June 2021
Volume 62, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2021
Comparison of IOP Response to Timolol Versus Latanoprost
Author Affiliations & Notes
  • Jeremy Reitinger
    Creighton University School of Medicine, Omaha, Nebraska, United States
  • David Reed
    Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan, United States
    Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States
  • Jesse Gilbert
    Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan, United States
    Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States
  • Tyler Kristoff
    Department of Ophthalmology, Case Western Reserve University, Cleveland, Ohio, United States
  • Vikas Gulati
    Stanley M Truhlsen Eye Institute, University of Nebraska Medical Center, Omaha, Nebraska, United States
  • Arash Kazemi
    Mayo Clinic Minnesota, Rochester, Minnesota, United States
  • Jay Mclaren
    Mayo Clinic Minnesota, Rochester, Minnesota, United States
  • Shan Fan
    Stanley M Truhlsen Eye Institute, University of Nebraska Medical Center, Omaha, Nebraska, United States
  • Carol B Toris
    Stanley M Truhlsen Eye Institute, University of Nebraska Medical Center, Omaha, Nebraska, United States
    Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States
  • Arthur J Sit
    Mayo Clinic Minnesota, Rochester, Minnesota, United States
  • Sayoko E Moroi
    Kellogg Eye Center, University of Michigan, Ann Arbor, Michigan, United States
    Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States
  • Footnotes
    Commercial Relationships   Jeremy Reitinger, None; David Reed, None; Jesse Gilbert, None; Tyler Kristoff, None; Vikas Gulati, None; Arash Kazemi, None; Jay Mclaren, None; Shan Fan, None; Carol Toris, None; Arthur Sit, None; Sayoko Moroi, None
  • Footnotes
    Support  NEI EY0022124, NEI P30 EY007003, NIH UL1TR000433, Unrestricted grant from Research to Prevent Blindness
Investigative Ophthalmology & Visual Science June 2021, Vol.62, 2769. doi:
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      Jeremy Reitinger, David Reed, Jesse Gilbert, Tyler Kristoff, Vikas Gulati, Arash Kazemi, Jay Mclaren, Shan Fan, Carol B Toris, Arthur J Sit, Sayoko E Moroi; Comparison of IOP Response to Timolol Versus Latanoprost. Invest. Ophthalmol. Vis. Sci. 2021;62(8):2769.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Prostaglandin analogues and beta-blockers are effective intraocular pressure (IOP) lowering drugs commonly used for glaucoma. However, there remain a sizeable number of nonresponders to these treatments. This study used both iCare and pneumatonometry to identify the IOP response to latanoprost and timolol under monotherapy.

Methods : We examined 212 eyes from 106 ocular normotensive, non-glaucomatous volunteers (76% female, 55.5 ± 8.9 years of age) from the EDEN consortium. At baseline, IOP was measured by iCare at 9AM and 11AM, and pneumatonometry at 11AM. Subjects were randomized and treated in both eyes (OU) with either 0.005% latanoprost once daily or 0.5% timolol twice daily for 7 days, with measurements repeated on day 8 of each treatment. After a 6-week washout, subjects switched drug arms. IOP-responders were those having an IOP reduction of >15% OU, while mixed responders had an IOP reduction of >15% in one eye (OD or OS). Treatment effects and intereye correlations on IOP were analyzed using Spearman’s rho, two-tailed paired t-tests and Fisher’s Exact Test.

Results : As compared to baseline, timolol and latanoprost effectively lowered IOP by 13% OD (14% OS) and 17% OD (18% OS), respectively (p < 0.0001, pneumatonometry). Twenty-two subjects (21%) failed to respond to either latanoprost or timolol OU. IOP response to timolol did not predict IOP response to latanoprost, however, latanoprost responders tended to also respond to timolol. More subjects were IOP-responders OU when taking latanoprost compared to timolol (p < 0.007), with 54% responding to latanoprost and 28% responding to timolol (pneumatonometry) (Figure 1). In patients given timolol, a higher non-response rate was found when measuring with pneumatonometry as opposed to iCare (p = 0.037) (Figure 1).

Conclusions : In this group of healthy subjects, a significant amount did not respond to either timolol or latanoprost. Even though the drugs represent two different mechanisms of action (timolol decreasing aqueous flow and latanoprost increasing uveoscleral outflow), non-response to one drug did not predict response to another. A new study is underway to determine if this pattern persists in patients with ocular hypertension.

This is a 2021 ARVO Annual Meeting abstract.

 

Figure 1. IOP response rates of latanoprost and timolol with iCare and Pneumatonometry. Responder, >15% decrease in IOP OU; Non-responder, <15% decrease in IOP OU; Mixed Responder, >15% decrease in IOP in one eye, OD or OS. * indicates p < 0.05.

Figure 1. IOP response rates of latanoprost and timolol with iCare and Pneumatonometry. Responder, >15% decrease in IOP OU; Non-responder, <15% decrease in IOP OU; Mixed Responder, >15% decrease in IOP in one eye, OD or OS. * indicates p < 0.05.

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