Longitudinal Growth Differentiation Factor 15 (GDF15) and Long-term Intraocular Pressure Fluctuation in Glaucoma: A Pilot Study

被引:1
|
作者
Lin, Jonathan B. [1 ,2 ]
Sheybani, Arsham [1 ,2 ]
Santeford, Andrea [1 ,2 ]
Apte, Rajendra S. [1 ,2 ,3 ,4 ]
机构
[1] Washington Univ, Dept Ophthalmol, St Louis, MO 63110 USA
[2] Washington Univ, Dept Vis Sci, St Louis, MO 63110 USA
[3] Washington Univ, Dept Dev Biol, St Louis, MO 63110 USA
[4] Washington Univ, Dept Med, St Louis, MO 63110 USA
关键词
GDF15; Glaucoma; Neurodegeneration; Molecular Markers; PROGRESSION; BIOMARKERS;
D O I
10.18502/jovr.v16i1.8245
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Growth Differentiation Factor 15 (GDF15) was previously identified as a molecular marker of retinal ganglion cell stress in rodent models of glaucoma and was elevated in the aqueous humor (AH) of patients with primary open-angle glaucoma as a possible risk factor for glaucoma progression. The purpose of this study was to determine whether changes in the AH GDF15 levels were associated with intraocular pressure (IOP) changes in eyes undergoing glaucoma surgery. Methods: Here, we performed a prospective, longitudinal pilot study in nine patients to determine whether changes in AH GDF15 levels from surgery to post-surgery follow-up were associated with IOP fluctuation. An initial AH sample was taken from the peripheral corneal paracentesis during planned glaucoma surgery, and a second sample was taken during an outpatient follow-up visit, approximately six months later. Results: There was a statistically significant correlation between GDF15 fold change and IOP standard deviation (r = 0.87, P = 0.003), IOP range (r = 0.87, P = 0.003), and maximum IOP (r = 0.86, P = 0.003). There was no correlation between the GDF15 fold change and baseline IOP (r = 0.50, P = 0.17), final IOP (r = 0.038, P = 0.92), or mean IOP (r = 0.40, P = 0.28). Conclusion: Our findings in this pilot study suggest that longitudinal changes in AH GDF15 may be associated with IOP fluctuation during the postoperative period. Further studies are necessary to corroborate these findings in a larger patient population and to explore the possibility that AH GDF15 may be used not only to improve treatment algorithms but also as a surrogate endpoint in clinical trials.
引用
收藏
页码:21 / 27
页数:7
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