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Free T3 values were variably reduced in sick sera by the seven
methods used by Sapin et al (9) (Figure 4). Free T3 estimates
were lowest in patients with the most reduced total T4 and total
T3 concentrations by all methods (9), presumably reflecting
the greater severity of illness. Free T3 values determined by
tracer or direct equilibrium dialysis, tracer ultrafiltration, and direct
Sephadex LH- 20 method in sick sera did not correlate with total T3
concentrations, and were reduced in all studies (1,9,19,21,23,26) except
three (22,27,28).
Faber et al. (22,27) used minimally diluted sera but did not
demonstrate that radioactivity in ultrafiltrates was T3 rather
than labeled contaminants; mean free T3 values in sick sera
were 104% and 92% of normal. The direct equilibrium dialysis method of
Chopra et al. (26,28) required addition of unlabelled T3
to sick serum samples (exogenous to endogenous T3 concentration
ratio of 4:1), to allow detectable levels of T3 to be measured
in dialysate. Using this method, mean free T3 estimates varied
from 46% to 96% of normal in sick sera in two different reports (26,28).
Surks et al (19) avoided the most obvious problems, by using undiluted
sera at pH 7.4 and 37 degrees Celsius, and identified T3 in
ultrafiltrates by paper chromatography, and observed free T3
values in critically ill patients to be modestly reduced to 80% of normal
values. Indeed, free T3 availability to tissue sites of action
may be normal in nonthyroidal disorders as indicated by normal T3
nuclear receptor proteins and normal thyroid hormone-regulated mRNAs (14).
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