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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 |
Appears in Collections: | Elements Staff Publications |
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