Familial Aggregation of Severity of Diabetic Retinopathy in Mexican Americans From Starr County, Texas
- D. Michael Hallman, PHD1,
- J. Charles Huber, Jr., PHD1,
- Victor H. Gonzalez, MD2,
- Barbara E.K. Klein, MD3,
- Ronald Klein, MD3 and
- Craig L. Hanis, PHD1
- 1Human Genetics Center, University of Texas Health Science Center at Houston, Houston, Texas
- 2Valley Retina Institute, McAllen, Texas
- 3Department of Ophthalmology and Visual Sciences, Madison Medical School, The University of Wisconsin, Madison, Wisconsin
- Address correspondence and reprint requests to Craig L. Hanis, The University of Texas Health Science Center at Houston, P.O. Box 20186, Houston, TX 77225. E-mail: craig.l.hanis{at}uth.tmc.edu
Abstract
OBJECTIVE—Diabetic retinopathy is a major cause of blindness. To determine whether retinopathy itself or only its severity aggregates in families, we examined the occurrence and severity of diabetic retinopathy in Mexican-American siblings with type 2 diabetes.
RESEARCH DESIGN AND METHODS—Using stereoscopic fundus photography of seven standard fields, we measured retinopathy in 656 type 2 diabetic patients from 282 Mexican-American families from Starr County, Texas. Retinopathy severity was scored using the Early Treatment of Diabetic Retinopathy Study system and classified as no retinopathy, early nonproliferative diabetic retinopathy (NPDR-E), moderate-to-severe nonproliferative diabetic retinopathy (NPDR-S), or proliferative diabetic retinopathy (PDR).
RESULTS—Of 249 siblings of randomly selected probands with retinopathy, 169 (67.9%) had retinopathy, compared with 95 of 125 siblings of unaffected probands (76.0%; P = 0.11). Proband retinopathy class was associated (P = 0.03) with sibling retinopathy class, with significant odds ratios (ORs) for NPDR-E versus no retinopathy (OR 0.57 [95% CI 0.35–0.93]) and PDR versus NPDR-E (2.02 [1.13–3.63]); the contrast of NPDR-S versus NPDR-E approached significance (1.78 [0.99–3.20]). With the more severe classes (PDR and NPDR-S) combined in one group and the less severe ones (none and NPDR-E) in another, more severe proband retinopathy was associated with more severe sibling retinopathy (1.72 [1.03–2.88]).
CONCLUSIONS—More severe diabetic retinopathy showed evidence of familial aggregation, but the occurrence of diabetic retinopathy per se did not. The factors involved in the onset of diabetic retinopathy may differ from those involved in its progression to more severe forms.
- NPDR-E, early nonproliferative diabetic retinopathy
- NPDR-S, moderate-to-severe nonproliferative diabetic retinopathy
- PDR, proliferative diabetic retinopathy
Footnotes
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A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
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- Accepted January 31, 2005.
- Received September 15, 2004.
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