Utzschneider Kristina M, Carr Darcy B, Hull Rebecca L, Kodama Keiichi, Shofer Jane B, Retzlaff Barbara M, Knopp Robert H, Kahn Steven E
Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, Veterans Affairs Puget Sound Health Care System (151), 1660 S. Columbian Way, Seattle, WA 98108, USA.
Diabetes. 2004 Nov;53(11):2867-72. doi: 10.2337/diabetes.53.11.2867.
The prevalence of glucose intolerance and type 2 diabetes increases with age. To determine whether the hyperbolic relationship between insulin sensitivity and the insulin response is affected by age and whether the decline in beta-cell function with age is related to increases in intra-abdominal fat or age per se, we studied 220 healthy subjects with fasting glucose <6.1 mmol/l (89 men and 131 women, aged 26-75 years, BMI 18.7-40.4 kg/m(2)). The insulin sensitivity index (S(i)) and the acute insulin response to glucose (AIRg) were determined, and from these beta-cell function was estimated as the disposition index (S(i) x AIRg). Intra-abdominal fat and subcutaneous fat areas were quantified by computed tomography. S(i) (5.40 +/- 0.5 vs. 7.86 +/- 0.7 x10(-5) min(-1)/[pmol/l]), P < 0.01) was decreased and intra-abdominal fat (117 +/- 10 vs. 81 +/- 9 cm(2), P < 0.05) was increased in the oldest (age 60-75 years) versus the youngest (age 26-44 years) quartile. The hyperbolic relationship between S(i) and AIRg was present independent of age; thus, beta-cell function measured as the disposition index (1,412 +/- 120 vs. 2,125 +/- 150 x10(-5) min(-1), P < 0.01) was lower in the oldest versus the youngest quartile. In multiple regression, intra-abdominal fat (r = -0.470, P < 0.001) but not age was associated with S(i), but both intra-abdominal fat (r = -0.198, P = 0.003) and age (r = -0.131, P = 0.05) were correlated with the disposition index. These data suggest that although intra-abdominal fat is a strong determinant of insulin sensitivity and beta-cell function, age has an independent effect on beta-cell function that may contribute to the increased prevalence of type 2 diabetes in older populations.
葡萄糖耐量异常和2型糖尿病的患病率随年龄增长而增加。为了确定胰岛素敏感性与胰岛素反应之间的双曲线关系是否受年龄影响,以及β细胞功能随年龄的下降是否与腹内脂肪增加或年龄本身有关,我们研究了220名空腹血糖<6.1 mmol/l的健康受试者(89名男性和131名女性,年龄26 - 75岁,BMI 18.7 - 40.4 kg/m²)。测定了胰岛素敏感性指数(S(i))和对葡萄糖的急性胰岛素反应(AIRg),并据此将β细胞功能估计为处置指数(S(i)×AIRg)。通过计算机断层扫描对腹内脂肪和皮下脂肪面积进行定量。与最年轻四分位数组(年龄26 - 44岁)相比,最年长四分位数组(年龄60 - 75岁)的S(i)降低(5.40±0.5对7.86±0.7×10⁻⁵ min⁻¹/[pmol/l],P<0.01),腹内脂肪增加(117±10对81±9 cm²,P<0.05)。S(i)与AIRg之间的双曲线关系不受年龄影响;因此,以处置指数衡量的β细胞功能在最年长四分位数组中低于最年轻四分位数组(1412±120对2125±150×10⁻⁵ min⁻¹,P<0.01)。在多元回归分析中,腹内脂肪(r = -0.470,P<0.001)而非年龄与S(i)相关,但腹内脂肪(r = -0.198,P = 0.003)和年龄(r = -0.131,P = 0.05)均与处置指数相关。这些数据表明,尽管腹内脂肪是胰岛素敏感性和β细胞功能的重要决定因素,但年龄对β细胞功能有独立影响,这可能导致老年人群中2型糖尿病患病率增加。