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
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu randomizované kontrolované studie, časopisecké články, práce podpořená grantem
PubMed
36841085
DOI
10.1016/j.jdiacomp.2023.108433
PII: S1056-8727(23)00031-4
Knihovny.cz E-zdroje
- Klíčová slova
- Albuminuria, Cardiovascular disease, Chronic kidney disease, Diabetic retinopathy, Risk stratification, Type 2 diabetes,
- MeSH
- albuminurie komplikace MeSH
- chronická renální insuficience * komplikace epidemiologie MeSH
- diabetes mellitus 2. typu * komplikace epidemiologie MeSH
- diabetická retinopatie * etiologie komplikace MeSH
- diabetické nefropatie * MeSH
- hodnoty glomerulární filtrace MeSH
- ledviny MeSH
- lidé MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
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/1.73m2); 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 HbA1c (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.
Bethesda Diabetes Research Center Hoogeveen the Netherlands
Department General Practice and Elderly Care Amsterdam the Netherlands
Department of Internal Medicine Charles University 3rd Faculty of Medicine Prague Czech Republic
Department of Internal Medicine Nephrology Ziekenhuisgroep Twente Hospital Almelo the Netherlands
Department of Nephrology Cyril and Methodius University in Skopje Skopje Macedonia
Department of Nephrology Ghent University Hospital Ghent Belgium
Diabetes Center Institute for Clinical and Experimental Medicine Prague Czech Republic
Diabetespraxis Leipzig Germany
Diabetologische Schwerpunktpraxis Diabetologen Hessen Marburg Germany
Instituto de Investigacion Sanitaria de la Fundacion Jiménez Díaz UAM Madrid Spain
Mosaiques Diagnostics GmbH Hannover Germany
Orgenesis Germany GmbH Munich Germany
School of Cardiovascular and Metabolic Health University of Glasgow Glasgow UK
School of Health and Wellbeing University of Glasgow Glasgow UK
Steno Diabetes Center Copenhagen Herlev Denmark
University Clinic of Endocrinology Diabetes and Metabolic Disorders Skopje Macedonia
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