Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0196465
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dc.titleA prospective evaluation of serum kynurenine metabolites and risk of pancreatic cancer
dc.contributor.authorHuang J.Y.
dc.contributor.authorButler L.M.
dc.contributor.authorMidttun Ø.
dc.contributor.authorUlvik A.
dc.contributor.authorWang R.
dc.contributor.authorJin A.
dc.contributor.authorGao Y.-T.
dc.contributor.authorUeland P.M.
dc.contributor.authorKoh W.-P.
dc.contributor.authorYuan J.-M.
dc.date.accessioned2019-11-01T08:15:40Z
dc.date.available2019-11-01T08:15:40Z
dc.date.issued2018
dc.identifier.citationHuang J.Y., Butler L.M., Midttun Ø., Ulvik A., Wang R., Jin A., Gao Y.-T., Ueland P.M., Koh W.-P., Yuan J.-M. (2018). A prospective evaluation of serum kynurenine metabolites and risk of pancreatic cancer. PLoS ONE 13 (5) : e0196465. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0196465
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161230
dc.description.abstractBackground Serum pyridoxal 5’-phosphate (PLP), the active form of vitamin B6, is associated with reduced risk of pancreatic cancer. Data on functional measures of vitamin B6 status and risk of pancreatic cancer is lacking. Methods A nested case-control study involving 187 incident cases of pancreatic cancer and 362 individually matched controls were conducted within two prospective cohorts to evaluate the associations between kynurenine metabolites in pre-diagnostic serum samples and risk of pancreatic cancer. Results Higher serum concentrations of 3-hydroxyanthranilic acid (HAA) and the HAA:3-hydroxyky-nurenine (HK) ratio (a measure for in vivo functional status of PLP) were significantly associated with reduced risk of pancreatic cancer. Compared with the lowest tertile, odds ratios (95% confidence intervals) of pancreatic cancer for the highest tertile was 0.62 (0.39, 1.01) for HAA, and 0.59 (0.35–0.98) for the HAA:HK ratio, after adjustment for potential confounders and serum PLP (both Ps for trend<0.05). The kynurenine:tryptophan ratio or neopterin was not significantly associated with pancreatic cancer risk. Conclusions The inverse association between HAA or the HAA:HK ratio and risk of pancreatic cancer supports the notion that functional status of PLP may be a more important measure than circulating PLP alone for the development of pancreatic cancer. © 2018 Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subject3 hydroxyanthranilic acid
dc.subject3 hydroxykynurenine
dc.subjectkynurenine
dc.subjectneopterin
dc.subjectpyridoxal 5 phosphate
dc.subjecttryptophan
dc.subject3 hydroxyanthranilic acid
dc.subject3-hydroxykynurenine
dc.subjectbiological marker
dc.subjectkynurenine
dc.subjectpyridoxal 5 phosphate
dc.subjectpyridoxine
dc.subjectadult
dc.subjectaged
dc.subjectamino acid blood level
dc.subjectArticle
dc.subjectcancer risk
dc.subjectcase control study
dc.subjectclinical evaluation
dc.subjectcohort analysis
dc.subjectconfidence interval
dc.subjectcontrolled study
dc.subjectfemale
dc.subjecthuman
dc.subjectin vivo study
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectodds ratio
dc.subjectpancreas cancer
dc.subjectprospective study
dc.subjectvitamin blood level
dc.subjectanalogs and derivatives
dc.subjectblood
dc.subjectChina
dc.subjectmetabolism
dc.subjectmiddle aged
dc.subjectpancreas tumor
dc.subjectrisk factor
dc.subject3-Hydroxyanthranilic Acid
dc.subjectBiomarkers
dc.subjectCase-Control Studies
dc.subjectChina
dc.subjectFemale
dc.subjectHumans
dc.subjectKynurenine
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectOdds Ratio
dc.subjectPancreatic Neoplasms
dc.subjectProspective Studies
dc.subjectPyridoxal Phosphate
dc.subjectRisk Factors
dc.subjectVitamin B 6
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1371/journal.pone.0196465
dc.description.sourcetitlePLoS ONE
dc.description.volume13
dc.description.issue5
dc.description.pagee0196465
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