Diminished urinary free cortisol excretion in patients with moderate and severe renal impairment.
Because plasma free cortisol is filtered through the glomeruli with partial tubular reabsorption, the amount of free cortisol appearing in the urine is theoretically dependent on the glomerular filtration rate. However, the high reliability of using 24-h urinary cortisol excretion for the diagnosis of Cushing syndrome implies that urinary excretion of cortisol is relatively unaffected by renal function. In patients with confirmed Cushing disease and severe renal impairment, the urinary free cortisol excretion rate reportedly is normal despite markedly increased plasma cortisol (4-6). The relationship between glomerular filtration rate and urinary cortisol excretion has not been documented in patients with different degrees of renal impairment.
We selected 100 leftover portions of urine samples that had been sent for the measurement of creatinine clearance (CrCI) in the Prince of Wales Hospital of Hong Kong during September, October, and November 2002. All patients were given clear instructions by an experienced nurse to ensure the completeness of 24-h urine collection. Simultaneous serum samples were also received for the determination of serum creatinine and were used for subsequent calculation of CrCI for each patient. The 24-h urinary protein excretion and random serum total cortisol were also measured. All blood samples were collected in the morning. Patient records were reviewed to exclude those samples from patients who were diagnosed to have Cushing syndrome or were taking steroids. The volume of each 24-h urine sample had previously been recorded. The concentration of free cortisol of the urine samples was determined by electrochemiluminescence immunoassay (E170 Analyzer; Roche Diagnostics GmbH) after centrifugation to remove urinary sediments and extraction with dichloromethane (7). This commercially available immunoassay measures cortisol and corticoid-like products (8) and is widely used in routine clinical chemistry laboratories. The 24-h urinary free cortisol excretion was then calculated based on the concentration and the initial volume of the 24-h urine sample. The reference intervals used for 24-h urinary free cortisol and morning serum total cortisol were 100-379 nmol/day and 171-536 nmol/L, respectively. The reference intervals for CrCI in males and females are 94-140 and 72-110 mL/min, respectively.
Among the 100 urine samples in which we measured free cortisol excretion, 18 were excluded from the subsequent analysis. Sixteen of them were excluded because patients were taking steroids, 1 patient was subsequently diagnosed to have Cushing syndrome, and another was found to be on peritoneal dialysis. The median volume of the 24-h urine collection was 2.175 L (range, 0.15-4.5 L).
The 24-h urinary cortisol excretion rates of the studied patients ranged from 2 to 440 nmol/day. The relationship between CrCI and 24-h urinary free cortisol excretion is shown in Fig. 1A. There appeared to be a correlation between 24-h urinary free cortisol excretion and CrCI for those patients with significant renal impairment. To further investigate this observation, we arbitrarily divided the patients into three groups according to their CrCI rates: mild or no renal impairment (CrCI >60 mL/min), moderate renal impairment (CrCI, 20-60 mL/min), and severe renal impairment (CrCI <20 mL/min). There were 49, 19, and 14 patients in the three groups, respectively. The median 24-h urinary free cortisol excretion rates of the three groups were 172 (interquartile range, 152-284) nmol/day, 109 (88-145) nmol/day, and 27.8 (6.9-36.4) nmol/day, respectively.
Patients with moderate or severe renal impairment had significantly lower urinary free cortisol excretion rates than those with no or mild renal impairment (P <0.001, Kruskal-Wallis test), and patients with severe renal impairment had significantly lower urinary cortisol excretion rates than those with moderate impairment (P <0.05, Mann-Whitney rank-sum test). Furthermore, in patients with severe renal impairment, there was a linear relationship between the urinary free cortisol excretion rate and CrCI ([r.sup.2] = 0.83, linear regression; Fig. 1B). On the other hand, we observed no linear relationship between urinary cortisol excretion rates and random total serum cortisol or the degree of proteinuria in the studied patients (data not shown). In contrast to the strong relationship between CrCI and urinary cortisol excretion rate, there was only a weak correlation between the volume of the 24-h urine collection and urinary free cortisol ([r.sup.2] = 0.16, Spearman correlation). Therefore, it is unlikely that the observed reduction in urinary free cortisol excretion was attributable to the incomplete collection of 24-h urine.
[FIGURE 1 OMITTED]
Because the estimation of CrCI involves collection of urine over 24 h, we further investigated whether the reduced urinary cortisol excretion could be predicted by use of the serum creatinine concentration alone. We performed a ROC curve analysis to determine the cutoff value for serum creatinine concentrations for the prediction of CrCI of <60 mL/min and found that the cutoff values for males and females were 126 and 94 [micro]mol/L, respectively. The distributions of urinary free cortisol excretion rates and CrCI in patients with normal and increased serum creatinine concentrations are shown in Fig. 1A. The mean urinary free cortisol excretion rates in individuals with normal and increased serum creatinine concentrations were 168 and 61 nmol/day, respectively (P <0.001, Mann-Whitney rank-sum test).
Our study has shown that CrCI is a major determinant for urinary cortisol excretion rate in patients with severe renal impairment. Because there is a theoretical possibility that the low urinary cortisol excretion rate may reflect the low blood cortisol concentrations in these patients, we compared the total random morning serum cortisol concentrations for patients with different degrees of renal impairment and found that serum total cortisol was significantly higher in patients with CrCI <20 mL/min (P = 0.002, Kruskal-Wallis test). This finding is consistent with previous reports that the serum cortisol concentrations of patients with end stage renal failure were higher than those of healthy individuals (9). Therefore, it is unlikely that the observed decrease in urinary free cortisol excretion in patients with moderate to severe renal impairment was attributable to hypoadrenalism.
In summary, the urinary free cortisol excretion rate is significantly reduced in patients with moderate to severe renal impairment (CrCI <60 mL/min) and consequently has diminished sensitivity in the diagnosis of Cushing syndrome in such patients. Moreover, this diminished urinary free cortisol excretion rate could be accurately predicted by the increased serum creatinine concentrations. Therefore, it would be more appropriate to use late-night serum salivary cortisol or other blood-based diagnostic tests for the screening and diagnosis of Cushing syndrome in patients with significantly impaired renal function as indicated by an increased serum creatinine concentration. The influence of impairment of renal function on the measurement of other urinary analytes, e.g., urinary steroid profile and urinary catecholamines, may need to be explored.
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(9.) Carlstrom K, Pousette A, Stege R, Lindholm A. Serum hormone levels in men with end stage renal disease. Scand J Urol Nephrol 1990;24:75-8. D01: 10.1373/ci i nchem.2003.029934
K.C. Allen Chan,  Lydia C.W. Lit,  Eric L.K. Law,  Morris H.L. Tai  C.U. Yung,  Michael H.M. Chan,  and Christopher W.K. Lam  *
 Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong Special Administrative Region, China;
 Department of Medicine, Alice Ho Miu Ling Nethersole Hospital, Tai Po, New Territories, Hong Kong Special Administrative Region, China;
* address correspondence to this author at: Department of Chemical Pathology, Chinese University of Hong Kong, Prince of Wales Hospital, 30-32 Ngan Shing St., Shatin, New Territories, Hong Kong SAR, China; fax 852-2636-5090, e-mail waikeilam~cuhk.edu.hk)
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|Title Annotation:||Technical Briefs|
|Author:||Chan, K.C. Allen; Lit, Lydia C.W.; Law, Eric L.K.; Tai, Morris H.L.; Yung, C.U.; Chan, Michael H.M.;|
|Date:||Apr 1, 2004|
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