Diabetes Care, Vol 18, Issue 8 1168-1173, Copyright © 1995 by American Diabetes Association
Reproducibility of the first-phase insulin response to intravenous glucose is not improved by retrograde cannulation and arterialization or the use of a lower glucose dose
PD McNair, PG Colman, FP Alford and LC Harrison
Royal Melbourne Hospital, Parkville, Victoria, Australia.
OBJECTIVE--To determine whether the reproducibility of the first-phase
insulin response (FPIR) measured during an intravenous glucose tolerance
test is improved by the use of a lower glucose dose or retrograde sampling
from an arterialized hand vein. RESEARCH DESIGN AND METHODS--Previous
studies have suggested that the high within-subject variation of FPIR
measurement of up to 110% could be reduced by sampling from a retrograde
cannulated and arterialized hand vein opposite to the cubital fossa vein
through which the glucose was injected or by the use of a lower dose of
glucose. Two low-dose (glucose, 5 g/m2 injected over 30 s) and two standard
Islet Cell Antibody Registry Users Study (ICARUS) (glucose, 0.5 g/kg
injected over 3 min) tests were performed on seven normal subjects at
2-week intervals. Samples were collected simultaneously from the cubital
fossa vein, through which the glucose was injected, and from a retrograde
cannulated, contralateral hand vein that was arterialized by heating. FPIR
was expressed as the sum of the insulin measurements 1 and 3 min after the
completion of the glucose injection and as the area under the insulin curve
between 0 and 10 min. RESULTS--Responses to the mean sum of serum insulin
concentrations at 1 and 3 min after intravenous glucose were significantly
lower for the low-dose test (mean 94 mU/l) than for the high-dose test
(mean 184 mU/l) for samples taken from the arm (P < 0.05); mean 0- to
10-min insulin areas were 367 and 596 mU/l for low- and high-dose tests,
respectively (P < 0.05). Within-subject coefficients of variation for
samples from the hand or the arm ranged from 0.33 to 17.5% and 1.3 to 38%
for successive ICARUS and low-dose tests, respectively. Reproducibility,
measured by the coefficient of variation between successive tests for each
protocol, was not significantly different using samples taken from the arm
or the contralateral hand. CONCLUSIONS--The intravenous glucose tolerance
test is reproducible when performed by the same operator over a short time
span. Reproducibility is not significantly improved by sampling from an
arterialized, retrograde cannulated, contralateral hand vein. There is no
case for changing the present ICARUS protocol to incorporate retrograde
cannulation or low-dose (5 g/m2) glucose.