L.) – name: 2 Research Institute for Bioactive-Metabolome Network, Konkuk University, Seoul 05029, Korea – name: 3 Department of Internal Medicine, Konkuk University School of Medicine, Seoul 05030, Korea |
Author_xml | – sequence: 1 givenname: Su-Young orcidid: 0000-0001-6519-1918 surname: Son fullname: Son, Su-Young organization: Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea – sequence: 2 givenname: Choong-Hwan surname: Lee fullname: Lee, Choong-Hwan organization: Research Institute for Bioactive-Metabolome Network, Konkuk University, Seoul 05029, Korea – sequence: 3 givenname: Sun-Young orcidid: 0000-0003-4146-6686 surname: Lee fullname: Lee, Sun-Young organization: Department of Internal Medicine, Konkuk University School of Medicine, Seoul 05030, Korea |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35327358$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.20892/j.issn.2095-3941.2019.0348 10.1111/jgh.12605 10.1001/jamanetworkopen.2021.14186 10.1038/s41395-018-0259-5 10.1016/j.dld.2010.04.006 10.1158/1055-9965.EPI-20-1633 10.1016/j.micpath.2017.05.027 10.1046/j.1365-2036.2001.00960.x 10.1016/j.gie.2016.03.791 10.1016/j.bbrc.2020.04.019 10.3389/fmicb.2017.00536 10.1177/10732748211041881 10.1111/j.1523-5378.2012.00972.x 10.1056/NEJMoa1708423 10.1128/IAI.00690-20 10.2174/1875039701407010001 10.1007/s10620-005-9030-z 10.1007/s10620-020-06659-8 10.1245/s10434-014-3886-0 10.1158/1940-6207.CAPR-13-0235 10.1046/j.1440-1746.2001.02541.x 10.1080/17474124.2021.1850259 10.1111/hel.12480 10.5009/gnl18399 10.1186/s12885-016-2356-4 10.1111/cas.14443 10.3390/jcm8030312 10.7704/kjhugr.2019.19.2.88 10.2169/internalmedicine.56.7775 10.3390/ijerph17020541 10.1007/s11306-011-0297-0 10.1111/hel.12464 10.1016/j.micpath.2018.08.033 |
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Keywords | gastric mucosa Helicobacter pylori gas chromatography metabolites |
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) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric mucosa according to the status of... Helicobacter pylori (H. pylori) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric... Helicobacter pylori ( H. pylori ) alters metabolism during the gastric carcinogenesis process. This study aimed to determine the metabolites in the gastric... |
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SubjectTerms | Alcohols Amino acids Biopsy Carcinogenesis Chromatography Data processing Discriminant analysis Endoscopy Fatty acids Gas chromatography Gastric cancer Gastric mucosa Gastroscopy Helicobacter pylori Infections Lipid metabolism Mass spectrometry Mass spectroscopy Metabolism Metabolites Organic acids Scientific imaging Serology Software Statistical analysis Variables Variance analysis |
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Title | Different Metabolites of the Gastric Mucosa between Patients with Current Helicobacter pylori Infection, Past Infection, and No Infection History |
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