Limited benefit of haemoglobin glycation index as risk factor for cardiovascular disease in type 2 diabetes patients

TY - JOUR

T1 - Limited benefit of haemoglobin glycation index as risk factor for cardiovascular disease in type 2 diabetes patients

AU - Østergaard, H. B.

AU - Mandrup-Poulsen, T.

AU - Berkelmans, G. F.N.

AU - van der Graaf, Y.

AU - Visseren, F. L.J.

AU - Westerink, J.

PY - 2019

Y1 - 2019

N2 - Background: The haemoglobin glycation index (HGI)has been proposed as a marker of interindividual differences in haemoglobin glycosylation. Previous studies have shown a relationship between high HGI and risk of cardiovascular disease (CVD)in patients with diabetes. However, no studies have investigated the role of previous CVD in this association. Methods: The study cohort comprised patients with type 2 diabetes mellitus (T2DM; n = 1910)included in the Second Manifestations of Arterial Disease (SMART)study. The relationship between either HGI or HbA1c and a composite of cardiovascular events as the primary outcome, and mortality, cardiovascular mortality, myocardial infarction and stroke as secondary outcomes, was investigated using Cox proportional-hazards models. Similar analyses were performed after stratification according to previous CVD. Results: A 1-unit higher HGI was associated with a 29% greater risk of a composite of cardiovascular events (HR: 1.29, 95% CI: 1.06–1.57)in patients without previous CVD, whereas no such relationship was seen in patients with previous CVD (HR: 0.96, 95% CI: 0.86–1.08). The direction and magnitude of the hazard ratios (HRs)of HGI and HbA1c in relation to outcomes were similar. Additional adjustment for HbA1c in the association between HGI and outcomes lowered the HRs. Conclusion: Similar to HbA1c, higher HGI is related to higher risk of cardiovascular events in patients with T2DM without CVD. As HbA1c has proved to be a comparable risk factor, and obtaining and interpreting the HGI is complicated, any additional benefit of applying the HGI in clinical settings is likely to be limited.

AB - Background: The haemoglobin glycation index (HGI)has been proposed as a marker of interindividual differences in haemoglobin glycosylation. Previous studies have shown a relationship between high HGI and risk of cardiovascular disease (CVD)in patients with diabetes. However, no studies have investigated the role of previous CVD in this association. Methods: The study cohort comprised patients with type 2 diabetes mellitus (T2DM; n = 1910)included in the Second Manifestations of Arterial Disease (SMART)study. The relationship between either HGI or HbA1c and a composite of cardiovascular events as the primary outcome, and mortality, cardiovascular mortality, myocardial infarction and stroke as secondary outcomes, was investigated using Cox proportional-hazards models. Similar analyses were performed after stratification according to previous CVD. Results: A 1-unit higher HGI was associated with a 29% greater risk of a composite of cardiovascular events (HR: 1.29, 95% CI: 1.06–1.57)in patients without previous CVD, whereas no such relationship was seen in patients with previous CVD (HR: 0.96, 95% CI: 0.86–1.08). The direction and magnitude of the hazard ratios (HRs)of HGI and HbA1c in relation to outcomes were similar. Additional adjustment for HbA1c in the association between HGI and outcomes lowered the HRs. Conclusion: Similar to HbA1c, higher HGI is related to higher risk of cardiovascular events in patients with T2DM without CVD. As HbA1c has proved to be a comparable risk factor, and obtaining and interpreting the HGI is complicated, any additional benefit of applying the HGI in clinical settings is likely to be limited.

KW - Cardiovascular disease

KW - Diabetes mellitus type 2

KW - Glycaemic control

KW - Haemoglobin glycation index

KW - HbA

KW - HGI

U2 - 10.1016/j.diabet.2018.04.006

DO - 10.1016/j.diabet.2018.04.006

M3 - Journal article

C2 - 29784563

AN - SCOPUS:85047219438

SN - 1262-3636

VL - 45

SP - 254

EP - 260

JO - Diabetes and Metabolism

JF - Diabetes and Metabolism

IS - 3

ER -