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Validation of nonradioactive chemiluminescent immunoassay methods for the analysis of thyroxine and cortisol in blood samples obtained from dogs, cats, and horses.

Abstract: The performances of a radioimmunoassay method, a chemiluminescent immunoassay method, and a chemiluminescent-enzyme immunoassay method were evaluated for the analysis of cortisol and total thyroxine in blood samples obtained from dogs, cats, horses, and humans (reference samples). The analysis of cortisol in human and animal samples exhibited good precision, linearity, and recovery. The 3 methods gave comparable values for the ACTH-induced increase and the dexamethasone-induced decrease in cortisol concentrations in animal samples. The recoveries of total thyroxine from human samples, analyzed by the 3 methods, were comparable. However, the basal total thyroxine concentrations determined by the chemiluminescent immunoassay method were 30-40% lower than those determined by the radioimmunoassay and the chemiluminescent-enzyme immunoassay methods in animal samples. In both human and animal samples, the plot of thyroxine values obtained by the radioimmunoassay method against those obtained by the chemiluminescent immunoassay method or the chemiluminescent-enzyme immunoassay method was linear. However, although the slope of the radioimmunoassay versus chemiluminescent-enzyme immunoassay curve was close to unity, the slope of the radioimmunoassay versus chemiluminescent immunoassay curve was 0.6. This result suggests that, compared with the radioimmunoassay method, the chemiluminescent immunoassay method underestimated thyroxine values in animal samples but not in human samples. Although all 3 methods yielded comparable changes in thyroxine concentrations in response to thyroid stimulating hormone, they did not yield comparable thyroxine concentrations in response to T3 suppression in dogs and cats.
Publication Date: 1997-07-01 PubMed ID: 9249165DOI: 10.1177/104063879700900307Google Scholar: Lookup
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study compares the effectiveness of three methods for measuring amounts of cortisol and thyroxine in blood samples from pets and livestock animals. The results suggest that all three methods provide accurate measurements for cortisol, but one method may underestimate levels of thyroxine in animal samples.

Evaluation of Three Immunoassay Methods

  • The research team aimed to compare the effectiveness of three different immunoassay methods, which are laboratory techniques used to measure the presence and quantity of specific substances in blood samples. These methods were radioimmunoassay, chemiluminescent immunoassay, and chemiluminescent-enzyme immunoassay.

Investigating Cortisol Levels

  • The first part of the study focused on analysing cortisol, a hormone that helps regulate stress responses in many organisms including humans and animals.
  • The tested animals include dogs, cats, horses, and the reference samples were from human beings.
  • The results showed that each of the three methods performed well in regard to precision, linearity, and recovery of cortisol in both human and animal samples.

Examining Thyroxine Measurements

  • The study also investigated measurements of total thyroxine, a hormone produced by the thyroid gland that regulates metabolism.
  • When thyroxine was analysed in human samples using each of the three methods, results demonstrated similar recoveries. However, in animal blood samples, the measurements using the chemiluminescent immunoassay method were 30-40% lower than those using the other two methods.
  • Even though chemiluminescent immunoassay method showed reliable linear relation with the radioimmunoassay and the chemiluminescent-enzyme immunoassay methods in both human and animal samples, it seemed to underestimate thyroxine values in animal samples, compared to the radioimmunoassay method.

Responses to Thyroid Stimulation

  • The study further evaluated how the three methods responded to changes in thyroxine concentrations caused by external influences such as thyroid stimulating hormone and T3 suppression.
  • All three methods showed comparable changes when thyroxine levels were shifted due to thyroid stimulating hormone.
  • However, the tested methods didn’t yield consistent concentrations results under T3 suppression in dogs and cats.

Cite This Article

APA
Singh AK, Jiang Y, White T, Spassova D. (1997). Validation of nonradioactive chemiluminescent immunoassay methods for the analysis of thyroxine and cortisol in blood samples obtained from dogs, cats, and horses. J Vet Diagn Invest, 9(3), 261-268. https://doi.org/10.1177/104063879700900307

Publication

ISSN: 1040-6387
NlmUniqueID: 9011490
Country: United States
Language: English
Volume: 9
Issue: 3
Pages: 261-268

Researcher Affiliations

Singh, A K
  • Department of Veterinary Diagnostic Medicine, College of Veterinary Medicine, University of Minnesota, St Paul 55108, USA.
Jiang, Y
    White, T
      Spassova, D

        MeSH Terms

        • Adrenocorticotropic Hormone / pharmacology
        • Animals
        • Cats
        • Dexamethasone / pharmacology
        • Dogs
        • Female
        • Horses
        • Humans
        • Hydrocortisone / blood
        • Immunoassay / methods
        • Immunoenzyme Techniques
        • Luminescent Measurements
        • Male
        • Radioimmunoassay / methods
        • Reference Values
        • Regression Analysis
        • Reproducibility of Results
        • Sensitivity and Specificity
        • Thyrotropin / pharmacology
        • Thyroxine / blood
        • Triiodothyronine / pharmacology

        Citations

        This article has been cited 34 times.
        1. Vecchiato CG, Golinelli S, Pinna C, Pilla R, Suchodolski JS, Tvarijonaviciute A, Rubio CP, Dorato E, Delsante C, Stefanelli C, Pagani E, Fracassi F, Biagi G. Fecal microbiota and inflammatory and antioxidant status of obese and lean dogs, and the effect of caloric restriction.. Front Microbiol 2022;13:1050474.
          doi: 10.3389/fmicb.2022.1050474pubmed: 36713218google scholar: lookup
        2. Yulianti ES, Rahman SF, Whulanza Y. Molecularly Imprinted Polymer-Based Sensor for Electrochemical Detection of Cortisol.. Biosensors (Basel) 2022 Nov 29;12(12).
          doi: 10.3390/bios12121090pubmed: 36551057google scholar: lookup
        3. Del Baldo F, Gerou Ferriani M, Bertazzolo W, Luciani M, Tardo AM, Fracassi F. Urinary cortisol-creatinine ratio in dogs with hypoadrenocorticism.. J Vet Intern Med 2022 Mar;36(2):482-487.
          doi: 10.1111/jvim.16358pubmed: 35150029google scholar: lookup
        4. Golinelli S, de Marco V, Leal RO, Barbarossa A, Aniballi C, Maietti E, Tardo AM, Galac S, Fracassi F. Comparison of methods to monitor dogs with hypercortisolism treated with trilostane.. J Vet Intern Med 2021 Nov;35(6):2616-2627.
          doi: 10.1111/jvim.16269pubmed: 34672018google scholar: lookup
        5. Korchia J, Freeman KP. Validation study of canine serum cortisol measurement with the Immulite 2000 Xpi cortisol immunoassay.. J Vet Diagn Invest 2021 Sep;33(5):844-863.
          doi: 10.1177/10406387211029247pubmed: 34292121google scholar: lookup
        6. Contalbrigo L, Borgi M, De Santis M, Collacchi B, Tuozzi A, Toson M, Redaelli V, Odore R, Vercelli C, Stefani A, Luzi F, Valle E, Cirulli F. Equine-Assisted Interventions (EAIs) for Children with Autism Spectrum Disorders (ASD): Behavioural and Physiological Indices of Stress in Domestic Horses (Equus caballus) during Riding Sessions.. Animals (Basel) 2021 May 27;11(6).
          doi: 10.3390/ani11061562pubmed: 34071859google scholar: lookup
        7. Tschoner T. Methods for Pain Assessment in Calves and Their Use for the Evaluation of Pain during Different Procedures-A Review.. Animals (Basel) 2021 Apr 25;11(5).
          doi: 10.3390/ani11051235pubmed: 33922942google scholar: lookup
        8. Zeugswetter FK, Carranza Valencia A, Glavassevich K, Schwendenwein I. Patterns of the low-dose dexamethasone suppression test in canine hyperadrenocorticism revisited.. Vet Clin Pathol 2021 Mar;50(1):62-70.
          doi: 10.1111/vcp.12958pubmed: 33728722google scholar: lookup
        9. Yu L, Lacorcia L, Finch S, Johnstone T. Assessment of serum symmetric dimethylarginine and creatinine concentrations in hyperthyroid cats before and after a fixed dose of orally administered radioiodine.. J Vet Intern Med 2020 Jul;34(4):1423-1431.
          doi: 10.1111/jvim.15831pubmed: 32506701google scholar: lookup
        10. Schechter DA, Lee HP, Kemppainen RJ, Behrend EN. Effect of EDTA on measurement of cortisol and thyroxine by chemiluminescent enzyme immunoassay in dogs.. J Vet Diagn Invest 2020 May;32(3):363-368.
          doi: 10.1177/1040638720911376pubmed: 32238057google scholar: lookup
        11. Wolff EDS, Bilbrough G, Moore G, Guptill L, Scott-Moncrieff JC. Comparison of 2 assays for measuring serum total thyroxine concentration in dogs and cats.. J Vet Intern Med 2020 Mar;34(2):607-615.
          doi: 10.1111/jvim.15703pubmed: 32017235google scholar: lookup
        12. Sieber-Ruckstuhl NS, Reusch CE, Hofer-Inteeworn N, Kuemmerle-Fraune C, Müller C, Hofmann-Lehmann R, Boretti FS. Evaluation of a low-dose desoxycorticosterone pivalate treatment protocol for long-term management of dogs with primary hypoadrenocorticism.. J Vet Intern Med 2019 May;33(3):1266-1271.
          doi: 10.1111/jvim.15475pubmed: 30865322google scholar: lookup
        13. Lottati M, Aucoin D, Bruyette DS. Expected total thyroxine (TT4) concentrations and outlier values in 531,765 cats in the United States (2014-2015).. PLoS One 2019;14(3):e0213259.
          doi: 10.1371/journal.pone.0213259pubmed: 30840691google scholar: lookup
        14. Boretti F, Musella C, Burkhardt W, Kuemmerle-Fraune C, Riond B, Reusch C, Sieber-Ruckstuhl N. Comparison of two prepill cortisol concentrations in dogs with hypercortisolism treated with trilostane.. BMC Vet Res 2018 Dec 27;14(1):417.
          doi: 10.1186/s12917-018-1750-3pubmed: 30591042google scholar: lookup
        15. Botsford A, Behrend EN, Kemppainen RJ, Gaillard PR, Oprandy F, Lee HP. Low-dose ACTH stimulation testing in dogs suspected of hypoadrenocorticism.. J Vet Intern Med 2018 Nov;32(6):1886-1890.
          doi: 10.1111/jvim.15256pubmed: 30230611google scholar: lookup
        16. Frye CW, Mann S, Joseph JL, Hansen C, Sass B, Wakshlag JJ. Serum Biochemistry and Inflammatory Cytokines in Racing Endurance Sled Dogs With and Without Rhabdomyolysis.. Front Vet Sci 2018;5:145.
          doi: 10.3389/fvets.2018.00145pubmed: 30073172google scholar: lookup
        17. Bennaim M, Shiel RE, Forde C, Mooney CT. Evaluation of individual low-dose dexamethasone suppression test patterns in naturally occurring hyperadrenocorticism in dogs.. J Vet Intern Med 2018 May;32(3):967-977.
          doi: 10.1111/jvim.15079pubmed: 29498108google scholar: lookup
        18. Bree L, Gallagher BA, Shiel RE, Mooney CT. Prevalence and risk factors for hyperthyroidism in Irish cats from the greater Dublin area.. Ir Vet J 2018;71:2.
          doi: 10.1186/s13620-017-0113-xpubmed: 29372047google scholar: lookup
        19. Tangyuenyong S, Nambo Y, Nagaoka K, Tanaka T, Watanabe G. Sensitive radioimmunoassay of total thyroxine (T4) in horses using a simple extraction method.. J Vet Med Sci 2017 Jul 28;79(7):1294-1300.
          doi: 10.1292/jvms.17-0133pubmed: 28603213google scholar: lookup
        20. Wakayama JA, Furrow E, Merkel LK, Armstrong PJ. A retrospective study of dogs with atypical hypoadrenocorticism: a diagnostic cut-off or continuum?. J Small Anim Pract 2017 Jul;58(7):365-371.
          doi: 10.1111/jsap.12649pubmed: 28247992google scholar: lookup
        21. Nagata N, Kojima K, Yuki M. Comparison of Survival Times for Dogs with Pituitary-Dependent Hyperadrenocorticism in a Primary-Care Hospital: Treated with Trilostane versus Untreated.. J Vet Intern Med 2017 Jan;31(1):22-28.
          doi: 10.1111/jvim.14617pubmed: 27906457google scholar: lookup
        22. Macfarlane L, Parkin T, Ramsey I. Pre-trilostane and three-hour post-trilostane cortisol to monitor trilostane therapy in dogs.. Vet Rec 2016 Dec 10;179(23):597.
          doi: 10.1136/vr.103744pubmed: 27803375google scholar: lookup
        23. Willems A, Paepe D, Marynissen S, Smets P, Van de Maele I, Picavet P, Duchateau L, Daminet S. Results of Screening of Apparently Healthy Senior and Geriatric Dogs.. J Vet Intern Med 2017 Jan;31(1):81-92.
          doi: 10.1111/jvim.14587pubmed: 27747924google scholar: lookup
        24. Bertin FR, Taylor SD, Bianco AW, Sojka-Kritchevsky JE. The Effect of Fasting Duration on Baseline Blood Glucose Concentration, Blood Insulin Concentration, Glucose/Insulin Ratio, Oral Sugar Test, and Insulin Response Test Results in Horses.. J Vet Intern Med 2016 Sep;30(5):1726-1731.
          doi: 10.1111/jvim.14529pubmed: 27481572google scholar: lookup
        25. Woolcock AD, Ward C. Successful treatment of a cat with primary hypoadrenocorticism and severe hyponatremia with desoxycorticosterone pivalate (DOCP).. Can Vet J 2015 Nov;56(11):1158-60.
          pubmed: 26538671
        26. Hoffman CJ, McKenzie HC 3rd, Furr MO, Desrochers A. Glucocorticoid receptor density and binding affinity in healthy horses and horses with systemic inflammatory response syndrome.. J Vet Intern Med 2015 Mar-Apr;29(2):626-35.
          doi: 10.1111/jvim.12558pubmed: 25818217google scholar: lookup
        27. Bovens C, Tennant K, Reeve J, Murphy KF. Basal serum cortisol concentration as a screening test for hypoadrenocorticism in dogs.. J Vet Intern Med 2014 Sep-Oct;28(5):1541-5.
          doi: 10.1111/jvim.12415pubmed: 25066405google scholar: lookup
        28. Lathan P, Scott-Moncrieff JC, Wills RW. Use of the cortisol-to-ACTH ratio for diagnosis of primary hypoadrenocorticism in dogs.. J Vet Intern Med 2014 Sep-Oct;28(5):1546-50.
          doi: 10.1111/jvim.12392pubmed: 24966067google scholar: lookup
        29. da Costa AN, Feitosa JV, Júnior PA, de Souza PT, de Araújo AA. Hormonal profiles, physiological parameters, and productive and reproductive performances of Girolando cows in the state of Ceará-Brazil.. Int J Biometeorol 2015 Feb;59(2):231-6.
          doi: 10.1007/s00484-014-0838-0pubmed: 24859822google scholar: lookup
        30. Williams TL, Elliott J, Syme HM. Effect on renal function of restoration of euthyroidism in hyperthyroid cats with iatrogenic hypothyroidism.. J Vet Intern Med 2014 Jul-Aug;28(4):1251-5.
          doi: 10.1111/jvim.12359pubmed: 24773059google scholar: lookup
        31. Proverbio D, Perego R, Spada E, Bagnagatti de Giorgi G, Belloli A, Pravettoni D. Comparison of VIDAS and radioimmunoassay methods for measurement of cortisol concentration in bovine serum.. ScientificWorldJournal 2013;2013:216569.
          doi: 10.1155/2013/216569pubmed: 24288466google scholar: lookup
        32. Hart KA, Barton MH, Vandenplas ML, Hurley DJ. Effects of low-dose hydrocortisone therapy on immune function in neonatal horses.. Pediatr Res 2011 Jul;70(1):72-7.
          doi: 10.1203/PDR.0b013e31821b502bpubmed: 21430601google scholar: lookup
        33. Wong DM, Vo DT, Alcott CJ, Stewart AJ, Peterson AD, Sponseller BA, Hsu WH. Adrenocorticotropic hormone stimulation tests in healthy foals from birth to 12 weeks of age.. Can J Vet Res 2009 Jan;73(1):65-72.
          pubmed: 19337398
        34. Hoh WP, Oh TH. Circadian variations of serum thyroxine, free thyroxine and 3,5,3'triiodothyronine concentrations in healthy dogs.. J Vet Sci 2006 Mar;7(1):25-9.
          doi: 10.4142/jvs.2006.7.1.25pubmed: 16434845google scholar: lookup