ANTITHYROID PEROXIDASE (ANTI-TPO) ANTIBODIES IN THYROID-DISEASES, NONTHYROIDAL ILLNESS AND CONTROLS - CLINICAL VALIDITY OF A NEW COMMERCIALMETHOD FOR DETECTION OF ANTI-TPO (THYROID MICROSOMAL) AUTOANTIBODIES
H. Engler et al., ANTITHYROID PEROXIDASE (ANTI-TPO) ANTIBODIES IN THYROID-DISEASES, NONTHYROIDAL ILLNESS AND CONTROLS - CLINICAL VALIDITY OF A NEW COMMERCIALMETHOD FOR DETECTION OF ANTI-TPO (THYROID MICROSOMAL) AUTOANTIBODIES, Clinica chimica acta, 225(2), 1994, pp. 123-136
The identification of the thyroid peroxidase (TPO) as the main antigen
of the thyroid microsomal fraction has enabled the development of a s
ensitive and specific assay for detection of the corresponding autoant
ibodies. We evaluated the diagnostic validity of the anti-TPO assay in
303 patients with different types of thyroid disease and in controls.
Clearly elevated anti-TPO values (anti-TPO > 500 units/ml) were found
in 59% of patients with thyroiditis but in none of the controls or th
e patients with non-thyroidal illness. The mean anti-TPO levels in the
se two control groups were 26 +/- 31 units/ml (mean +/- S.D.) and 39 /- 34 units/ml, respectively. The highest frequency of positive result
s (88%) was obtained in patients with autoimmune hypothyroidism (clini
cal diagnosis: Hashimoto's thyroiditis) followed by patients with Grav
es' disease (53%). With a cut-off point of 200 units/ml, a sensitivity
of 96% was obtained for Hashimoto's thyroiditis and of 59% for Graves
' disease with a specificity of 100% (50 cases). The new method (anti-
TPO, Dynotest) was compared with three conventional methods (35 sample
s). The results for all measurements were in general agreement. In two
cases the results were clearly discordant: one sample contained high
anti-thyroglobulin antibody concentrations, the other was obtained fro
m a patient with non-thyroidal illness. In both instances the 'classic
al' assays yielded false-positive results. Treatment of autoimmune hyp
erthyroidism resulted in a median decrease in anti-TPO levels of over
50% after reaching the euthyroid state (P < 0.05), whereas in persiste
nt hyperthyroidism no consistent changes were observed. In autoimmune
hypothyroidism a marked variability in anti-TPO levels was noted. Some
patients showed a clear decrease in anti-TPO levels during T4 substit
ution whereas in others no consistent changes were observed.