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dc.contributor.authorKönig, Carola S
dc.contributor.authorMann, Amar
dc.contributor.authorMcFarlane, Rob
dc.contributor.authorMarriott, John
dc.contributor.authorPrice, Malcolm
dc.contributor.authorRamachandran, Sudarshan
dc.date.accessioned2024-01-24T12:38:32Z
dc.date.available2024-01-24T12:38:32Z
dc.date.issued2023-12-02
dc.identifier.citationKönig CS, Mann A, McFarlane R, Marriott J, Price M, Ramachandran S. Age and the Residual Risk of Cardiovascular Disease following Low Density Lipoprotein-Cholesterol Exposure. Biomedicines. 2023 Dec 2;11(12):3208. doi: 10.3390/biomedicines11123208.en_US
dc.identifier.issn2227-9059
dc.identifier.doi10.3390/biomedicines11123208
dc.identifier.pmid38137429
dc.identifier.urihttp://hdl.handle.net/20.500.14200/3423
dc.description.abstractWe believe that there is sufficient evidence from basic science, longitudinal cohort studies and randomised controlled trials which validates the low-density lipoprotein cholesterol (LDL-C) or lipid hypothesis. It is important that we can communicate details of the cardiovascular disease (CVD) risk reduction that the average patient could expect depending on the scale of LDL-C decrease following lipid lowering therapy. It is also essential that residual risk (ResR) of CVD be highlighted. To achieve this aim by using existing trial evidence, we developed mathematical models initially for relative risk reduction (RRR) and absolute risk (AR) reduction and then showed that despite optimising LDL-C levels, a considerable degree of ResR remains that is dependent on AR. Age is significantly associated with AR (odds ratio: 1.02, 95% confidence intervals: 1.01-1.04) as was previously demonstrated by analysing the Whickham study cohort using a logistic regression model (age remaining significant even when all the other significant risk factors such as sex, smoking, systolic blood pressure, diabetes and family history were included in the regression model). A discussion of a paper by Ference et al. provided detailed evidence of the relationship between age and AR, based on lifetime LDL-C exposure. Finally, we discussed non-traditional CVD risk factors that may contribute to ResR based on randomised controlled trials investigating drugs improving inflammation, thrombosis, metabolic and endothelial status.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.urlhttp://www.mdpi.com/journal/biomedicinesen_US
dc.subjectCardiologyen_US
dc.subjectOncology. Pathology.en_US
dc.subjectVascular diseases
dc.titleAge and the residual risk of cardiovascular disease following low density lipoprotein-cholesterol exposureen_US
dc.typeArticle
dc.source.journaltitleBiomedicines
dc.source.volume11
dc.source.issue12
dc.source.countrySwitzerland
rioxxterms.versionNAen_US
dc.contributor.trustauthorRamachandran, Sudarshan
dc.contributor.departmentPathologyen_US
dc.contributor.roleMedical and Dentalen_US
oa.grant.openaccessnaen_US


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