Printer Friendly

Changes in Retinal and Choroidal Vascular Blood Flow after Oral Sildenafil: An Optical Coherence Tomography Angiography Study.

1. Introduction

Optical coherence tomography angiography (OCT-A) is a new noninvasive diagnostic tool that allows visualization of the retinal and choroidal circulation in real time. The study allows the estimation of the ocular vascular flow [1] and the theoretical quantification of the capillary density at different retinal anatomical zones. Although its role in patient care is still debatable, the study has shown promising results in demonstrating vascular changes occurring in common retinal pathologies like diabetic retinopathy, vascular occlusions, and choroidal neovascularization [2].

Sildenafil is a phosphodiesterase 5 and 6 (PDE-5, PDE-6) inhibitors that induce vasodilation. It is used in the treatment of pulmonary arterial hypertension and is currently the pharmacological first line treatment for erectile dysfunction. The drug achieves its biological effect by inducing the degradation of cyclic guanosine monophosphate (cGMP), enhancing the effect of nitric oxide and the inhibition of transmembrane influx of calcium and cell membrane hyperpolarization.

The result is smooth muscle relaxation [3]. The recommended oral dose is 25-50 mg to 100 mg qd, three times per week. Doses above 100 mg can increase the risk of systemic adverse effects like headaches, nasal congestion, and flushing. Some ocular adverse effects are changes in color and light perception, blurred vision, conjunctival hyperemia, ocular pain, and photophobia [4]. Less common ocular adverse effects are nonarteritic ischemic optic neuropathy [5], reversible increase in intraocular pressure [6], idiopathic serous macular detachment, central serous chorioretinopathy [7, 8], and ERG disturbances [4, 9, 10].

A precise explanation of the ocular adverse effects is still unknown. However, it has been hypothesized that changes in the vascular flow of the retina and choroid could have an important role. Several studies have yielded mixed results. Those studies supporting this theory have shown that oral sildenafil can induce changes in choroidal thickness [11, 12], vascular flow [13-16], and alteration in retinal electroretinogram [17] and others that did not find changes in perimetry [18], flowmetry [19], and Doppler echography [20]. Therefore, the purpose of the current study is to assess vascular changes in the retinal and choroidal circulation, by taking advantage all the capabilities of the OCT-A, after the oral ingestion of sildenafil in healthy volunteers.

2. Method

Case and control, single center study. The study was conducted at the Asociacion para Evitar la Ceguera en Mexico IAP, Mexico City, Mexico and approved by the local Internal Review Board. The study was conducted according to the tenets of the Declaration of Helsinki and Good Clinical Practices guidelines. All sensitive data were managed according to the Mexican Federal Law for Protection of Personal Data in Possession of Individuals (NOM-024-SSA3-2010), which is the equivalent of the Health Insurance Portability and Accountability Act (HIPAA) rules of 1996. All participants signed an informed consent form before enrollment.

We included patients between 18 and 40 years of age, with no relevant medical history. Patients with history of a hypersensitivity reaction to phosphodiesterase inhibitors or history of past adverse effect with oral sildenafil were excluded. General demographic data and biometric data (weight and height) were recorded at baseline. All participants were stratified randomized into two groups with a proportion of 2: 1. Patients assigned to the study group received 50 mg of oral sildenafil (Viagra[R], Pfizer, New York, NY) and patients assigned to the control group received a sham pill the same size, color, and form.

Retinal and choroidal images were captured at baseline and 1 hours after the pill ingestion. Central macular thickness (CMT) and central choroidal thickness (CCT) were measured with optical coherent tomography (OCT) and enhanced depth imaging-OCT (Spectralis HRA-OCT; Heidelberg Engineering, Heidelberg, Germany). Central choroidal thickness was measured using the measuring tool built in the OCT software. The measurements were done in three locations: subfoveal, 1000 fim temporal to the fovea, and 1000 fim nasal to the fovea. All three measurements were averaged into a single central choroidal thickness value per patient. All measurements were done in triplicates. Choroidal flow (CF), outer retina flow (ORF), retinal vascular density (RVD), and choroidal vascular density (CVD) were measured with OCT-A (AngioVue OCT-A system, Optovue Inc., Fremont, CA).

All OCT-A images were taken using the default setting of the system (70,000 A scans per second, =5 fim on optical axial resolution, and =15 fim on optical transversal resolution). Segmentation of the images was done with the automatic segmentation tool build in the software. All values were derived directly from the calculation made by the system and shown on the screen.

Statistical analysis was done using an Excel spreadsheet (Excel 2010; Microsoft Corp., Redmond, WA) with and XLSTAT application v18.06 (Addinsoft, New York, NY). Continuous variables were compared using a Mann-Whitney U test with an alpha value of 0.05 for statistical significance.

3. Results

We enrolled 20 eyes into the study group (sildenafil 50 mg) and 10 eyes into the control group (sham). In the study group, the mean age was 28.1 years, the mean weight was 73.6 kg, and the mean height was 1.76 meters. In the control group, the mean age was 29.2 years, the mean weight was 70.4 kg, and the mean height was 1.75 meters.

Results from the study and control group are summarized in Table 1. In the study group, CCT increased significantly after 1 hour of sildenafil ingestion (p <0.01). The rest of the assessed variables in the study group did not have a significant change after sildenafil. In the control group, none of the assessed variables had a significant change after sham.

Intergroup comparison between study and control group are summarized in Table 2. The analysis showed that 1 hour after pills ingestion, the outer retinal flow increased significantly in the study group (p < 0.01). The rest of the assessed variables between groups did not have a significant difference between them.

4. Discussion

Optical coherence tomography angiography is a novel diagnostic tool that can potentially impact ocular medical therapies in the future. It has been tried as an early diagnostic and assessment tool for age-related macular degeneration (AMD) [21-24], as a research tool in order to improve the current understanding of ischemic diseases that affects the different layers of the retinal microcirculation (diabetic retinopathy) [25, 26], cotton wool spots, acute macular neuroretinopathy, paracentral acute middle maculopathy, and macular telangiectasia type 2 among others [27-29].

The role of vascular flow changes in choroidal diseases is unknown. Evidence from peer-reviewed manuscripts has found a relationship between flow changes among different retinal layers and choroid with the pathogenesis of some of the most common chorioretinal diseases [30-33]. Changes in choroidal thickness (reduction) and in the density of superficial and deep retinal vessels have been associated with choroidal neovascularization [34-36]. A reduction in the total retinal and choroidal flow has been observed in patients with macular edema [37, 38], and finally, an increase in the total choroidal flow has been observed in patients with central serous retinopathy [39]. Since most of the ocular side effects of oral sildenafil are thought to be secondary to an idiosyncratic dilation of the retinal and choroidal vessels, the potential impact of this pharmacologic effect on the total vascular flow should be assessed. A major understanding of the mechanisms associated with this phenomenon could aid us in preventing such adverse effects as well as improving our current understanding of the relationship of vascular flow and others chorioretinal diseases like central serous retinopathy.

The results of the current study are similar to previous reports reporting a significant increase in choroidal thickness measured by EDI-OCT. However, OCT-A results failed to demonstrate a significant change in choroidal blood flow.

Outer retinal blood flow increased after sildenafil, but the capillary density of the retina remained unchanged. Nevertheless, our results may suggest that despite a local pharmacological effect secondary to sildenafil, the autoregulation mechanisms of the retinal and choroidal vasculature may prevent significant changes in vascular hemodynamics, at least in the short term, ensuring a constant blood flow and preventing blood stagnation and ischemic changes in healthy patients.

The current study has several limitations that we would like to address. First, an error type 2 is highly likely due to the small sample. The high variability in biometric values could affect the distribution volume of the drug among patients. Therefore, our patients could have responded differently to a fixed dose. There is a possibility that an ocular vascular effect could have been demonstrated if we had adjusted the dose according to weight and height. Finally, all our patients were first-time users of sildenafil. Most of the ocular adverse effects of the drug occur in chronic users. There is a possibility that ocular changes due to sildenafil are due to the continued exposition to the drug or to the association of a preexisting ocular condition with exposition to the drug. Finally, it is important to note that the AngioVue OCT-A default setting is programmed to measure the choroidal flow solely at the level of the choriocapillaris, while EDI software is designed to measure the whole choroidal thickness. This is an important difference to consider since this might be the reason why there was no change observed in choroidal flow measurements after sildenafil intake.

In summary, our study found an increase in choroidal thickness and in the outer retinal flow that suggests a vascular effect of sildenafil in the eye. No measurable data was found regarding the change in choroidal flow, despite the increase in choroidal thickness. The results may suggest that even with a local pharmacological effect of sildenafil, the vascular autoregulation mechanisms of the retina and choroid may prevent a significant change in vascular hemodynamics, at least in the short term, ensuring a constant blood flow and preventing blood stagnation and ischemia. Further studies with longer follow-up are needed in order to assess the role of the chronic use of sildenafil on retinal vascular hemodynamics in healthy and diseased patients.

https://doi.org/10.1155/2017/7174540

Conflicts of Interest

The authors do not have any economic, proprietary, or financial interest to disclose in the publication of this paper. There were no funds allocated to the realization of this research. The authors state that they have full control of all primary data, and they agreed to allow the journal to review their data upon request.

References

[1] J. Maram, S. Srinivas, and S. R. Sadda, "Evaluating ocular blood flow," Indian Journal of Ophthalmology, vol. 65, pp. 337-346, 2017.

[2] K. Sambhav, S. Grover, and K. V. Chalam, "The application of optical coherence tomography angiography in retinal diseases," Survey of Ophthalmology, 2017.

[3] H. Sperling, M. C. Michel, and H. Rubben, "Sildenafil (Viagra[R]). Tolerance, contraindications, drug interactions," Der Urologe, vol. 38, pp. 124-127, 1999.

[4] M. M. Moschos and E. Nitoda, "Pathophysiology of visual disorders induced by phosphodiesterase inhibitors in the treatment of erectile dysfunction," Drug Design, Development and Therapy, vol. 8, pp. 3407-3413, 2016.

[5] H. Almuhtaseb, O. Kanavati, and A. Lotery, "Branch retinal vein occlusion secondary to sildenafil," BMJ, vol. 356, p. j753, 2017.

[6] R. Gerometta, L. J. Alvarez, and O. A. Candia, "Effect of sildenafil citrate on intraocular pressure and blood pressure in human volunteers," Experimental Eye Research, vol. 93, pp. 103-107, 2011.

[7] F. W. Fraunfelder and F. T. Fraunfelder, "Central serous chorioretinopathy associated with sildenafil," Retina, vol. 28, pp. 606-609, 2008.

[8] E. Damar, Y. Toklu, A. Tuncel et al., "Does therapeutic dose of sildenafil citrate treatment lead to central serous chorioretinopathy in patients with erectile dysfunction?," American Journal of Men's Health, vol. 7, pp. 439-443, 2013.

[9] A. Stockman, L. T. Sharpe, A. Tufail, P. D. Kell, C. Ripamonti, and G. Jeffery, "The effect of sildenafil citrate (Viagra[R]) on visual sensitivity," Journal of Vision, vol. 7, p. 4, 2007.

[10] J. Martins, B. Kolomiets, R. Caplette et al., "Sildenafil acutely decreases visual responses in ON and OFF retinal ganglion cells," Investigative Opthalmology & Visual Science, vol. 56, pp. 2639-2648, 2015.

[11] D. Y. Kim, R. H. Silverman, R. V. Chan et al., "Measurement of choroidal perfusion and thickness following systemic sildenafil (Viagra[R])," Acta Ophthalmologica, vol. 91, pp. 183-188, 2013.

[12] S. K. Vance, Y. Imamura, and K. B. Freund, "The effects of sildenafil citrate on choroidal thickness as determined by enhanced depth imaging optical coherence tomography," Retina, vol. 31, pp. 332-335, 2011.

[13] E. Kurtulan, A. Gulcu, M. Secil, I. Celebi, G. Aslan, and A. A. Esen, "Effects of sildenafil on ocular perfusion demonstrated by color Doppler ultrasonography," International Journal of Impotence Research, vol. 16, pp. 244-248, 2004.

[14] M. Koksal, H. Ozdemir, S. Kargi et al., "The effects of sildenafil on ocular blood flow," Acta Ophthalmologica Scandinavica, vol. 83, pp. 355-359, 2005.

[15] Z. Yuan, T. W. Hein, R. H. Rosa Jr., and L. Kuo, "Sildenafil (Viagra) evokes retinal arteriolar dilation: dual pathways via NOS activation and phosphodiesterase inhibition," Investigative Ophthalmology & Visual Science, vol. 49, pp. 720-725, 2008.

[16] A. Harris, L. Kagemann, R. Ehrlich, Y. Ehrlich, C. R. Lopez, and V. A. Purvin, "The effect of sildenafil on ocular blood flow," British Journal of Ophthalmology, vol. 92, pp. 469-473, 2008.

[17] J. K. Luu, A. V. Chappelow, T. J. McCulley, and M. F. Marmor, "Acute effects of sildenafil on the electroretinogram and multifocal electroretinogram," American Journal of Ophthalmology, vol. 132, pp. 388-394, 2001.

[18] S. O. Dundar, A. Topalo Gcaron Lu, M. Dundar, and I. Kocak, "Effects of sildenafil on blue-on-yellow and white-on-white Humphrey perimetry in 3 months regular use," Eye, vol. 20, pp. 810-813, 2006.

[19] T. I. Metelitsina, J. E. Grunwald, J. C. DuPont, and G. S. Ying, "Effect of Viagra on the foveolar choroidal circulation of AMD patients," Experimental Eye Research, vol. 81, pp. 159-164, 2005.

[20] A. P. Costa, A. M. Lima, L. H. da Silva, R. de Oliveira Alves Carvalho, A. V. do Amaral, and N. C. Borges, "Ocular perfusion pressure and color Doppler imaging of the external ophthalmic artery of rabbits treated with sildenafil citrate," BMC Veterinary Research, vol. 12, p. 149, 2016.

[21] Y. Jia, S. T. Bailey, D. J. Wilson et al., "Quantitative optical coherence tomography angiography of choroidal neovascularization in age-related macular degeneration," Ophthalmology, vol. 121, pp. 1435-1444, 2014.

[22] E. Moult, W. Choi, N. K. Waheed et al., "Ultrahigh-speed swept-source OCT angiography in exudative AMD," Ophthalmic Surgery, Lasers and Imaging Retina, vol. 45, pp. 496-505, 2014.

[23] M. M. Castillo, G. Mowatt, A. Elders et al., "Optical coherence tomography for the monitoring of neovascular age-related macular degeneration: a systematic review," Ophthalmology, vol. 122, pp. 399-406, 2015.

[24] D. Y. Kim, J. Fingler, R. J. Zawadzki et al., "Optical imaging of the chorioretinal vasculature in the living human eye," Proceedings of the National Academy of Sciences, vol. 110, pp. 14354-14359, 2013.

[25] N. Takase, M. Nozaki, A. Kato, H. Ozeki, M. Yoshida, and Y. Ogura, "Enlargement of foveal avascular zone in diabetic eyes evaluated by en face optical coherence tomography angiography," Retina, vol. 35, pp. 2377-2383, 2015.

[26] G. Coscas, M. Lupidi, and F. Coscas, "Optical coherence tomography angiography in diabetic maculopathy," Developments in Ophthalmology, vol. 60, pp. 38-49, 2017.

[27] A. Nagiel, S. R. Sadda, and D. Sarraf, "A promising future for optical coherence tomography angiography," JAMA Ophthalmology, vol. 133, pp. 629-630, 2015.

[28] E. Rahimy, D. Sarraf, M. L. Dollin, J. D. Pitcher, and A. C. HoParacentral acute middle maculopathy in nonischemic central retinal vein occlusion," American Journal of Ophthalmology, vol. 158, pp. 372-380 e1, 2014.

[29] R. F. Spaide, J. M. Klancnik Jr., and M. J. Cooney, "Retinal vascular layers in macular telangiectasia type 2 imaged by optical coherence tomographic angiography," JAMA Ophthalmology, vol. 133, pp. 66-73, 2015.

[30] N. V. Palejwala, Y. Jia, S. S. Gao et al., "Detection of non-exudative choroidal neovascularization in age-related macular degeneration with optical coherence tomography angiography," Retina, vol. 35, pp. 2204-2211, 2015.

[31] L. Roisman, Q. Zhang, R. K. Wang et al., "Optical coherence tomography angiography of asymptomatic neovascularization in intermediate age-related macular degeneration," Ophthalmology, vol. 123, pp. 1309-1319, 2016.

[32] G. Querques, M. Srour, N. Massamba et al., "Functional characterization and multimodal imaging of treatment-naive "quiescent" choroidal neovascularization," Investigative Ophthalmology & Visual Science, vol. 54, pp. 6886-6892, 2013.

[33] J. D. Gass, "Serous retinal pigment epithelial detachment with a notch. A sign of occult choroidal neovascularization," Retina, vol. 4, pp. 205-220, 1984.

[34] L. Toto, E. Borrelli, L. Di Antonio, P. Carpineto, and R. Mastropasqua, "Retinal vascular plexuses' changes in dry age-related macular degeneration, evaluated by means of optical coherence tomography angiography," Retina, vol. 36, pp. 1566-1572, 2016.

[35] D. J. Coleman, R. H. Silverman, M. J. Rondeau, H. O. Lloyd, A. A. Khanifar, and R. V. Chan, "Age-related macular degeneration: choroidal ischaemia?," British Journal of Ophthalmology, vol. 97, pp. 1020-1023, 2013.

[36] R. W. Flower, C. von Kerczek, L. Zhu, A. Ernest, C. Eggleton, and L. D. Topoleski, "Theoretical investigation of the role of choriocapillaris blood flow in treatment of subfoveal choroidal neovascularization associated with age-related macular degeneration," American Journal of Ophthalmology, vol. 132, pp. 85-93, 2001.

[37] M. Okamoto, M. Yamashita, T. Sakamoto, and N. Ogata, "Choroidal blood flow and thickness as predictors for response to anti-vascular endothelial growth factor therapy in macular edema secondary to branch retinal vein occlusion," Retina, 2017.

[38] B. Lee, E. A. Novais, N. K. Waheed et al., "En face Doppler optical coherence tomography measurement of total retinal blood flow in diabetic retinopathy and diabetic macular edema," JAMA Ophthalmology, vol. 135, p. 244, 2017.

[39] M. Nicolo, R. Rosa, D. Musetti, M. Musolino, M. Saccheggiani, and C. E. Traverso, "Choroidal vascular flow area in central serous chorioretinopathy using swept-source optical coherence tomography angiography," Investigative Ophthalmology & Visual Science, vol. 58, p. 2002, 2017.

David Berrones, (1) Guillermo Salcedo-Villanueva, (2) Virgilio Morales-Canton, (2) and Raul Velez-Montoya (2)

(1) Ophthalmology Department, Asociacion para Evitar la Ceguera en Mexico IAP, Mexico City, Mexico (2) Retina Department, Asociacion para Evitar la Ceguera en Mexico IAP, Mexico City, Mexico

Correspondence should be addressed to Guillermo Salcedo-Villanueva; salcedovilla@gmail.com

Received 28 July 2017; Revised 16 September 2017; Accepted 25 September 2017; Published 9 October 2017

Academic Editor: Giuseppe Querques
Table 1: Change in OCT before and after sildenafil/sham.
Comparison of variables before and after the ingestion of the pill
for both groups. CMT: central macular thickness; CCT: central
choroidal thickness; CF: choroidal flow; ORF: outer retinal flow;
RVD: retinal vascular density; CVD: choroidal vascular density.
* p < 0.01.

                 Before                            After

Sildenafil group

CMT  280.4 [+ or -] 23.69 [micro]m    279.85 [+ or -] 22.80 [micro]m
CCT  354.45 [+ or -] 67.17 [micro]m   429.30 [+ or -] 82.87 [micro]m *
CF   1.95 [+ or -] 0.04 [mm.sup.2]    1.87 [+ or -] 0.22 [mm.sup.2]
ORF  1.21 [+ or -] 0.20 [mm.sup.2]    1.31 [+ or -] 0.27 [mm.sup.2]
RVD       52.6 [+ or -] 3.50%              53.6 [+ or -] 3.21%
CVD       66.6 [+ or -] 1.48%              67.28 [+ or -] 1.02%

Sham group

CMT  266.60 [+ or -] 19.28 [micro]m   266.20 [+ or -] 19.02 [micro]m
CCT  397.10 [+ or -] 72.81 [micro]m   396.50 [+ or -] 68.48 [micro]m
CF   1.96 [+ or -] 0.05 [mm.sup.2]    1.95 [+ or -]  0.05 [mm.sup.2]
ORF  1.06 [+ or -] 0.23 [mm.sup.2]    1.03 [+ or -]  0.23 [mm.sup.2]
RVD       53.9 [+ or -] 2.16%              53.3 [+ or -] 3.45%
CVD      66.98 [+ or -] 1.06%              66.90 [+ or -] 1.50%

Table 2: Results after pill administration for both groups.
Comparison of the variables for the study and control group 1
hour after the ingestion of sildenafil/sham. CMT: central macular
thickness; CCT: central choroidal thickness; CF: choroidal flow;
ORF: outer retinal flow; RVD: retinal vascular density; CVD:
choroidal vascular density. * p < 0.01.

     Posttreatment sildenafil group        Posttreatment sham group

CMT  279.85 [+ or -] 22.80 [micro]m     266.20 [+ or -] 19.02 [micro]m
CCT  429.30 [+ or -] 82.87 [micro]m       396.50 [+ or -] 68.48 f m
CF    1.87 [+ or -] 0.22 [mm.sup.2]     1.95 [+ or -] 0.05 [mm.sup.2]
ORF   1.31 [+ or -] 0.27 [mm.sup.2]    1.03 [+ or -] 0.23 [mm.sup.2] *
RVD        53.6 [+ or -] 3.21%               53.3 [+ or -] 3.45%
CVD       67.28 [+ or -] 1.02%               66.90 [+ or -] 1.50%
COPYRIGHT 2017 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research Article
Author:Berrones, David; Salcedo-Villanueva, Guillermo; Morales-Canton, Virgilio; Velez-Montoya, Raul
Publication:Journal of Ophthalmology
Article Type:Report
Date:Jan 1, 2017
Words:3373
Previous Article:High-Intensity Focused Ultrasound Circular Cyclocoagulation in Glaucoma: A Step Forward for Cyclodestruction?
Next Article:Neovascular Age-Related Macular Degeneration in the Very Old ([greater than or equal to] 90 Years): Epidemiology, Adherence to Treatment, and...
Topics:

Terms of use | Privacy policy | Copyright © 2020 Farlex, Inc. | Feedback | For webmasters