Reduced insulin secretion in normoglycaemic patients with β-thalassaemia major

Aims  To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with β‐thalassaemia major with normal glucose response during an oral glucose tolerance test and to estimate its possible relation to iron overload. Methods  We measured fasting glucose, insulin a...

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Published inDiabetic medicine Vol. 23; no. 12; pp. 1327 - 1331
Main Authors Angelopoulos, N. G., Zervas, A., Livadas, S., Adamopoulos, I., Giannopoulos, D., Goula, A., Tolis, G.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.12.2006
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Abstract Aims  To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with β‐thalassaemia major with normal glucose response during an oral glucose tolerance test and to estimate its possible relation to iron overload. Methods  We measured fasting glucose, insulin and C‐peptide levels in 24 patients with β‐thalassaemia major and 18 control subjects matched for age and body mass index. Insulin sensitivity and insulin release index were calculated according to the homeostasis model assessment (HOMA). Correlations with age, body mass index and serum ferritin were also calculated. Results  Fasting glucose levels in patients were increased compared with control subjects (5.5 ± 0.12 vs. 4.7 ± 0.13 mmol/l, mean ± sem, P < 0.001). Pancreatic B‐cell insulin secretion in the fasting state (estimated by SCHOMA) was lower in thalassaemic patients (SCHOMA 88.5 ± 11.11 vs. 184.3 ± 23.72 in control subjects, P < 0.001). Patients were then divided into those with impaired (IFG) and normal (NFG) fasting glucose. SCHOMA was higher in the patients with NFG compared with those with IFG patients (110.6 ± 17.63 vs. 66.3 ± 10.88, respectively, P < 0.05) but estimated insulin sensitivity (ISIHOMA) was similar. Plasma values of C‐peptide correlated positively with ferritin (r = 0.42, P = 0.04) and SCHOMA (r = 0.45, P = 0.02) and negatively with ISIHOMA (r = −0.43, P = 0.03). Conclusions  These results support the concept that impaired B‐cell function, as reflected by a reduction in the insulin secretion index, is present in β‐thalassaemic patients with normoglycaemia before changes in oral glucose tolerance tests are apparent.
AbstractList Aims  To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with β‐thalassaemia major with normal glucose response during an oral glucose tolerance test and to estimate its possible relation to iron overload. Methods  We measured fasting glucose, insulin and C‐peptide levels in 24 patients with β‐thalassaemia major and 18 control subjects matched for age and body mass index. Insulin sensitivity and insulin release index were calculated according to the homeostasis model assessment (HOMA). Correlations with age, body mass index and serum ferritin were also calculated. Results  Fasting glucose levels in patients were increased compared with control subjects (5.5 ± 0.12 vs. 4.7 ± 0.13 mmol/l, mean ± sem, P < 0.001). Pancreatic B‐cell insulin secretion in the fasting state (estimated by SCHOMA) was lower in thalassaemic patients (SCHOMA 88.5 ± 11.11 vs. 184.3 ± 23.72 in control subjects, P < 0.001). Patients were then divided into those with impaired (IFG) and normal (NFG) fasting glucose. SCHOMA was higher in the patients with NFG compared with those with IFG patients (110.6 ± 17.63 vs. 66.3 ± 10.88, respectively, P < 0.05) but estimated insulin sensitivity (ISIHOMA) was similar. Plasma values of C‐peptide correlated positively with ferritin (r = 0.42, P = 0.04) and SCHOMA (r = 0.45, P = 0.02) and negatively with ISIHOMA (r = −0.43, P = 0.03). Conclusions  These results support the concept that impaired B‐cell function, as reflected by a reduction in the insulin secretion index, is present in β‐thalassaemic patients with normoglycaemia before changes in oral glucose tolerance tests are apparent.
To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with beta-thalassaemia major with normal glucose response during an oral glucose tolerance test and to estimate its possible relation to iron overload. We measured fasting glucose, insulin and C-peptide levels in 24 patients with beta-thalassaemia major and 18 control subjects matched for age and body mass index. Insulin sensitivity and insulin release index were calculated according to the homeostasis model assessment (HOMA). Correlations with age, body mass index and serum ferritin were also calculated. Fasting glucose levels in patients were increased compared with control subjects (5.5 +/- 0.12 vs. 4.7 +/- 0.13 mmol/l, mean +/- SEM, P < 0.001). Pancreatic B-cell insulin secretion in the fasting state (estimated by SC(HOMA)) was lower in thalassaemic patients (SC(HOMA) 88.5 +/- 11.11 vs. 184.3 +/- 23.72 in control subjects, P < 0.001). Patients were then divided into those with impaired (IFG) and normal (NFG) fasting glucose. SC(HOMA) was higher in the patients with NFG compared with those with IFG patients (110.6 +/- 17.63 vs. 66.3 +/- 10.88, respectively, P < 0.05) but estimated insulin sensitivity (ISI(HOMA)) was similar. Plasma values of C-peptide correlated positively with ferritin (r = 0.42, P = 0.04) and SC(HOMA) (r = 0.45, P = 0.02) and negatively with ISI(HOMA) (r = -0.43, P = 0.03). These results support the concept that impaired B-cell function, as reflected by a reduction in the insulin secretion index, is present in beta-thalassaemic patients with normoglycaemia before changes in oral glucose tolerance tests are apparent.
Abstract Aims  To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with β‐thalassaemia major with normal glucose response during an oral glucose tolerance test and to estimate its possible relation to iron overload. Methods  We measured fasting glucose, insulin and C‐peptide levels in 24 patients with β‐thalassaemia major and 18 control subjects matched for age and body mass index. Insulin sensitivity and insulin release index were calculated according to the homeostasis model assessment (HOMA). Correlations with age, body mass index and serum ferritin were also calculated. Results  Fasting glucose levels in patients were increased compared with control subjects (5.5 ± 0.12 vs. 4.7 ± 0.13 mmol/l, mean ±  sem , P  < 0.001). Pancreatic B‐cell insulin secretion in the fasting state (estimated by SC HOMA ) was lower in thalassaemic patients (SC HOMA 88.5 ± 11.11 vs. 184.3 ± 23.72 in control subjects, P  < 0.001). Patients were then divided into those with impaired (IFG) and normal (NFG) fasting glucose. SC HOMA was higher in the patients with NFG compared with those with IFG patients (110.6 ± 17.63 vs. 66.3 ± 10.88, respectively, P  < 0.05) but estimated insulin sensitivity (ISI HOMA ) was similar. Plasma values of C‐peptide correlated positively with ferritin ( r =  0.42, P  = 0.04) and SC HOMA ( r =  0.45, P  = 0.02) and negatively with ISI HOMA ( r =  −0.43, P  = 0.03). Conclusions  These results support the concept that impaired B‐cell function, as reflected by a reduction in the insulin secretion index, is present in β‐thalassaemic patients with normoglycaemia before changes in oral glucose tolerance tests are apparent.
AIMSTo assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with beta-thalassaemia major with normal glucose response during an oral glucose tolerance test and to estimate its possible relation to iron overload.METHODSWe measured fasting glucose, insulin and C-peptide levels in 24 patients with beta-thalassaemia major and 18 control subjects matched for age and body mass index. Insulin sensitivity and insulin release index were calculated according to the homeostasis model assessment (HOMA). Correlations with age, body mass index and serum ferritin were also calculated.RESULTSFasting glucose levels in patients were increased compared with control subjects (5.5 +/- 0.12 vs. 4.7 +/- 0.13 mmol/l, mean +/- SEM, P < 0.001). Pancreatic B-cell insulin secretion in the fasting state (estimated by SC(HOMA)) was lower in thalassaemic patients (SC(HOMA) 88.5 +/- 11.11 vs. 184.3 +/- 23.72 in control subjects, P < 0.001). Patients were then divided into those with impaired (IFG) and normal (NFG) fasting glucose. SC(HOMA) was higher in the patients with NFG compared with those with IFG patients (110.6 +/- 17.63 vs. 66.3 +/- 10.88, respectively, P < 0.05) but estimated insulin sensitivity (ISI(HOMA)) was similar. Plasma values of C-peptide correlated positively with ferritin (r = 0.42, P = 0.04) and SC(HOMA) (r = 0.45, P = 0.02) and negatively with ISI(HOMA) (r = -0.43, P = 0.03).CONCLUSIONSThese results support the concept that impaired B-cell function, as reflected by a reduction in the insulin secretion index, is present in beta-thalassaemic patients with normoglycaemia before changes in oral glucose tolerance tests are apparent.
Author Livadas, S.
Angelopoulos, N. G.
Adamopoulos, I.
Zervas, A.
Giannopoulos, D.
Tolis, G.
Goula, A.
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Issue 12
Keywords Endocrinopathy
Human
fasting glycaemia
Hemoglobinopathy
Pancreatic hormone
Secretion
Diabetes mellitus
Homeostasis
Tolerance
Hemopathy
Glucose
Insulin
Genetic disease
Hemolytic anemia
β-Thalassemia
β-thalassaemia major
Models
glucose tolerance
Fast
Glycemia
homeostasis model assessment
Language English
License CC BY 4.0
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PublicationDate December 2006
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PublicationTitle Diabetic medicine
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Snippet Aims  To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with β‐thalassaemia major with normal glucose response...
To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with beta-thalassaemia major with normal glucose response...
Abstract Aims  To assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with β‐thalassaemia major with normal glucose...
AIMSTo assess insulin sensitivity and secretion in the fasting state in regularly transfused patients with beta-thalassaemia major with normal glucose response...
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StartPage 1327
SubjectTerms Adult
Anemias. Hemoglobinopathies
beta-Thalassemia - blood
beta-Thalassemia - complications
Biological and medical sciences
Blood Glucose - metabolism
C-Peptide - metabolism
Case-Control Studies
Diabetes Mellitus - blood
Diabetes Mellitus - etiology
Diabetes Mellitus - metabolism
Diabetes. Impaired glucose tolerance
Diseases of red blood cells
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
fasting glycaemia
Female
glucose tolerance
Glucose Tolerance Test
Hematologic and hematopoietic diseases
Homeostasis
homeostasis model assessment
Humans
Insulin - deficiency
Insulin - metabolism
Insulin Secretion
Male
Medical sciences
Models, Biological
β-thalassaemia major
Title Reduced insulin secretion in normoglycaemic patients with β-thalassaemia major
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https://www.ncbi.nlm.nih.gov/pubmed/17116183
https://search.proquest.com/docview/68178724
Volume 23
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