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首页> 外文期刊>American Journal of Ophthalmology: The International Journal of Ophthalmology >Risk factors associated with reticular pseudodrusen versus large soft drusen
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Risk factors associated with reticular pseudodrusen versus large soft drusen

机译:网状假性软疣与大面积软疣相关的危险因素

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Purpose To investigate genetic, environmental, and systemic risk factors in prospectively identified subjects with the age-related macular degeneration (AMD) phenotypes of (1) reticular pseudodrusen without large soft drusen and (2) large soft drusen without reticular pseudodrusen. Design Prospective case-case comparison. Methods In a clinical practice setting, patients with AMD were sequentially screened using clinical examination and scanning laser ophthalmoscopy imaging to prospectively identify subjects (n = 73) with the phenotypes of (1) reticular pseudodrusen without large soft drusen (n = 30) or (2) large soft drusen without reticular pseudodrusen (n = 43). Subjects were genotyped for 2 alleles associated with AMD, age-related maculopathy susceptibility 2 (ARMS2) and complement factor H (CFH). A questionnaire was administered to collect history of smoking, hypertension, diabetes, and hyperlipidemia, as well as personal and family history of AMD. Results The reticular pseudodrusen group was older (median age 87 vs 81 years, P =.04) and had more female subjects (83.3% vs 48.8%, P =.003), later ages of AMD onset (83 vs 70 years, P =.0005), and a greater frequency of hypertension (76.7% vs 55.8%, P =.08). No significant differences were found in the distribution of the ARMS2 risk allele (P =.4) between the reticular pseudodrusen (homozygous = 20.0%; heterozygous = 56.7%) and large soft drusen (homozygous = 19.0%; heterozygous = 42.9%) phenotypes, or in the distribution of the CHF risk allele (P =.7) between the reticular pseudodrusen (homozygous = 26.7%; heterozygous = 56.7%) and large soft drusen (homozygous = 21.4%; heterozygous = 66.7%) phenotypes. Conclusions The reticular pseudodrusen phenotype was associated with increased age, later age of AMD onset, and female sex.
机译:目的探讨前瞻性鉴定的具有年龄相关性黄斑变性(AMD)表型的受试者的遗传,环境和系统性危险因素,这些表型为(1)没有大的软性玻璃膜疣的网状假性玻璃疣和(2)没有大的软性玻璃膜疣的大性软性玻璃疣。设计前瞻性案例与案例的比较。方法在临床实践中,依次采用临床检查和扫描激光眼底镜检查对AMD患者进行筛查,以前瞻性鉴定具有(1)网状假性软疣但无大的软性玻璃膜疣(n = 30)或( 2)大的软性玻璃膜疣,无网状假性鼻疣(n = 43)。对受试者的2个与AMD相关的等位基因,年龄相关性黄斑病变易感性2(ARMS2)和补体因子H(CFH)进行基因分型。进行了问卷调查以收集吸烟,高血压,糖尿病和高脂血症的病史,以及AMD的个人和家族病史。结果网状假性督察组年龄较大(中位年龄为87岁对81岁,P = .04),女性受试者较多(83.3%对48.8%,P = .003),AMD发病年龄较高(83岁对70岁,P = .0005),并且高血压发生率更高(76.7%vs 55.8%,P = .08)。网状假性鼻疣(纯合子= 20.0%;杂合子= 56.7%)和大的软性玻璃疣(纯合子= 19.0%;杂合子= 42.9%)表型之间的ARMS2风险等位基因分布没有显着差异(P = .4)。 ,或在网状假性鼻疣(纯合子= 26.7%;杂合子= 56.7%)和大的软性玻璃疣(纯合子= 21.4%;杂合子= 66.7%)表型之间的CHF风险等位基因分布(P = .7)。结论网状假性表型与年龄增加,AMD发病年龄增加和女性有关。

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