The purpose of this study was to evaluate the association of the insulin re
sistance syndrome with both blood pressure and target organ damage in black
s and whites with essential hypertension. Eighty-two black and 63 white Fre
nch Canadian patients were studied. None had diabetes, and antihypertensive
medications had been discontinued for greater than or equal to1 week. Meas
urements included 24-hour blood pressure monitoring, fasting plasma lipids,
insulin sensitivity determined with the Bergman minimal model, echocardiog
ram, microalbumin excretion, and inulin and lithium clearances. Compared wi
th the white French Canadians, black patients had an attenuated nighttime r
eduction in blood pressure (P<0.02), increased cardiac dimensions (P<0.001)
, greater microalbumin excretion (P<0.05), increased inulin clearance (indi
cative of glomerular hyperfiltration; P<0.001), and decreased lithium clear
ance (indicative of increased sodium reabsorption in the proximal tubule; P
<0.001). Blood pressure levels were not related to insulin resistance; alth
ough in blacks, the nighttime reduction in systolic blood pressure was inve
rsely related to fasting plasma insulin (r= -0.18, P<0.04). In a stepwise m
ultivariate analysis (including blood pressure levels and components of the
insulin resistance syndrome as independent variables), race was the strong
est predictor of left ventricular mass (r=0.53, P<0.000), relative wall thi
ckness (r=0.49, P<0.000), and both inulin (r=0.53, P<0.000) and lithium (r=
0.41, P<0.000) clearances. Nighttime systolic blood pressure was also a sig
nificant determinant of concentric left ventricular hypertrophy (r=0.37, P<
0.000). In blacks, microalbumin excretion was related to insulin resistance
. These observations are consistent with the hypothesis that there is a gen
etic contribution to cardiac hypertrophy, glomerular hyperfiltration, and s
odium retention in blacks with essential hypertension.