Exp Clin Endocrinol Diabetes 2010; 118(3): 151-157
DOI: 10.1055/s-0029-1202275
Article

© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York

The low-dose (1 μg) Cosyntropin Test (LDT) for Primary Adrenocortical Insufficiency: Defining the Normal Cortisol Response and Report on First Patients with Addison Disease Confirmed with LDT

M. Pura 1 ,  Kreze 2 A. Jr. , P. Kentoš 1 , P. Vaňuga 1
  • 1Department of Endocrinology, National Institute of Endocrinology and Diabetology, Lubochna, Slovakia
  • 2IInd Internal Department, Bulovka Faculty Hospital, Prague, Czech Republic
Further Information

Publication History

received 22.06.2008 first decision 30.10.2008

accepted 22.01.2009

Publication Date:
08 April 2009 (online)

Abstract

Background: The validity of low-dose 1 μg cosyntropin test (LDT) is reported mainly for the assessment of secondary adrenocortical insufficiency (AI). Likewise the hypothalamic-pituitary disorders, early diagnosis of the initial or partial stages of primary AI has an important role.

Objective: The aim of study was to: 1) establish the normal cut-off level at which the stimulated plasma cortisol (FP) in LDT excludes primary AI; 2) compare the results in elderly subjects to those in younger ones; 3) compare the results between normal and obese subjects; and 4) verify the established cut-off values on the sample of patients suspected to have primary AI.

Subjects and Methods: 110 subjects (99 women and 11 men, aged 19–80 years, mean 46.2±16.1 years, without suspicion for impairment of the hypothalamo-pituitary-adrenal axis were recruited to undergo the LDT in standard conditions. Control group consists of 30 patients (22 women and 8 men, aged 7–58 years, mean 38.4±10.6 years) evaluated in whom for suspicion of primary AI as suggested by LDT was confirmed by supplemental investigations (elevated ACTH levels, positive autoantibodies against 21-hydroxylase, mutational analysis of corresponding genes).

Results: The mean peak FP level at 30 min (FP30) of the subjects was 675±85 nmol/L (95% CI=659 to 691 nmol/L), thus reference values expressed as mean±2 SD were 505–845 nmol/L. There was a significant negative correlation between basal FP values (FP0) (434±105 nmol/L) and the absolute FP incremental (FPΔ) response varying from 52 to 553 nmol/L (median 230 nmol/L) (r=–0.71; P<0.001). FP30 was higher in elderly subjects (n=27) in comparison to younger subjects (n=25) (689±88 nmol/L vs. 642±63 nmol/L, u=2.11, P<0.05) due to higher FPΔ (274±116 nmol/L vs. 175±112 nmol/L; u=4.02, P<0.01) ; FP30 levels in obese subjects (n=27) did not differ from those with normal BMI (n=33) (694±100 nmol/L vs. 667±65 nmol/L, u=1.31, P>0.05). We did not find any correlation between body weight or body surface area and FP0, FP30 or FPΔ. Post-stimulation FP30 levels in the control group varied from 0 to 354 nmol/L with median 64 nmol/L (25th percentile 10 nmol/L; 75th percentile 165 nmol/L) and were entirely distinctive from those of the subjects without adrenal impairment (P<0.001).

Conclusions: Taking the mean –2 SD result as a threshold, FP value of 500 nmol/L can be consider as cut-off at 30 min in the LDT for defining the intact adrenocortical function, independently of age and body weight, body surface area.

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Correspondence

M. PuraMD 

Department of Endocrinology

National Institute of Endocrinology and Diabetology

034 91 Lubochna

Slovakia

Phone: +421/44/4306 113 214

Fax: +421/44/4306 322

Email: mikulas.pura@nedu.sk

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