Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/35400
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dc.contributor.authorRajendrakumar, Aravind Lathikaen_UK
dc.contributor.authorHapca, Simona Men_UK
dc.contributor.authorNair, Anand Thakarakkattil Narayananen_UK
dc.contributor.authorHuang, Yuen_UK
dc.contributor.authorChourasia, Mehul Kumaren_UK
dc.contributor.authorKwan, Ryan Shun-Yuenen_UK
dc.contributor.authorNangia, Charvien_UK
dc.contributor.authorSiddiqui, Moneeza Ken_UK
dc.contributor.authorVijayaraghavan, Prathibaen_UK
dc.contributor.authorMatthew, Shona Zen_UK
dc.contributor.authorLeese, Graham Pen_UK
dc.contributor.authorMohan, Viswanathanen_UK
dc.contributor.authorPearson, Ewan Ren_UK
dc.contributor.authorDoney, Alexander S Fen_UK
dc.contributor.authorPalmer, Colin N Aen_UK
dc.date.accessioned2023-09-25T00:01:54Z-
dc.date.available2023-09-25T00:01:54Z-
dc.date.issued2023-08-10en_UK
dc.identifier.other304en_UK
dc.identifier.urihttp://hdl.handle.net/1893/35400-
dc.description.abstractBackground Diabetic retinopathy (DR) is a major sight-threatening microvascular complication in individuals with diabetes. Systemic inflammation combined with oxidative stress is thought to capture most of the complexities involved in the pathology of diabetic retinopathy. A high level of neutrophil–lymphocyte ratio (NLR) is an indicator of abnormal immune system activity. Current estimates of the association of NLR with diabetes and its complications are almost entirely derived from cross-sectional studies, suggesting that the nature of the reported association may be more diagnostic than prognostic. Therefore, in the present study, we examined the utility of NLR as a biomarker to predict the incidence of DR in the Scottish population. Methods The incidence of DR was defined as the time to the first diagnosis of R1 or above grade in the Scottish retinopathy grading scheme from type 2 diabetes diagnosis. The effect of NLR and its interactions were explored using a competing risks survival model adjusting for other risk factors and accounting for deaths. The Fine and Gray subdistribution hazard model (FGR) was used to predict the effect of NLR on the incidence of DR. Results We analysed data from 23,531 individuals with complete covariate information. At 10 years, 8416 (35.8%) had developed DR and 2989 (12.7%) were lost to competing events (death) without developing DR and 12,126 individuals did not have DR. The median (interquartile range) level of NLR was 2.04 (1.5 to 2.7). The optimal NLR cut-off value to predict retinopathy incidence was 3.04. After accounting for competing risks at 10 years, the cumulative incidence of DR and deaths without DR were 50.7% and 21.9%, respectively. NLR was associated with incident DR in both Cause-specific hazard (CSH = 1.63; 95% CI: 1.28–2.07) and FGR models the subdistribution hazard (sHR = 2.24; 95% CI: 1.70–2.94). Both age and HbA1c were found to modulate the association between NLR and the risk of DR. Conclusions The current study suggests that NLR has a promising potential to predict DR incidence in the Scottish population, especially in individuals less than 65 years and in those with well-controlled glycaemic status.en_UK
dc.language.isoenen_UK
dc.publisherSpringer Science and Business Media LLCen_UK
dc.relationRajendrakumar AL, Hapca SM, Nair ATN, Huang Y, Chourasia MK, Kwan RS, Nangia C, Siddiqui MK, Vijayaraghavan P, Matthew SZ, Leese GP, Mohan V, Pearson ER, Doney ASF & Palmer CNA (2023) Competing risks analysis for neutrophil to lymphocyte ratio as a predictor of diabetic retinopathy incidence in the Scottish population. <i>BMC Medicine</i>, 21, Art. No.: 304. https://doi.org/10.1186/s12916-023-02976-7en_UK
dc.rightsOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectDiabetic retinopathyen_UK
dc.subjectNeutrophil-lymphocyte rationen_UK
dc.subjectCompeting risksen_UK
dc.subjectSubdistribution hazard rationen_UK
dc.subjectCause-specific hazard ratioen_UK
dc.titleCompeting risks analysis for neutrophil to lymphocyte ratio as a predictor of diabetic retinopathy incidence in the Scottish populationen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1186/s12916-023-02976-7en_UK
dc.identifier.pmid37563596en_UK
dc.citation.jtitleBMC Medicineen_UK
dc.citation.issn1741-7015en_UK
dc.citation.volume21en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNational Institute for Health Researchen_UK
dc.author.emailsimona.hapca@stir.ac.uken_UK
dc.citation.date10/08/2023en_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationComputing Scienceen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationMadras Diabetes Research Foundationen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationMadras Diabetes Research Foundationen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.identifier.isiWOS:001048237900001en_UK
dc.identifier.scopusid2-s2.0-85168336485en_UK
dc.identifier.wtid1930127en_UK
dc.contributor.orcid0000-0003-3148-9657en_UK
dc.contributor.orcid0000-0002-6415-6560en_UK
dc.date.accepted2023-07-11en_UK
dcterms.dateAccepted2023-07-11en_UK
dc.date.filedepositdate2023-09-22en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorRajendrakumar, Aravind Lathika|en_UK
local.rioxx.authorHapca, Simona M|0000-0003-3148-9657en_UK
local.rioxx.authorNair, Anand Thakarakkattil Narayanan|en_UK
local.rioxx.authorHuang, Yu|en_UK
local.rioxx.authorChourasia, Mehul Kumar|en_UK
local.rioxx.authorKwan, Ryan Shun-Yuen|en_UK
local.rioxx.authorNangia, Charvi|en_UK
local.rioxx.authorSiddiqui, Moneeza K|en_UK
local.rioxx.authorVijayaraghavan, Prathiba|en_UK
local.rioxx.authorMatthew, Shona Z|en_UK
local.rioxx.authorLeese, Graham P|en_UK
local.rioxx.authorMohan, Viswanathan|en_UK
local.rioxx.authorPearson, Ewan R|en_UK
local.rioxx.authorDoney, Alexander S F|en_UK
local.rioxx.authorPalmer, Colin N A|0000-0002-6415-6560en_UK
local.rioxx.projectProject ID unknown|National Institute for Health Research|http://dx.doi.org/10.13039/501100000272en_UK
local.rioxx.freetoreaddate2023-09-22en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2023-09-22|en_UK
local.rioxx.filenames12916-023-02976-7.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1741-7015en_UK
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