Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study

Abstract Background Early diagnosis and relapse prediction in Graves’ disease influences treatment. We assessed the abilities of four TSH-receptor antibody tests [TRAb] and one cyclic adenosine monophosphate bioassay to predict relapse of Graves’ disease. Methods Observational study investigating pa...

Full description

Bibliographic Details
Main Authors: Tristan Struja, Rebecca Jutzi, Noemi Imahorn, Marina Kaeslin, Fabienne Boesiger, Alexander Kutz, Esther Mundwiler, Andreas Huber, Marius Kraenzlin, Beat Mueller, Christian Meier, Luca Bernasconi, Philipp Schuetz
Format: Article
Language:English
Published: BMC 2019-04-01
Series:BMC Endocrine Disorders
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12902-019-0363-6
_version_ 1828900565016379392
author Tristan Struja
Rebecca Jutzi
Noemi Imahorn
Marina Kaeslin
Fabienne Boesiger
Alexander Kutz
Esther Mundwiler
Andreas Huber
Marius Kraenzlin
Beat Mueller
Christian Meier
Luca Bernasconi
Philipp Schuetz
author_facet Tristan Struja
Rebecca Jutzi
Noemi Imahorn
Marina Kaeslin
Fabienne Boesiger
Alexander Kutz
Esther Mundwiler
Andreas Huber
Marius Kraenzlin
Beat Mueller
Christian Meier
Luca Bernasconi
Philipp Schuetz
author_sort Tristan Struja
collection DOAJ
description Abstract Background Early diagnosis and relapse prediction in Graves’ disease influences treatment. We assessed the abilities of four TSH-receptor antibody tests [TRAb] and one cyclic adenosine monophosphate bioassay to predict relapse of Graves’ disease. Methods Observational study investigating patients presenting with Graves’ disease at a Swiss hospital endocrine referral center or an endocrine outpatient clinic. Main outcomes were diagnosis and relapse of Graves’ disease after stop of anti-thyroid drugs. We used Cox regression to study associations of TRAb levels with relapse risk and calculated c-statistics [AUC] to assess discrimination. Blood draws took place as close as possible to treatment initiation. Results AUCs ranged from 0.90 (TSAb Biossay by RSR) to 0.97 (IMMULITE TSI by Siemens). Highest sensitivity (94.0%) was observed for IMMULITE TSI and RSR TRAb Fast, while the greatest specificity (97.9%) was found with the EliA anti-TSH-R (by Thermo Fisher). In Cox regression analysis comparing the highest versus the lower quartiles, the highest hazard ratio [HR] for relapse was found for BRAHMS TRAK (by Thermo Fisher) (2.98, 95% CI 1.13–7.84), IMMULITE TSI (2.40, 95% CI 0.91–6.35), EliA anti-TSH-R (2.05, 95% CI 0.82–5.10), RSR Fast TRAb (1.80, 95% CI 0.73–4.43), followed by RSR STIMULATION (1.18, 95% CI 0.46–2.99). Discrimination analyses showed respective AUCs of 0.68, 0.65, 0.64, 0.64, and 0.59. Conclusion The assays tested had good diagnostic power and relapse risk prediction with few differences among the new assays. Due to the small sample size and retrospective design with possible selection bias, our data need prospective validation.
first_indexed 2024-12-13T15:49:14Z
format Article
id doaj.art-d2e4adb29b424e78bb38f47a03875e34
institution Directory Open Access Journal
issn 1472-6823
language English
last_indexed 2024-12-13T15:49:14Z
publishDate 2019-04-01
publisher BMC
record_format Article
series BMC Endocrine Disorders
spelling doaj.art-d2e4adb29b424e78bb38f47a03875e342022-12-21T23:39:35ZengBMCBMC Endocrine Disorders1472-68232019-04-0119111110.1186/s12902-019-0363-6Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot studyTristan Struja0Rebecca Jutzi1Noemi Imahorn2Marina Kaeslin3Fabienne Boesiger4Alexander Kutz5Esther Mundwiler6Andreas Huber7Marius Kraenzlin8Beat Mueller9Christian Meier10Luca Bernasconi11Philipp Schuetz12Medical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauDepartment of Laboratory Medicine, Kantonsspital AarauDepartment of Laboratory Medicine, Kantonsspital AarauEndonetMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauMedical Faculty of the University of BaselDepartment of Laboratory Medicine, Kantonsspital AarauMedical University Department, Clinic for Endocrinology, Diabetes & Metabolism, Kantonsspital AarauAbstract Background Early diagnosis and relapse prediction in Graves’ disease influences treatment. We assessed the abilities of four TSH-receptor antibody tests [TRAb] and one cyclic adenosine monophosphate bioassay to predict relapse of Graves’ disease. Methods Observational study investigating patients presenting with Graves’ disease at a Swiss hospital endocrine referral center or an endocrine outpatient clinic. Main outcomes were diagnosis and relapse of Graves’ disease after stop of anti-thyroid drugs. We used Cox regression to study associations of TRAb levels with relapse risk and calculated c-statistics [AUC] to assess discrimination. Blood draws took place as close as possible to treatment initiation. Results AUCs ranged from 0.90 (TSAb Biossay by RSR) to 0.97 (IMMULITE TSI by Siemens). Highest sensitivity (94.0%) was observed for IMMULITE TSI and RSR TRAb Fast, while the greatest specificity (97.9%) was found with the EliA anti-TSH-R (by Thermo Fisher). In Cox regression analysis comparing the highest versus the lower quartiles, the highest hazard ratio [HR] for relapse was found for BRAHMS TRAK (by Thermo Fisher) (2.98, 95% CI 1.13–7.84), IMMULITE TSI (2.40, 95% CI 0.91–6.35), EliA anti-TSH-R (2.05, 95% CI 0.82–5.10), RSR Fast TRAb (1.80, 95% CI 0.73–4.43), followed by RSR STIMULATION (1.18, 95% CI 0.46–2.99). Discrimination analyses showed respective AUCs of 0.68, 0.65, 0.64, 0.64, and 0.59. Conclusion The assays tested had good diagnostic power and relapse risk prediction with few differences among the new assays. Due to the small sample size and retrospective design with possible selection bias, our data need prospective validation.http://link.springer.com/article/10.1186/s12902-019-0363-6ThyroidGraves’ diseaseTRAbBioassay
spellingShingle Tristan Struja
Rebecca Jutzi
Noemi Imahorn
Marina Kaeslin
Fabienne Boesiger
Alexander Kutz
Esther Mundwiler
Andreas Huber
Marius Kraenzlin
Beat Mueller
Christian Meier
Luca Bernasconi
Philipp Schuetz
Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study
BMC Endocrine Disorders
Thyroid
Graves’ disease
TRAb
Bioassay
title Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study
title_full Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study
title_fullStr Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study
title_full_unstemmed Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study
title_short Comparison of Five TSH-Receptor Antibody Assays in Graves’ disease: results from an observational pilot study
title_sort comparison of five tsh receptor antibody assays in graves disease results from an observational pilot study
topic Thyroid
Graves’ disease
TRAb
Bioassay
url http://link.springer.com/article/10.1186/s12902-019-0363-6
work_keys_str_mv AT tristanstruja comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT rebeccajutzi comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT noemiimahorn comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT marinakaeslin comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT fabienneboesiger comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT alexanderkutz comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT esthermundwiler comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT andreashuber comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT mariuskraenzlin comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT beatmueller comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT christianmeier comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT lucabernasconi comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy
AT philippschuetz comparisonoffivetshreceptorantibodyassaysingravesdiseaseresultsfromanobservationalpilotstudy