Chiu K C, Lee N P, Cohan P, Chuang L M
Division of Endocrinology, Diabetes and Hypertension, University of California, Los Angeles, School of Medicine, Los Angeles, California, USA.
Clin Endocrinol (Oxf). 2000 Nov;53(5):569-75. doi: 10.1046/j.1365-2265.2000.01132.x.
As type 2 diabetes results from an imbalance between insulin sensitivity and beta cell function, either or both may worsen with age. However, existing data are controversial on the effect of ageing on both insulin sensitivity and beta cell function.
We enrolled 149 healthy, glucose tolerant and normotensive Caucasians (age 35 +/- 1 years, body mass index 26.07 +/- 0.44 kg/m2, waist-hip ratio 0.842 +/- 0.009 cm/cm, mean +/- standard error). A cross-sectional study was designed to examine the impact of age on insulin sensitivity and beta cell function. Their beta cell function (percentage B [%B]) and insulin sensitivity (percentage S [%S]) were estimated using the homeostasis model assessment.
Simple regression analysis revealed that %B declined with age (P = 0.008) while no relation was found between %S and age (P = 0.769). A stepwise regression analysis revealed that body mass index and diastolic blood pressure explained 14.7% of variation in %S, while age, waist-hip ratio, gender, and systolic blood pressure had no influence on %S. Age, body mass index and diastolic blood pressure together accounted for 21.7% of variation in %B, with age being an independent variable.
In the present study, we showed that beta cell function declined with age at a rate of about 1% per year. In contrast, insulin sensitivity was not affected by ageing. Our observations suggest that the age-related decline in glucose tolerance is primarily related to the loss of beta-cell function.
由于2型糖尿病是由胰岛素敏感性和β细胞功能之间的失衡所致,其中任何一个因素或两者都可能随年龄增长而恶化。然而,现有数据对于衰老对胰岛素敏感性和β细胞功能的影响存在争议。
我们招募了149名健康、糖耐量正常且血压正常的高加索人(年龄35±1岁,体重指数26.07±0.44kg/m²,腰臀比0.842±0.009cm/cm,均值±标准误)。设计了一项横断面研究以检验年龄对胰岛素敏感性和β细胞功能的影响。使用稳态模型评估来估计他们的β细胞功能(B百分比[%B])和胰岛素敏感性(S百分比[%S])。
简单回归分析显示%B随年龄下降(P = 0.008),而未发现%S与年龄之间存在关联(P = 0.769)。逐步回归分析显示体重指数和舒张压解释了%S变异的14.7%,而年龄、腰臀比、性别和收缩压对%S没有影响。年龄、体重指数和舒张压共同解释了%B变异的21.7%,其中年龄是一个独立变量。
在本研究中,我们表明β细胞功能随年龄下降,每年下降速率约为1%。相比之下,胰岛素敏感性不受衰老影响。我们的观察结果表明,与年龄相关的糖耐量下降主要与β细胞功能丧失有关。