University of Bordeaux, Inserm, Bordeaux Population Health Research Center, Team LEHA, UMR 1219, Bordeaux, France.
Service d'Ophtalmologie, CHU de Bordeaux, Bordeaux, France.
Retina. 2019 Jan;39(1):34-43. doi: 10.1097/IAE.0000000000002237.
To study the associations of subfoveal choroidal thickness with vascular risk factors and age-related macular degeneration.
Two hundred sixty-one participants of the Alienor study had gradable enhanced-depth imaging optical coherence tomography scans of the macula and available data on vascular and genetic risk factors (assessed through face-to-face interview and fasting blood samples) and age-related macular degeneration status (assessed from retinal photographs and optical coherence tomography). Subfoveal choroidal thickness was measured manually on one horizontal scan passing through the fovea.
In a multivariate mixed linear model, subfoveal choroidal thickness was independently associated with age greater than 80 years (-21.77 μm, P = 0.02), axial length (-21.77 μm, P < 0.0001), heavy smoking (≥20 pack-years: -24.89 μm, P = 0.05), fasting blood glucose higher than 7 mmol/L (-53.17 μm, P = 0.02), and lipid-lowering treatment (+18.23, P = 0.047). After multivariate adjustment for age, sex, axial length, and vascular and genetic risk factors, subfoveal choroidal thickness was thinner in eyes with central hyperpigmentation (-45.39 μm, P = 0.006), central hypopigmentation (-44.99 μm, P = 0.001), and central pigmentary abnormalities (-44.50 μm, P = 0.001), but not in eyes with late age-related macular degeneration (-18.05 μm, P = 0.33) or soft drusen.
These findings indicate a relationship between vascular risk factors and choroidal thinning and suggest an early involvement of the choroid in the pathogenesis of age-related macular degeneration.
研究脉络膜下厚度与血管危险因素和年龄相关性黄斑变性的相关性。
在 Alienor 研究中,261 名参与者进行了黄斑增强深度成像光学相干断层扫描检查,并且有血管和遗传危险因素(通过面对面访谈和空腹血样评估)以及年龄相关性黄斑变性的相关数据(通过视网膜照片和光学相干断层扫描评估)。在一个水平扫描中,手动测量黄斑中心凹下脉络膜厚度。
在多元混合线性模型中,脉络膜下厚度与年龄大于 80 岁(-21.77μm,P=0.02)、眼轴长度(-21.77μm,P<0.0001)、重度吸烟(≥20 包/年:-24.89μm,P=0.05)、空腹血糖高于 7mmol/L(-53.17μm,P=0.02)和降脂治疗(+18.23μm,P=0.047)独立相关。在多元调整年龄、性别、眼轴长度以及血管和遗传危险因素后,中心性色素沉着(-45.39μm,P=0.006)、中心性色素减退(-44.99μm,P=0.001)和中心性色素异常(-44.50μm,P=0.001)的眼中脉络膜下厚度变薄,但在晚期年龄相关性黄斑变性(-18.05μm,P=0.33)或软性玻璃膜疣的眼中没有变薄。
这些发现表明血管危险因素与脉络膜变薄之间存在关系,并提示脉络膜在年龄相关性黄斑变性的发病机制中早期受累。