Long-term stability of thyroid peroxidase antibody (anti-TPO) in serum in the Danish General Suburban Population Study

Author:

Jensen Christian Z.1,Nygaard Birte12,Faber Jens12,Pedersen Palle L.3,Larsen Morten K.24,Kanters Jørgen K.5,Poulsen Henrik E.267,Kellogg Mark89,Ellervik Christina28910ORCID

Affiliation:

1. Center for Endocrinology and Metabolism , Copenhagen University Hospital – Herlev and Gentofte , Herlev , Denmark

2. Department of Clinical Medicine, Faculty of Health and Medical Sciences , University of Copenhagen , Copenhagen , Denmark

3. Department of Clinical Biochemistry, Region Zealand Biobank , Region Zealand University Hospital , Naestved , Denmark

4. Department of Hematology , Region Zealand University Hospital , Roskilde , Denmark

5. Department of Biomedical Sciences, Faculty of Health and Medical Sciences , University of Copenhagen , Copenhagen , Denmark

6. Department Endocrinology , Copenhagen University Hospital , Bispebjerg Frederiksberg , Denmark

7. Department Cardiology , Copenhagen University Hospital, Nordsjællands Hospital Hillerød , Hillerød , Denmark

8. Department of Laboratory Medicine , Boston Children’s Hospital , Boston , MA , USA

9. Department of Pathology , Harvard Medical School , Boston , MA , USA

10. Department of Data Support , Region Zealand , Sorø , Denmark

Abstract

Abstract Objectives We evaluated the long-term stability of thyroid peroxidase antibody (anti-TPO). Methods In the Danish General Suburban Population Study (GESUS), serum samples were biobanked at −80 °C during 2010–2013. In a paired design with 70 subjects, we compared anti-TPO (30–198 U/mL) measured on fresh serum on Kryptor Classic in 2010–2011 (anti-TPOfresh) with anti-TPO remeasured on frozen serum (anti-TPOfrozen) on Kryptor Compact Plus in 2022. Both instruments used the same reagents and the anti-TPOn automated immunofluorescent assay, which was calibrated against the international standard NIBSC 66/387, based on the Time Resolved Amplified Cryptate Emission (TRACE) technology from BRAHMS. Values greater than 60 U/mL are regarded as positive in Denmark with this assay. Statistical comparisons included Bland-Altman, Passing-Bablok regression, and Kappa statistic. Results The mean follow-up time was 11.9 years (SD: 0.43). For anti-TPOfrozen vs. anti-TPOfresh, the line of equality was within the confidence interval of the absolute mean difference [5.71 (−0.32; 11.7) U/mL] and the average percentage deviation [+2.22% (−3.89%; +8.34%)]. The average percentage deviation of 2.22% did not exceed analytical variability. Passing-Bablok regression revealed both a statistically significant systematic and proportional difference: Anti-TPOfrozen=−22.6 + 1.22*(anti-TPOfresh). Frozen samples were correctly classified as positive in 64/70 (91.4%; Kappa=71.8%). Conclusions Anti-TPO serum samples in the range 30–198 U/mL were stable after 12-years of storage at −80 °C with an estimated nonsignificant average percentage deviation of +2.22%. This comparison is based on Kryptor Classic and Kryptor Compact Plus, which used identical assays, reagents, and calibrator, but for which the agreement in the range 30–198 U/mL is unclarified.

Funder

The Local Government Denmark Foundation

Naestved Hospital

The National Board of Health

Johannes Fog’s Foundation

Region Sjælland

Stofskifteforeningen

The Danish Ministry of Health

Naestved Municipality

Johan and Lise Boserup Foundation

Region Zealand Research Foundation

Naestved Hospital Foundation

Laboratory Medicine Endowment Fund of Boston Children’s Hospital

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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