A radioimmunoassay procedure for the measurement of urinary
18-oxocortisol was developed. The antibody was raised against
18-oxocortisol 3-carboxymethyloxime-BSA and had relatively high specificity, except for
aldosterone (26.3%). The RIA required a preliminary HPLC purification using a Lichrosorb diol column eluted with
toluene:
acetonitrile:
isopropanol:
acetic acid (83:11.9:5.1:0.01). The eluate portion corresponding to
18-oxocortisol was evaporated and subjected to RIA. The RIA procedure had an intraassay variability of 11% when using a pool containing 10.8 micrograms/24 hr (n = 6) and 17% with a pool containing 3.28 micrograms/24 hr. The interassay variability was 11% (n = 4). The recovery of added
18-oxocortisol was 90 +/- 10%. The urinary excretion of
18-oxocortisol in 22 white normal subjects was 3.26 +/- 1.98 (SD) micrograms/24 hr (range 0.8 to 7.1 micrograms/24 hr). The mean excretion of
18-oxocortisol in 4 patients with
glucocorticoid-suppressible
aldosteronism (GSA) was 38.6 micrograms/24 hr (range 25.5 to 54.6 micrograms/24 hr). The excretion of
18-oxocortisol in 3 patients with
adenomas producing primary
aldosteronism (APA) varied between 11.1 to 17.3 micrograms/24 hr and in 3 patients with idiopathic
aldosteronism (IA) varied between 2.5 to 10.6 micrograms/24 hr.
18-Oxocortisol excretion is increased markedly in the urine of patients with GSA: what role this relatively weak
mineralocorticoid plays in the pathogenesis of their
hypertension is unknown. Its elevation is probably a reflection of a postulated lack of involution of the 18-methyloxidase in the inner layers of the adrenal.