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Amarante et al., Sao Paulo, Brasil, studied if urinary collagen cross-links
excretion, correlates with free hormone levels in 23 patients with untreated
Graves' disease. They measured excretion of pyridinolin and deoxypyridinolin
in urine and found a better correlation with free T3 than with free T4.
The exretion of these collagens is correlated with bone turnover in hyperthyroidism.
Mercuro et al., Cagliari, Sardinia, Italy, studied cardiac function
and skeletal muscle performance in 14 patients before treatment of hyperthyroidism
and at several instances during and after treatment. They found that impaired
exercise tolerance was caused both by decreased cardiac performance and
skeletal muscle performance (presumably due to decreased muscular oxidative
capacity). In addition it appeared the faster hyperthyroidism was corrected,
the longer it took to restore muscular function, whereas a slow and progressive
return to euthyroidism normalized muscular function earlier.
Nystrom et al., Goteborg, Sweden, studied bone mineral density and body
composition in 8 patients with hyperthyroidism before and one year after
treatment. They found that after one year all subjects increased in bodyweight,
bone mineral content and total calcium. However, urinary calcium excretion
was still low after one year in 5/8 patients, while the mean parathyroid
hormone level was increased. These findings point to a negative calcium
balance still one year after treatment and the authors question if these
patients should not receive calcium supplementation after treatment.
Vaisman et al., Rio de Janeiro, Brasil, investigated muscle performance
and did anthropometric measurements in 9 patients before and after medical
treatment for Graves' disease. They found that the increase in bodyweight
was mainly due to increase in lean body mass and that the improvement in
muscle performance resulted both from enhanced intrinsic muscle function
as well as increased muscle mass.
Gerasimov et al., Moscow, Russia, measured left ventricular contractility
before and after treatment for hyperthyroidism in 19 patients with Graves'
disease. They found that parameters of left ventricular contractility like
stroke volume, cardiac output, left ventricular ejection fraction all correlated
with FT4. They also found 8% of patients having mitral valve prolaps before,
but only 4% after treatment.
Hüfner et al., Göttingen, Germany, tested the efficacy of
prophylactic administration of 20 mg methimazole or 900 mg perchlorate
to prevent iodine induced thyrotoxicosis in patients with autonomy of thyroid
function (low TSH and normal FT3 and FT4). Treatment was started 12h before
coronary angiography and continued for 14 days. In total 51 patients were
included in the study. They found that either of these medical regimens
could not prevent mild hyperthyroidism in some cases as measured 30 days
after angiography. The lab results however indicate some protection against
excess of iodine. (Comment: In the experience of the authors it is in most
instances possible to prevent even mild thyrotoxicosis when 60 mg methimazole
and 1200 mg perchlorate daily are given together until 1 week after iodine
excess, after which perchlorate can be discontinued completely and methimazole
tapered off in the course of a few weeks.)
Jarlof et al., Odense, Denmark, compared two regimens of RAI treatment
for hyperthyroidism. The first regimen consisted of administration of 185,
370, 555 mBq for small (< 30ml), medium (30-60 ml), or large glands
(> 60 ml) (volumes were assessed by palpation) versus a so-called compensated
l3lI therapy based on type of thyroid gland, accurate thyroid volume and
24h RAI uptake determinations. In total 163 patients were studied and no
differences in therapeutic outcome were found in any of the three types
of hyperthryoidism (Graves' disease, multinodular toxic goiter, and toxic
adenoma). They conclude that the first semiquantative approach is probably
as good as the more elaborate one and is clearly more cost-effective.
Cortelazzi et al., Milan, Italy, report the first patient with a toxic
nodule who was treated with ethanol injections during pregnancy in the
13th week of gestation. Four injections of 3 ml ethanol (95%) one, every
3 days, were given, successfully resulting in euthyroidism 3 weeks after
the first injection. The nodule reduced to 1/3 of its original volume.
Apart from a transient pain and a burning sensation no adverse affects
were seen, either in the mother or in the fetus.
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