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Study · Not a test of the peptide alone · 1998

4 results

A high-sensitivity test in the assessment of adrenocortical insufficiency: 10 microg vs 250 microg cosyntropin dose assessment of adrenocortical insufficiency.

González-González JG, De la Garza-Hernández NE, Mancillas-Adame LG, Montes-Villarreal J, Villarreal-Pérez JZ

The Journal of endocrinology1 Nov 1998Cited by 20 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study4

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone4

In this study, Cosyntropin was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Cosyntropin.

  1. 01HumanNot a test of Cosyntropin aloneNon-randomized trialOther

    In healthy subjects, peak cortisol did not differ significantly between low-dose and standard-dose cosyntropin tests.

    In plain wordsIn healthy people, peak cortisol did not differ significantly between low-dose and standard-dose cosyntropin tests.

    Outcome
    No significant changePeak serum cortisol
    Study

    n = 46

    Comparator
    250 microg cosyntropin
    Outcome group
    Diagnostic test performance · Endocrine and hormones

    Source sentences

    Summary
    On comparing low- and standard-dose cosyntropin testing in healthy subjects there were no statistical differences in baseline and peaks of serum cortisol.
    1 context sentence
    Summary · context
    The subjects were 83 healthy people and 37 patients, the latter having Addison's disease (11), pituitary adenomas (7), Sheehan's syndrome (9) and recent use of glucocorticoid therapy (10). Forty-six healthy subjects and all patients underwent low- and standard-dose cosyntropin testing. In addition,…

    In this study, Cosyntropin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Cosyntropin.

  2. 02HumanNot a test of Cosyntropin aloneNon-randomized trialOther

    In Addison's disease, low-dose cosyntropin identified abnormal cortisol in 2 of 11 cases with normal standard-test values.

    In plain wordsIn Addison's disease, low-dose cosyntropin identified abnormal cortisol in cases with normal standard-test results.

    Outcome
    Not applicableAbnormal cortisol classification in Addison's disease
    Study

    n = 11

    Comparator
    250 microg cosyntropin
    Outcome group
    Diagnostic test performance · Endocrine and hormones

    Measurements

    Discordant cases
    2 cases
    11 Addison's disease cases

    Source sentences

    Summary
    In the group of patients, 2 out of 11 cases of Addison's disease showed normal cortisol criterion values during the standard test but abnormal during the low-dose test.
    1 context sentence
    Summary · context
    The subjects were 83 healthy people and 37 patients, the latter having Addison's disease (11), pituitary adenomas (7), Sheehan's syndrome (9) and recent use of glucocorticoid therapy (10). Forty-six healthy subjects and all patients underwent low- and standard-dose cosyntropin testing. In addition,…

    In this study, Cosyntropin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Cosyntropin.

  3. 03HumanNot a test of Cosyntropin aloneNon-randomized trialOther

    In patients and controls, low-dose cosyntropin had better sensitivity than standard-dose testing at 30 min.

    In plain wordsIn patients and controls, low-dose cosyntropin was more sensitive than standard-dose testing at 30 min.

    Outcome
    IncreaseSensitivity at 30 min
    Study

    n: not reported in source

    Comparator
    250 microg cosyntropin
    Outcome group
    Diagnostic test performance · Endocrine and hormones

    Source sentences

    Summary
    In our group of patients and controls, the statistical analysis displayed a better sensitivity of the low-dose vs standard-dose ACTH test at 30 and 60 min.
    1 context sentence
    Summary · context
    The subjects were 83 healthy people and 37 patients, the latter having Addison's disease (11), pituitary adenomas (7), Sheehan's syndrome (9) and recent use of glucocorticoid therapy (10). Forty-six healthy subjects and all patients underwent low- and standard-dose cosyntropin testing. In addition,…

    In this study, Cosyntropin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Cosyntropin.

  4. 04HumanNot a test of Cosyntropin aloneNon-randomized trialOther

    In patients and controls, low-dose cosyntropin had better sensitivity than standard-dose testing at 60 min.

    In plain wordsIn patients and controls, low-dose cosyntropin was more sensitive than standard-dose testing at 60 min.

    Outcome
    IncreaseSensitivity at 60 min
    Study

    n: not reported in source

    Comparator
    250 microg cosyntropin
    Outcome group
    Diagnostic test performance · Endocrine and hormones

    Source sentences

    Summary
    In our group of patients and controls, the statistical analysis displayed a better sensitivity of the low-dose vs standard-dose ACTH test at 30 and 60 min.
    1 context sentence
    Summary · context
    The subjects were 83 healthy people and 37 patients, the latter having Addison's disease (11), pituitary adenomas (7), Sheehan's syndrome (9) and recent use of glucocorticoid therapy (10). Forty-six healthy subjects and all patients underwent low- and standard-dose cosyntropin testing. In addition,…

    In this study, Cosyntropin was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Cosyntropin.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:37 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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