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Ringold et al., Los Angeles, CA, USA, found 99 twin pairs indicating a
history of Graves' disease from a population of 13.726 twin pairs that
responded to a written questionnaire. The pairwise concordance for GD was
estimated at 17% in monozygotic (MZ) twins and 1.9% in dizygotic (DZ) twins.
These results were in close agreement with those of a recent Danish twin
registry report. GD/chronic thyroiditis concordance, in twins not concordant
for GD, was observed in 17.2% of MZ twins vs. 2.1% in DZ twins. Concordance
rates for GD/non-thyroidal autoimmune, in twins not concordant for GD, were
13.8% and 4.3% respectively. The authors state that the here reported
concordance rates for GD in twin pairs are lower than from some other reports
and suggest that apart from genetic factors, environmental factors may play a
more substantial role in the etiology of GD. Furthermore, the results imply that
thyroidal and non-thyroidal autoimmune diseases may share a common genetic
substrate. Wallaschofski et al., Leipzig and Erfurt, Germany, studied thyrotropin
binding inhibiting immunoglobulins (TBII), thyroid stimulating antibodies (TSAB),
and thyrotropin stimulating blocking antibodies (TSBAB) in 64 patients with GD,
at the time antithyroid drug treatment (given for 2 years) was stopped and 1 year
later. Twenty-eight patients stayed in remission, whereas 36 patients were in a
relapse. In patients in remission, there was a significant decrease in TSAB whereas
TBII and TSBAB were not changed one year after discontinuation of drug treatment.
Combined measurement of TSAB and TSBAB (loss of TSAB and transition of TSAB to
TSBAB and vice versa) showed a higher prognostic significance for remission
prediction (P = 0.0001) than measurement of TSAB alone. In relapsed patients no
significant changes were seen in activities of the three parameters. Pegoraro et
al., Sao Paulo, Brasil, measured IL-1 beta, soluble (s) IL-2R, IL-6, IL-8, and
TNF-alpha in 31 patients with GD before and after 16-20 weeks of treatment with
methimazole with or without L-T3 addition. In untreated GD, IL-1 beta, sIL-2R,
and IL-6 were elevated (p < 0.001) while IL-8 and TNF-alpha were not. After
restoring euthyroidism sIL-2R and TNF-alpha decreased significantly (p < 0.001
and p < 0.01 respectively) but no alteration was present with regard to IL-1
beta and IL-8. sIL-2R and IL-6 levels were positively correlated with serum T3,
while this was only the case for sIL-2R with regard to serum free T4. The decrease
of TNF-alpha was explained by a direct effect of methimazole. (Comment: The authors
suggest that sIL-2R and IL-6 could be of clinical use in prediction of GD recurrence,
however this hypothesis was not actually tested in this report.) Miyake et al.,
Kurume, Japan, measured velocity (V), pulsative index (PI), resistance index (RI),
and flow volume (FV) of the superior thyroid artery, using colour pulse Doppler
ultrasonography (CPDU) in 22 patients with Hashimoto's disease (HT), 4 patients
with subacute thyroiditis (SAT), 16 patients with untreated GD (uGD), 23 patients
with treated GD (tGD), and 15 healthy controls (C). Sixteen uGD were followed during
treatment. V was significantly greater in uGD than in HT, SAT, and C. Positive
correlations were found between V and FT3, FT4, TBII, and TSAB in uGD. PI showed
significant correlations with FT3, FT4, TBII, and TSAB levels the same patients group.
The authors conclude that CPDU may be of aid in the diagnosis of Graves' disease.
(Comment: The technique may rather be useful in differentiating uGD from other
causes of thyrotoxicosis.) Three reports were presented on the effect of
antithyroid drugs (ATD) treatment on the subsequent efficacy of radioiodine
therapy in GD. Andrade et al., Porto Allegre, RS, Brasil, prospectively
pretreated 24 patients with Graves'disease with methimazole until euthyroidism
and subsequently with I-131 and 24 GD patients with I-131 without pretreatment.
In this randomized trial no differences between the two groups were present
regarding age, gender, thyroid volume, 24h I-131 uptake, TRAb or basal thyroid hormone
levels. Methimazole was stopped 4 days before I-131 administration. After one year no
statistical difference between the two treatment groups was present with respect to
persistent hyperthyroidism, euthyroidism or hypothyroidism. The authors suggest that
methimazole pretreatment does not affect the efficacy of I-131 treatment. Asamoah et
al., Providence, RI, USA, analyzed results of I-131 treatment in 161 patients
(140 females) with Graves'disease. 17/161 Patients (12/140 females; 8%, and 5/21
males; 24%) needed a second dose. Mean goiter size of retreated patients versus
non-retreated patients was 57.6 vs. 44.8 (p = 0.009). There was no significant
difference with regard to mean age at the time of initial treatment between the
two groups. Also pretreatment with ATD did not influence the efficacy of therapy.
(Comment: Unfortunately the type of ATD used was not mentioned.) Santos et al.,
Campinas, SP, Brazil, evaluated 67 patients with GD, 3 and 6 months after I-131
treatment who were randomly assigned to pretreatment with propylthiouracil, methimazole,
or no ATD. No differences between the three subgroups were present with regard to sex,
age, thyroid weight and 24h I-131 thyroid uptake. Cure (eu- or hypothyroidism) was
similar in methimazole group and no-ATD group being 72 and 75% respectively, whereas
only 35% (p < 0.05) were cured of the propylthiourcil group. (Comment: Both abstracts
are in favour of using methimazole if pre-treatment with ATD is desired. Another advantage
of methimazole over propylthyouracil is its longer half-life.)
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