Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/105889
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dc.contributorDepartment of Applied Social Sciences-
dc.creatorChan, KLen_US
dc.creatorLo, CKMen_US
dc.creatorChen, XYen_US
dc.creatorIp, Pen_US
dc.creatorLeung, WCen_US
dc.creatorShiels, PGen_US
dc.creatorPell, JPen_US
dc.creatorMinnis, Hen_US
dc.creatorHo, FKen_US
dc.date.accessioned2024-04-23T04:32:02Z-
dc.date.available2024-04-23T04:32:02Z-
dc.identifier.issn2045-7960en_US
dc.identifier.urihttp://hdl.handle.net/10397/105889-
dc.language.isoenen_US
dc.publisherCambridge University Pressen_US
dc.rights© The Author(s), 2023. Published by Cambridge University Press. This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.en_US
dc.rightsThe following publication Chan KL, Lo CKM, Chen X-Y, et al. Association between intimate partner violence and leukocyte telomere length: a retrospective cohort study of 144 049 UK Biobank participants. Epidemiology and Psychiatric Sciences. 2023;32:e26 is available at https://doi.org/10.1017/S2045796023000112.en_US
dc.subjectDepressionen_US
dc.subjectIntimate partner violenceen_US
dc.subjectPTSDen_US
dc.subjectTelomere lengthen_US
dc.titleAssociation between intimate partner violence and leukocyte telomere length : a retrospective cohort study of 144 049 UK Biobank participantsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume32en_US
dc.identifier.doi10.1017/S2045796023000112en_US
dcterms.abstractAims: Intimate partner violence (IPV) is a public health challenge negatively affecting victims’ health. Telomere length (TL), a marker for biological ageing, might be reflective of the mechanisms through which IPV leads to adverse health outcomes. The objective of the current study was to explore the association between IPV and leucocyte TL.-
dcterms.abstractMethods: We conducted an analysis using a subset of the UK Biobank (N = 144 049). Physical, sexual and emotional IPV were reported by the participants. DNA was extracted from peripheral blood leukocytes. TL was assayed by quantitative polymerase chain reaction. We used multivariable linear regressions to test the associations between IPV and TL adjusted for age, sex, ethnicity, deprivation, education, as well as symptoms of depression and post-traumatic stress disorder in a sensitivity analysis.-
dcterms.abstractResults: After adjusting for sociodemographic factors, any IPV was associated with 0.02-S.D. shorter TL (β = −0.02, 95% CI −0.04 to −0.01). Of the three types of IPV, physical violence had a marginally stronger association (β = −0.05, 95% CI −0.07 to −0.02) than the other two types. The associations of numbers of IPV and TL showed a dose–response pattern whereby those who experienced all three types of IPV types had the shortest TL (β = −0.07, 95% CI −0.12 to −0.03), followed by those who experienced two types (β = −0.04, 95% CI −0.07 to −0.01). Following additional adjustment for symptoms of depression and PTSD, the associations were slightly attenuated but the general trend by number of IPVs remained.-
dcterms.abstractConclusions: Victims of IPV, particularly those exposed to multiple types of IPVs, had shorter TL indicative of accelerated biological ageing. Given that all three types of IPV are linked to TL, clinical practitioners need to comprehensively identify all types of IPV and those who received multiple types. Further studies should explore the association of violence with changes in TL over time, as well as to which extent biological ageing is a mechanistic factor.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationEpidemiology and psychiatric sciences, 2023, v. 32, e26en_US
dcterms.isPartOfEpidemiology and psychiatric sciencesen_US
dcterms.issued2023-
dc.identifier.scopus2-s2.0-85156114665-
dc.identifier.eissn2045-7979en_US
dc.identifier.artne26en_US
dc.description.validate202404 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextGlasgow Children’s Hospital Charity; Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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