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1From the Doheny Eye Institute and the Department of Ophthalmology, and the 2Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California; and the 3Department of Ophthalmology and Visual Sciences, University of Wisconsin, School of Medicine and Public Health, Madison, Wisconsin.
| Abstract |
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METHODS. This was a population-based, cross-sectional study comprising 6357 Latinos, 40 years of age and older, from six census tracts in La Puente, Los Angeles, California. An interviewer-administered questionnaire assessed sociodemographic factors and medical history. Color fundus photographs were taken and graded in a masked manner according to a modified Airlie House Classification Grading System. Participants underwent a physical examination that included height, weight, blood pressure, random serum glucose, and glycosylated hemoglobin measurements. Univariate and multivariate logistic regression analyses were used to assess associations between sociodemographic and clinical characteristics and retinopathy in persons without diabetes.
RESULTS. The prevalence of retinopathy among individuals without diabetes in the Los Angeles Latino Eye Study (LALES) population was 6.6% (95% confidence interval 5.9%–7.4%). Stepwise logistic regression indicated that stage II hypertension (World Health Organization 2003 Guidelines), male gender, current smoking status, and obesity (body mass index
30 kg/m2) were associated with retinopathy (odds ratio = 4.3, 1.6, 1.4, and 1.3, respectively). No statistically significant associations with retinopathy were present for Native American ancestry; country of origin; health insurance status; history of cardiovascular disease; or history of aspirin, oral contraceptive, or hormone replacement therapy.
CONCLUSIONS. The data suggest that the prevalence of retinopathy in nondiabetic individuals among Latinos of primarily Mexican ancestry is significant. Independent risk indicators for retinopathy in the study population are hypertension, male gender, current smoking status, and obesity.
Studies have been undertaken to investigate factors contributing to incident retinopathy as well, including blood glucose, hypertension, age, and abdominal obesity.5 14 15 Separately, others have associated the presence of retinopathy in persons without diabetes with an increased incidence of stroke and stroke-related mortality, decreased renal function, hypertension, and diabetes.16 17 18 19 20 Together, these findings support the theory that cardiovascular risk factors are significant in the development of nondiabetic retinopathy, and that retinopathy may, in turn, be an independent predictive marker of cardiovascular, cerebrovascular, and other diseases.
Only one report of nondiabetic retinopathy in adult Latinos has been published to date21 This study of adult Latinos living in Arizona reported a higher prevalence of nondiabetic retinopathy than that in other population-based studies and also reported a lack of association between hypertension and retinopathy in its population. The Los Angeles Latino Eye Study (LALES) is a large, population-based survey designed to evaluate the prevalence of ocular disease in adult Latinos from six census tracts in La Puente, California. One of its primary goals is to obtain an accurate estimate of the prevalence of disease that is generalizable to Mexican-Americans in the United States.22 The purpose of our study was to assess the prevalence and relationship of retinopathy to sociodemographic and clinical characteristics in our population-based cohort of adult Latinos in Los Angeles without diabetes.
| Subjects and Methods |
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Clinical Procedures
Participants underwent interviews, ophthalmic examinations, and brief physical examinations.22 Interview questions included inquiries regarding sociodemographic factors such as age, gender, country of birth, degree of acculturation, Native American ancestry, and possession of health insurance. Medical history queries included a history of atherosclerotic disease/myocardial infarction or stroke; use of aspirin, oral contraceptives, or hormone replacement therapy; and history of alcohol and tobacco use. During the ophthalmic examination, visual acuity was measured with the revised Early Treatment of Diabetic Retinopathy Study (ETDRS) charts 1, 2, and 3, and Lea symbol charts were used for the illiterate participants. Fundus photography was performed (TRC 50EX Retinal Camera; Topcon Corp. of America, Paramus, NJ, with Ektachrome 100 film; Eastman-Kodak, Rochester, NY). Three color fundus photographs were taken in all participants without diabetes: stereo fundus 30° photographs centered on the disc (Diabetic Retinopathy Study [DRS] standard field 1) and macula (DRS standard field 2) and a nonstereo photograph temporal to, but including the fovea (DRS standard field 3).23 Additional fundus photographs were taken if any lesions were found outside these fields. The physical examination included weight, height, and blood pressure measurements. Participants removed excess clothing and shoes, and weight measurements were recorded to the nearest 0.1 kg and height to the nearest 0.5 cm. Blood pressure was measured with participants seated with both feet flat on the floor and after they had been quiet for at least 5 minutes. Their right arms were bared, supported, and positioned at heart level, and measurements were taken using a sphygmomanometer (Random Zero; Hawksley & Sons Ltd., West Sussex, UK) with a Baum cuff of appropriate size. Twenty minutes later, the blood pressure measurement was repeated. Random blood glucose and glycosylated hemoglobin were measured (B-Glucose Analyzer; Hemocue Inc., Lake Forest, CA, and the DCA 2000+ System; Bayer Corp., Tarrytown, NY, respectively). Other clinical procedures are described in detail elsewhere.22
Definition of Diabetes Mellitus
Participants were categorized into three groups: no diabetes, questionable diabetes, and definite diabetes. They were identified as being without diabetes mellitus if they had all the following: (1) no history of diabetes; (2) a hemoglobin A1c level less than 6.5%; and (3) random blood glucose less than 200 mg/dL. Participants who had all the following were considered to have questionable diabetes: (1) no history of diabetes; (2) hemoglobin A1c level of between 6.5% and 6.9%; and (3) random blood glucose less than 200 mg/dL. As described elsewhere,24 participants were considered to have definite diabetes if they had any one of the following: (1) history of diabetes with treatment by oral hypoglycemic medications, insulin, or diet alone; (2) hemoglobin A1c of 7.0% or higher; or (3) random blood glucose of 200mg/dL or higher.
Definition and Grading of Nondiabetic Retinopathy
Fundus photographs were used to determine the presence of retinopathy. Participants were defined as having retinopathy if any one of the following lesions were present in either eye: retinal microaneurysms, blot hemorrhages, cotton-wool spots, hard exudates, intraretinal microvascular abnormalities, venous beading, new retinal vessels, preretinal or vitreous hemorrhages, or macular edema. Graders identified lesions as "definite" if they were at least 90% certain the lesion was present and as "questionable" if they could make the determination with only 50% to 89% certainty. Retinopathy from an otherwise identifiable etiology including artery and vein occlusions, macroaneurysms, retinal cholesterol emboli, and epiretinal membranes were marked separately. Grading was performed at the Ocular Epidemiology Grading Center at the University of Wisconsin, Madison, Wisconsin, and the graders were masked to the diabetic status of the participants.
Other Definitions
Hypertension was defined according to The Seventh Report of the Joint Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC7) criteria. The categories are normal, less than 120 mm Hg systolic blood pressure (SBP) and less than 80 mm Hg diastolic blood pressure (DBP); prehypertension, 120 to 139 mm Hg SBP or 80 to 89 mm Hg DBP; stage I hypertension, 140 to 159 mm Hg SBP or 90 to 99 mm Hg DBP; and stage II hypertension,
160 mm Hg SBP or
100 mm Hg DBP.25 Definitions of sociodemographic factors are described in detail elsewhere.26 Relevant to this study, alcohol use was defined as the following: nondrinker (less than 12 drinks in the past), ex-drinker (at least 12 drinks in the past with no alcoholic beverage use in the past year), partial drinker (fewer than 5 drinks of beer, wine, or hard liquor per day), and regular drinker (at least 5 drinks of beer, wine, or hard liquor per day). A participant was described as a nonsmoker (smoking no more than 100 cigarettes in the past), an ex-smoker (>100 cigarettes in the past and not currently smoking), or a current smoker (>100 cigarettes and smoking at the time of the questionnaire). Aspirin, oral contraceptives, and hormone replacement use was noted if participants reported taking the respective medications for at least the past 6 months.
Statistical Analysis
Prevalence of nondiabetic retinopathy was calculated as the ratio of the number of participants without diabetes who have evidence of definite retinopathy in either eye to the total number of participants without diabetes. Univariate logistic regression was used to assess the association of sociodemographic and cardiovascular factors with retinopathy. Multiple logistic regression analyses with forward step-wise selection were used to evaluate the independent relationship of significant variables (using a P
0.5 criterion) with retinopathy. All confidence intervals (CIs) presented are 95%, and all analyses were conducted at a less than 0.05 significance level (Statistical Analysis System 8; SAS Institute Inc., Cary, NC).
| Results |
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30 k/m2) was also a significant risk factor for retinopathy (OR = 1.3, P = 0.04). Waist-hip ratio was not a significant risk factor by univariate analysis (data not shown). In addition, a history of myocardial infarction and stroke did not appear to be associated risk factors, nor did the use of aspirin, oral contraceptives, or hormone replacement therapy.
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| Discussion |
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Although certain systemic risk factors for vascular disease including hypertension, male gender, current smoking status, and obesity were significantly and independently associated with nondiabetic retinopathy by univariate and stepwise multivariate logistic regression analysis, other factors, such as history of atherosclerotic disease, myocardial infarction, stroke, and history of aspirin, oral contraceptive, or hormone replacement therapy were not significantly associated. In contrast to the Proyecto VER finding, which showed a lack of association between hypertension status and retinopathy,21 our finding that hypertension is significantly associated with retinopathy is consistent with that of several other studies.1 2 4 10 Male gender was also significantly associated with prevalent retinopathy both by univariate and stepwise logistic regression analysis. The Beaver Dam Eye Study reported that after adjustment for age, men had a significantly higher prevalence of retinopathy than did women,4 but the Hoorn study, which did not control for age, reported that gender was not a significant risk factor in prevalent retinopathy.10 Notably, both subsequent incidence studies report no statistically significant male gender risk after adjustment for age.5 15 Incident studies in our population may be needed to elucidate this association further.
Prior studies have adjusted for smoking status in the multivariate analysis of risk factors of retinopathy,1 13 but we found that current smoking status is itself independently associated with prevalent retinopathy in our population. The Hoorn Study of Incident Retinopathy showed that cigarette smokers and ex-smokers had higher but nonsignificant odds ratios compared with those of individuals who had never smoked.5 10 It is possible that their inclusion of ex-smokers with current smokers diluted the significance of the difference in the comparison to current smokers.
Although we did not find a significant association between older age and prevalent retinopathy, there was a significant trend across increasing age groups. This lack of significant association was consistent with findings from some studies of prevalent and incident retinopathy5 10 15 ; however, the 5-year incidence study in the Blue Mountains Eye Study population reported a significant association with increasing age.14 Notably, age was a significant risk factor for arteriolar narrowing and arteriovenous nicking.15 Other factors thought to have an effect on retinal vasculature, such as aspirin, oral contraceptive, and hormone replacement use were investigated. In a recent study, regular aspirin use has been associated with wider retinal arteriolar diameter,27 but we found no significant association with aspirin and retinopathy in our population. Further evaluation of the affects of age and medication on retinal microvasculature is warranted.
One of the most clinically useful implications to arise from these population studies is the association of retinopathy with systemic diseases, including coronary heart disease, incident congestive heart failure, clinical stroke and stroke mortality, nephropathy, carotid artery thickening, and incident diabetes.9 16 17 18 19 28 29 Of note, we did not find a significant association with patient-reported histories of atherosclerotic disease, myocardial infarction, or stroke, but objective measurements such as ultrasound determination of carotid artery intima–media thickening or medical chart documentation of disease may be needed to detect the subclinical or clinical cardiovascular disease in our population and its relationship to retinopathy. In addition, it will be useful to examine incident cardiovascular disease and its relationship to previously documented retinopathy.
To characterize better the type of retinopathy observed in our study, we reported the frequency of specific retinal lesions and their laterality. The most common lesions were microaneurysms and retinal hemorrhages, and most were unilateral. This is consistent with the Beaver Dam Eye Study findings that when retinopathy was present, it was more likely to be bilateral (60.1%) in persons with known diabetes mellitus compared with those without diabetes (9.5%, P < 0.0001).30 There is evidence that nondiabetic retinal lesions are more ephemeral than are diabetic retinal lesions. In the Blue Mountains Eye Study, although there was a 10% incidence of nondiabetic retinopathy over 5 years, there was also a 72% regression in baseline lesions.14 Thus, given the cross-sectional nature of this report, it would be important to examine the progression and profile of our lesions in a follow-up incidence study. In addition, it would be useful to study the correlation between the incidence of retinopathy and the development of visual impairment, to identify visually significant and possibly treatable retinal lesions.
A limitation to our study is the use of random blood glucose and hemoglobin A1c levels, rather than oral glucose tolerance testing, in determining the definition of diabetes. A recent study by the Diabetes Prevention Program used oral glucose tolerance testing to identify a 7.9% prevalence of retinopathy in participants with subdiabetic levels of glycemia.11 It is likely that this subdiabetic cohort was included in our study population, although they were not specifically identified by oral glucose tolerance testing. However, as noted in prior studies, a hemoglobin A1c level of 7% or higher has good sensitivity and specificity when compared with results of oral glucose tolerance testing.24 31 Definitions similar to ours were used by other large population-based studies, including the Beaver Dam Eye Study and Proyecto VER, allowing us to compare our findings accordingly.4 21 Another limitation is the possible misclassification of subtle retinal lesions. Although we were careful to exclude retinal lesions of identifiable etiologies, including artery and vein occlusions, macroaneurysms, retinal cholesterol emboli, and epiretinal membranes, it is possible that graders could have missed small branched vein occlusions that appear clinically similar to nondiabetic retinopathy. Finally, because we graded our retinopathy based on the three retinal field photographs described earlier, we cannot exclude the possibility that there were lesions outside of these fields that were not included in our retinopathy classification.
In conclusion, the results of this study demonstrate that the prevalence of retinopathy in nondiabetic participants in the LALES is similar to that reported by other large population-based studies. We report that hypertension, male gender, history of current smoking status, and greater body mass index are significantly associated with prevalent retinopathy. In addition, we elucidate the unilateral nature of retinal lesions found in nondiabetic retinopathy. Long-term follow-up studies are needed to determine the visual and systemic significance of nondiabetic retinopathy in the LALES population.
| Appendix 1 |
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Battelle Survey Research Center, St. Louis, MO: Sonia Chico, Lisa John, Michael Preciado, and Karen Tucker.
Ocular Epidemiology Grading Center, University of Wisconsin, Madison, WI: Ronald Klein.
| Footnotes |
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Supported by National Eye Institute Grants U10-EY11753 and EY03040 and an unrestricted grant from Research to Prevent Blindness.
Submitted for publication February 16, 2007; revised May 4, 2007; accepted June 11, 2007.
Disclosure: J.R. Chao, None; M.-Y. Lai, None; S.P. Azen, None; R. Klein, None; R. Varma, None
The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C.
1734 solely to indicate this fact.
Corresponding author: Rohit Varma, Doheny Eye Institute, 1450 San Pablo Street, DEI Suite 4900, Los Angeles, CA 90033; rvarma{at}usc.edu.
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