Internal Medicine, Hopital de la Croix-Rousse, Lyon, France.
Pneumology, Centre Hospitalier Universitaire de Lyon, Lyon, France.
Br J Ophthalmol. 2019 Dec;103(12):1690-1694. doi: 10.1136/bjophthalmol-2018-312949. Epub 2019 Mar 14.
Uveitis is a frequent and early feature of sarcoidosis. As BTNL2 (butyrophilin-like 2) gene polymorphism was found linked with the susceptibility to sarcoidosis, we investigated whether a specific genotype of BTNL2 gene G16071A (or rs2076530) single-nucleotide polymorphism (SNP) would be associated with the risk of sarcoid uveitis in all patient subgroups.
The study compared the genotype frequencies of SNP G16071A of 135 patients with sarcoid uveitis (SaUv) with those of 196 patients with sarcoidosis without uveitis (SaUv), 81 patients with uveitis without sarcoidosis (SaUv), and 271 controls with no sarcoidosis nor uveitis (SaUv). Three hypothetical subgroups of patients with sarcoid uveitis (SaUv cases) were considered: (1) subgroup I: patients aged <45 years of both sexes and all ethnic origins; (2) subgroup II: Caucasian women aged >45 years; and (3) subgroup III: all other patients.
A statistically significant difference in genotype frequencies was found between the groups SaUv and SaUv (p=3.2×10) and between the groups SaUv and SaUv (p=7.1×10). There was no difference between the three subgroups of SaUv patients. There was a statistically significant difference in genotype frequencies between SaUv and SaUv subgroup II (p=0.005) but no difference between SaUv and SaUv subgroup I.
No association was found between G16071A and the susceptibility to sarcoid uveitis. BTNL2 gene G16071A SNP seems to be a predisposing factor for sarcoidosis except in Caucasian postmenopausal women with sarcoid uveitis in whom the GG genotype prevails. These and future results will help in understanding differences between particular subgroups of patients with sarcoid uveitis.
葡萄膜炎是结节病的常见且早期特征。由于 BTNL2(丁酰膦蛋白样 2)基因多态性与结节病易感性相关,我们研究了 BTNL2 基因 G16071A(或 rs2076530)单核苷酸多态性(SNP)的特定基因型是否与所有患者亚组的结节病性葡萄膜炎(SaUv)风险相关。
该研究比较了 135 例结节病性葡萄膜炎(SaUv)患者的 SNP G16071A 基因型频率与 196 例无葡萄膜炎(SaUv)的结节病患者、81 例无葡萄膜炎(SaUv)的葡萄膜炎患者和 271 例无结节病或葡萄膜炎(SaUv)的对照者。考虑了三组假设的 SaUv 患者亚组:(1)亚组 I:所有种族的男性和女性年龄<45 岁;(2)亚组 II:年龄>45 岁的白种人女性;和(3)亚组 III:所有其他患者。
SaUv 组与 SaUv 组(p=3.2×10)和 SaUv 组与 SaUv 组(p=7.1×10)之间的基因型频率存在统计学差异。SaUv 患者的三个亚组之间没有差异。SaUv 患者与 SaUv 亚组 II 之间的基因型频率存在统计学差异(p=0.005),但 SaUv 与 SaUv 亚组 I 之间无差异。
未发现 G16071A 与结节病性葡萄膜炎易感性之间存在关联。BTNL2 基因 G16071A SNP 似乎是结节病的易感因素,但白种绝经后女性除外,她们患有结节病性葡萄膜炎,GG 基因型占优势。这些和未来的结果将有助于理解结节病性葡萄膜炎特定患者亚组之间的差异。