Biological variation data for lipid cardiovascular risk assessment biomarkers. A systematic review applying the biological variation data critical appraisal checklist (BIVAC)

dc.contributor.authorDiaz-Garzon, Jorge
dc.contributor.authorFernandez Calle, Pilar
dc.contributor.authorMinchinela, Joana
dc.contributor.authorAarsand, Aasne K.
dc.contributor.authorBartlett, William A.
dc.contributor.authorAslan, Berna
dc.contributor.authorBoned, Beatriz
dc.contributor.authorBraga, Federica
dc.contributor.authorCarobene, Anna
dc.contributor.authorCoskun, Abdurrahman
dc.contributor.authorGonzalez-Lao, Elisabet
dc.contributor.authorJonker, Niels
dc.contributor.authorMarques-Garcia, Fernando
dc.contributor.authorPerich, Carmen
dc.contributor.authorRicos, Carmen
dc.contributor.authorSimon, Margarita
dc.contributor.authorSandberg, Sverre
dc.date.accessioned2023-02-21T12:41:40Z
dc.date.available2023-02-21T12:41:40Z
dc.date.issued2019-01-01
dc.description.abstractBackground: Biological variation (BV) data can be used to set analytical performance specifications (APS) for lipid assays. Poor performance will impact upon the efficacy of international guidelines for cardiovascular risk assessment (CVR) and relevant clinical decision limits. This systematic review applies the Biological Variation Data Critical Appraisal Checklist (BIVAC) to published studies of BV of CVR biomarkers enabling metanalysis of the data. Methods: Studies of BV of total cholesterol, HDL-cholesterol, LDL-cholesterol, triglycerides and apolipoproteins A(1) and B, retrieved using a systematic literature search, were evaluated and graded using the BIVAC. Meta analysis of CV1 and CVG estimates were performed utilizing weightings based upon BIVAC grades and the width of the data confidence intervals. Results: Applying the BIVAC, ten publications were graded as D, 43 as C, 5 as B and 1 as A (fully compliant). A total of 196 CV1 and 87 CVG estimates were available for the different lipid measurands. The meta-analysis-derived BV data estimates were generally concordant with those in the online 2014 BV database. Conclusions: Application of BIVAC identifies BV data suitable for many important applications including setting APS. Additionally, this review identifies a need for new BIVAC compliant studies to deliver BV reference data in different subpopulations.
dc.description.issueAUG
dc.description.pages467-475
dc.description.volume495
dc.identifier.doi10.1016/j.cca.2019.05.013
dc.identifier.urihttps://hdl.handle.net/11443/2740
dc.identifier.urihttp://dx.doi.org/10.1016/j.cca.2019.05.013
dc.identifier.wosWOS:000476964200070
dc.publisherELSEVIER
dc.relation.ispartofCLINICA CHIMICA ACTA
dc.subjectBiological variation
dc.subjectMeta-analysis
dc.subjectLipids
dc.subjectCardiovascular risk
dc.subjectAnalytical performance specifications
dc.titleBiological variation data for lipid cardiovascular risk assessment biomarkers. A systematic review applying the biological variation data critical appraisal checklist (BIVAC)
dc.typeArticle

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