Adverse association between diabetic retinopathy and cardiac structure and function

David Aguilar, D. Michael Hallman, Linda B. Piller, Barbara E.K. Klein, Ronald Klein, Richard B. Devereux, Donna K. Arnett, Victor H. Gonzalez, Craig L. Hanis

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Background: Recent work has demonstrated a link between retinopathy, a marker of microvascular disease, and the development of heart failure, a finding particularly relevant in individuals with diabetes. Our objective was to assess the relationship between retinopathy and cardiac structure and function in a cohort of individuals with type 2 diabetes mellitus. Methods: Stereoscopic fundus photography of 7 standard fields was obtained in 531 Mexican American adults with type 2 diabetes mellitus recruited as sibships from Starr County, Texas. Retinopathy was centrally scored and classified as no retinopathy, early nonproliferative diabetic retinopathy, moderate to severe nonproliferative diabetic retinopathy, or proliferative diabetic retinopathy. Echocardiography was used to assess cardiac structure and function. Multilevel mixed models were used to assess associations of clinical and echocardiographic variables with retinopathy while accounting for correlations among siblings. Results: More severe diabetic retinopathy was associated with the presence of hypertension, previous cardiovascular disease, longer duration of diabetes, elevated glycosylated hemoglobin, and greater albuminuria. With worsening severity of diabetic retinopathy, left ventricular (LV) mass and left atrial dimension increased, and LV ejection fraction and LV fractional shortening decreased, independent of potential confounding variables. Conclusions: More severe diabetic retinopathy was associated with worse cardiac structure and function by echocardiography independent of potential confounding variables. These data suggest a possible microvascular contribution to the development of diabetes-associated cardiac enlargement and dysfunction. Alternatively, common pathways may be leading to both disorders.

Original languageEnglish
Pages (from-to)563-568
Number of pages6
JournalAmerican Heart Journal
Volume157
Issue number3
DOIs
StatePublished - Mar 2009

Bibliographical note

Funding Information:
This study was supported in part by the National Heart, Lung, and Blood Institute Family Blood Pressure Program (HL54504), the National Eye Institute (EY12386), and an NIH Mentored Clinical Investigator Award (5K12RR017665-05) to Dr Aguilar.

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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