The use of dried blood spot sampling for the measurement of HbA1c: a cross-sectional study

dc.contributor.authorMastronardi, Claudio A.
dc.contributor.authorWhittle, Belinda
dc.contributor.authorTunningley, Robert
dc.contributor.authorNeeman, Teresa
dc.contributor.authorPaz-Filho, Gilberto
dc.date.accessioned2015-09-03T05:04:28Z
dc.date.available2015-09-03T05:04:28Z
dc.date.issued2015-07-08
dc.date.updated2016-02-24T08:06:39Z
dc.description.abstractBACKGROUND: The use of dried blood spot (DBS) sampling is an alternative to traditional venous blood collection, and particularly useful for people living in rural and remote areas, and for those who are infirm, house-bound or time-poor. The objective of this study was to assess whether the measurement of glycated haemoglobin A1c (HbA1c) in DBS samples provided comparative and acceptably precise results. METHODS: Venous and capillary blood samples were collected from 115 adult participants. After proper instruction, each participant punctured his/her own finger and collected capillary blood samples on pieces of a proprietary cellulose filter paper. Each filter paper was subsequently placed inside a breathable envelope, stored at room temperature, and processed on the same day (D0), four (D4), seven (D7) and fourteen (D14) days after collection. HbA1c was measured in duplicates/triplicates in whole venous blood (WB), capillary blood (capDBS) and venous blood placed on the matrix paper (venDBS), by turbidimetric inhibition immunoassay. Intra-assay coefficients of variation (CV) were calculated. DBS values were compared to WB results using linear regression, Bland-Altman plots and cross-validation models. RESULTS: Eleven and 56 patients had type 1 and type 2 diabetes mellitus, respectively. Mean HbA1c levels were 6.22 ± 1.11 % for WB samples (n = 115). The median intra-assay CV was lower than 3 % for WB and capDBS on all days. Results from capDBS and venDBS showed high correlation and agreement to WB results, with narrow 95 % limits of agreement (except for results from D14 samples), as observed in Bland-Altman plots. When capDBS values were applied to equations derived from regression analyses, results approached those of WB values. A cross-validation model showed that capDBS results on D0, D4 and D7 were close to the WB results, with prediction intervals that were narrow enough to be clinically acceptable. CONCLUSIONS: The measurement of HbA1c from DBS samples provided results that were comparable to results from WB samples, if measured up to seven days after collection. Intra-assay coefficients of variation were low, results were in agreement with the gold-standard, and prediction intervals were clinically acceptable. The measurement of HbA1c through DBS sampling may be considered in situations where traditional venipuncture is not available.
dc.description.sponsorshipThis study was funded by MyHealthTest Pty, including the article-processing charge.en_AU
dc.identifier.issn1472-6890en_AU
dc.identifier.urihttp://dx.doi.org/10.1186/s12907-015-0013-5
dc.identifier.urihttp://hdl.handle.net/1885/15149
dc.language.rfc3066en
dc.publisherBioMed Central
dc.rights© 2015 Mastronardi et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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.
dc.rights.holderMastronardi et al.
dc.sourceBMC Clinical Pathology
dc.titleThe use of dried blood spot sampling for the measurement of HbA1c: a cross-sectional study
dc.typeJournal article
dcterms.dateAccepted2015-06-24
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.startpage13en_AU
local.contributor.affiliationMastronardi, C. A., The John Curtin School of Medical Research, The Australian National Universityen_AU
local.contributor.affiliationPaz-Filho, G., The John Curtin School of Medical Research, The Australian National Universityen_AU
local.contributor.authoruidU4763468en_AU
local.identifier.absfor060400 - GENETICS
local.identifier.absfor111799 - Public Health and Health Services not elsewhere classified
local.identifier.absfor110316 - Pathology
local.identifier.ariespublicationa383154xPUB2654
local.identifier.citationvolume15en_AU
local.identifier.doi10.1186/s12907-015-0013-5en_AU
local.identifier.essn1472-6890en_AU
local.identifier.scopusID2-s2.0-84935424150
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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