Song Zeyuan, Pany Satyabrata, Guo Shengru, Mazumder Arpan G, Itakura Tatsuo, Huang Jonathan, Magarychoff Evan, Gurinovich Anastasia, Benchek Penelope H, Stamer W Daniel, Price Francis W, Willoughby Colin E, Senthilkumari Srinivasan, George Ronnie J, Chitipothu Srujana, Lass Jonathan H, Iyengar Sudha K, Schwartz Stephen G, Griswold Anthony J, Sebastiani Paola, Price Marianne O, Fini M Elizabeth
Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.
Tufts University Clinical and Translational Science Institute, Boston, MA, USA.
medRxiv. 2025 Aug 13:2025.08.11.25333245. doi: 10.1101/2025.08.11.25333245.
Adverse drug reactions are a frequent cause of worldwide morbidity and mortality. Glucocorticoids (GCs), commonly used to treat inflammatory diseases, alter gene expression with both beneficial and adverse consequences. When used in the eye, GCs cause steroid-induced ocular hypertension (SIOH) in 30-50% of patients, leading to steroid-induced glaucoma. Evidence suggests that predisposition to SIOH is genetically determined. Here we took a pharmacogenomic approach to discover DNA variants associated with SIOH. We identified 44 SNPs of genome-wide significance (p<5E-08) located at 26 risk loci out of a total of 531 SNPs of suggestive significance (p<5E-06) at 262 risk loci. Unlike SNPs identified in complex disease which are overwhelmingly common in frequency, most SNPs found here were rare or of low frequency, likely discoverable because of their large effect sizes. Follow-up analyses provide insight into the pathogenetic relationship of SIOH to high-tension glaucomas and suggest a new mechanistic paradigm for SIOH pathophysiology.
药物不良反应是全球发病和死亡的常见原因。糖皮质激素(GCs)常用于治疗炎症性疾病,可改变基因表达,既有有益的结果,也有不良的后果。当用于眼部时,GCs在30%至50%的患者中会导致类固醇性高眼压(SIOH),进而引发类固醇性青光眼。有证据表明,SIOH的易感性是由基因决定的。在此,我们采用药物基因组学方法来发现与SIOH相关的DNA变异。我们在262个风险位点上共531个具有提示意义(p<5E-06)的单核苷酸多态性(SNP)中,鉴定出位于26个风险位点的44个具有全基因组意义(p<5E-08)的SNP。与在复杂疾病中鉴定出的频率极高的SNP不同,这里发现的大多数SNP都是罕见的或低频的,可能由于其较大的效应大小而可被发现。后续分析深入了解了SIOH与高眼压性青光眼的发病机制关系,并为SIOH病理生理学提出了一种新的机制范式。