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(Hypertension. 1998;31:110.)
© 1998 American Heart Association, Inc.
Scientific Contributions |
From the Internal Medicine and Hypertension Centre, University of Palermo, Italy.
AbstractBoth
microalbuminuria (>0.290 nmol/min [20 µg/min]) and
high sodium-lithium countertransport (SLC) in diabetic or hypertensive
humans are predictive of overt nephropathy and more
aggressive cardiovascular complications, perhaps
induced by insulin resistance. To analyze the relationships
between microalbuminuria, SLC,
microalbuminuria, and insulin in essential hypertension, we
studied 90 hypertensive white patients, 25 of whom had
microalbuminuria and 32 of whom were healthy. When urine
sampling was completed for albuminuria determination, SLC
was measured; all patients then underwent standard (75 g) oral glucose
load to measure basal (0 minutes) and 2-hour glucose and insulin serum
levels. Glucose-insulin ratio was used as insulin sensitivity index
(ISI). In both hypertensive patients with normal
microalbuminuria and those with pathological
microalbuminuria, plasma insulin at 120 minutes was
significantly higher than in control subjects. When the patients with
pathological microalbuminuria were divided into thirds on
the basis of their microalbuminuria, in the lower third, we
found statistically significant less fasting insulin and higher basal
ISI. SLC was higher in hypertensives than normotensives and, among
hypertensives, higher in the subgroup with elevated
microalbuminuria. In hypertensives, we found a weak but
significant correlation between SLC and microalbuminuria,
independent of insulin or ISI. The prevalence of high value of SLC
(
0.383 mmol · L-1 · h-1)
was significantly lower in hypertensives with normal rather than
abnormal urinary albumin excretion. Our results indicate that
in nondiabetic hypertensive whites, higher microalbuminuria
is accompanied by signs of insulin resistance; moreover, a link exists
between SLC and microalbuminuria, both predictive of
aggressive complications of hypertension.
Key Words: insulin sodium-lithium countertransport microalbuminuria insulin resistance cardiovascular risk nephropathy
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