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Insulin sensitivity, vascular reactivity, and clamp-induced vasodilatation in essential hypertension

Insulin resistance and vascular abnormalities have both been described in patients with essential hypertension. Whether these defects are associated with one another in the same individual has not been established. Whole-body insulin sensitivity (by the insulin clamp technique), forearm minimal vasc...

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Published in:Circulation (New York, N.Y.) N.Y.), 1997-08, Vol.96 (3), p.849-855
Main Authors: NATALI, A, TADDEI, S, QUINONES GALVAN, A, CAMASTRA, S, BALDI, S, FRASCERRA, S, VIRDIS, A, SUDANO, I, SALVETTI, A, FERRANNINI, E
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Language:English
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Summary:Insulin resistance and vascular abnormalities have both been described in patients with essential hypertension. Whether these defects are associated with one another in the same individual has not been established. Whole-body insulin sensitivity (by the insulin clamp technique), forearm minimal vascular resistances, and the dose-response curve to acetylcholine, sodium-nitroprusside, and norepinephrine were measured in a group of 29 male patients with untreated essential hypertension. When the patients were divided into tertiles according to their level of insulin sensitivity, resistant and sensitive hypertensives were matched on several potential confounders of insulin action and vascular function. These subgroups showed similar minimal vascular resistances (2.5+/-0.2 versus 3.2+/-0.6 mm Hg per mL x min(-1) x dL(-1)) and superimposable responses to graded intraarterial infusions of acetylcholine, sodium-nitroprusside, and norepinephrine. No correlation was found between the vascular parameters (slope of the curve or maximal response) and insulin-mediated glucose uptake in the whole group. During the clamp, insulin sensitive patients tended to have greater increments in forearm blood flow when compared to their insulin resistant counterparts (+53+/-21 versus +9+/-7%, P=.06); in the whole group, clamp-induced vasodilatation was weakly related to insulin-mediated glucose uptake (r=.44, P
ISSN:0009-7322
1524-4539
DOI:10.1161/01.cir.96.3.849