Department of Endocrinology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Department of Internal Medicine, Isala Hospital, Zwolle, The Netherlands.
Diagnosis (Berl). 2024 Feb 29;11(3):312-320. doi: 10.1515/dx-2024-0017. eCollection 2024 Aug 1.
Type 2 diabetes (T2DM) is associated with increased risk for cardiovascular disease (CVD). Whether screen-detected T2DM, based on fasting plasma glucose (FPG) or on HbA, are associated with different risks of incident CVD in high-risk populations and which one is preferable for diabetes screening in these populations, remains unclear.
A total of 8,274 high-risk CVD participants were included from the UCC-SMART cohort. Participants were divided into groups based on prior T2DM diagnosis, and combinations of elevated/non-elevated FPG and HbA (cut-offs at 7 mmol/L and 48 mmol/mol, respectively): Group 0: known T2DM; group 1: elevated FPG/HbA; group 2: elevated FPG, non-elevated HbA; group 3: non-elevated FPG, elevated HbA; group 1 + 2: elevated FPG, regardless of HbA; group 1 + 3: elevated HbA, regardless of FPG; and group 4 (reference), non-elevated FPG/HbA.
During a median follow-up of 6.3 years (IQR 3.3-9.8), 712 cardiovascular events occurred. Compared to the reference (group 4), group 0 was at increased risk (HR 1.40; 95 % CI 1.16-1.68), but group 1 (HR 1.16; 95 % CI 0.62-2.18), 2 (HR 1.18; 95 % CI 0.84-1.67), 3 (HR 0.61; 95 % CI 0.15-2.44), 1 + 2 (HR 1.17; 95 % CI 0.86-1.59) and 1 + 3 (HR 1.01; 95 % CI 0.57-1.79) were not. However, spline interpolation showed a linearly increasing risk with increasing HbA/FPG, but did not allow for identification of other cut-off points.
Based on current cut-offs, FPG and HbA at screening were equally related to incident CVD in high-risk populations without known T2DM. Hence, neither FPG, nor HbA, is preferential for diabetes screening in this population with respect to risk of incident CVD.
2 型糖尿病(T2DM)与心血管疾病(CVD)风险增加有关。基于空腹血糖(FPG)或糖化血红蛋白(HbA)筛查出的 T2DM 是否与高危人群中 CVD 事件的发生风险不同,以及哪种方法更适合该人群的糖尿病筛查,目前仍不清楚。
本研究共纳入了 UCC-SMART 队列中的 8274 名高危 CVD 参与者。参与者根据既往 T2DM 诊断以及 FPG 和 HbA 的升高/不升高情况(分别以 7mmol/L 和 48mmol/mol 为截断值)分为以下几组:组 0:已知的 T2DM;组 1:升高的 FPG/HbA;组 2:升高的 FPG,不升高的 HbA;组 3:不升高的 FPG,升高的 HbA;组 1+2:无论 HbA 如何,FPG 均升高;组 1+3:无论 FPG 如何,HbA 均升高;组 4(参照组):FPG 和 HbA 均不升高。
在中位随访 6.3 年(IQR 3.3-9.8)期间,发生了 712 例心血管事件。与参照组(组 4)相比,组 0 的风险增加(HR 1.40;95%CI 1.16-1.68),但组 1(HR 1.16;95%CI 0.62-2.18)、组 2(HR 1.18;95%CI 0.84-1.67)、组 3(HR 0.61;95%CI 0.15-2.44)、组 1+2(HR 1.17;95%CI 0.86-1.59)和组 1+3(HR 1.01;95%CI 0.57-1.79)的风险则无显著增加。然而,样条插值显示,随着 HbA/FPG 的升高,风险呈线性增加,但无法确定其他截断值。
基于目前的截断值,在无已知 T2DM 的高危人群中,FPG 和 HbA 在筛查时与 CVD 事件的发生风险同样相关。因此,FPG 和 HbA 均不能作为该人群 CVD 事件发生风险的首选筛查指标。