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A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
被引:9
|作者:
Qassim, Ayub
[1
]
Mullany, Sean
[1
]
Awadalla, Mona S.
[1
]
Hassall, Mark M.
[1
]
Nguyen, Thi
[1
]
Marshall, Henry
[1
]
Kolovos, Antonia
[1
]
Schulz, Angela M.
[2
]
Han, Xikun
[3
]
Gharahkhani, Puya
[3
]
Galanopoulos, Anna
[4
]
Agar, Ashish
[5
]
Healey, Paul R.
[6
]
Hewitt, Alex W.
[7
]
Landers, John
[1
]
Casson, Robert J.
[8
]
Graham, Stuart L.
[2
]
MacGregor, Stuart
[3
]
Souzeau, Emmanuelle
[1
]
Siggs, Owen M.
[1
]
Craig, Jamie E.
[1
]
机构:
[1] Flinders Univ S Australia, Flinders Med Ctr, Dept Ophthalmol, Bedford Pk, SA, Australia
[2] Macquarie Univ, Fac Med Hlth & Human Sci, N Ryde, NSW, Australia
[3] QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia
[4] Royal Adelaide Hosp, South Australian Inst Ophthalmol, Adelaide, SA, Australia
[5] Prince Wales Hosp, Dept Ophthalmol, Randwick, NSW, Australia
[6] Univ Sydney, Westmead Inst Med Res, Ctr Vis Res, Sydney, NSW, Australia
[7] Univ Tasmania, Menzies Inst Med Res, Hobart, Tas, Australia
[8] Univ Adelaide, South Australian Inst Ophthalmol, Adelaide, SA, Australia
来源:
基金:
英国医学研究理事会;
关键词:
Diurnal IOP;
Genetic risk prediction;
Glaucoma;
Home tonometry;
iCare HOME;
Intraocular pressure;
Polygenic risk score;
FALSE DISCOVERY RATE;
GLAUCOMA;
D O I:
10.1016/j.ogla.2020.12.002
中图分类号:
R77 [眼科学];
学科分类号:
100212 ;
摘要:
Purpose: Intraocular pressure (IOP) elevations may occur in early morning or outside office hours and can be missed during routine in-clinic IOP measurements. Such fluctuations or peaks likely contribute to glaucoma progression. We sought to investigate the relationship between an IOP polygenic risk score (PRS) and short-term IOP profile. Design: Cross-sectional study. Participants: Four hundred seventy-three eyes from 239 participants with suspected or established primary open-angle glaucoma sampled from 4 outpatient clinics in Australia between August 2016 and December 2019. Methods: Participants underwent Icare HOME (Icare Oy, Vanda, Finland) tonometer measurements to record IOP 4 times daily for 5 days. Unreliable measurements were excluded. A minimum of 2 days with at least 3 reliable measurements were required. We used a validated IOP PRS derived from 146 IOP-associated variants in a linear regression model adjusted for central corneal thickness and age. Main Outcome Measures: Highest recorded early morning IOP and mean IOP within and outside office hours. Early morning IOP spikes were defined by a higher early morning IOP than the maximum in-office hours IOP. Results: Reliable measurements were obtained from 334 eyes of 176 participants (mean age, 64 +/- 9 years). Eyes in the highest IOP PRS quintile showed an early morning IOP increase of 4.3 mmHg (95% confidence interval [CI], 1.4-7.3; P = 0.005) and mean increase in IOP outside office hours of 2.7 mmHg (95% CI, 0.61-4.7; P = 0.013) than the lowest quintile, which were significant independently after accounting for a recent in-clinic IOP measured by Goldmann applanation tonometry. Eyes in the highest PRS quintile were 5.4-fold more likely to show early morning IOP spikes than the lowest quintile (odds ratio 95% CI, 1.3-23.6; P = 0.023). Conclusions: A validated IOP PRS was associated with higher early morning IOP and mean IOP outside office hours. These findings support a role for genetic risk prediction of susceptibility to elevated IOP that may not be apparent during in-clinic hours, requiring more detailed clinical phenotyping using home tonometry, the results of which may guide additional interventions to improve IOP control. (C) 2020 by the American Academy of Ophthalmology
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页码:411 / 420
页数:10
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