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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0011860,
umls-concept:C0022885,
umls-concept:C0026336,
umls-concept:C0030274,
umls-concept:C0031809,
umls-concept:C0039593,
umls-concept:C0205307,
umls-concept:C0681850,
umls-concept:C1518321,
umls-concept:C1550501,
umls-concept:C1704410,
umls-concept:C1706203,
umls-concept:C1998602,
umls-concept:C2349001,
umls-concept:C2697811
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pubmed:issue |
3
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pubmed:dateCreated |
1998-4-14
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pubmed:abstractText |
A model-based method was developed to quantify pancreatic beta-cell responsiveness during a meal tolerance test (MTT). C peptide secretion was related in a linear fashion to glucose concentration, whereas the standard population model was used to derive transfer rate constants of the two compartmental model of C peptide kinetics. Two indexes of pancreatic beta-cell responsiveness were defined: 1) postprandial sensitivity M(I) (ability of postprandial glucose to stimulate beta-cell), and 2) basal sensitivity M0 (ability of fasting glucose to stimulate beta-cell). The method was evaluated using plasma glucose and C peptide measured over 180 min with a 10- to 30-min sampling interval during a MTT (75 g carbohydrates; 500 Cal) performed in 16 normal subjects (7 men and 9 women; age, 50 +/- 10 yr; body mass index, 29.2 +/- 3.6 kg/m2; fasting plasma glucose, 5.1 +/- 0.5 mmol/L; mean +/- SD) and 16 body mass index-matched subjects with newly diagnosed noninsulin-dependent diabetes mellitus (NIDDM; 15 men and 1 woman; age, 50 +/- 9 yr; body mass index, 29.3 +/- 3.7 kg/m2; fasting plasma glucose, 12.6 +/- 3.2 mmol/L). M(I) and M0 indexes were estimated with very good precision (coefficient of variation, < 15%). Subjects with NIDDM demonstrated lower postprandial sensitivity M(I) (17.7 +/- 11.4 vs. 90.0 +/- 43.3 x 10(-9)/min; NIDDM vs. normal, P < 0.001) and basal sensitivity M0 (5.4 +/- 2.2 vs. 10.3 +/- 4.9 x 10(-9)/min; P < 0.005). Deconvolution analysis documented that the relationship between C peptide secretion and glucose concentration is approximately linear during MTT in both normal subjects (plasma glucose range, 5-8 mmol/L) and subjects with NIDDM (12-17 mmol/L). We conclude that pancreatic responsiveness during glucose stimulation (M(I)) and under basal conditions (M0) can be obtained from this novel method during MTT in healthy and disease states.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0021-972X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
744-50
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:9506719-Adult,
pubmed-meshheading:9506719-Blood Glucose,
pubmed-meshheading:9506719-C-Peptide,
pubmed-meshheading:9506719-Diabetes Mellitus, Type 2,
pubmed-meshheading:9506719-Eating,
pubmed-meshheading:9506719-Female,
pubmed-meshheading:9506719-Glucose,
pubmed-meshheading:9506719-Humans,
pubmed-meshheading:9506719-Insulin,
pubmed-meshheading:9506719-Islets of Langerhans,
pubmed-meshheading:9506719-Male,
pubmed-meshheading:9506719-Methods,
pubmed-meshheading:9506719-Middle Aged,
pubmed-meshheading:9506719-Models, Biological,
pubmed-meshheading:9506719-Reference Values,
pubmed-meshheading:9506719-Sensitivity and Specificity
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pubmed:year |
1998
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pubmed:articleTitle |
Pancreatic beta-cell responsiveness during meal tolerance test: model assessment in normal subjects and subjects with newly diagnosed noninsulin-dependent diabetes mellitus.
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pubmed:affiliation |
Metabolic Modelling Group, Center for Measurement and Information in Medicine, City University, London, United Kingdom. r.hovorka@city.ac.uk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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