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Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia

Purpose: To determine the prevalence and underlying pathology of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia (NTDT). Patients and methods: In this study, we enrolled 211 patients aged 4–63 years with NTDT, including 79 β thalassemia intermedia patients...

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Autores principales: Luo, Yunchen, Bajoria, Rekha, Lai, Yongrong, Pan, Hongfei, Li, Qiaochuan, Zhang, Zhongming, Yang, Pijian, Chatterjee, Ratna, Liang, Yuzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489622/
https://www.ncbi.nlm.nih.gov/pubmed/31114275
http://dx.doi.org/10.2147/DMSO.S194591
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author Luo, Yunchen
Bajoria, Rekha
Lai, Yongrong
Pan, Hongfei
Li, Qiaochuan
Zhang, Zhongming
Yang, Pijian
Chatterjee, Ratna
Liang, Yuzhen
author_facet Luo, Yunchen
Bajoria, Rekha
Lai, Yongrong
Pan, Hongfei
Li, Qiaochuan
Zhang, Zhongming
Yang, Pijian
Chatterjee, Ratna
Liang, Yuzhen
author_sort Luo, Yunchen
collection PubMed
description Purpose: To determine the prevalence and underlying pathology of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia (NTDT). Patients and methods: In this study, we enrolled 211 patients aged 4–63 years with NTDT, including 79 β thalassemia intermedia patients, 114 Hb H disease patients and 18 Hb E/β thalassemia patients. All had oral glucose tolerance test, serum ferritin (SF), homeostasis model assessment (HOMA) and liver iron concentration (LIC) measurement. One hundred and twenty healthy age-matched controls were also used for the comparative purpose. Iron load was assessed by using SF and hepatic load by LIC using validated MRI techniques. Results: The 211 patients were divided into three groups according to their fasting and 2 hrs postprandial blood glucose levels: hypoglycemic, normal glucose tolerance (NGT) and hyperglycemic groups. In this study, 149 patients had NGT, 33 had hypoglycemia, 4 had diabetes and 25 had impaired glucose tolerance (IGT). None had impaired fasting glucose. There was a significant correlation between 2 hrs postprandial blood glucose levels and age, PINS120, HOMA-IR, alanine aminotransferase and LIC (P<0.05). Risk factors for IGT in NTDT patients were older age (≥24 years) and SF concentration of ≥2,500 ng/mL. Conclusion: Age ≥24 years and SF ≥2,500 ng/mL of NTDT patients were at a greater risk for impaired glucose tolerance.
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spelling pubmed-64896222019-05-21 Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia Luo, Yunchen Bajoria, Rekha Lai, Yongrong Pan, Hongfei Li, Qiaochuan Zhang, Zhongming Yang, Pijian Chatterjee, Ratna Liang, Yuzhen Diabetes Metab Syndr Obes Original Research Purpose: To determine the prevalence and underlying pathology of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia (NTDT). Patients and methods: In this study, we enrolled 211 patients aged 4–63 years with NTDT, including 79 β thalassemia intermedia patients, 114 Hb H disease patients and 18 Hb E/β thalassemia patients. All had oral glucose tolerance test, serum ferritin (SF), homeostasis model assessment (HOMA) and liver iron concentration (LIC) measurement. One hundred and twenty healthy age-matched controls were also used for the comparative purpose. Iron load was assessed by using SF and hepatic load by LIC using validated MRI techniques. Results: The 211 patients were divided into three groups according to their fasting and 2 hrs postprandial blood glucose levels: hypoglycemic, normal glucose tolerance (NGT) and hyperglycemic groups. In this study, 149 patients had NGT, 33 had hypoglycemia, 4 had diabetes and 25 had impaired glucose tolerance (IGT). None had impaired fasting glucose. There was a significant correlation between 2 hrs postprandial blood glucose levels and age, PINS120, HOMA-IR, alanine aminotransferase and LIC (P<0.05). Risk factors for IGT in NTDT patients were older age (≥24 years) and SF concentration of ≥2,500 ng/mL. Conclusion: Age ≥24 years and SF ≥2,500 ng/mL of NTDT patients were at a greater risk for impaired glucose tolerance. Dove 2019-04-11 /pmc/articles/PMC6489622/ /pubmed/31114275 http://dx.doi.org/10.2147/DMSO.S194591 Text en © 2019 Luo et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Luo, Yunchen
Bajoria, Rekha
Lai, Yongrong
Pan, Hongfei
Li, Qiaochuan
Zhang, Zhongming
Yang, Pijian
Chatterjee, Ratna
Liang, Yuzhen
Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia
title Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia
title_full Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia
title_fullStr Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia
title_full_unstemmed Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia
title_short Prevalence of abnormal glucose homeostasis in Chinese patients with non-transfusion-dependent thalassemia
title_sort prevalence of abnormal glucose homeostasis in chinese patients with non-transfusion-dependent thalassemia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489622/
https://www.ncbi.nlm.nih.gov/pubmed/31114275
http://dx.doi.org/10.2147/DMSO.S194591
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