Relationship Between Diabetic Retinopathy Stages and Risk of Major Lower-Extremity Arterial Disease in Patients With Type 2 Diabetes

Author:

Foussard Ninon1ORCID,Saulnier Pierre-Jean234ORCID,Potier Louis567ORCID,Ragot Stéphanie234,Schneider Fabrice28,Gand Elise3,Monlun Marie1ORCID,Baillet-Blanco Laurence1,Velho Gilberto7ORCID,Marre Michel679ORCID,Roussel Ronan567ORCID,Rigalleau Vincent11011,Mohammedi Kamel11012ORCID,Hadjadj Samy13ORCID

Affiliation:

1. Hôpital Haut-Lévêque, Département d’Endocrinologie, Diabétologie, Nutrition, Pessac, Bordeaux, France

2. Université de Poitiers, UFR de Médecine et Pharmacie, Poitiers, France

3. CHU de Poitiers, Centre d’Investigation Clinique, Poitiers, France

4. INSERM, CIC 1402, Poitiers, France

5. Assistance Publique–Hôpitaux de Paris, Bichat Hospital, Département de Diabétologie, Endocrinologie, Nutrition, Paris, France

6. Université de Paris, Paris, France

7. Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, Paris, France

8. Département de Chirurgie Vasculaire, CHU de Poitiers, Poitiers, France

9. CMC Ambroise Paré, Neuilly-sur-Seine, France

10. Université de Bordeaux, UFR de Médecine, Bordeaux, France

11. INSERM U1219 “Bordeaux Population Health,” Bordeaux, France

12. INSERM U1034, Biologie des Maladies Cardiovasculaires, Bordeaux, France

13. Institut du Thorax, INSERM, CNRS, Université de Nantes, Nantes, France

Abstract

OBJECTIVE We evaluated the association between diabetic retinopathy stages and lower-extremity arterial disease (LEAD), its prognostic value, and the influence of potential contributors to this relationship in a prospective cohort of patients with type 2 diabetes. RESEARCH DESIGN AND METHODS Diabetic retinopathy was staged at baseline as absent, nonproliferative, or proliferative. A Cox regression model was fitted in order to compute the hazard ratio (HR) (95% CI) for major LEAD (lower-limb amputation or revascularization) during follow-up by baseline retinopathy stages. The retinopathy-LEAD association was assessed in subgroups by age, sex, diabetes duration, HbA1c, systolic blood pressure, diabetic kidney disease, smoking, and macrovascular disease at baseline. The performance of retinopathy in stratifying LEAD risk was assessed by using the C statistic, integrated discrimination improvement (IDI), and net reclassification improvement (NRI). RESULTS Among 1,320 participants without a history of LEAD at baseline, 94 (7.1%) developed a major LEAD during a 7.1-year median follow-up (incidence rate 9.6 per 1,000 person-years [95% CI 7.8–11.7]). The LEAD incidence rate (per 1,000 person-years) increased as retinopathy worsened: it was 5.5 (95% CI 3.9–7.8) in participants in whom retinopathy was absent, 14.6 (11.1–19.3) in those with nonproliferative retinopathy, and 20.1 (11.1–36.3) in those with proliferative retinopathy. Nonproliferative retinopathy (adjusted HR 2.31 [95% CI 1.43–3.81], P = 0.0006) and proliferative retinopathy (3.14 [1.40–6.15], P = 0.007) remained associated with major LEAD. No heterogeneity was observed across subgroups. Retinopathy enhanced the C statistic (+0.023 [95% CI 0.003–0.044], P = 0.02), IDI (0.209 [0.130–0.321], P < 0.001), and NRI (0.562 [0.382–0.799], P < 0.001) values for risk of LEAD, beyond traditional risk factors. CONCLUSIONS An independent dose-response relationship was identified between diabetic retinopathy stages and major LEAD. Retinopathy yielded incremental prognostic information for stratifying risk of LEAD, suggesting its usefulness as a predictor of LEAD.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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