The present study investigates the possible relationship between human β-cell secretory capacity and polymorphism in the 5′-flanking region of the human insulin gene. The glucose potentiation slope was measured in normal and non-insulin-dependent diabetic subjects (NIDDM). This slope, as reported previously (Ward, W. K., et al., Am. J. Physiol. 1984; 246:E405–11), is an index of the ability of hyperglycemia to potentiate the insulin response to arginine and as such is a measure of β-cell responsiveness to glucose. Restriction enzyme analysis using a human insulin gene probe was performed on leukocyte DNA isolated from the same individuals. We conclude that a 1.6 kb polymorphism in the 5′-flanking region of the human insulin gene in both normal and NIDDM subjects has no association with insulin secretory responses as defined here by the glucose potentiation Slope.
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Original Contributions|
April 01 1985
Islet β-Cell Function and Polymorphism in the 5′-Flanking Region of the Human Insulin Gene
M Alan Permutt;
M Alan Permutt
Metabolism Division, Washington University School of Medicine
St. Louis, Missouri
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Peter Rotwein;
Peter Rotwein
Metabolism Division, Washington University School of Medicine
St. Louis, Missouri
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Teresa Andreone;
Teresa Andreone
Metabolism Division, Washington University School of Medicine
St. Louis, Missouri
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W Kenneth Ward;
W Kenneth Ward
Division of Endocrinology and Metabolism, University of Washington Medical School
Seattle, Washington
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Danil Porte, Jr
Danil Porte, Jr
Division of Endocrinology and Metabolism, University of Washington Medical School
Seattle, Washington
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Address reprint requests to M. A. Permutt, M.D., Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, Missouri 63110.
Citation
M Alan Permutt, Peter Rotwein, Teresa Andreone, W Kenneth Ward, Danil Porte; Islet β-Cell Function and Polymorphism in the 5′-Flanking Region of the Human Insulin Gene. Diabetes 1 April 1985; 34 (4): 311–314. https://doi.org/10.2337/diab.34.4.311
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