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年龄相关性黄斑变性继发地图样萎缩中眼底自发荧光增强与病情进展:GAIN研究

Increased Fundus Autofluorescence and Progression of Geographic Atrophy Secondary to Age-Related Macular Degeneration: The GAIN Study.

作者信息

Biarnés Marc, Arias Luis, Alonso Jordi, Garcia Míriam, Hijano Míriam, Rodríguez Anabel, Serrano Anna, Badal Josep, Muhtaseb Hussein, Verdaguer Paula, Monés Jordi

机构信息

Institut de la màcula i de la retina (Centro Médico Teknon), Barcelona, Spain; Universitat Pompeu Fabra (UPF), Barcelona, Spain.

Hospital Universitari de Bellvitge, Barcelona, Spain.

出版信息

Am J Ophthalmol. 2015 Aug;160(2):345-353.e5. doi: 10.1016/j.ajo.2015.05.009. Epub 2015 May 15.

Abstract

PURPOSE

To define the role of increased fundus autofluorescence (FAF), a surrogate for lipofuscin content, as a risk factor for progression of geographic atrophy (GA).

DESIGN

Prospective natural history cohort study, the GAIN (Characterization of geographic atrophy progression in patients with age-related macular degeneration).

METHODS

setting: Single-center study conducted in Barcelona, Spain.

PATIENTS

After screening of 211 patients, 109 eyes of 82 patients with GA secondary to age-related macular degeneration and a minimum follow-up of 6 months were included.

OBSERVATION PROCEDURES

Lipofuscin content was classified independently by 2 masked observers according to FAF patterns described previously. Bivariate, stratified, and multivariable analyses were used to explore the associations between GA growth and independent variables. Mediation analysis was used to evaluate the contribution of FAF patterns to GA progression.

MAIN OUTCOME

Progression of GA in mm(2)/year as measured with FAF.

RESULTS

Median follow-up was 18 months (range, 6-42). Median GA growth was 1.61 mm(2)/year. FAF, baseline area of atrophy, and time of follow-up were independently associated with GA progression (P < .004). FAF patterns and baseline area of atrophy were strongly associated (P < .0001), suggesting potential confounding. Mediation analysis suggested that most of the effect of FAF patterns on GA growth was actually caused by baseline area of atrophy.

CONCLUSIONS

FAF patterns, baseline area of atrophy, and time of follow-up were associated with GA progression. However, FAF patterns seem to be a consequence (not a cause) of enlarging atrophy and their effect on GA progression seems mostly driven by baseline area of atrophy.

摘要

目的

确定作为脂褐质含量替代指标的眼底自发荧光(FAF)增加作为地图样萎缩(GA)进展危险因素的作用。

设计

前瞻性自然史队列研究,即GAIN(年龄相关性黄斑变性患者地图样萎缩进展的特征研究)。

方法

地点:在西班牙巴塞罗那进行的单中心研究。

患者

在对211例患者进行筛查后,纳入了82例年龄相关性黄斑变性继发GA且随访至少6个月的患者的109只眼。

观察程序

2名盲法观察者根据先前描述的FAF模式独立对脂褐质含量进行分类。采用双变量、分层和多变量分析来探讨GA生长与自变量之间的关联。采用中介分析来评估FAF模式对GA进展的作用。

主要结局

用FAF测量的GA以mm²/年为单位的进展情况。

结果

中位随访时间为18个月(范围6 - 42个月)。GA的中位生长速度为1.61 mm²/年。FAF、萎缩的基线面积和随访时间与GA进展独立相关(P < 0.004)。FAF模式与萎缩的基线面积密切相关(P < 0.0001),提示可能存在混杂因素。中介分析表明,FAF模式对GA生长的大部分影响实际上是由萎缩的基线面积引起的。

结论

FAF模式、萎缩的基线面积和随访时间与GA进展相关。然而,FAF模式似乎是萎缩扩大的结果(而非原因),其对GA进展的影响似乎主要由萎缩的基线面积驱动。

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