Laspa E, Christen A, Efstathiadou Z, Johnston D G, Godsland I F
Endocrinology and Metabolic Medicine, Division of Medicine, Faculty of Medicine, Imperial College School of Science, Technology and Medicine, London, UK.
Diabet Med. 2007 Nov;24(11):1269-78. doi: 10.1111/j.1464-5491.2007.02225.x. Epub 2007 Sep 26.
To determine whether rate of change and variability in risk factors provides insight into the development of impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or Type 2 diabetes (DM).
In a nested case-control study, repeated risk factor measurements (mean number 4.3, duration 11.4 years) culminated in 59 men developing IFG (n = 37), IGT (n = 14) and/or DM (n = 11). For each case, two control subjects were matched for age and equivalence of follow-up. Rates of change and variability in diabetes risk factors prior to diagnosis were quantified by regression analysis. Changes between penultimate and diagnostic visits were also analysed.
The age-related rise in body mass index (BMI) was attenuated prior to IFG compared with control subjects (+0.102 vs. +0.772 kg/m2/decade, P = 0.02). There was also some evidence for this prior to IGT and DM (IGT: -1.530 vs. +0.158 kg/m2/decade, P = 0.09; DM: -1.146 vs. +0.332 kg/m2/decade, non-significant). Prior to onset, IGT cases were distinguished by higher inflammatory marker levels, a decline in insulinogenic index and greater variability in oral glucose tolerance test (OGTT) insulin, and DM cases by lower insulin sensitivity and higher liver enzyme activities. Fasting and OGTT glucose levels changed little during the mean 8.9 years prior to onset of IFG, IGT or DM. The transition to IGT or DM was accompanied by a fall in insulin sensitivity.
Except for BMI, change or variability in risk factor levels appears relatively unimportant in the development of clinically elevated glucose levels. Deterioration in glucose levels to IGT or DM occurs as a rapid, incremental increase accompanied by a decline in insulin sensitivity.
确定风险因素的变化率和变异性是否有助于深入了解空腹血糖受损(IFG)、糖耐量受损(IGT)或2型糖尿病(DM)的发生发展情况。
在一项巢式病例对照研究中,对风险因素进行多次测量(平均4.3次,持续11.4年),最终有59名男性发展为IFG(n = 37)、IGT(n = 14)和/或DM(n = 11)。对于每个病例,匹配两名年龄和随访时间相当的对照受试者。通过回归分析量化诊断前糖尿病风险因素的变化率和变异性。还分析了倒数第二次就诊和诊断就诊之间的变化。
与对照受试者相比,IFG发生前体重指数(BMI)随年龄的增长有所减缓(+0.102 vs. +0.772 kg/m²/十年,P = 0.02)。在IGT和DM发生前也有一些相关证据(IGT:-1.530 vs. +0.158 kg/m²/十年,P = 0.09;DM:-1.146 vs. +0.332 kg/m²/十年,无显著性差异)。发病前,IGT病例的特点是炎症标志物水平较高、胰岛素生成指数下降以及口服葡萄糖耐量试验(OGTT)胰岛素变异性较大,而DM病例的特点是胰岛素敏感性较低和肝酶活性较高。在IFG、IGT或DM发病前的平均8.9年期间,空腹和OGTT血糖水平变化不大。向IGT或DM的转变伴随着胰岛素敏感性的下降。
除BMI外,风险因素水平的变化或变异性在临床血糖水平升高的发生发展中似乎相对不重要。血糖水平恶化至IGT或DM是一个快速、渐进的过程,同时伴有胰岛素敏感性下降。