TY - JOUR
T1 - Presence of retinopathy and incident kidney and cardiovascular events in type 2 diabetes with normoalbuminuria - A post-hoc analysis of the PRIORITY randomized clinical trial
AU - Curovic, Viktor Rotbain
AU - Tofte, N
AU - Lindhardt, M
AU - Adamova, K
AU - Bakker, Stephan J.L.
AU - Beige, J
AU - Beulens, JWJ
AU - Birkenfeld, AL
AU - Currie, G
AU - Delles, C
AU - Dimos, I
AU - Francová, L
AU - Frimodt-Moller, M
AU - Girman, P
AU - Göke, R
AU - Hansen, TW
AU - Havrdova, T
AU - Kooy, A
AU - Laverman, Gozewijn D.
AU - Mischak, H
AU - Navis, G
AU - Nijpels, G
AU - Noutsou, M
AU - Ortiz, A
AU - Parvanova, A
AU - Persson, F
AU - Petrie, JR
AU - Ruggenenti, PL
AU - Rutters, F
AU - Rychlík, I
AU - Siwy, J
AU - Spasovski, G
AU - Speeckaert, M
AU - Trillini, M
AU - Zürbig, P
AU - von der Leyen, H
AU - Rossing, P
AU - PRIORITY Study Grp
PY - 2023/4
Y1 - 2023/4
N2 - Aims: Baseline diabetic retinopathy (DR) and risk of development of microalbuminuria, kidney function decline, and cardiovascular events (CVEs) in type 2 diabetes. Methods: Post-hoc analysis of the PRIORITY study including 1758 persons with type 2 diabetes and normoalbuminuria followed for a median of 2.5 (IQR: 2.0–3.0) years. DR diagnosis included non-proliferative and proliferative abnormalities, macular oedema, or prior laser treatment. Cox models were fitted to investigate baseline DR presence with development of persistent microalbuminuria (urinary albumin-creatinine ratio > 30 mg/g); chronic kidney disease (CKD) G3 (eGFR <60 ml/min/1.73m
2); and CVE. Models were adjusted for relevant risk factors. Results: At baseline, 304 (17.3 %) had DR. Compared to persons without DR, they were older (mean ± SD: 62.7 ± 7.7 vs 61.4 ± 8.3 years, p = 0.019), had longer diabetes duration (17.9 ± 8.4 vs. 10.6 ± 7.0 years, p < 0.001), and higher HbA
1c (62 ± 13 vs. 56 ± 12 mmol/mol, p < 0.001). The adjusted hazard ratios of DR at baseline for development of microalbuminuria (n = 197), CKD (n = 166), and CVE (n = 64) were: 1.50 (95%CI: 1.07, 2.11), 0.87 (95%CI: 0.56, 1.34), and 2.61 (95%CI: 1.44, 4.72), compared to without DR. Conclusions: Presence of DR in normoalbuminuric type 2 diabetes was associated with an increased risk of developing microalbuminuria and CVE, but not with kidney function decline.
AB - Aims: Baseline diabetic retinopathy (DR) and risk of development of microalbuminuria, kidney function decline, and cardiovascular events (CVEs) in type 2 diabetes. Methods: Post-hoc analysis of the PRIORITY study including 1758 persons with type 2 diabetes and normoalbuminuria followed for a median of 2.5 (IQR: 2.0–3.0) years. DR diagnosis included non-proliferative and proliferative abnormalities, macular oedema, or prior laser treatment. Cox models were fitted to investigate baseline DR presence with development of persistent microalbuminuria (urinary albumin-creatinine ratio > 30 mg/g); chronic kidney disease (CKD) G3 (eGFR <60 ml/min/1.73m
2); and CVE. Models were adjusted for relevant risk factors. Results: At baseline, 304 (17.3 %) had DR. Compared to persons without DR, they were older (mean ± SD: 62.7 ± 7.7 vs 61.4 ± 8.3 years, p = 0.019), had longer diabetes duration (17.9 ± 8.4 vs. 10.6 ± 7.0 years, p < 0.001), and higher HbA
1c (62 ± 13 vs. 56 ± 12 mmol/mol, p < 0.001). The adjusted hazard ratios of DR at baseline for development of microalbuminuria (n = 197), CKD (n = 166), and CVE (n = 64) were: 1.50 (95%CI: 1.07, 2.11), 0.87 (95%CI: 0.56, 1.34), and 2.61 (95%CI: 1.44, 4.72), compared to without DR. Conclusions: Presence of DR in normoalbuminuric type 2 diabetes was associated with an increased risk of developing microalbuminuria and CVE, but not with kidney function decline.
KW - Albuminuria
KW - Cardiovascular disease
KW - Chronic kidney disease
KW - Diabetic retinopathy
KW - Risk stratification
KW - Type 2 diabetes
KW - n/a OA procedure
U2 - 10.1016/j.jdiacomp.2023.108433
DO - 10.1016/j.jdiacomp.2023.108433
M3 - Article
C2 - 36841085
SN - 1056-8727
VL - 37
JO - Journal of diabetes and its complications
JF - Journal of diabetes and its complications
IS - 4
M1 - 108433
ER -