If a single gene produced insulin resistance, with environmental effects creating some additional variance, insulin action might be distributed as a mixture of two normal distributions if the gene is dominant or recessive or as a mixture of three normal distributions if the gene is codominant. To estimate maximal insulin-stimulated glucose uptake rates (MaxMs), hyperinsulinemic-euglycemic clamps were performed on 245 nondiabetic Pima Indians (126 men, 119 women). Five models (for 1, 2, 3, 4, or 5 components each, normally distributed with a common variance) were fitted to the frequency distribution of MaxM by iterative maximum-likelihood estimation. The three-component model fit the data significantly better than a single normal distribution (χ2 = 14.3 with 4 df P < .01) or a mixture of two normal distributions (χ2 = 9.9 with 2 df, P < .01). Mixtures of four or five normal distributions did not fit the data significantly better than a mixture of three normal distributions. The first component of the distribution comprised 23%, the second 48%, and the third 29% of the total distribution. Similarly, the frequency distributions of fasting plasma insulin concentrations and a principal component score derived from MaxM and fasting insulin were best fitted by a mixture of three normal distributions. These results are consistent with the hypothesis that among Pimas, insulin resistance is determined by a single gene with a codominant mode of inheritance. Segregation analyses of studies performed in pedigrees are indicated to prove or disprove this genetic hypothesis.
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Original Articles|
November 01 1989
Distribution of In Vivo Insulin Action in Pima Indians as Mixture of Three Normal Distributions Free
Clifton Bogardus;
Clifton Bogardus
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Stephen Lillioja;
Stephen Lillioja
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Bulangu Lukuki Nyomba;
Bulangu Lukuki Nyomba
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Francesco Zurlo;
Francesco Zurlo
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Boyd Swinburn;
Boyd Swinburn
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Antonella Esposito-Del Puente;
Antonella Esposito-Del Puente
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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William C Knowler;
William C Knowler
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Eric Ravussin;
Eric Ravussin
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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David M Mott;
David M Mott
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Peter H Bennett
Peter H Bennett
Clinical Diabetes and Nutrition Section, Phoenix Epidemiology and Clinical Research Branch, and the Diabetes and Arthritis Epidemiology Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health
Phoenix, Arizona
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Address correspondence and reprint requests to Clifton Bogardus, MD, Clinical Diabetes and Nutrition Section, NIDDK/NIH, 4212 North 16th Street, Room 5-41, Phoenix, AZ 85016.
Diabetes 1989;38(11):1423–1432
Article history
Received:
November 30 1988
Revision Received:
July 06 1989
Accepted:
July 06 1989
PubMed:
2695375
Citation
Clifton Bogardus, Stephen Lillioja, Bulangu Lukuki Nyomba, Francesco Zurlo, Boyd Swinburn, Antonella Esposito-Del Puente, William C Knowler, Eric Ravussin, David M Mott, Peter H Bennett; Distribution of In Vivo Insulin Action in Pima Indians as Mixture of Three Normal Distributions. Diabetes 1 November 1989; 38 (11): 1423–1432. https://doi.org/10.2337/diab.38.11.1423
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