Diabet. Med. 29, 12791284 (2012) Abstract Aims The mixed meal tolerance test is the gold standard measure of endogenous insulin secretion. Practical issues limit the routine clinical use of this test, including omitting insulin prior to the ingestion of a high-carbohydrate liquid mixed meal, which can result in marked hyperglycaemia. We aimed to assess whether insulin omission is necessary during the mixed meal tolerance test and whether fasting C-peptide was a practical alternative to the test. Methods Ninety-one adults with insulin-treated diabetes (Type 1 n = 56, Type 2 n = 35) underwent two mixed meal tolerance tests; one standard without insulin and one with the patients usual morning insulin. Results The 90-min serum C-peptide was highly correlated in the standard mixed meal tolerance test and the test with insulin (r = 0.98, P < 0.0001). There was a 20% reduction in the peak C-peptide value when insulin was given {test with insulin [0.39 (0.011.16) vs. test without insulin 0.48 (0.011.36) nmol/l, P = 0.001]}, but the original serum C-peptide cut-off for significant endogenous insulin secretion (= 0.2 nmol/l) still correctly classified 90/91 patients (98% sensitivity/100% specificity). Fasting serum C-peptide was highly correlated to 90-min serum C-peptide during the test (r = 0.97, P < 0.0001). A fasting serum C-peptide = 0.07 nmol/l was the optimal cut-off (100% sensitivity and 97% specificity) for significant endogenous insulin secretion (defined as 90-min stimulated serum C-peptide = 0.2 nmol/l). Conclusions Insulin omission may not always be necessary during a mixed meal tolerance test and fasting serum C-peptide may offer a practical alternative in insulin-treated patients.
机构:
Benaroya Res Inst, Diabet Res Program, Seattle, WA USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Greenbaum, Carla J.
Anderson, Andrea M.
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Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Anderson, Andrea M.
Dolan, Lawrence M.
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Cincinnati Childrens Hosp & Med Ctr, Cincinnati, OH USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Dolan, Lawrence M.
Mayer-Davis, Elizabeth J.
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Univ N Carolina, Dept Nutr, Chapel Hill, NC USA
Univ S Carolina, Dept Epidemiol & Biostat, Columbia, SC 29208 USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Mayer-Davis, Elizabeth J.
Dabelea, Dana
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Univ Colorado, Dept Epidemiol, Colorado Sch Publ Hlth, Denver, CO 80202 USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Dabelea, Dana
Imperatore, Giuseppina
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Ctr Dis Control & Prevent, Natl Ctr Chron Dis Prevent & Hlth Promot, Div Diabet Translat, Atlanta, GA USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Imperatore, Giuseppina
Marcovina, Santica
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Univ Washington, Dept Med, Seattle, WA USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
机构:
Benaroya Res Inst, Diabet Res Program, Seattle, WA USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Greenbaum, Carla J.
Anderson, Andrea M.
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机构:
Wake Forest Univ, Bowman Gray Sch Med, Winston Salem, NC USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Anderson, Andrea M.
Dolan, Lawrence M.
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Cincinnati Childrens Hosp & Med Ctr, Cincinnati, OH USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Dolan, Lawrence M.
Mayer-Davis, Elizabeth J.
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h-index: 0
机构:
Univ N Carolina, Dept Nutr, Chapel Hill, NC USA
Univ S Carolina, Dept Epidemiol & Biostat, Columbia, SC 29208 USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Mayer-Davis, Elizabeth J.
Dabelea, Dana
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机构:
Univ Colorado, Dept Epidemiol, Colorado Sch Publ Hlth, Denver, CO 80202 USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Dabelea, Dana
Imperatore, Giuseppina
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h-index: 0
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Ctr Dis Control & Prevent, Natl Ctr Chron Dis Prevent & Hlth Promot, Div Diabet Translat, Atlanta, GA USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA
Imperatore, Giuseppina
Marcovina, Santica
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Univ Washington, Dept Med, Seattle, WA USABenaroya Res Inst, Diabet Res Program, Seattle, WA USA