TY - JOUR
T1 - HbA1c and fasting plasma glucose levels are equally related to incident cardiovascular risk in a high CVD risk population without known diabetes
AU - UCC-SMART Study Group
AU - Been, Riemer A
AU - Noordstar, Ellen
AU - Helmink, Marga A G
AU - van Sloten, Thomas T
AU - de Ranitz-Greven, Wendela L
AU - van Beek, André P
AU - Houweling, Sebastiaan T
AU - van Dijk, Peter R
AU - Westerink, Jan
N1 - © 2024 the author(s), published by De Gruyter, Berlin/Boston.
PY - 2024/8
Y1 - 2024/8
N2 - OBJECTIVES: 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
1c, 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.
METHODS: 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
1c (cut-offs at 7 mmol/L and 48 mmol/mol, respectively): Group 0: known T2DM; group 1: elevated FPG/HbA
1c; group 2: elevated FPG, non-elevated HbA
1c; group 3: non-elevated FPG, elevated HbA
1c; group 1 + 2: elevated FPG, regardless of HbA
1c; group 1 + 3: elevated HbA
1c, regardless of FPG; and group 4 (reference), non-elevated FPG/HbA
1c.
RESULTS: 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
1c/FPG, but did not allow for identification of other cut-off points.
CONCLUSIONS: Based on current cut-offs, FPG and HbA
1c at screening were equally related to incident CVD in high-risk populations without known T2DM. Hence, neither FPG, nor HbA
1c, is preferential for diabetes screening in this population with respect to risk of incident CVD.
AB - OBJECTIVES: 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
1c, 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.
METHODS: 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
1c (cut-offs at 7 mmol/L and 48 mmol/mol, respectively): Group 0: known T2DM; group 1: elevated FPG/HbA
1c; group 2: elevated FPG, non-elevated HbA
1c; group 3: non-elevated FPG, elevated HbA
1c; group 1 + 2: elevated FPG, regardless of HbA
1c; group 1 + 3: elevated HbA
1c, regardless of FPG; and group 4 (reference), non-elevated FPG/HbA
1c.
RESULTS: 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
1c/FPG, but did not allow for identification of other cut-off points.
CONCLUSIONS: Based on current cut-offs, FPG and HbA
1c at screening were equally related to incident CVD in high-risk populations without known T2DM. Hence, neither FPG, nor HbA
1c, is preferential for diabetes screening in this population with respect to risk of incident CVD.
U2 - 10.1515/dx-2024-0017
DO - 10.1515/dx-2024-0017
M3 - Article
C2 - 38414181
SN - 2194-8011
VL - 11
SP - 312
EP - 320
JO - Diagnosis
JF - Diagnosis
IS - 3
ER -