Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/30170
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dc.contributor.authorPhillips, Anna C.en_UK
dc.contributor.authorCarroll, Douglasen_UK
dc.contributor.authorDrayson, Mark T.en_UK
dc.contributor.authorDer, Geoffen_UK
dc.date.accessioned2019-09-26T00:02:21Z-
dc.date.available2019-09-26T00:02:21Z-
dc.date.issued2015-12-23en_UK
dc.identifier.othere0145083en_UK
dc.identifier.urihttp://hdl.handle.net/1893/30170-
dc.description.abstractImmunoglobulins are essential for combating infectious disease although very high levels can indicate underlying pathology. The present study examined associations between secretory immunoglobulin A (sIgA) in saliva and mortality rates in the general population. Participants were 639 adults from the eldest cohort of the West of Scotland Twenty-07 Study aged 63 years at the time of saliva sampling in 1995. From unstimulated 2-minute saliva samples, saliva volume and S-IgA concentration were measured, and S-IgA secretion rate determined as their product. Mortality data were tracked for 19 years. Cox proportional hazard models were applied to compute hazard ratios (HR) for all-cause mortality from sIgA secretion rate. Associations were adjusted for gender, assay batch, household occupational group, smoking, medication usage, and self-reported health. There was a negative association between log sIgA secretion rate and all-cause mortality, HR = 0.81, 95%CI = 0.73–0.91, p < .001. Further analysis of specific causes of mortality revealed that the all-cause association was due to an underlying association with cancer mortality and in particular with cancers other than lung cancer. The HR for non-lung cancer was 0.68 (95%CI = 0.54 to 0.85) implying a 32% reduction in mortality risk per standard deviation rise in log sIgA secretion rate. Effects were stronger for men than women. For deaths from respiratory diseases, sIgA secretion had a non-linear relationship with mortality risk whereby only the very lowest levels of secretion were associated with elevated risk. SIgA concentration revealed a similar but weaker pattern of association. In the present study, higher secretion rates of sIgA were associated with a decreased risk of death from cancer, specifically non-lung cancer, as well as from respiratory disease. Thus, it appears that sIgA plays a protective role among older adults, and could serve as a marker of mortality risk, specifically cancer mortality.en_UK
dc.language.isoenen_UK
dc.publisherPublic Library of Science (PLoS)en_UK
dc.relationPhillips AC, Carroll D, Drayson MT & Der G (2015) Salivary Immunoglobulin A Secretion Rate Is Negatively Associated with Cancer Mortality: The West of Scotland Twenty-07 Study. PLOS ONE, 10 (12), Art. No.: e0145083. https://doi.org/10.1371/journal.pone.0145083en_UK
dc.rights© 2015 Phillips et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are crediteden_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.titleSalivary Immunoglobulin A Secretion Rate Is Negatively Associated with Cancer Mortality: The West of Scotland Twenty-07 Studyen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1371/journal.pone.0145083en_UK
dc.identifier.pmid26699127en_UK
dc.citation.jtitlePLoS ONEen_UK
dc.citation.issn1932-6203en_UK
dc.citation.volume10en_UK
dc.citation.issue12en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderMedical Research Councilen_UK
dc.author.emaila.c.whittaker@stir.ac.uken_UK
dc.citation.date23/12/2015en_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Birminghamen_UK
dc.contributor.affiliationUniversity of Glasgowen_UK
dc.identifier.isiWOS:000367092600045en_UK
dc.identifier.scopusid2-s2.0-84957549122en_UK
dc.identifier.wtid1420029en_UK
dc.contributor.orcid0000-0002-5461-0598en_UK
dc.date.accepted2015-11-28en_UK
dcterms.dateAccepted2015-11-28en_UK
dc.date.filedepositdate2019-07-30en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorPhillips, Anna C.|0000-0002-5461-0598en_UK
local.rioxx.authorCarroll, Douglas|en_UK
local.rioxx.authorDrayson, Mark T.|en_UK
local.rioxx.authorDer, Geoff|en_UK
local.rioxx.projectProject ID unknown|Medical Research Council|http://dx.doi.org/10.13039/501100000265en_UK
local.rioxx.freetoreaddate2019-09-25en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2019-09-25|en_UK
local.rioxx.filenamejournal.pone.0145083.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1932-6203en_UK
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