4.6 Article

P-selectin Plasma Levels and Genetic Variant Associated With Diabetic Retinopathy in African Americans

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AMERICAN JOURNAL OF OPHTHALMOLOGY
卷 159, 期 6, 页码 1152-1160

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajo.2015.03.008

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资金

  1. National Eye Institute, Bethesda, Maryland [K12-EY16335]
  2. Research to Prevent Blindness Career Development Award and William & Mary Greve Special Scholar Award, New York, New York
  3. Harvard Catalyst \ The Harvard Clinical and Translations Science Center Faculty Fellowship, Boston, Massachusetts
  4. Massachusetts Lions Eye Research Fund, Abington, Massachusetts
  5. Eleanor and Miles Shore Fellowship, Boston, Massachusetts
  6. Sara Elizabeth O'Brien Trust, Boston, Massachusetts
  7. National Heart, Lung and Blood Institute [HHSN268201300046C, HHSN268201300047C, HHSN268201300048C, HHSN268201300049C, HHSN268201300050C]
  8. National Institute on Minority Health and Health Disparities, Bethesda, Maryland

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PURPOSE: To report the prevalence and risk factors for retinopathy in African Americans with impaired fasting glucose (IFG) and type 2 diabetes in the Jackson Heart Study and to determine if P-selectin plasma levels are independently associated with retinopathy in this population. DESIGN: Prospective, cross-sectional observational study. METHODS: SETTING: Community-based epidemiologic study. STUDY POPULATION: Total of 629 patients with type 2 diabetes and 266 participants with impaired fasting glucose. OBSERVATION PROCEDURES: Bilateral, 7-field fundus photographs were scored by masked readers for diabetic retinopathy (DR) level. Covariate data including P-selectin plasma levels and genotypes were collected in a standardized fashion. MAIN OUTCOME MEASURES: Association between risk factors, including P-selectin plasma levels and genotypes, and retinopathy. RESULTS: The prevalences of any retinopathy among participants with IFG and type 2 diabetes were 9.4% and 32.4%, respectively. Among those with type 2 diabetes, in multivariate models adjusted for age, sex, and other traditional risk factors, higher P-selectin levels were associated with any DR (odds ratio = 1.11, 95% confidence interval = 1.02-1.21, P =.02) and proliferative DR (odds ratio = 1.23, 95% confidence interval = 1.03-1.46, P =.02). To further investigate the relationship between P-selectin and DR, we examined the association between P-selectin genotype and DR. Minor allele homozygotes for the variant rs6128 were less likely to develop DR (P after Bonferroni correction = 0.03). CONCLUSIONS: Both serologic and genetic data show an association between P-selectin and DR in the Jackson Heart Study. If confirmed in other studies, this association may provide insight into the pathogenesis of retinopathy. (C) 2015 by Elsevier Inc. All rights reserved.)

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