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Letters to the Editor |
Bnai Zion Medical Center Haifa, 31048, Israel
In their paper, Shankar et al. (1) claim that they found no improvement in the sensitivity of the low dose ACTH test for the evaluation of the HPA axis. However, they use the term "low dose ACTH test" wrongly.
The dose of ACTH in the low dose test was defined previously as being 1.0 µg for adults (2, 3, 4), or 0.5 µg/1.73 m2 for children (5, 6). These were the doses proven to increase sensitivity. Tordjman et al. (3) have shown that 5.0 µg (which equals 0.061.0 µg/kg) is too high a dose for this purpose. The dose the authors use in the current study is much higher, equaling about 15 µg for adults and about 10.0 µg/1.73 m2 for children. All that this paper shows is that such a dose does not increase the sensitivity of the ACTH test, which is not surprising, knowing that even lower doses do not.
However, the term "low dose ACTH test" should not have been used in this study, as readers might wrongly think that their low dose ACTH test is similar to the one used in the past and proven to increase sensitivity.
We have also a comment regarding the study design. We find that both ACTH tests (high dose and so called low dose) should not have been done on the same day, and definitely not in the order they were. The correct way should be either to perform tests in random order, as we did (2), or start with the lower dose, as the higher one might prime the adrenal gland, rather than deplete it. Actually, the fact that one patient did not respond to the huge dose of 250 µg but responded to the lower ACTH later in the same day suggests that this is really the case. However, considering the too large ACTH dose used as a low dose, this point is minor in the current study.
Footnotes
1 Received June 19, 1997. Address
correspondence to: Gabriel Dickstein, Division of Endocrinology, Oregon
Health Sciences University L607, 3181 SW Sam Jackson Park Road,
Portland, Oregon 97201-3098. ![]()
References
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