Delayed ß-cell response and glucose intolerance in young women with Turner syndrome

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Delayed ß-cell response and glucose intolerance in young women with Turner syndrome. / Hjerrild, Britta Eilersen; Holst, Jens Juul; Juhl, Claus; Christiansen, Jens Sandahl; Schmitz, Ole; Gravholt, Claus Højbjerg.

I: B M C Endocrine Disorders, Bind 11, 2011, s. 11-6.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hjerrild, BE, Holst, JJ, Juhl, C, Christiansen, JS, Schmitz, O & Gravholt, CH 2011, 'Delayed ß-cell response and glucose intolerance in young women with Turner syndrome', B M C Endocrine Disorders, bind 11, s. 11-6. https://doi.org/10.1186/1472-6823-11-6

APA

Hjerrild, B. E., Holst, J. J., Juhl, C., Christiansen, J. S., Schmitz, O., & Gravholt, C. H. (2011). Delayed ß-cell response and glucose intolerance in young women with Turner syndrome. B M C Endocrine Disorders, 11, 11-6. https://doi.org/10.1186/1472-6823-11-6

Vancouver

Hjerrild BE, Holst JJ, Juhl C, Christiansen JS, Schmitz O, Gravholt CH. Delayed ß-cell response and glucose intolerance in young women with Turner syndrome. B M C Endocrine Disorders. 2011;11:11-6. https://doi.org/10.1186/1472-6823-11-6

Author

Hjerrild, Britta Eilersen ; Holst, Jens Juul ; Juhl, Claus ; Christiansen, Jens Sandahl ; Schmitz, Ole ; Gravholt, Claus Højbjerg. / Delayed ß-cell response and glucose intolerance in young women with Turner syndrome. I: B M C Endocrine Disorders. 2011 ; Bind 11. s. 11-6.

Bibtex

@article{4e066161356a44bcbdd501f1d59fb0d9,
title = "Delayed {\ss}-cell response and glucose intolerance in young women with Turner syndrome",
abstract = "BACKGROUND: To investigate glucose homeostasis in detail in Turner syndrome (TS), where impaired glucose tolerance (IGT) and type 2 diabetes are frequent.METHODS: Cross sectional study of women with Turner syndrome (TS)(n = 13) and age and body mass index matched controls (C) (n = 13), evaluated by glucose tolerance (oral and intravenous glucose tolerance test (OGTT and IVGTT)), insulin sensitivity (hyperinsulinemic, euglycemic clamp), beta-cell function (hyperglycaemic clamp, arginine and GLP-1 stimulation) and insulin pulsatility.RESULTS: Fasting glucose and insulin levels were similar. Higher glucose responses was seen in TS during OGTT and IVGTT, persisting after correction for body weight or muscle mass, while insulin responses were similar in TS and C, despite the higher glucose level in TS, leading to an insufficient increase in insulin response during dynamic testing. Insulin sensitivity was comparable in the two groups (TS vs. control: 8.6 ± 1.8 vs. 8.9 ± 1.8 mg/kg*30 min; p = 0.6), and the insulin responses to dynamic {\ss}-cell function tests were similar. Insulin secretion patterns examined by deconvolution analysis, approximate entropy, spectral analysis and autocorrelation analysis were similar. In addition we found low IGF-I, higher levels of cortisol and norepinephrine and an increased waist-hip ratio in TS.CONCLUSIONS: Young normal weight TS women show significant glucose intolerance in spite of normal insulin secretion during hyperglycaemic clamping and normal insulin sensitivity. We recommend regularly testing for diabetes in TS",
author = "Hjerrild, {Britta Eilersen} and Holst, {Jens Juul} and Claus Juhl and Christiansen, {Jens Sandahl} and Ole Schmitz and Gravholt, {Claus H{\o}jbjerg}",
year = "2011",
doi = "10.1186/1472-6823-11-6",
language = "English",
volume = "11",
pages = "11--6",
journal = "BMC Endocrine Disorders",
issn = "1472-6823",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Delayed ß-cell response and glucose intolerance in young women with Turner syndrome

AU - Hjerrild, Britta Eilersen

AU - Holst, Jens Juul

AU - Juhl, Claus

AU - Christiansen, Jens Sandahl

AU - Schmitz, Ole

AU - Gravholt, Claus Højbjerg

PY - 2011

Y1 - 2011

N2 - BACKGROUND: To investigate glucose homeostasis in detail in Turner syndrome (TS), where impaired glucose tolerance (IGT) and type 2 diabetes are frequent.METHODS: Cross sectional study of women with Turner syndrome (TS)(n = 13) and age and body mass index matched controls (C) (n = 13), evaluated by glucose tolerance (oral and intravenous glucose tolerance test (OGTT and IVGTT)), insulin sensitivity (hyperinsulinemic, euglycemic clamp), beta-cell function (hyperglycaemic clamp, arginine and GLP-1 stimulation) and insulin pulsatility.RESULTS: Fasting glucose and insulin levels were similar. Higher glucose responses was seen in TS during OGTT and IVGTT, persisting after correction for body weight or muscle mass, while insulin responses were similar in TS and C, despite the higher glucose level in TS, leading to an insufficient increase in insulin response during dynamic testing. Insulin sensitivity was comparable in the two groups (TS vs. control: 8.6 ± 1.8 vs. 8.9 ± 1.8 mg/kg*30 min; p = 0.6), and the insulin responses to dynamic ß-cell function tests were similar. Insulin secretion patterns examined by deconvolution analysis, approximate entropy, spectral analysis and autocorrelation analysis were similar. In addition we found low IGF-I, higher levels of cortisol and norepinephrine and an increased waist-hip ratio in TS.CONCLUSIONS: Young normal weight TS women show significant glucose intolerance in spite of normal insulin secretion during hyperglycaemic clamping and normal insulin sensitivity. We recommend regularly testing for diabetes in TS

AB - BACKGROUND: To investigate glucose homeostasis in detail in Turner syndrome (TS), where impaired glucose tolerance (IGT) and type 2 diabetes are frequent.METHODS: Cross sectional study of women with Turner syndrome (TS)(n = 13) and age and body mass index matched controls (C) (n = 13), evaluated by glucose tolerance (oral and intravenous glucose tolerance test (OGTT and IVGTT)), insulin sensitivity (hyperinsulinemic, euglycemic clamp), beta-cell function (hyperglycaemic clamp, arginine and GLP-1 stimulation) and insulin pulsatility.RESULTS: Fasting glucose and insulin levels were similar. Higher glucose responses was seen in TS during OGTT and IVGTT, persisting after correction for body weight or muscle mass, while insulin responses were similar in TS and C, despite the higher glucose level in TS, leading to an insufficient increase in insulin response during dynamic testing. Insulin sensitivity was comparable in the two groups (TS vs. control: 8.6 ± 1.8 vs. 8.9 ± 1.8 mg/kg*30 min; p = 0.6), and the insulin responses to dynamic ß-cell function tests were similar. Insulin secretion patterns examined by deconvolution analysis, approximate entropy, spectral analysis and autocorrelation analysis were similar. In addition we found low IGF-I, higher levels of cortisol and norepinephrine and an increased waist-hip ratio in TS.CONCLUSIONS: Young normal weight TS women show significant glucose intolerance in spite of normal insulin secretion during hyperglycaemic clamping and normal insulin sensitivity. We recommend regularly testing for diabetes in TS

U2 - 10.1186/1472-6823-11-6

DO - 10.1186/1472-6823-11-6

M3 - Journal article

C2 - 21406078

VL - 11

SP - 11

EP - 16

JO - BMC Endocrine Disorders

JF - BMC Endocrine Disorders

SN - 1472-6823

ER -

ID: 40321220