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Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus

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Standard

Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus. / Rasmussen, Søren K.; Lautier, Corinne; Hansen, Lars; Echwald, Søren M.; Hansen, Torben; Ekstrøm, Claus T.; Urhammer, Søren A.; Borch-Johnsen, Knut; Grigorescu, Florin; Smith, Robert J.; Pedersen, Oluf.

I: Journal of Clinical Endocrinology and Metabolism, Bind 85, Nr. 4, 01.12.2000, s. 1606-1610.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Rasmussen, SK, Lautier, C, Hansen, L, Echwald, SM, Hansen, T, Ekstrøm, CT, Urhammer, SA, Borch-Johnsen, K, Grigorescu, F, Smith, RJ & Pedersen, O 2000, 'Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus', Journal of Clinical Endocrinology and Metabolism, bind 85, nr. 4, s. 1606-1610. https://doi.org/10.1210/jc.85.4.1606

APA

Rasmussen, S. K., Lautier, C., Hansen, L., Echwald, S. M., Hansen, T., Ekstrøm, C. T., ... Pedersen, O. (2000). Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus. Journal of Clinical Endocrinology and Metabolism, 85(4), 1606-1610. https://doi.org/10.1210/jc.85.4.1606

Vancouver

Rasmussen SK, Lautier C, Hansen L, Echwald SM, Hansen T, Ekstrøm CT o.a. Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus. Journal of Clinical Endocrinology and Metabolism. 2000 dec 1;85(4):1606-1610. https://doi.org/10.1210/jc.85.4.1606

Author

Rasmussen, Søren K. ; Lautier, Corinne ; Hansen, Lars ; Echwald, Søren M. ; Hansen, Torben ; Ekstrøm, Claus T. ; Urhammer, Søren A. ; Borch-Johnsen, Knut ; Grigorescu, Florin ; Smith, Robert J. ; Pedersen, Oluf. / Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus. I: Journal of Clinical Endocrinology and Metabolism. 2000 ; Bind 85, Nr. 4. s. 1606-1610.

Bibtex

@article{159444e0827740598e91cc85f815ce30,
title = "Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus",
abstract = "Insulin-like growth factor I (IGF-I) is an important regulator of many aspects of growth, differentiation, and development, and as low birth weight has been associated with impaired glucose tolerance and overt type 2 diabetes in adult life, we considered the genes encoding the IGF-I and the IGF-I receptor (IGF-IR) as candidates for low birth weight, insulin resistance, and type 2 diabetes. Here we report the mutational analysis of the coding regions of the IGF-I and IGF-IR performed on genomic DNA from probands of 82 Danish type 2 diabetic families. No mutations predicting changes in the amino acid sequences of the IGF-I or IGF-IR genes were detected, but several silent and intronic polymorphisms were found. The impact of the most prevalent polymorphism, GAG1013GAA of the IGF-IR, was evaluated in a population-based sample of 349 young healthy subjects, where the variant had an allele frequency of 0.44 (95{\%} confidence interval, 0.40-0.48). No significant relationships between this variant and birth weight, birth length, or insulin sensitivity index were detected. In addition, we did not observe any significant differences in allelic frequencies of the codon 1013 variant between 395 type 2 diabetic patients (allele frequency, 0.52; 95{\%} confidence interval, 0.49-0.55) and 238 matched glucose-tolerant control subjects (allelic frequency, 0.47; 95{\%} confidence interval, 0.43-0.50). In conclusion, variability in the coding regions of IGF-I and the IGF-IR does not associate with reduced birth weight, insulin sensitivity index, or type 2 diabetes in the Danish population.",
author = "Rasmussen, {S{\o}ren K.} and Corinne Lautier and Lars Hansen and Echwald, {S{\o}ren M.} and Torben Hansen and Ekstr{\o}m, {Claus T.} and Urhammer, {S{\o}ren A.} and Knut Borch-Johnsen and Florin Grigorescu and Smith, {Robert J.} and Oluf Pedersen",
year = "2000",
month = "12",
day = "1",
doi = "10.1210/jc.85.4.1606",
language = "English",
volume = "85",
pages = "1606--1610",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "4",

}

RIS

TY - JOUR

T1 - Studies of the variability of the genes encoding the insulin-like growth factor I receptor and its ligand in relation to type 2 diabetes mellitus

AU - Rasmussen, Søren K.

AU - Lautier, Corinne

AU - Hansen, Lars

AU - Echwald, Søren M.

AU - Hansen, Torben

AU - Ekstrøm, Claus T.

AU - Urhammer, Søren A.

AU - Borch-Johnsen, Knut

AU - Grigorescu, Florin

AU - Smith, Robert J.

AU - Pedersen, Oluf

PY - 2000/12/1

Y1 - 2000/12/1

N2 - Insulin-like growth factor I (IGF-I) is an important regulator of many aspects of growth, differentiation, and development, and as low birth weight has been associated with impaired glucose tolerance and overt type 2 diabetes in adult life, we considered the genes encoding the IGF-I and the IGF-I receptor (IGF-IR) as candidates for low birth weight, insulin resistance, and type 2 diabetes. Here we report the mutational analysis of the coding regions of the IGF-I and IGF-IR performed on genomic DNA from probands of 82 Danish type 2 diabetic families. No mutations predicting changes in the amino acid sequences of the IGF-I or IGF-IR genes were detected, but several silent and intronic polymorphisms were found. The impact of the most prevalent polymorphism, GAG1013GAA of the IGF-IR, was evaluated in a population-based sample of 349 young healthy subjects, where the variant had an allele frequency of 0.44 (95% confidence interval, 0.40-0.48). No significant relationships between this variant and birth weight, birth length, or insulin sensitivity index were detected. In addition, we did not observe any significant differences in allelic frequencies of the codon 1013 variant between 395 type 2 diabetic patients (allele frequency, 0.52; 95% confidence interval, 0.49-0.55) and 238 matched glucose-tolerant control subjects (allelic frequency, 0.47; 95% confidence interval, 0.43-0.50). In conclusion, variability in the coding regions of IGF-I and the IGF-IR does not associate with reduced birth weight, insulin sensitivity index, or type 2 diabetes in the Danish population.

AB - Insulin-like growth factor I (IGF-I) is an important regulator of many aspects of growth, differentiation, and development, and as low birth weight has been associated with impaired glucose tolerance and overt type 2 diabetes in adult life, we considered the genes encoding the IGF-I and the IGF-I receptor (IGF-IR) as candidates for low birth weight, insulin resistance, and type 2 diabetes. Here we report the mutational analysis of the coding regions of the IGF-I and IGF-IR performed on genomic DNA from probands of 82 Danish type 2 diabetic families. No mutations predicting changes in the amino acid sequences of the IGF-I or IGF-IR genes were detected, but several silent and intronic polymorphisms were found. The impact of the most prevalent polymorphism, GAG1013GAA of the IGF-IR, was evaluated in a population-based sample of 349 young healthy subjects, where the variant had an allele frequency of 0.44 (95% confidence interval, 0.40-0.48). No significant relationships between this variant and birth weight, birth length, or insulin sensitivity index were detected. In addition, we did not observe any significant differences in allelic frequencies of the codon 1013 variant between 395 type 2 diabetic patients (allele frequency, 0.52; 95% confidence interval, 0.49-0.55) and 238 matched glucose-tolerant control subjects (allelic frequency, 0.47; 95% confidence interval, 0.43-0.50). In conclusion, variability in the coding regions of IGF-I and the IGF-IR does not associate with reduced birth weight, insulin sensitivity index, or type 2 diabetes in the Danish population.

UR - http://www.scopus.com/inward/record.url?scp=17744393626&partnerID=8YFLogxK

U2 - 10.1210/jc.85.4.1606

DO - 10.1210/jc.85.4.1606

M3 - Journal article

C2 - 10770205

AN - SCOPUS:17744393626

VL - 85

SP - 1606

EP - 1610

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 4

ER -

ID: 203910183