| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
ORIGINAL ARTICLES |
From the University of Medicine and Dentistry (M.S.R.), New Jersey Medical School, Institute of Ophthalmology and Visual Science, Newark, New Jersey; Psychiatry Service (A.R.), Veterans Administration Medical Center, East Orange, New Jersey; and Department of Mathematics (M.A.), Kean University, Union, New Jersey.
Address correspondence and reprint requests to Monique S. Roy, Department of Ophthalmology, UMDNJ-New Jersey Medical School, 90 Bergen Street, Room 6164, Newark, NJ 07101-1709. E-mail address: Roymo{at}umdnj.edu
Objective: To examine longitudinal data about depression in relationship to glycemic control and as a risk factor for diabetic retinopathy (DR). Depression is a common psychiatric disorder among diabetic persons and has been shown in cross-sectional studies to be associated with the vascular complications of diabetes.
Methods: A total of 483 African-American patients with Type 1 diabetes had a baseline examination and 6-year follow-up examination. Evaluations at both visits included administering the Beck Depression Inventory (BDI), a detailed ophthalmologic examination, retinal photographs, and measurement of glycosylated hemoglobin as an index of glycemic control. Six-year progression of DR between baseline and follow-up visits was evaluated from the change in retinopathy severity using the Early Treatment of Diabetic Retinopathy Study grading scale.
Results: Patients with high BDI scores at both baseline and 6-year follow-up visits had significantly higher baseline glycosylated hemoglobin values (p = .01), and were more likely to show progression of DR (odds ratio (OR) = 2.44; 95% confidence interval (CI): 1.01–5.88; p = .049) and progression to proliferative diabetic retinopathy (PDR) (OR = 3.19; 95% CI: 1.30–7.87; p = .01) than patients with low BDI scores at both visits. This was independent of baseline medical risk factors for DR.
Conclusion: Six-year longitudinal data indicate that depression is significantly associated with both poor glycemic control and higher 6-year progression to PDR in African-Americans with Type 1 diabetes.
Key Words: depression diabetes glycemic control retinopathy
Abbreviations: AER = albumin excretion rate; BDI = Beck Depression Inventory; CI = confidence interval; DR = diabetic retinopathy; HbA1C = hemoglobin A1C; HPA = hypothalamo-pituitary-adrenal; OR = odds ratio; PDR = proliferative diabetic retinopathy.
This article has been cited by other articles:
![]() |
M. S. Roy and M. N. Janal High Caloric and Sodium Intakes as Risk Factors for Progression of Retinopathy in Type 1 Diabetes Mellitus Arch Ophthalmol, January 1, 2010; 128(1): 33 - 39. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Echeverry, P. Duran, C. Bonds, M. Lee, and M. B. Davidson Effect of Pharmacological Treatment of Depression on A1C and Quality of Life in Low-Income Hispanics and African Americans With Diabetes: A randomized, double-blind, placebo-controlled trial Diabetes Care, December 1, 2009; 32(12): 2156 - 2160. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Roy, D. M. Hallman, Y.-P. Fu, M. Machado, and C. L. Hanis Assessment of 193 Candidate Genes for Retinopathy in African Americans With Type 1 Diabetes Arch Ophthalmol, May 1, 2009; 127(5): 605 - 612. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Gendelman, J. K. Snell-Bergeon, K. McFann, G. Kinney, R. Paul Wadwa, F. Bishop, M. Rewers, and D. M. Maahs Prevalence and Correlates of Depression in Individuals With and Without Type 1 Diabetes Diabetes Care, April 1, 2009; 32(4): 575 - 579. [Abstract] [Full Text] [PDF] |
||||
![]() |
J Ding, N Patton, I J Deary, M W J Strachan, F G R Fowkes, R J Mitchell, and J F Price Retinal microvascular abnormalities and cognitive dysfunction: a systematic review Br J Ophthalmol, August 1, 2008; 92(8): 1017 - 1025. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |