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埃及β地中海贫血患者的葡萄糖耐量异常:与基因分型的可能关联。

Abnormal glucose tolerance in Egyptian beta-thalassemic patients: possible association with genotyping.

作者信息

Khalifa A S, Salem Mona, Mounir Eman, El-Tawil M M, El-Sawy Mohamed, Abd Al-Aziz Manal M

机构信息

Department of Pediatrics, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

出版信息

Pediatr Diabetes. 2004 Sep;5(3):126-32. doi: 10.1111/j.1399-543X.2004.00051.x.

Abstract

BACKGROUND

Type 1 diabetes mellitus (DM) is a frequent complication in patients with beta-thalassemia. It is believed to be due to the damage inflicted by iron overload of the pancreatic beta cells. Liver disorders and genetic influences seem to be additional predisposing factors.

OBJECTIVE

To study the prevalence of diabetes and impaired glucose tolerance (IGT) in transfusion-dependent Egyptian beta-thalassemic patients and to evaluate the possible role of genotyping in the pathogenesis of diabetes associated with beta-thalassemia.

RESEARCH DESIGN AND METHODS

A total of 56 transfusion-dependent beta-thalassemic patients aged 10-31 (mean age=15.9 +/- 5.7 yr), 32 males and 24 females, including 48 thalassemia major and eight thalassemia intermedia; compared to 15 age- and sex-matched controls. All were subjected to history and examination, laboratory investigations: complete blood count (CBC), serum ferritin, liver function tests, hepatitis B and C markers, fasting blood glucose, oral glucose tolerance test (OGTT) and fasting C-peptide. Genotyping for 16 mutations was assessed in thalassemic patients with abnormal glucose tolerance.

RESULTS

The prevalence of diabetes was 10.4% (5 of 48) and IGT was 14.6% (7 of 48) among thalassemia major, whereas, none of thalassemia intermedia had abnormal glucose tolerance. Fasting C-peptide was lower in beta-thalassemic patients compared to controls (p <0.001); the level was significantly higher in patients complicated by diabetes or IGT compared with other thalassemic patients (p <0.001). Chronic hepatitis C was detected in all patients (100%) with abnormal glucose tolerance. Genotyping showed that IVS II nt 745 was detected in 77.7% of cases with abnormal glucose tolerance.

CONCLUSIONS

Abnormal glucose tolerance is common in multiply transfused beta-thalassemia major patients, which could be attributed to progressive and early loss of beta-cell mass, along with persistent insulin resistance. Chronic hepatitis C may play a role in the development of abnormal glucose tolerance. An association between diabetes and genotyping IVS II nt 745 was found. Patients with this particular genotype are advised to check their blood glucose every 6 months to detect early occurrence of diabetes.

摘要

背景

1型糖尿病(DM)是β地中海贫血患者常见的并发症。据信这是由于胰腺β细胞铁过载造成的损害所致。肝脏疾病和遗传因素似乎是另外的易感因素。

目的

研究依赖输血的埃及β地中海贫血患者中糖尿病和糖耐量受损(IGT)的患病率,并评估基因分型在与β地中海贫血相关的糖尿病发病机制中的可能作用。

研究设计与方法

共纳入56例年龄在10 - 31岁(平均年龄 = 15.9 ± 5.7岁)的依赖输血的β地中海贫血患者,其中男性32例,女性24例,包括48例重型地中海贫血和8例中间型地中海贫血;与15例年龄和性别匹配的对照者进行比较。所有研究对象均接受病史采集、体格检查及实验室检查:全血细胞计数(CBC)、血清铁蛋白、肝功能检查、乙肝和丙肝标志物、空腹血糖、口服葡萄糖耐量试验(OGTT)及空腹C肽。对糖耐量异常的地中海贫血患者进行16种突变的基因分型评估。

结果

重型地中海贫血患者中糖尿病患病率为10.4%(48例中有5例),IGT患病率为14.6%(48例中有7例),而中间型地中海贫血患者均无糖耐量异常。与对照组相比,β地中海贫血患者的空腹C肽水平较低(p < 0.001);与其他地中海贫血患者相比,合并糖尿病或IGT的患者C肽水平显著更高(p < 0.001)。所有糖耐量异常的患者(100%)均检测出慢性丙型肝炎。基因分型显示,77.7%糖耐量异常的病例中检测到IVS II nt 745。

结论

多次输血的重型β地中海贫血患者糖耐量异常常见,这可能归因于β细胞数量的渐进性早期丧失以及持续的胰岛素抵抗。慢性丙型肝炎可能在糖耐量异常的发生中起作用。发现糖尿病与IVS II nt 745基因分型之间存在关联。建议具有这种特定基因型的患者每6个月检查一次血糖,以早期发现糖尿病的发生。

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