We describe three patients who have
polydipsia and
polyuria due to an abnormality in the
osmoregulation of thirst. The clinical manifestations of the
syndrome are similar to those of neurogenic diabetes insipidus. Thus, under
basal conditions the patients have thirst, normal to high normal levels of
plasma osmolality, and low levels of plasma vasopressin. Moreover,
antidiuretic therapy greatly reduces thirst and
polydipsia as well as
polyuria. The only clinically distinguishing feature of the response is that thirst and water intake decrease less rapidly than water excretion. As a consequence, the patients with this
syndrome develop variable degrees of dilutional
hyponatremia and hypoosmolemia during treatment. The plasma vasopressin response to osmotic stimulation is relatively normal. In most of the patients, the
osmotic threshold for
vasopressin release is at the upper limit of normal, but this finding only explains their modest elevation in basal plasma osmolality. Thirst and water intake also change as a function of
plasma osmolality. However, the
threshold or "set" of the thirst osmostat appears to be abnormally low. The degree of downward resetting varies from patient to patient, but is always sufficient to stimulate thirst and water intake at levels of
plasma osmolality below the normal range. This abnormality can account not only for the thirst and
polyuria under
basal conditions but also for the overhydration that occurs during
antidiuretic therapy. The
pathogenesis of the osmoregulatory abnormality is unknown but may be due to disruption of one or more of the afferent pathways that
regulate the "set" of the thirst and
vasopressin osmostats.