超重对患有β-地中海贫血(β-TM)的年轻成年女性血糖稳态的影响:一项初步回顾性研究。

Vincenzo De Sanctis, Shahina Daar, Ashraf T Soliman, Ploutarchos Tzoulis, Mohamed Yassin, Christos Kattamis
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引用次数: 0

摘要

背景:随着全球肥胖患病率的上升,尽早发现糖代谢紊乱以预防2型糖尿病(T2D)的发展变得至关重要。研究设计:本回顾性观察性研究旨在评估超重(BMI 25-29.9 kg/m2)的β-TM女性患者的BMI与糖代谢、胰岛素分泌和糖耐量试验(OGTT)得出的敏感指数之间的关系,并随着时间的推移跟踪其结果。受试者和方法:招募11名超重女性和11名具有理想体重和β-TM的女性,年龄匹配。进行OGTT,计算β细胞功能、胰岛素敏感性和胰岛素分泌的不同指标。结果:首次评估时,11名超重的β-TM患者中有7名(63.6%)和11名正常体重的β-TM患者中有3名(27.2%)在OGTT期间出现葡萄糖调节障碍(GD)。超重的β-TM患者HOMA-IR和QUICKI指数升高,Matsuda WBISI指数降低。随访时间平均为4.5±1.2年。在最后的观察中,2/11名超重患者发生了T2D(18.1%)。在体重正常的患者中,GD从3/11(27.2%)增加到5/11(45.4%),但没有发生T2DM。第一次和最后一次观察时的SF之间的差异(1220±702 vs.1991±454 ng/mL;P:0.61)没有显著性。结论:超重似乎是β-TM患者发生GD的额外危险因素。由于缺乏专门针对这类患者的适当指南,这在临床实践中尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of excess weight on glucose homeostasis in young adult females with β-thalassemia major (β-TM): a preliminary retrospective study.

Background: With the rising prevalence of obesity worldwide, it is becoming imperative to detect disturbed glucose metabolism as early as possible in order to prevent type 2 diabetes (T2D) development.

Study design: The present retrospective observational study aimed to evaluate the relationship between BMI and glucose metabolism, insulin secretion and sensitivity indices, derived from glucose tolerance test (OGTT), in β -TM female patients who were overweight (BMI 25-29.9 kg/m2) and follow its outcome over time.

Subjects and methods: Eleven overweight and 11 females with ideal weight and β -TM, matched for age, were recruited. OGTT was undertaken and different indices for β-cell function, insulin sensitivity and insulin secretion were calculated.

Results: At first evaluation, 7 of 11 overweight β -TM patients (63.6%) and 3 of 11 normal weight β-TM patients (27.2%) had glucose dysregulation (GD) during OGTT. Overweight patients with β-TM had increased HOMA-IR and QUICKI indices associated with decreased Matsuda WBISI index. The mean ± SD duration of follow-up was 4.5 ± 1.2 years. At last observation, 2/11 overweight patients had developed T2D (18.1%). In patients with normal weight, GD increased from 3/11 (27.2%) to 5/11 (45.4%), but none developed T2DM. The difference between SF at first and last observation (1,220 ± 702 vs.1,091 ± 454 ng/mL; P: 0.61) was not significant.

Conclusion: Overweight seems to be an additional risk factor for the development of GD in β-TM patients. This is particularly important in clinical practice, due to the lack of appropriate guidelines dedicated to this group of patients.

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