Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0071315
Title: Filter Paper Blood Spot Enzyme Linked Immunoassay for Adiponectin and Application in the Evaluation of Determinants of Child Insulin Sensitivity
Authors: Martin R.M.
Patel R.
Oken E.
Thompson J.
Zinovik A.
Kramer M.S. 
Vilchuck K.
Bogdanovich N.
Sergeichick N.
Foo Y.
Gusina N.
Keywords: adiponectin
glucose
insulin
adolescent
article
blood analysis
blood sampling
body height
body mass
child
controlled study
dried blood spot testing
enzyme linked immunospot assay
fat mass
female
filter paper
human
insulin sensitivity
intermethod comparison
male
medical device
protein determination
protein localization
school child
skinfold thickness
validation process
waist circumference
Adiponectin
Adolescent
Adult
Child
Dried Blood Spot Testing
Enzyme-Linked Immunosorbent Assay
Female
Filtration
Humans
Insulin Resistance
Male
Paper
Reproducibility of Results
Issue Date: 2013
Citation: Martin R.M., Patel R., Oken E., Thompson J., Zinovik A., Kramer M.S., Vilchuck K., Bogdanovich N., Sergeichick N., Foo Y., Gusina N. (2013). Filter Paper Blood Spot Enzyme Linked Immunoassay for Adiponectin and Application in the Evaluation of Determinants of Child Insulin Sensitivity. PLoS ONE 8 (8) : e71315. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0071315
Rights: Attribution 4.0 International
Abstract: Background:Adiponectin is an adipocyte-derived hormone that acts as a marker of insulin sensitivity. Bloodspot sampling by fingerstick onto filter paper may increase the feasibility of large-scale studies of the determinants of insulin sensitivity. We first describe the validation of an enzyme-linked immunoassay (ELISA) for quantifying adiponectin from dried blood spots and then demonstrate its application in a large trial (PROBIT).Methods:We quantified adiponectin from 3-mm diameter discs (?3 ?L of blood) punched from dried blood spots obtained from: i) whole blood standards (validation); and ii) PROBIT trial samples (application) in which paediatricians collected blood spots from 13,879 children aged 11.5 years from 31 sites across Belarus. We examined the distribution of bloodspot adiponectin by demographic and anthropometric factors, fasting insulin and glucose.Results:In the validation study, mean intra-assay coefficients of variation (n = 162) were 15%, 13% and 10% for 'low' (6.78 ?g/ml), 'medium' (18.18 ?g/ml) and 'high' (33.13 ?g/ml) internal quality control (IQC) samples, respectively; the respective inter-assay values (n = 40) were 23%, 21% and 14%. The correlation coefficient between 50 paired whole bloodspot versus plasma samples, collected simultaneously, was 0.87 (95% CI: 0.78 to 0.93). Recovery of known quantities of adiponectin (between 4.5 to 36 ?g/ml) was 100.3-133%. Bloodspot adiponectin was stable for at least 30 months at -80°C. In PROBIT, we successfully quantified fasting adiponectin from dried blood spots in 13,329 of 13,879 (96%) children. Mean adiponectin (standard deviation) concentrations were 17.34 ?g/ml (7.54) in boys and 18.41 ?g/ml (7.92) in girls and were inversely associated with body mass index, fat mass, triceps and subscapular skin-fold thickness, waist circumference, height and fasting glucose.Conclusions:Bloodspot ELISA is suitable for measuring adiponectin in very small volumes of blood collected on filter paper and can be applied to large-scale studies. © 2013 Martin et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161284
ISSN: 19326203
DOI: 10.1371/journal.pone.0071315
Rights: Attribution 4.0 International
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