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1.
PLoS One ; 7(6): e39300, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22723992

RESUMEN

Lattice degeneration of the retina is a vitreoretinal disorder characterized by a visible fundus lesion predisposing the patient to retinal tears and detachment. The etiology of this degeneration is still uncertain, but it is likely that both genetic and environmental factors play important roles in its development. To identify genetic susceptibility regions for lattice degeneration of the retina, we performed a genome-wide association study (GWAS) using a dense panel of 23,465 microsatellite markers covering the entire human genome. This GWAS in a Japanese cohort (294 patients with lattice degeneration and 294 controls) led to the identification of one microsatellite locus, D2S0276i, in the collagen type IV alpha 4 (COL4A4) gene on chromosome 2q36.3. To validate the significance of this observation, we evaluated the D2S0276i region in the GWAS cohort and in an independent Japanese cohort (280 patients and 314 controls) using D2S0276i and 47 single nucleotide polymorphisms covering the region. The strong associations were observed in D2S0276i and rs7558081 in the COL4A4 gene (Pc = 5.8 × 10(-6), OR = 0.63 and Pc = 1.0 × 10(-5), OR = 0.69 in a total of 574 patients and 608 controls, respectively). Our findings suggest that variants in the COL4A4 gene may contribute to the development of lattice degeneration of the retina.


Asunto(s)
Colágeno Tipo IV/genética , Predisposición Genética a la Enfermedad , Variación Genética , Degeneración Retiniana/genética , Desprendimiento de Retina/genética , Alelos , Estudios de Casos y Controles , Regulación de la Expresión Génica , Frecuencia de los Genes , Estudio de Asociación del Genoma Completo , Haplotipos , Humanos , Desequilibrio de Ligamiento , Repeticiones de Microsatélite , Polimorfismo de Nucleótido Simple , Serina Endopeptidasas/genética
2.
Nat Genet ; 42(8): 703-6, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20622879

RESUMEN

Behçet's disease is a chronic systemic inflammatory disorder characterized by four major manifestations: recurrent ocular symptoms, oral and genital ulcers and skin lesions. We conducted a genome-wide association study in a Japanese cohort including 612 individuals with Behçet's disease and 740 unaffected individuals (controls). We identified two suggestive associations on chromosomes 1p31.3 (IL23R-IL12RB2, rs12119179, P = 2.7 x 10(-8)) and 1q32.1 (IL10, rs1554286, P = 8.0 x 10(-8)). A meta-analysis of these two loci with results from additional Turkish and Korean cohorts showed genome-wide significant associations (rs1495965 in IL23R-IL12RB2, P = 1.9 x 10(-11), odds ratio = 1.35; rs1800871 in IL10, P = 1.0 x 10(-14), odds ratio = 1.45).


Asunto(s)
Síndrome de Behçet/genética , Estudio de Asociación del Genoma Completo , Estudios de Casos y Controles , Susceptibilidad a Enfermedades , Ojo , Humanos , Interleucina-10/genética , Oportunidad Relativa , Enfermedades de la Piel/genética , Turquía
3.
Mol Vis ; 16: 462-6, 2010 Mar 17.
Artículo en Inglés | MEDLINE | ID: mdl-20309402

RESUMEN

PURPOSE: To investigate whether the GLC1F locus is associated with normal tension glaucoma (NTG) in Japanese patients. METHODS: We recruited 242 unrelated Japanese subjects, including, 141 NTG patients and 101 healthy controls. The patients exhibiting a comparatively early onset were selected as they suggest that genetic factors may show stronger involvement. Genotyping and assessment of allelic diversity was performed on 11 highly polymorphic microsatellite markers in and around the GLC1F locus. RESULTS: Individuals carrying the 163 allele of D7S1277i had a statistically significant increased risk of NTG (p=0.0013, pc=0.016, OR=2.47, 95%CI=1.42-4.30). None of the other markers identified significant loci (pc>0.05) after Bonferroni's correction. CONCLUSIONS: These findings suggested that the genes in the GLC1F locus may be associated with the pathogenesis of NTG.


Asunto(s)
Pueblo Asiatico/genética , Sitios Genéticos , Glaucoma de Baja Tensión/genética , Repeticiones de Microsatélite/genética , Polimorfismo de Nucleótido Simple/genética , Estudios de Casos y Controles , Proteínas del Ojo , Femenino , Frecuencia de los Genes , Humanos , Masculino , Persona de Mediana Edad , Fenotipo , Proteínas Supresoras de la Señalización de Citocinas
4.
Hum Genet ; 122(2): 151-7, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17557158

RESUMEN

The collagen type Iota alpha Iota (COL1A1) gene encodes the extracellular matrix component, collagen, and resides in candidate MYP5 for high myopia on the chromosome 17q22-q23.3. This locus has recently been implicated in playing an important role in the pathogenesis of experimental myopia. We investigated the association of disruptions of COL1A1 gene with high myopia by analyzing the frequency of ten SNPs in a Japanese population of 330 subjects with high myopia of -9.25 D or less and 330 randomized controls without high myopia. Two SNPs (rs2075555 and rs2269336) were significantly associated with high myopia (P < 0.05, Pc < 0.1). Two different haplotype blocks in COL1A1 were observed by the pair-wise linkage disequilibrium between the SNPs. The frequency of GGC/GGC diplotype constructed by the three SNPs (rs2075555, rs2269336, rs1107946) was significantly high (OR = 1.6) and associated with high myopia (P = 0.028, Pc< 0.084). Together our results provide the first evidence for COL1A1 as a gene associated with high myopia.


Asunto(s)
Pueblo Asiatico/genética , Cromosomas Humanos Par 17/genética , Colágeno Tipo I/genética , Predisposición Genética a la Enfermedad/genética , Miopía/genética , Adulto , Secuencia de Bases , Cadena alfa 1 del Colágeno Tipo I , Bases de Datos Genéticas , Femenino , Frecuencia de los Genes , Humanos , Japón , Desequilibrio de Ligamiento , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular , Polimorfismo de Nucleótido Simple/genética , Análisis de Secuencia de ADN
5.
Eye Contact Lens ; 31(5): 225-30, 2005 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16163016

RESUMEN

PURPOSE: To investigate whether daily-disposable and 2-week disposable soft contact lenses are being used correctly. METHODS: The number of purchases made and brands selected by the 44,566 consumers who purchased daily-disposable and 2-week disposable soft contact lenses in Okada Eye Clinic institutions between April 1, 2002 and November 1, 2002 were monitored. From the 7,759 respondents to a survey conducted in the clinic between November 1, 2002 and March 31, 2003, the number of purchases made and brands selected by the 1,584 respondents, whose sales records could be traced, were analyzed in further detail. RESULTS: The total number of consumers purchasing daily-disposable soft contact lenses was 14,909, and their annual average purchase was 10.56 boxes. Most purchases were of two boxes followed by purchases of four and then six. Only 6.4% of consumers purchased 24 boxes at a time. Consumers purchasing four or fewer boxes at a time accounted for 37.8%. A total of 25,705 consumers purchased 2-week disposable soft contact lenses, with an annual average purchase of 6.37 boxes per consumer. Nineteen percent of the consumers purchased eight boxes of 2-week disposable soft contact lenses per year. Most consumers tended to purchase their contact lenses in even numbers for daily-disposable and 2-week disposable soft contact lenses. Johnson & Johnson Vision Care (Jacksonville, FL) was the most popular manufacturer. According to the survey, 86.6% of the 2-week disposable soft contact lens wearers followed instructions correctly, whereas 13.4% did not. That is, they exceeded the instructed 14 days of wear. CONCLUSIONS: Annual average purchases of daily-disposable and 2-week disposable soft contact lenses tended to be in even numbers and showed differences in their sales depending on contact lens brands. The results obtained from the survey and the actual sales records correlated.


Asunto(s)
Lentes de Contacto de Uso Prolongado/estadística & datos numéricos , Lentes de Contacto Hidrofílicos/estadística & datos numéricos , Equipos Desechables , Soluciones para Lentes de Contacto , Humanos , Japón , Satisfacción del Paciente , Prescripciones/estadística & datos numéricos , Ajuste de Prótesis
6.
Eye Contact Lens ; 31(5): 231-7, 2005 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16163017

RESUMEN

PURPOSE: To investigate the relationships between contact lens wearers, their lens wear, and treatment to provide correct instructions for use. METHOD: A total of 55,056 consumers, who purchased contact lenses in the two institutions of Okada Eye Clinic in the 1-year period from April 1, 2002 to March 31, 2003, were analyzed with regard to age, sex, contact lens brands, treatments and lens-solution combinations purchased, and patterns of wear. RESULTS: The 2-week frequent-replacement soft contact lenses were the most popular type of contact lens, and most wearers of these lenses were those in their 20s. Saline solution was the treatment purchased most often with conventional soft contact lenses. Hard contact lens wearers tended to buy treatments of the same brand as their hard contact lenses. Hydrogen peroxide was the most purchased product with the 2-week frequent-replacement soft contact lenses and multipurpose treatment the next, especially with consumers in their 20s. There were no significant sex gaps. CONCLUSIONS: The survey was conducted on a wide age range of more than 50,000 people and can be assumed to accurately reflect the tendencies of contact lens wearers in Japan. The results clearly show the actual use of contact lenses and treatments of each age group and will be useful in instructing wearers to the correct use of their treatments.


Asunto(s)
Lentes de Contacto/estadística & datos numéricos , Adolescente , Adulto , Distribución por Edad , Anciano , Anciano de 80 o más Años , Niño , Preescolar , Soluciones para Lentes de Contacto , Femenino , Humanos , Japón , Masculino , Persona de Mediana Edad , Ajuste de Prótesis , Distribución por Sexo
7.
FEBS Lett ; 542(1-3): 105-8, 2003 May 08.
Artículo en Inglés | MEDLINE | ID: mdl-12729907

RESUMEN

The effects of isoproterenol on sialidase activity in rat cardiomyocytes were examined. Administration of isoproterenol to rats (0.2 or 2 mg/kg body weight) produced an increase in sialidase activity in total membrane fraction of heart tissue within 120 min (121+/-13% of the control at 120 min after administration of 0.2 mg isoproterenol/kg, n=5, P<0.05). Sialidase activity in cardiomyocyte-derived H9c2 cells was also increased by treatment with isoproterenol (10 microM) for 60 min. The effect of isoproterenol on sialidase activity was amplified by the addition of 3-isobutyl-1-methylxanthine (IBMX). Sialidase activity in H9c2 cells was elevated by treatment with dibutyryl cAMP plus IBMX without isoproterenol. The content of N-acetylneuraminic acid in cells decreased by 22% after treatment with isoproterenol plus IBMX. These results suggest that sialidase activity in rat cardiomyocytes is regulated by beta-adrenergic stimulators via a cAMP-dependent process. The increased activity of sialidase may account for the reduction of sialic acid content of cells.


Asunto(s)
Agonistas Adrenérgicos beta/farmacología , Isoproterenol/farmacología , Miocardio/enzimología , Miocitos Cardíacos/enzimología , Neuraminidasa/metabolismo , 1-Metil-3-Isobutilxantina/farmacología , Animales , Línea Celular , Relación Dosis-Respuesta a Droga , Sinergismo Farmacológico , Activación Enzimática , Cinética , Masculino , Miocitos Cardíacos/química , Miocitos Cardíacos/efectos de los fármacos , Ácido N-Acetilneuramínico/análisis , Inhibidores de Fosfodiesterasa/farmacología , Ratas , Ratas Sprague-Dawley
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