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From the Department of Medicine (W.R.L., N.D.L.F., G.H.W.), Brigham and
Women's Hospital and Harvard Medical School, Boston, Mass; the
Department of Medicine (S.H., P.H., R.W.), University of Utah, Salt Lake City,
Utah; and the Department of Molecular Hypertension and Clinical Investigative
Center (X.J., P.C.), Hospital Broussais, Paris, France.
AbstractWe evaluated urinary
cortisol excretion as a potential intermediate phenotype of
essential hypertension in 153 white patients with essential
hypertension and 18 normotensive white control subjects.
Analyses were controlled for dietary sodium and gender to
adjust for potential confounding effects of these variables on
cortisol excretion. Urinary cortisol excretion measured on both high-
and low-salt diets was significantly related to hypertension by
repeated measures ANCOVA (P=.02). Additional
determinants of urinary free cortisol included dietary sodium intake
and gender; cortisol excretion was significantly higher in men
(P=.0006) and during a high-sodium diet
(P=.0001). Maximum likelihood analysis showed
urinary cortisol to have a bimodal distribution on both 200-mmol
(P<.01) and 10-mmol (P<.002) sodium
diets in hypertensive subjects. On the low-salt diet, the mean urinary
cortisol in normotensive subjects (108.7±44.7 nmol/d) was similar to
the mean of hypertensive subjects in the low mode (127.2±43.0 nmol/d).
The high mode comprised 31.2% of the hypertensive population and had a
mean urinary cortisol of 224.3±93.8 nmol/d. Subjects with the highest
urinary free cortisol showed the least sensitivity of blood pressure to
dietary sodium loading (P<.05). These data suggest that
there is an association between salt-resistant hypertension and
high urine cortisol levels. This association may have a genetic
basis.
© 1998 American Heart Association, Inc.
Scientific Contributions
Increased Urinary Free Cortisol
A Potential Intermediate Phenotype of Essential Hypertension
Key Words: cortisol genetics phenotype, intermediate sodium bimodality
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