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1.
Invest Ophthalmol Vis Sci ; 48(9): 4002-6, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17724179

RESUMEN

PURPOSE: To determine the heritability of refractive error and familial aggregation of myopia and hyperopia in an elderly Old Order Amish (OOA) population. METHODS: Nine hundred sixty-seven siblings (mean age, 64.2 years) in 269 families were recruited for the Amish Eye Study in the Lancaster County area of Pennsylvania. Refractive error was determined by noncycloplegic manifest refraction. Heritability of refractive error was estimated with multivariate linear regression as twice the residual sibling-sibling correlation after adjustment for age and gender. Logistic regression models were used to estimate the sibling recurrence odds ratio (OR(s)). Myopia and hyperopia were defined with five different thresholds. RESULTS: The age- and gender-adjusted heritability of refractive error was 70% (95% CI: 48%-92%) in the OOA. Age and gender-adjusted OR(s) and sibling recurrence risk (lambda(s)), with different thresholds defining myopia ranged from 3.03 (95% CI: 1.58-5.80) to 7.02 (95% CI: 3.41-14.46) and from 2.36 (95% CI: 1.65-3.19) to 5.61 (95% CI: 3.06-9.34). Age and gender-adjusted OR(s) and lambda(s) for different thresholds of hyperopia ranged from 2.31 (95% CI: 1.56-3.42) to 2.94 (95% CI: 2.04-4.22) and from 1.33 (95% CI: 1.22-1.43) to 1.85 (95% CI: 1.18-2.78), respectively. Women were significantly more likely than men to have hyperopia. There was no significant gender difference in the risk of myopia. CONCLUSIONS: In the OOA, refractive error is highly heritable. Hyperopia and myopia aggregate strongly in OOA families.


Asunto(s)
Etnicidad/genética , Predisposición Genética a la Enfermedad , Hiperopía/genética , Miopía/genética , Carácter Cuantitativo Heredable , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Oportunidad Relativa , Pennsylvania , Población Blanca/genética
2.
J Cell Sci ; 117(Pt 14): 3049-59, 2004 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-15197244

RESUMEN

The hypothesis is tested that enhanced green fluorescent protein (EGFP) can be used to quantify the aqueous spaces of living cells, using as a model transgenic Xenopus rods. Consistent with the hypothesis, regions of rods having structures that exclude EGFP, such as the mitochondrial-rich ellipsoid and the outer segments, have highly reduced EGFP fluorescence. Over a 300-fold range of expression the average EGFP concentration in the outer segment was approximately half that in the most intensely fluorescent regions of the inner segment, in quantitative agreement with prior X-ray diffraction estimates of outer segment cytoplasmic volume. In contrast, the fluorescence of soluble arrestin-EGFP fusion protein in the dark adapted rod outer segment was approximately threefold lower than predicted by the EGFP distribution, establishing that the fusion protein is not equilibrated with the cytoplasm. Arrestin-EGFP mass was conserved during a large-scale, light-driven redistribution in which approximately 40% of the protein in the inner segment moved to the outer segment in less than 30 minutes.


Asunto(s)
Arrestina/metabolismo , Citoplasma/metabolismo , Proteínas Fluorescentes Verdes/metabolismo , Proteínas Recombinantes de Fusión/metabolismo , Células Fotorreceptoras Retinianas Bastones/citología , Animales , Animales Modificados Genéticamente , Arrestina/genética , Células CHO , Compartimento Celular , Cricetinae , Cricetulus , Adaptación a la Oscuridad , Proteínas Fluorescentes Verdes/genética , Luz , Microscopía Confocal , Proteínas Recombinantes de Fusión/genética , Células Fotorreceptoras Retinianas Bastones/metabolismo , Xenopus
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