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1 index and individuals with normal or altered oral glucose tolerance.
2 aired fasting plasma glucose and/or impaired oral glucose tolerance.
3 a levels of GLP-1 and insulin and diminished oral glucose tolerance.
5 gotes for ABCA1 mutations exhibited enhanced oral glucose tolerance and dramatically increased beta-c
7 F508 mutants had lower body weight, improved oral glucose tolerance, and a trend toward higher insuli
8 , Simple Index Assessing Insulin Sensitivity Oral Glucose Tolerance, and HOMA-IR were high, and did n
9 tein can use RT to improve body composition, oral glucose tolerance, and skeletal muscle aPKC zeta/la
10 mic-hyperinsulinemic clamp) 442% (P < 0.01), oral glucose tolerance (area under the curve for 3-h ora
12 polypeptide (GIP), and insulin, and improved oral glucose tolerance in an RU486-insensitve manner in
17 eight, visceral and subcutaneous fat depots, oral glucose tolerance, insulin sensitivity, and the pla
18 tor for 10 d was well tolerated and improved oral glucose tolerance, it increased the expression of t
19 lation-based Ely Study, had glycemic status (oral glucose tolerance), lipids, insulin, anthropometry,
20 nt in those with diabetes; those with normal oral glucose tolerance lost 9.1+/-3.7 kg of fat (18+/-3
22 ycemia, preferred strategies were the 2-hour oral glucose tolerance test (100% effectiveness; $390 pe
23 g therapy at any examination, or with a 75-g oral glucose tolerance test (1980 World Health Organizat
24 spectroscopy, and glucose turnover during an oral glucose tolerance test ([14C]glucose given with the
25 rement (DeltaI(30-0)/DeltaG(30-0)) during an oral glucose tolerance test (a surrogate for insulin sec
26 4 and glucose area under the curve during an oral glucose tolerance test (additive model, P = 0.022;
27 d increased fasting plasma insulin during an oral glucose tolerance test (all P < 0.01), as well as a
28 38; P = .03), plasma glucose levels after an oral glucose tolerance test (Hedges g = 0.61; 95% CI, 0.
29 icting to identifying IGT/NODAT using 2-hour oral glucose tolerance test (n = 66), fructosamine was t
30 these autoantibodies (Ab-), had an abnormal oral glucose tolerance test (OGTT) (P = 0.03) before and
31 years from prediabetes onset and the average oral glucose tolerance test (OGTT) 2-h glucose measureme
32 Study participants were phenotyped by an oral glucose tolerance test (OGTT) and an intravenous gl
33 mpared beta-cell function assessed during an oral glucose tolerance test (OGTT) and an isoglycemic in
34 s with varying glucose tolerance received an oral glucose tolerance test (OGTT) and euglycemic insuli
35 20 type 2 diabetic patients received a 75-g oral glucose tolerance test (OGTT) and euglycemic insuli
36 cose tracer and labeled glucose infusion and oral glucose tolerance test (OGTT) before and 6 months a
37 owing glucose beverage consumption during an oral glucose tolerance test (OGTT) for 400 northern Euro
38 litus (GDM) is conventionally confirmed with oral glucose tolerance test (OGTT) in 24 to 28 weeks of
39 venous glucose tolerance test (IVGTT) and by oral glucose tolerance test (OGTT) in 3 different sessio
40 , based on insulin levels measured during an oral glucose tolerance test (OGTT) in 552 nondiabetic pa
41 c evaluation of biochemical changes after an oral glucose tolerance test (OGTT) in a community-based
42 on lower (P < 0.05) during the meal than the oral glucose tolerance test (OGTT) in all subgroups rega
44 as a compound that displayed activity in an oral glucose tolerance test (OGTT) in normal and diabeti
45 fasting and postprandial lipids and after an oral glucose tolerance test (OGTT) in the European Ather
47 ell function and insulin sensitivity from an oral glucose tolerance test (OGTT) over a 4-year period
48 e obtained, in addition to 0-hour and 2-hour oral glucose tolerance test (OGTT) results, with measure
50 /dl relative to control HF animals during an oral glucose tolerance test (OGTT) such that levels were
52 zed by the following: 1) associations with 5 oral glucose tolerance test (OGTT) traits in 427 nondiab
53 in and glucose were monitored weekly, and an oral glucose tolerance test (OGTT) was performed at stud
55 h positive O'Sullivan test (POT) results, an oral glucose tolerance test (OGTT) was performed to diag
57 ons of glucose, insulin, and GLP-1 during an oral glucose tolerance test (OGTT) were analyzed in indi
58 the insulin-to-glucose ratio (IGR) at 30-min oral glucose tolerance test (OGTT), a frequently used su
59 atched control participants and underwent an oral glucose tolerance test (OGTT), a hypoglycemia quest
60 at reducing peak glucose levels in an acute oral glucose tolerance test (OGTT), but this effect was
61 e in blood glucose measured 2 h after a 75 g oral glucose tolerance test (OGTT), compared first betwe
62 by blood glucose and insulin responses to an oral glucose tolerance test (OGTT), insulin sensitivity
63 s with wild-type genotype (CC) underwent 5-h oral glucose tolerance test (OGTT), isoglycemic intraven
76 nal age at delivery, parity, maternal age at oral glucose tolerance test (OGTT); Model 2 adjusted for
77 with glucose area under the curve during an oral glucose tolerance test (P = 0.035 and 0.013, respec
78 n in the insulinogenic index derived from an oral glucose tolerance test (risk allele homozygotes hav
80 560887 was significantly associated with the oral glucose tolerance test 30-min incremental insulin r
81 ly diagnosed diabetes by 2-h glucose from an oral glucose tolerance test [OGTT] [DM2h], n = 80; newly
82 ting plasma glucose, hemoglobin A1c, and the oral glucose tolerance test all predict diabetic complic
83 ts and 10 healthy control subjects to a 75-g oral glucose tolerance test and a corresponding isoglyce
84 estionnaire, color Doppler echocardiography, oral glucose tolerance test and blood biomarkers analyse
85 d as the suppression of plasma FFA during an oral glucose tolerance test and by a low-dose insulin in
86 were gestational diabetes (diagnosed with an oral glucose tolerance test and by criteria from the Int
87 jection not only improved the response to an oral glucose tolerance test and corrected insulin signal
89 ose tissue biopsy, in addition to metabolic (oral glucose tolerance test and hyperinsulinemic euglyce
90 a, and disposition index were measured after oral glucose tolerance test and isoglycemic IV glucose i
93 o glucose during the first 30 minutes of the oral glucose tolerance test and using the area under the
95 ant recipients without diabetes underwent an oral glucose tolerance test and were observed until prim
97 es of maternal metabolism obtained during an oral glucose tolerance test at approximately 28 weeks' g
98 054 adults aged 30-74 years who underwent an oral glucose tolerance test at baseline (1976-1980).
101 glucose below 7 mmol/L, 2 hour glucose after oral glucose tolerance test below 11.1 mmol/L, and glyca
102 utcome measures were difference in change in oral glucose tolerance test between the groups and betwe
103 lin level, Matsuda index, and area under the oral glucose tolerance test curve (AUC) of insulin.
104 e and glucose area under the curve on 2-hour oral glucose tolerance test differed across arms (1-way
105 mes were glucose tolerance (measured with an oral glucose tolerance test given after 90 min) and meal
106 y homeostasis model assessment, and 2-h post-oral glucose tolerance test glucose and insulin levels.
107 bese adolescents with high-"normal" 2-h post-oral glucose tolerance test glucose levels display defec
108 ur plasma glucose >/=200 mg/dL during a 75-g oral glucose tolerance test had a definite diagnosis of
109 c ICA positivity had to be confirmed, and an oral glucose tolerance test had to result in nondiabetic
110 enge test (GCT) followed by a 75-gram 2-hour oral glucose tolerance test if GCT result was >/=7.8 mmo
111 -5.2]) and with 30-min plasma insulin during oral glucose tolerance test in 287 nondiabetic individua
112 ivo activity in rodents and was active in an oral glucose tolerance test in mice following oral admin
114 ervous system activity at rest and during an oral glucose tolerance test in obese metabolic syndrome
120 = 292), and Hispanics (n = 34) underwent an oral glucose tolerance test to assess whole-body insulin
121 e levels in healthy adults during a standard oral glucose tolerance test via exhaled VOC analysis.
126 sensitivity and rate sensitivity during the oral glucose tolerance test were measured with the model
127 and 2-hour glucose levels measured during an oral glucose tolerance test were used to assess glycemic
128 control participants underwent a 6-hour 75-g oral glucose tolerance test with ECG recording and blood
129 A total of 1,437 individuals underwent an oral glucose tolerance test with measurements of circula
130 of NAFLD patients underwent liver biopsy, an oral glucose tolerance test with minimal model analysis
131 okines, and cytokeratin-18 fragments, and an oral glucose tolerance test with minimal model analysis
132 cose tolerance (area under the curve for 3-h oral glucose tolerance test) 28% (P < 0.05), and plasma
133 (including results of a 26-28 week gestation oral glucose tolerance test) of women from the Born in B
134 G) ingested a labeled meal and 75 g glucose (oral glucose tolerance test) on separate occasions.
135 d ALT, AST, and GGT in 451 nondiabetic (75-g oral glucose tolerance test) Pima Indians (aged 30 +/- 6
136 rum resistin levels in 113 nondiabetic (75-g oral glucose tolerance test) Pima Indians (ages 29 +/- 7
137 ulinemic clamp), and glucose tolerance (75-g oral glucose tolerance test) were measured in 55 Pima In
138 absorptiometry), glucose tolerance (by 75-g oral glucose tolerance test), insulin action (M; by hype
139 nd indirect calorimetry), glucose tolerance (oral glucose tolerance test), serum lipid profile, and d
143 Of 1319 people who were screened with an oral glucose tolerance test, 196 (15%) had impaired gluc
145 y insulin area under the curve (AUC) from an oral glucose tolerance test, aerobic fitness (peak oxyge
146 asured after an overnight fast and during an oral glucose tolerance test, and abdominal, thoracic, an
147 se in the glucose area under the curve in an oral glucose tolerance test, and AcAc predicted the conv
148 ions, 2-hour glucose concentrations using an oral glucose tolerance test, and an HbA1c level were sim
149 glucose and lipid levels, the results of an oral glucose tolerance test, and blood pressure were use
150 ulation (O-BP) using a clinical examination, oral glucose tolerance test, and gene expression and DNA
151 glucose (G-AUC) area under the curve during oral glucose tolerance test, and the Belfiore and Stumvo
152 bA1c and plasma glucose concentrations in an oral glucose tolerance test, and thus impaired beta cell
153 rwent clinical laboratory testing, including oral glucose tolerance test, and ultrasonographic invest
154 lucose sensitivity) were derived from a 75-g oral glucose tolerance test, and whole-body insulin sens
155 g insulin and glucagon concentrations during oral glucose tolerance test, and, in vitro, by measuring
156 were evaluated annually for 4 years with an oral glucose tolerance test, applying American Diabetes
158 excursion between the groups of mice during oral glucose tolerance test, but insulin concentrations
159 hour glucose (beta = 0.46, P = 0.00090) post oral glucose tolerance test, but only the latter passed
160 glucose area under the curve (AUC) during an oral glucose tolerance test, correlated with MFAUp (r=0.
161 mnography, a multiple sleep latency test, an oral glucose tolerance test, determination of body fat b
162 ucose levels, plasma glucose levels after an oral glucose tolerance test, fasting plasma insulin leve
163 ucose levels, plasma glucose levels after an oral glucose tolerance test, fasting plasma insulin leve
165 clinical and anthropometric examinations, an oral glucose tolerance test, overnight urine collection,
168 years of age, without diabetes by history or oral glucose tolerance test, was done between 1992 and 1
169 asma glucose and hemoglobin A1c than for the oral glucose tolerance test, we suggest an alternative d
170 ts (5 men), as determined by a standard 75-g oral glucose tolerance test, were recruited to determine
171 ulin clearance were estimated by means of an oral glucose tolerance test, whereas peripheral insulin
172 tly associated with glucose levels during an oral glucose tolerance test, with the same SNP (rs642734
173 odel assessment of insulin resistance and an oral glucose tolerance test-based index (Matsuda insulin
174 with euglycemic-hyperinsulinemic clamp- and oral glucose tolerance test-based measures of insulin re
198 rves of glucose and insulin levels during an oral glucose tolerance test; levels of low-density lipop
199 r flowmetry), and glucose metabolism status (oral glucose tolerance test; normal glucose metabolism [
200 rimester of pregnancy (2-h glucose after the oral glucose tolerance test; r(s) </= -0.21, P < 0.05).
202 tes mellitus (i.e., an abnormal result on an oral glucose-tolerance test but a fasting glucose level
203 28; aged 26 +/- 2 y) were tested with a 5-h oral-glucose-tolerance test (OGTT) and a euvolemic, euen
204 Intravenous-glucose-tolerance tests and oral-glucose-tolerance test (OGTT) and hyperinsulinemic-
205 itivity was measured by fasting and 2-h post-oral-glucose-tolerance test (OGTT) insulin, the homeosta
206 g/m(2)) of 22.4 +/- 0.8 were subjected to an oral-glucose-tolerance test (OGTT) on 4 separate days wi
207 consumption (P = 0.07) and glycemia after an oral-glucose-tolerance test (P = 0.10) trended toward be
208 he curve of insulin and glucose after a 75-g oral-glucose-tolerance test after 4 mo of treatment.
210 inistered questionnaires, by fasting and 2-h oral-glucose-tolerance test blood glucose measurement at
211 nsulin and glucose concentrations during the oral-glucose-tolerance test increased significantly afte
212 (P = 0.02), and the fasting insulin and the oral-glucose-tolerance test insulin area under the curve
213 ept for a reduced insulinemic response to an oral-glucose-tolerance test over time with daily breakfa
214 and 2-h glucose and insulin areas during the oral-glucose-tolerance test were similar across treatmen
215 NAFLD patients underwent a liver biopsy, an oral-glucose-tolerance test with minimal model analysis
217 , a fasting blood glucose measurement, a 2-h oral-glucose-tolerance test, and record linkage to a rei
224 inistered questionnaires; by fasting and 2-h oral-glucose-tolerance-test blood glucose measurement at
227 .3 kg/m(2), 66 women, 35 men) underwent 75-g oral glucose tolerance testing (OGTT), body composition
229 screening in the early postpartum period via oral glucose tolerance testing after GDM, which is a tim
231 definition, despite not requiring the use of oral glucose tolerance testing or measures of IR or micr
232 is unique because diabetes was determined by oral glucose tolerance testing rather than by self-repor
233 ment was associated with the need to perform oral glucose tolerance testing upon study completion, by
235 tly correlated with glucose responses during oral glucose tolerance testing, HbA1c, beta-cell functio
236 lipids, we performed lipid profiling during oral glucose tolerance testing, pharmacologic interventi
241 ow-up for 2 years that included 2-hour, 75-g oral glucose tolerance testing; anthropometry; and inter
242 15 centers in nine countries underwent 75-g oral glucose-tolerance testing at 24 to 32 weeks of gest
244 persons without diabetes) was determined by oral-glucose-tolerance testing of the sample aged 40-74
245 abetic renal transplant recipients underwent oral glucose tolerance tests (OGTT) in 2005 to 2006 (bas
246 after death and who had undergone 2 or more oral glucose tolerance tests (OGTT) using grouped analys
247 pharmacodynamic endpoints were explored with oral glucose tolerance tests (OGTT), serum lipid profile
250 To examine this possibility, we performed oral glucose tolerance tests (OGTTs) and euglycemic-insu
254 their associations with glucose levels from oral glucose tolerance tests (OGTTs) in pregnancy have n
255 sma glucose was measured every 3 months, and oral glucose tolerance tests (OGTTs) were performed annu
256 subjects with the E/E genotype underwent 5-h oral glucose tolerance tests (OGTTs), graded glucose inf
257 n of postchallenge change in glucagon during oral glucose tolerance tests (OGTTs), hypothesizing that
259 insulinemia, by combining microdialysis with oral glucose tolerance tests and euglycemic-hyperinsulin
260 female obese Zucker (fa/fa) rats using both oral glucose tolerance tests and hyperinsulinemic-euglyc
261 nd enhanced suppression of plasma FFA during oral glucose tolerance tests and insulin clamp in obese
262 insulin, and C-peptide concentrations during oral glucose tolerance tests at baseline and study end.
266 and demonstrated blood glucose reductions in oral glucose tolerance tests in both C57BL/6J mice and h
267 significantly improved glycemic response to oral glucose tolerance tests in CNTF(Ax15)-treated UCP1-
268 sma glucose responses were higher during the oral glucose tolerance tests in patients with IDCM (p <
269 receiving neuroleptic medication were given oral glucose tolerance tests involving serial glucose an
270 We studied this progression using biennial oral glucose tolerance tests performed in the Baltimore
274 od samples were collected in the morning and oral glucose tolerance tests were done in accordance wit
276 Fasting glucose was measured quarterly, and oral glucose tolerance tests were performed annually.
281 ed; and (3) peak blood glucose levels during oral glucose tolerance tests were significantly reduced.
283 ed insulin sensitivity, show improvements in oral glucose tolerance tests, display reduced adipose ti
284 asting or non-fasting plasma glucose levels, oral glucose tolerance tests, hemoglobin A1C levels, and
288 We measured steroids in serum and performed oral glucose-tolerance tests before and after the oral a
290 h measures collected from frequently sampled oral-glucose-tolerance tests (OGTTs).Twenty-seven of 29
291 se, insulin, and C-peptide measured by using oral-glucose-tolerance tests at the end of each diet.
292 resistance and sensitivity were defined from oral-glucose-tolerance tests in 86 overweight and obese
293 d hormone concentrations, and results of 3-h oral-glucose-tolerance tests were examined in obese and
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