来自系统综述和荟萃分析的证据:根据进展为糖尿病的风险,应将经典的糖耐量受损分为单独的糖耐力受损和糖耐量损伤合并空腹血糖受损的亚组

IF 2.781 The Journal of Physical Chemistry Pub Date : 2022-02-18 eCollection Date: 2022-01-01 DOI:10.3389/fendo.2022.835460
Yupu Liu, Juan Li, Yuchao Wu, Han Zhang, Qingguo Lv, Yuwei Zhang, Xiaofeng Zheng, Nanwei Tong
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引用次数: 0

摘要

背景美国糖尿病协会(ADA)2003年诊断标准将糖耐量受损(IGT)分为单独的空腹血糖正常的糖耐量异常(I-IGT,IGT+NFG)和空腹血糖受损的糖耐度受损(IGT+IFG),而世界卫生组织(世界卫生组织)1999年标准则没有。这项荟萃分析的目的是评估IGT是否应根据其发展为2型糖尿病的风险分为I-IGT(IGT+NFG)或IGT+IFG。方法检索MEDLINE和EMBASE,以确定2020年4月18日之前以英语发表的前瞻性队列研究。Review Manager 5.3用于计算合并风险比(RR)和95%置信区间(CI),作为每个纳入研究的汇总统计数据。结果16项符合条件的研究(n=147006)被纳入分析。I-IGT(IGT+NFG)组的2型糖尿病后续发病率低于IGT+IFG组(根据世界卫生组织1999年标准为0.45[95%CI 0.37,0.55],根据ADA 2003年标准为0.59[95%CI 0.54,0.66])。I-IFG、I-IGT(IGT+NFG)和IGT+IFG组的发病率高于血糖正常组(根据世界卫生组织1999年标准,95%CI为5.53[3.78,8.08]、5.21[3.70,7.34]和11.87[7.33,19.20],根据ADA 2003标准,95%CI2.66[2.00,3.54]、3.34[2.81,3.97]和6.10[4.72,7.88])。一般来说,IGT+IFG组的糖尿病发病率在糖尿病前期人群中最高。结论目前的荟萃分析表明,应修订世界卫生组织制定的IGT诊断标准,以分别识别IGT+NFG或IGT+IFG个体。
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Evidence From a Systematic Review and Meta-Analysis: Classical Impaired Glucose Tolerance Should Be Divided Into Subgroups of Isolated Impaired Glucose Tolerance and Impaired Glucose Tolerance Combined With Impaired Fasting Glucose, According to the Risk of Progression to Diabetes.

Background: The American Diabetes Association (ADA) 2003 diagnostic criteria divide impaired glucose tolerance (IGT) into isolated impaired glucose tolerance with normal fasting glucose (I-IGT, IGT+NFG) and impaired glucose tolerance combined with impaired fasting glucose (IGT+IFG), while the World Health Organization (WHO) 1999 criteria do not. The aim of this meta-analysis was to evaluate whether IGT should be divided into I-IGT (IGT+NFG) or IGT+IFG according to their risk of progression to type 2 diabetes.

Methods: The MEDLINE and EMBASE were searched to identify prospective cohort studies published in English prior to April 18, 2020. Review Manager 5.3 was used to calculate the pooled risk ratios (RRs) and 95% confidence intervals (CIs) as summary statistics for each included study.

Results: Sixteen eligible studies (n = 147,006) were included in the analysis. The subsequent incidence of type 2 diabetes was lower in the I-IGT (IGT+NFG) group than in the IGT+IFG group (0.45 [95% CI 0.37, 0.55] according to WHO 1999 criteria and 0.59 [95% CI 0.54, 0.66] according to ADA 2003 criteria). It was higher in the I-IFG, I-IGT (IGT+NFG), and IGT+IFG groups than in the normoglycemic group (95% CI of 5.53 [3.78, 8.08], 5.21 [3.70, 7.34], and 11.87 [7.33, 19.20] according to the WHO 1999 criteria and 95% CI of 2.66 [2.00, 3.54], 3.34 [2.81, 3.97], and 6.10 [4.72, 7.88] according to the ADA 2003 criteria). In general, the incidence of diabetes in the IGT+IFG group was the highest in the prediabetic population.

Conclusions: The present meta-analysis suggested that the established WHO diagnostic criteria for IGT should be revised to separately identify individuals with IGT+NFG or IGT+IFG.

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