Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus

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Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus. / Møller, A M; Jensen, N M; Pildal, J; Drivsholm, T; Borch-Johnsen, K; Urhammer, S A; Hansen, T; Pedersen, O.

I: Journal of Clinical Endocrinology and Metabolism, Bind 86, Nr. 5, 01.05.2001, s. 2181-6.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Møller, AM, Jensen, NM, Pildal, J, Drivsholm, T, Borch-Johnsen, K, Urhammer, SA, Hansen, T & Pedersen, O 2001, 'Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus', Journal of Clinical Endocrinology and Metabolism, bind 86, nr. 5, s. 2181-6.

APA

Møller, A. M., Jensen, N. M., Pildal, J., Drivsholm, T., Borch-Johnsen, K., Urhammer, S. A., Hansen, T., & Pedersen, O. (2001). Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus. Journal of Clinical Endocrinology and Metabolism, 86(5), 2181-6.

Vancouver

Møller AM, Jensen NM, Pildal J, Drivsholm T, Borch-Johnsen K, Urhammer SA o.a. Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus. Journal of Clinical Endocrinology and Metabolism. 2001 maj 1;86(5):2181-6.

Author

Møller, A M ; Jensen, N M ; Pildal, J ; Drivsholm, T ; Borch-Johnsen, K ; Urhammer, S A ; Hansen, T ; Pedersen, O. / Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus. I: Journal of Clinical Endocrinology and Metabolism. 2001 ; Bind 86, Nr. 5. s. 2181-6.

Bibtex

@article{b92eac2b2fea409db14cf368ae6b7ede,
title = "Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus",
abstract = "This study was performed to test the hypothesis that genetic variation in the promoter of the glucose transporter 2 (GLUT2) might predispose to prediabetic phenotypes or type 2 diabetes. A total of 1611 bp comprising the minimal promoter region of the GLUT2 gene were examined by combined single-strand conformational polymorphism and heteroduplex analysis followed by direct sequencing of identified variants on genomic DNA from 96 randomly recruited Danish type 2 diabetic patients. We identified 4 nucleotide variants, -447g-->a, -149c-->a, -122t-->c, and -44g-->a. None of the variants were positioned in known or presumed transcription factor binding sites, TATA-box, or transcriptional start site. Association studies of the -149c-->a, -122t-->c, and -44g-->a variants revealed that the variants were as prevalent in 320 type 2 diabetic patients [11.0% (95% confidence interval, 8.4-13.6), 9.8% (7.4-12.2), and 29.0% (24.4-33.6), respectively] as in 241 age-matched glucose-tolerant subjects [13.1% (9.8-16.4), 11.2% (8.3-14.1), and 33.4% (28.8-38.0), respectively]. The -447g-->a mutation was only identified in a single diabetic patient and did not show cosegregation with diabetes in the family of the proband. The three common variants showed in a primary genotype-phenotype study comprising 241 glucose-tolerant middle-aged subjects association to increased plasma glucose levels during an oral glucose tolerance test. However, this result could not be replicated in a second sample of 298 60-yr-old glucose-tolerant subjects. In conclusion, we found no evidence supporting the hypothesis that genetic variability in the minimal promoter of the GLUT2 is associated with type 2 diabetes or prediabetic phenotypes in the Danish population.",
keywords = "Adult, Aged, Denmark, Diabetes Mellitus, Type 2, European Continental Ancestry Group, Female, Genetic Variation, Glucose Tolerance Test, Glucose Transporter Type 2, Humans, Male, Middle Aged, Monosaccharide Transport Proteins, Promoter Regions, Genetic",
author = "M{\o}ller, {A M} and Jensen, {N M} and J Pildal and T Drivsholm and K Borch-Johnsen and Urhammer, {S A} and T Hansen and O Pedersen",
year = "2001",
month = may,
day = "1",
language = "English",
volume = "86",
pages = "2181--6",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "5",

}

RIS

TY - JOUR

T1 - Studies of genetic variability of the glucose transporter 2 promoter in patients with type 2 diabetes mellitus

AU - Møller, A M

AU - Jensen, N M

AU - Pildal, J

AU - Drivsholm, T

AU - Borch-Johnsen, K

AU - Urhammer, S A

AU - Hansen, T

AU - Pedersen, O

PY - 2001/5/1

Y1 - 2001/5/1

N2 - This study was performed to test the hypothesis that genetic variation in the promoter of the glucose transporter 2 (GLUT2) might predispose to prediabetic phenotypes or type 2 diabetes. A total of 1611 bp comprising the minimal promoter region of the GLUT2 gene were examined by combined single-strand conformational polymorphism and heteroduplex analysis followed by direct sequencing of identified variants on genomic DNA from 96 randomly recruited Danish type 2 diabetic patients. We identified 4 nucleotide variants, -447g-->a, -149c-->a, -122t-->c, and -44g-->a. None of the variants were positioned in known or presumed transcription factor binding sites, TATA-box, or transcriptional start site. Association studies of the -149c-->a, -122t-->c, and -44g-->a variants revealed that the variants were as prevalent in 320 type 2 diabetic patients [11.0% (95% confidence interval, 8.4-13.6), 9.8% (7.4-12.2), and 29.0% (24.4-33.6), respectively] as in 241 age-matched glucose-tolerant subjects [13.1% (9.8-16.4), 11.2% (8.3-14.1), and 33.4% (28.8-38.0), respectively]. The -447g-->a mutation was only identified in a single diabetic patient and did not show cosegregation with diabetes in the family of the proband. The three common variants showed in a primary genotype-phenotype study comprising 241 glucose-tolerant middle-aged subjects association to increased plasma glucose levels during an oral glucose tolerance test. However, this result could not be replicated in a second sample of 298 60-yr-old glucose-tolerant subjects. In conclusion, we found no evidence supporting the hypothesis that genetic variability in the minimal promoter of the GLUT2 is associated with type 2 diabetes or prediabetic phenotypes in the Danish population.

AB - This study was performed to test the hypothesis that genetic variation in the promoter of the glucose transporter 2 (GLUT2) might predispose to prediabetic phenotypes or type 2 diabetes. A total of 1611 bp comprising the minimal promoter region of the GLUT2 gene were examined by combined single-strand conformational polymorphism and heteroduplex analysis followed by direct sequencing of identified variants on genomic DNA from 96 randomly recruited Danish type 2 diabetic patients. We identified 4 nucleotide variants, -447g-->a, -149c-->a, -122t-->c, and -44g-->a. None of the variants were positioned in known or presumed transcription factor binding sites, TATA-box, or transcriptional start site. Association studies of the -149c-->a, -122t-->c, and -44g-->a variants revealed that the variants were as prevalent in 320 type 2 diabetic patients [11.0% (95% confidence interval, 8.4-13.6), 9.8% (7.4-12.2), and 29.0% (24.4-33.6), respectively] as in 241 age-matched glucose-tolerant subjects [13.1% (9.8-16.4), 11.2% (8.3-14.1), and 33.4% (28.8-38.0), respectively]. The -447g-->a mutation was only identified in a single diabetic patient and did not show cosegregation with diabetes in the family of the proband. The three common variants showed in a primary genotype-phenotype study comprising 241 glucose-tolerant middle-aged subjects association to increased plasma glucose levels during an oral glucose tolerance test. However, this result could not be replicated in a second sample of 298 60-yr-old glucose-tolerant subjects. In conclusion, we found no evidence supporting the hypothesis that genetic variability in the minimal promoter of the GLUT2 is associated with type 2 diabetes or prediabetic phenotypes in the Danish population.

KW - Adult

KW - Aged

KW - Denmark

KW - Diabetes Mellitus, Type 2

KW - European Continental Ancestry Group

KW - Female

KW - Genetic Variation

KW - Glucose Tolerance Test

KW - Glucose Transporter Type 2

KW - Humans

KW - Male

KW - Middle Aged

KW - Monosaccharide Transport Proteins

KW - Promoter Regions, Genetic

M3 - Journal article

C2 - 11344224

VL - 86

SP - 2181

EP - 2186

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 5

ER -

ID: 33030840