Filter Paper Blood Spot Enzyme Linked Immunoassay for Insulin and Application in the Evaluation of Determinants of Child Insulin Resistance 英文参考文献.docVIP
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Filter Paper Blood Spot Enzyme Linked Immunoassay for Insulin and Application in the Evaluation of Determinants of Child Insulin Resistance 英文参考文献
FilterPaperBloodSpotEnzymeLinkedImmunoassayfor
InsulinandApplicationintheEvaluationof
DeterminantsofChildInsulinResistance
RichardM.Martin1,2*,RitaPatel1,AlexanderZinovik3,MichaelS.Kramer4,5,EmilyOken6,
KonstantinVilchuck3,NataliaBogdanovich3,NataliaSergeichick3,RobertGunnarsson7,LisaGrufman7,
YingFoo1,NinaGusina3
1SchoolofSocialandCommunityMedicine,UniversityofBristol,Bristol,UnitedKingdom, 2MRCCentreforCausalAnalysesinTranslationalEpidemiology, Schoolof
SocialandCommunityMedicine,UniversityofBristol,Bristol,UnitedKingdom,3NationalResearchandAppliedMedicine,MotherandChildCentre,Minsk,Republicof
Belarus,4DepartmentofEpidemiology,BiostatisticsandOccupationalHealth,McGillUniversity,Montreal,Canada,5DepartmentofPediatrics,McGillUniversity,Montreal,
Canada, 6Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts, United States of America,
7MercodiaAB,Uppsala,Sweden
Abstract
Background: In large-scale epidemiology, bloodspot sampling by fingerstick onto filter paper has many advantages,
includingeaseandlowcostsofcollection,processingandtransport.Wedescribethedevelopmentofanenzyme-linked
immunoassay(ELISA)forquantifyinginsulinfromdriedbloodspotsanddemonstrateitsapplicationinalargetrial.
Methods:Weadaptedanexistingcommercialkit(MercodiaHumanInsulinELISA,10-1113-01)toquantifyinsulinfromtwo3-
mmdiameterdiscs(6mLofblood)punchedfromwholebloodstandardsandfromtrialsamples.Paediatricianscollected
driedbloodspotsinafollow-upof13,879fastedchildrenaged11.5years(interquartilerange11.3–11.8years)from31trial
sites across Belarus. We quantified bloodspot insulin levels and examined their distribution by demography and
anthropometry.
Results: Meanintra-assay(n=157)coefficientsofvariationwere15%and6%for ‘low’(6.7mU/L) and‘high’ (23.1mU/L)
values, respectively; the respective inter-assay values (n=33) were 23% and 11%. The intraclass correlation coefficient
between 50 paired whole bloodspot versus serum
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