Effect of triiodothyronine on thyroid function after stopping long-term treatment of thyrotoxicosis with antithyroid drugs

Metabolism ◽  
1967 ◽  
Vol 16 (8) ◽  
pp. 741-743 ◽  
Author(s):  
W.Donald Alexander ◽  
Ronald McG. Harden ◽  
Donald McLarty ◽  
Paul McGill
1962 ◽  
Vol 25 (3) ◽  
pp. 343-350 ◽  
Author(s):  
G. HANNO ◽  
H. K. AWWAD

SUMMARY The mechanism of the antithyroid effect of tolbutamide was investigated by studying its effect on thyroid iodine trapping, the salivary secretion of 131I and the organic binding of thyroid 131I. No inhibitory effect was noted on iodine trapping. After prolonged therapy a defect in the organic binding of 131I was observed in some cases. There was a significant correlation between thyroid function as measured by the 2 hr. neck:thigh ratio and the total drug dose in patients on long-term treatment. Recovery of the gland from this defect after withdrawal of the drug seemed to be slower than the recovery from other antithyroid drugs having the same mode of action.


1998 ◽  
pp. 281-285 ◽  
Author(s):  
M Akuzawa ◽  
M Murakami ◽  
M Yamada ◽  
T Satoh ◽  
H Shimizu ◽  
...  

Clinical evaluation was conducted to ascertain whether thyrotropin receptor antibody (TRAb) in the normal range may still be involved in the regulation of thyroid function after prolonged treatment for Graves' disease. All patients (n = 33) were treated with antithyroid drugs for an average of 10.6 years and were under euthyroid conditions in which normal blood levels of tri-iodothyronine (T3) were significantly correlated with blood thyrotropin (TSH) levels, but not with titers of TRAb. A significant correlation was observed between TRAb titer and thyroid-stimulating antibody (TSAb) activity. In contrast, this correlation was not found in normal subjects. After administration of T3 (75 microg daily for 8 days), the patients showed increased levels of T3 with concomitant suppression of TSH levels. Under these conditions, linear regression analysis showed significant correlations of TRAb titer and TSAb activity with 24-h thyroid radioiodine uptake (r = 0.641 and 0.621 respectively, P < 0.01), in contrast to declining blood thyroxine levels. Moreover, the immunoglobulin G (IgG) of the patients precipitated to a greater extent than IgG from normal subjects a peptide consisting of the amino acid sequence near the terminus of the human TSH receptor. These findings indicated that TRAb at normal levels possessed significant unremitting activities on thyroid function despite long-term treatment in euthyroid patients with Graves' disease.


Dermatology ◽  
1997 ◽  
Vol 195 (2) ◽  
pp. 69-72 ◽  
Author(s):  
K. Nobukuni ◽  
N. Hayakawa ◽  
R. Namba ◽  
Y. Ihara ◽  
K. Sato ◽  
...  

1999 ◽  
Vol 50 (1) ◽  
pp. 127-132 ◽  
Author(s):  
D. Maugendre ◽  
A. Gatel ◽  
L. Campion ◽  
C. Massart ◽  
I. Guilhem ◽  
...  

1966 ◽  
Vol 26 (4) ◽  
pp. 397-401 ◽  
Author(s):  
R. MCG. HARDEN ◽  
W. D. ALEXANDER ◽  
D. A. KOUTRAS ◽  
M. T. HARRISON ◽  
EDWARD WAYNE

Author(s):  
Ramin Malboosbaf ◽  
Fereidoun Azizi

Context: Medical therapy of hyperthyroidism has been the Astwood’s gift to medicine. However, controversy remains about its mechanisms of action, the ideal treatment duration, and its proper use in pregnancy. The concept that hyperthyroidism could be controlled ‘indefinitely’ with antithyroid drugs (ATDs) is also a topic of current debate. The purpose of this review was to highlight the pros and cons of long-term ATD therapy. Evidence Acquisition: PubMed, Scopus, Web of Science, and Google Scholar databases were searched for retrieving studies conducted on long-term treatment with ATDs up to Jan 2020. The final selection of the papers was made based on their relevancy with the safety and efficacy of long-term treatment with ATDs. Results: The main drawback of the ATD treatment is the high relapse rate after drug discontinuation. On the other hand, ATDs may have a favorable immunosuppressive effect, either primarily, in the diminution of thyroid-specific autoimmunity, or secondarily, as a result of controlling the hyperthyroid state, hence keeping patients in a euthyroid state for a prolonged period to diminish autoimmunity and hyperthyroid relapse. This often calls for long-term use of methimazole, but with the lowest possible dose to minimize the risk of side effects. Emerging evidence demonstrates that the long-term treatment with ATDs has relatively few adverse events, most of which arise within the starting months of treatment and in subjects on larger doses. Hence, once we have reached the end of a conventional course of ATD treatment (12 - 18 months), the hazard is eliminated, and adverse events are very rare to occur. Therefore, by continuing low-dose ATD, we could safely maintain the patient’s euthyroid status. Conclusions: Long-term ATD treatment is safe, especially at a low dose. It can be considered as the preferred treatment for selected hyperthyroid patients.


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