Balkau Beverley, Lange Céline, Fezeu Leopold, Tichet Jean, de Lauzon-Guillain Blandine, Czernichow Sebastien, Fumeron Frederic, Froguel Philippe, Vaxillaire Martine, Cauchi Stephane, Ducimetière Pierre, Eschwège Eveline
INSERM U780-IFR69, Villejuif, France/University Paris-Sud, Orsay, France.
Diabetes Care. 2008 Oct;31(10):2056-61. doi: 10.2337/dc08-0368. Epub 2008 Aug 8.
To provide a simple clinical diabetes risk score and to identify characteristics that predict later diabetes using variables available in the clinic setting as well as biological variables and polymorphisms.
Incident diabetes was studied in 1,863 men and 1,954 women, 30-65 years of age at baseline, with diabetes defined by treatment or by fasting plasma glucose >or=7.0 mmol/l at 3-yearly examinations over 9 years. Sex-specific logistic regression equations were used to select variables for prediction.
A total of 140 men and 63 women developed diabetes. The predictive clinical variables were waist circumference and hypertension in both sexes, smoking in men, and diabetes in the family in women. Discrimination, as measured by the area under the receiver operating curves (AROCs), were 0.713 for men and 0.827 for women, a little higher than for the Finish Diabetes Risk (FINDRISC) score, with fewer variables in the score. Combining clinical and biological variables, the predictive equation included fasting glucose, waist circumference, smoking, and gamma-glutamyltransferase for men and fasting glucose, BMI, triglycerides, and diabetes in family for women. The number of TCF7L2 and IL6 deleterious alleles was predictive in both sexes, but after including the above clinical and biological variables, this variable was only predictive in women (P < 0.03) and the AROC statistics increased only marginally.
The best clinical predictor of diabetes is adiposity, and baseline glucose is the best biological predictor. Clinical and biological predictors differed marginally between men and women. The genetic polymorphisms added little to the prediction of diabetes.
提供一个简单的临床糖尿病风险评分,并利用临床可用变量、生物学变量及多态性来确定预测未来糖尿病的特征。
对1863名男性和1954名女性进行新发糖尿病研究,基线年龄为30 - 65岁,通过治疗或在9年期间每3年一次的检查中空腹血糖≥7.0 mmol/l来定义糖尿病。使用性别特异性逻辑回归方程选择预测变量。
共有140名男性和63名女性患糖尿病。预测性临床变量在男性中为腰围和高血压、吸烟,在女性中为腰围和高血压、家族糖尿病史。用受试者工作特征曲线下面积(AROC)衡量的辨别力,男性为0.713,女性为0.827,略高于芬兰糖尿病风险(FINDRISC)评分,且评分中的变量更少。结合临床和生物学变量,预测方程对男性包括空腹血糖、腰围、吸烟和γ-谷氨酰转移酶,对女性包括空腹血糖、体重指数、甘油三酯和家族糖尿病史。TCF7L2和IL6有害等位基因的数量在两性中均具有预测性,但在纳入上述临床和生物学变量后,该变量仅在女性中具有预测性(P < 0.03),且AROC统计量仅略有增加。
糖尿病的最佳临床预测指标是肥胖,基线血糖是最佳生物学预测指标。临床和生物学预测指标在男性和女性之间略有差异。基因多态性对糖尿病预测的贡献不大。