This work was supported by NIH K08EY027006, R01EY030564, UH3NS100614, Research Grants from Carl Zeiss Meditec Inc (Dublin, CA) and Unrestricted Department Funding from Research to Prevent Blindness (New York, NY).

This study was approved by the University of Southern California Institutional Review Board and adhered to the tenets of the Declaration of Helsinki.
1. Setup of Gas Non-rebreathing Apparatus
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/60948/60948fig1v2.jpg" /> 
Figure 1: Diagram of the non-rebreathing apparatus.&#160;The full setup has been broken into three separate units according to their function and the frequency with which they are dealt with independently. These include: the Air-Control Unit, the Non-rebreathing Unit, and the Subject/Imaging Device Unit <a href="https://www.jove.com/files/ftp_upload/60948/60948fig1v2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<ol>
	<li>Apparatus assembly
	<ol>
		<li>Connect the Douglas bag (Figure 1, #1) to the three-way valve (#3) at a selective inlet port via the 35 mm inner-diameter tube (#2; see Table of Materials) with adapter (#2*). This combination will be called the &#8220;Air Control Unit&#8221; as shown in Figure 1.</li>
		<li>Connect the two-way non-rebreathing valve (#6) to the elbow joint connector (#7) at the non-rebreathing valve&#8217;s mouth port. Form the connection using a rubber tube (#5) fitted with an adapter (#4).</li>
		<li>Connect the elbow joint to the gas delivery tubing (#8). This setup, including the non-rebreathing valve (#6), in-house tubing (#5), adapters (#4), elbow joint (#7), and gas delivery tubing (#8) will be called the &#8220;Non-rebreathing Unit&#8221;. 
		NOTE: Minimize the amount of dead space between the subject&#8217;s mouth and the diaphragm of the two-way non-rebreathing valve (#6).</li>
		<li>Connect the Air Control Unit at the outlet port of the three-way valve (#3) to the Non-rebreathing Unit at the inlet port of the two-way non-rebreathing valve (#6). Make the connection using additional rubber tubing (#5) and adapters (#4) as those described earlier that allow the pieces to be inserted into one another.</li>
		<li>Seal all&#160;loose connections by wrapping the joints with sealing tape to ensure a hermetic fit.</li>
		<li>Connect the gas delivery tubing (#8) at its open end to a mouthpiece (#9) as shown in the Subject/Imaging Device Unit of Figure 1. 
		NOTE: This step (1.1.6) can be deferred until the subject testing is ready to begin (Step 3.5).</li>
	</ol>
	</li>
	<li>Preparation of the Air Control Unit for gas non-rebreathing
	<ol>
		<li>Isolate the Air Control Unit by disconnecting it from any in-house tubing (#5) or adapters (#4) if it is not already separated.</li>
		<li>Ensure the Douglas bag (#1) is empty or empty the Douglas bag (#1) of any air by systematically rolling-up the bag from the distal end towards the bag&#8217;s inlet port with the three-way valve (#3) set to Configuration 1 as shown in Figure 1.</li>
		<li>Fill the Douglas bag (#1) with the appropriate gas mixture.
		<ol>
			<li>If only room-air non-rebreathing is intended, set the three-way valve to Configuration 2 (shown in Figure 1) and do not fill the Douglas bag (#1). Otherwise continue with the steps that comprise Step 1.2.3.</li>
			<li>Connect the Air Control Unit (shown in Figure 1) at the outlet port of the three-way valve (#3) to a gas-cylinder (containing the desired air-mixture) using the appropriate adapters and tubing. Use a cuff adapter to mount a 1/8&#8221; gas filling tube to the outer diameter of the three-way valve (#3).</li>
			<li>Set the three-way valve assembly to Configuration 1 (as shown in Figure 1) to allow the intended gas to flow from the storage cylinder into the Douglas bag (#1). Open the gas cylinder.</li>
			<li>Once the Douglas bag (#1) is filled to the intended volume (usually half-filled), close the gas cylinder outlet and set the three-way valve to Configuration 2, which isolates the gas within the Douglas bag (#1). Disconnect the Air Control Unit from any tubing used to fill the Douglas bag (#1).</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
2. Preparing the Subject for Imaging
<ol>
	<li>After the subject consents to participate in the study, sit the subject behind the OCTA imaging device. Explain the testing procedures to the subject.</li>
	<li>Confirm the subject&#8217;s medical history to ensure that the subject has no existing medical conditions that increase the risk of participating in the study. 
	NOTE: Pre-existing cardiovascular or pulmonary diseases are risk factors for which subjects may be excluded from participating. It is essential that the subject understand that they can stop the procedure at any time for any reason such as feeling lightheaded or some additional unexpected discomfort.</li>
	<li>Determine the eye to be assessed as per the testing protocol. One eye only may be imaged to limit the testing time and minimize the potential discomforts from the gas non-rebreathing.</li>
	<li>Consider eye dilation if the subject has a pupil size of about 2.5 mm or less. Although dilation is not mandatory, it enhances the chances of acquiring good quality images. To dilate, instill one drop each of 0.5% proparacaine hydrochloride ophthalmic solution, 1% tropicamide ophthalmic solution and 2.5% phenylephrine hydrochloride ophthalmic solution. Full dilation should occur within 10&#8211;15 min.</li>
</ol>
3. Gas Provocation Experiment and Image Acquisition
<ol>
	<li>Create a profile for the patient in the OCTA machine.</li>
	<li>Wear gloves.</li>
	<li>Wipe down the OCTA head and chin rest with an alcohol swab to disinfect the setup.</li>
	<li>Free the mouthpiece (#9) from its sterile packaging. 
	NOTE: Refrain from touching the mouthpiece as much as possible as this component makes direct contact with the mucus lining of the mouth of the subject</li>
	<li>Connect the mouthpiece (#9) to gas delivery tubing (#8)</li>
	<li>Place a pulse oximeter on the subjects&#8217; finger and begin monitoring oxygen saturation levels and pulse. 
	NOTE: Once the subject begins breathing the desired air mixture, the pulse oximeter should be continuously monitored by the examiner. If the oxygen saturation of the subject drops below 94%, the experiment should be stopped, as a safety precaution, and the subject observed until they return to baseline.</li>
	<li>Adjust the height of the OCTA setup so that the subject can easily rest their chin on the chinrest (#11) without overextending or flexing their neck.</li>
	<li>Loop the gas delivery tubing (#8) with mouthpiece (#9) attachment through the head and chin rest with the mouthpiece (#9) facing the patient. Have the tubing loop through the machine oppposite the side of the eye that the subject is having imaged.</li>
	<li>Insert the mouthpiece into the patient&#8217;s mouth. Encourage the subject to practice breathing through the non-rebreathing setup to create familiarity with the apparatus. Ensure the subject takes deep breathes to facilitate gas exchange.</li>
	<li>Place the nose clip (#10) on the subject to ensure they are breathing through the mouthpiece.</li>
	<li>Keep the three-way valve on Configuration 2 or change it to Configuration 1 depending on whether images are being acquired for exposure to room air or a specific gas mixture, respectively. For future reference, note the time as the start of gas inhalation.</li>
	<li>Have the subject place their chin on the right or left section of the chinrest (#11) according to the eye selected for imaging.</li>
	<li>Ensure they move their head forward until their forehead is in firm contact with the headrest (#11).</li>
	<li>Capture the OCTA scan of interest as determined by the testing protocol. In this study, three 3 mm x 3 mm images centered on the fovea were captured after 1 min of gas breathing.
	<ol>
		<li>Have the subject keep their head facing forward and still while fixating on the target in the center of their view</li>
		<li>In the live image seen in the iris view, center the scan.</li>
		<li>Bring the iris into focus by moving the chinrest in or out using the left-right arrows.</li>
		<li>Make sure the foveal dip is centered in the OCT scan, which should occur by default.</li>
		<li>Take an image. Scanning will usually last several seconds on an OCTA machine.</li>
		<li>View the OCTA image after the completion of the scan and ensure it is of adequate quality. Signal strength should be a 7 or better on a 10-point scale provided by the OCTA manufacturer.</li>
		<li>Select save or rescan the eye.</li>
		<li>Repeat steps 3.14.1&#8211;3.14.7 for as many scans are desired.</li>
		<li>Allow the subject to sit back from the machine. Remove the nose clip (#10) and the mouthpiece (#9) when no more scans of the eye with this gas mixture are needed.</li>
	</ol>
	</li>
	<li>Allow subjects a 2 min break before starting CO2 gas provocation experiments.</li>
	<li>Fill the Douglas bag with the first desired air mixture (consisting of 5% CO2, 21% oxygen and 74% nitrogen) as specified in step 1.2. The three-way valve will be in Configuration 2 after this step.</li>
	<li>Complete gas non-rebreathing apparatus setup by connecting the Air Control Unit to the Non-rebreathing Unit as shown in Figure 1 and described in step 1.1.4. Make sure all joints are airtight with sealing tape.</li>
	<li>Repeat steps 3.9&#8211;3.14, but now set the three-way valve to Configuration 1 when directed in step 3.11.</li>
	<li>Give subjects a 10 min break after the CO2 gas provocation to allow a return to baseline.</li>
	<li>While the subject is on break, fill the Douglas bag with 100% O2 according to step 1.2.</li>
	<li>Repeat steps 3.17&#8211;3.18 to perform the experiment under 100% O2 gas provocation conditions.</li>
</ol>
4. Experimental Clean Up
<ol>
	<li>Discard the disposable elements of the setup: the subject&#8217;s mouthpiece (#9) and nose clip (#10).</li>
	<li>Clean the head and chin rest (#11) using an alcohol swab. Wipe the subject chair, OCTA table and OCTA handles with a disinfectant wipe to remove any errant saliva.</li>
	<li>Disconnect the setup into its base components&#8212;the Air Control Unit and Non-rebreathing Unit&#8212;at the three-way valve (#3).</li>
	<li>As no air exhaled from the subject should have reached the elements of the Air Control Unit, empty the Douglas bag according to step 1.2.2 and place in a location for future retrieval. Disconnect the clean-bor tube (#2) with adapter (#2*) and three-way valve (#3) from the Douglas bag if desired for easier storage. This completes the Air Control Unit clean up.</li>
	<li>Remove the gas delivery tubing (#8) from the Non-rebreathing Unit by disconnecting it from the elbow joint (#7). Disconnect the in-house rubber tubing (#5) and tubing adapters (#4), from the two-way non-rebreathing valve (#6). Then do the same from the elbow joint (#7) by removing the sealing tape and detaching the parts by pulling them apart. 
	NOTE: More extensive cleaning of the two-way non-rebreathing valve may be facilitated by disassembling it to remove the internal diaphragms for additional care.</li>
	<li>Prepare a disinfectant bath for cleanup of the reusable components
	<ol>
		<li>Fill a container large enough to submerge the gas delivery tubing (#8) with an appropriately diluted and well mixed detergent disinfectant. In this case, dilute the detergent with water to a ratio of 1:6425.</li>
	</ol>
	</li>
	<li>Soak the gas delivery tubing (#8), two-way non-rebreathing valve (#6), elbow joint (#7), in-house rubber tubing (#5) and tubing adapters (#4) in the prepared disinfectant bath for at least 10 min.</li>
	<li>Remove all parts after the bath is over and rinse them thoroughly with water.</li>
	<li>Place them on a paper towel on a clean countertop to be air-dried.</li>
	<li>Once air drying has completed, dispose of the paper towel and place all components away for storage.</li>
</ol>
5. OCTA Data Export and Analysis
<ol>
	<li>OCTA data export
	<ol>
		<li>Export OCTA data by inserting a removable media device of choice into the OCTA computer. Find the subject and scan of interest.</li>
		<li>Select Export to create a zip folder containing the subject of interest&#8217;s data in a .bmp format on the removable media device.</li>
	</ol>
	</li>
	<li>OCTA data analysis
	<ol>
		<li>Organize the OCTA data on a laboratory computer with the ability to perform additional image analysis and processing.</li>
		<li>Use a custom script to suppress noise with a global thresholding technique and perform additional feature extraction. Binarize and skeletonize the OCTA images.</li>
		<li>On the post-processed images, calculate the vessel skeleton density (VSD)19,26, a dimensionless measure of the total linear length of vessels in an image calculated by the following equation performed on a binarized skeletonized image of the OCTA: 
		<img alt="Equation 1" src="/files/ftp_upload/60948/60948equ01.jpg" /> 
		where i and j refer to pixel coordinate (i,j), L(i,j) refers to white pixels representing decorrelation, X(i,j) refers to all pixels, and n refers to the dimensions of the pixel array, which can be assumed to be n x n pixels19,26. The denominator of this equation represents the total number of pixels which is calculated as written from the skeletonized image, but can be thought of as representing the physical area of the entire image.</li>
	</ol>
	</li>
</ol>

Carl Zeiss Meditec has provided grant funding, equipment and financial support to AHK related to the topic of this article.

The methodology just described is the complete protocol for a gas breathing provocation experiment that allows for the measurement of a subject&#8217;s RVR in a controlled environment at specific timepoints with no modifications to the OCTA imaging device and minimal discomfort or risk to the subject. This setup is described in a way that allows for easy modifications to fit the needs of the researcher. It can accommodate additional tubing to fit different clinic rooms and certain elements such as the in-house tubing or ...

The metabolic demand of the retina is dependent on an adequate and constant supply of oxygen provided by a well-regulated system of arterioles, capillaries and venules1. Several studies have demonstrated that the function of larger caliber human retinal vessels can be assessed in vivo with various physiologic2,3,4,5 and pharmacologic6,7 stimuli. In addition, abnormal function of this vascular system is common in retinal vascular diseases such as diabetic retinopathy where retinal vascular reactivity (RVR) has been shown to be attenuated even in its earliest stages8,9 through both gas provocation9 and flickering light experiments5,10,11. Retinal vascular risk factors such as smoking have also been correlated with impaired RVR12 and retinal blood flow13. These findings are important since the clinical symptoms of retinal vascular disease occur relatively late in the disease process and proven early clinical markers of disease are lacking14. Thus, assessing RVR can provide useful measures of vascular integrity for the early assessment of abnormalities that can initiate or exacerbate retinal degenerative diseases.
Previous RVR experiments have usually relied upon devices such as a laser blood flowmeter9 or fundus cameras equipped with special filters15 for retinal image acquisition. However, these technologies are optimized for larger diameter vessels such as arterioles16 and venules15, which are not where gas, micronutrient and molecular exchange occur. A more recent study was able to quantify the RVR of capillaries using adaptive optics imaging17, but despite the improved spatial resolution, these images have a smaller field size and are not FDA approved for clinical use18.
The recent advent of optical coherence tomography angiography (OCTA) has provided an FDA approved, noninvasive and dyeless angiographic method of assessing capillary level changes in human patients and subjects in vivo. OCTA is widely accepted in clinical practice as an effective tool for assessing impairment in capillary perfusion in retinal vascular diseases such as diabetic retinopathy19, retinal venous occlusions20, vasculitis21 and many others22. OCTA therefore provides an excellent opportunity for the evaluation of capillary level changes, which can have significant spatial and temporal heterogeneity23 as well as pathologic changes, in a clinical setting. Our group recently demonstrated that OCTA can be used to quantify the responsiveness of retinal vessels at the capillary level2 to physiologic changes in inspired oxygen, which is a retinal vasoconstrictive stimulus16,24, and carbon dioxide, which is a retinal vasodilatory stimulus3,5.
The goal of this article is to describe a protocol that will allow the reader to assess the retinal vascular reactivity of the smaller arterioles and capillary bed using OCTA. The methods are adapted from those presented in Lu et al.25 who described the measurement of cerebrovascular reactivity with magnetic resonance imaging. Although the present methods were developed and used during OCTA imaging2, they are applicable to other retinal imaging devices with relatively simple and obvious modifications.

<table><tbody><tr><td>5% CO&lt;sub&gt;2&lt;/sub&gt; gas [5% CO&lt;sub&gt;2&lt;/sub&gt;, 21% O&lt;sub&gt;2&lt;/sub&gt;, 74% N&lt;sub&gt;2&lt;/sub&gt;] (Compressed)</td><td>Institution Dependent (Praxair)</td><td></td><td></td></tr><tr><td>Bacdown Disinfectant Detergent</td><td>Decon Labs</td><td>8001</td><td>https://deconlabs.com/products/disinfectant-bdd/</td></tr><tr><td>Clean-Bor Tubes (35 mm Inner Diameter)</td><td>Vacumed</td><td>1011-108</td><td>http://www.vacumed.com/zcom/product/Product.do?compid=27&amp;amp;skuid=1197</td></tr><tr><td>Cuff adapter for Douglas bag filling</td><td>Vacumed</td><td>22254</td><td>http://www.vacumed.com/zcom/product/Product.do?compid=27&amp;amp;prodid=343</td></tr><tr><td>Douglas bag (200 L capacity)</td><td>Harvard Apparatus</td><td>500942</td><td>https://www.harvardapparatus.com/douglas-bag.html</td></tr><tr><td>Elbow Joint (Inner Diameter 19 mm/Outer Diameter 22 mm), Modified in House</td><td></td><td></td><td></td></tr><tr><td>Fingertip Pulse Oximeter (Pro-Series)</td><td>CMS</td><td>CMS 500DL</td><td>https://www.walmart.com/ip/Pro-Series-CMS-500DL-Fingertip-Pulse-Oximeter-Blood-Oxygen-Saturation-Monitor-with-silicon-cover-batteries-and-lanyard/479049154</td></tr><tr><td>Gas Delivery Tube (22 mm Inner Diameter) Modified in House</td><td></td><td></td><td></td></tr><tr><td>Gas filling tube (1/8&quot; for compressed gas)</td><td></td><td></td><td></td></tr><tr><td>Hydrogen Peroxide Cleaner Disinfectant Wipes</td><td>Clorox Healthcare</td><td>30824</td><td>https://www.cloroxpro.com/products/clorox-healthcare/hydrogen-peroxide-cleaner-disinfectants/?gclid=EAIaIQobChMIk-KG4vi15QIVcRh9Ch0NNwLPEAAYASAAEgJIa_D_BwE&amp;amp;gclsrc=aw.ds</td></tr><tr><td>Lubricant Eye Drops</td><td>Refresh</td><td>Refresh Plus</td><td>https://www.refreshbrand.com/Products/refresh-plus</td></tr><tr><td>Manual Directional Control Valves: Three-Way T-Shape Stopcock Type (Inner Diameter 28.6 mm, Outer Diameter 35 mm)</td><td>Hans Rudolph</td><td>2100C Series</td><td>www.rudolphkc.com</td></tr><tr><td>Medical O&lt;sub&gt;2&lt;/sub&gt; (Compressed)</td><td>Institution Dependent</td><td></td><td></td></tr><tr><td>Mouth piece (Silicone, Model #9061)</td><td>Hans Rudolph</td><td>602076</td><td>www.rudolphkc.com</td></tr><tr><td>OCTA Imaging Device (PLEX Elite 9000)</td><td>Carl Zeiss Meditec, Dublin, CA, USA</td><td></td><td>https://www.zeiss.com/meditec/int/product-portfolio/optical-coherence-tomography-devices/plex-elite-9000-swept-source-oct.html</td></tr><tr><td>Phenylephrine Hydrochloride Ophthalmic Solution, USP 2.5%</td><td>Paragon Bioteck, Inc</td><td>NDC 42702-102-15</td><td>https://paragonbioteck.com/products/diagnostics/phenylephrine-hydrochloride-ophthalmic-solution-usp-2-5/</td></tr><tr><td>Plastic Nose Clip Sterile Foam CS100</td><td>Sklar Sterile</td><td>96-2951</td><td>https://www.sklarcorp.com/disposables/plastic/plastic-nose-clip-sterile-foam-box-of-100.html</td></tr><tr><td>Proparacaine Hydrochloride Ophthalmic Solution, USP .5%</td><td>Bausch + Lomb</td><td>NDC 24208-730-06</td><td>https://www.bausch.com/ecp/our-products/rx-pharmaceuticals/generics</td></tr><tr><td>Regulator (tank dependent- 5% CO&lt;sub&gt;2&lt;/sub&gt;: Fisherbrand Mulitstage Gas Cylinder Regulators)</td><td>Genstar Technologies Company</td><td>10575150</td><td>https://www.fishersci.com/shop/products/fisherbrand-multistage-cylinder-regulators-22/10575150?keyword=true</td></tr><tr><td>Regulator (tank dependent- Oxygen: Fisherbrand Multistage Gas Cylinder Regulators)</td><td>Genstar Technologies Company</td><td>10575145</td><td>https://www.fishersci.com/shop/products/fisherbrand-multistage-cylinder-regulators-22/10575145?keyword=true</td></tr><tr><td>Rubber Tubing (Inner diameter 19 mm, Outer diameter 27 mm), Made in House</td><td></td><td></td><td></td></tr><tr><td>Sealing tape- Parafilm Wrap (2&quot; Wide)</td><td>Cole Parmer</td><td>PM992</td><td>https://www.coleparmer.com/i/parafilm-pm992-wrap-2-wide-250-ft-roll/0672050?PubID=VV&amp;amp;persist=True&amp;amp;ip=no&amp;amp;gclid=EAIaIQobChMInY3vqomz5QIVfyCtBh1VSg64EAAYASAAEgJ9n_D_BwE</td></tr><tr><td>Sterile Alcohol Prep Pads</td><td>Medline</td><td>MDS090670</td><td>https://www.medline.com/product/Sterile-Alcohol-Prep-Pads/Swab-Pads/Z05-PF03816</td></tr><tr><td>Tropicamide Ophthalmic Solution, USP 1%</td><td>Akorn</td><td>NDC 17478-102-12</td><td>http://www.akorn.com/prod_detail.php?ndc=17478-102-12</td></tr><tr><td>Tubing Adapter, Made in House</td><td></td><td></td><td></td></tr><tr><td>Two-way non-rebreathing valve (2600 Series- Inner Diameter 28.6 mm, Outer Diameter 35 mm)</td><td>Hans Rudolph</td><td>2600 Series, UM-112078</td><td>www.rudolphkc.com</td></tr></tbody></table>

retinal vascular reactivity as assessed by optical coherence tomography angiography

The vascular supply to the retina has been shown to dynamically adapt through vasoconstriction and vasodilation to accommodate the metabolic demands of the retina. This process, referred to as retinal vascular reactivity (RVR), is mediated by neurovascular coupling, which is impaired very early in retinal vascular diseases such as diabetic retinopathy. Therefore, a clinically feasible method of assessing vascular function may be of significant interest in both research and clinical settings. Recently, in vivo imaging of the retinal vasculature at the capillary level has been made possible by the FDA approval of optical coherence tomography angiography (OCTA), a noninvasive, minimal risk and dyeless angiography method with capillary level resolution. Concurrently, physiological and pathological changes in RVR have been shown by several investigators. The method shown in this manuscript is designed to investigate RVR using OCTA with no need for alterations to the clinical imaging procedures or device. It demonstrates real time imaging of the retina and retinal vasculature during exposure to hypercapnic or hyperoxic conditions. The exam is easily performed with two personnel in under 30 min with minimal subject discomfort or risk. This method is adaptable to other ophthalmic imaging devices and the applications may vary based on the composition of the gas mixture and patient population. A strength of this method is that it allows for an investigation of retinal vascular function at the capillary level in human subjects in vivo. Limitations of this method are largely those of OCTA and other retinal imaging methods including imaging artifacts and a restricted dynamic range. The results obtained from the method are OCT and OCTA images of the retina. These images are amenable to any analysis that is possible on commercially available OCT or OCTA devices. The general method, however, can be adapted to any form of ophthalmic imaging.

The output from this experiment consists of the manual readings taken from the pulse oximeter, the timing noted for gas exposure or OCTA scanning and the raw OCTA imaging data. An OCTA image consists of the OCT B-scans and the decorrelation signal associated with each B-scan. The data parameters are given by the specifications of the device. A swept source laser platform OCTA machine with a central wavelength of 1040&#8211;1060 nm was used. The images provide a transverse resolution of 20 &#181;m and optical axial resolu...

Watch this Scientific Journal Video about Retinal Vascular Reactivity as Assessed by Optical Coherence Tomography Angiography at JoVE.com

Retinal Vascular Reactivity as Assessed by Optical Coherence Tomography Angiography

This article describes a method for measuring retinal vasculature reactivity in vivo with human subjects using a gas breathing provocation technique to deliver vasoactive stimuli while acquiring retinal images.

The vascular supply to the retina has been shown to dynamically adapt through vasoconstriction and vasodilation to accommodate the metabolic demands of ...

retinal-vascular-reactivity-as-assessed-optical-coherence-tomography

Research

JoVE Journal

Neuroscience

7.1K Views.  USC Roski Eye Institute. ROCTA-gebaseerde beoordeling van retinale vasculaire reactiviteit zal onderzoekers en clinici in staat stellen om retinale vasculaire functie te onderzoeken op het capillaire niveau op een niet-invasieve en veilige manier. Omdat OCTA een door de FDA goedgekeurde beeldvormingsmodaliteit is, kan onze techniek in toekomstige klinische proeven van toepassing zijn als een eindpuntmaat van retinale capillaire functie. De retinale versiculaire reactiviteit van een onderwerp weerspiegelt waarschijnli...

Video: Retinal Vascular Reactivity as Assessed by Optical Coherence Tomography Angiography

Doppler Optical Coherence Tomography of Retinal Circulation

Noncontact retinal blood flow measurements are performed with a Fourier domain optical coherence tomography (OCT) system using a circumpapillary double circular scan (CDCS) that scans around the optic nerve head at 3.40 mm and 3.75 mm diameters. The double concentric circles are performed 6 times consecutively over 2 sec. The CDCS scan is saved with Doppler shift information from which flow can be calculated. The standard clinical protocol calls for 3 CDCS scans made with the OCT beam passing through the superonasal edge of the pupil and 3 CDCS scan through the inferonal pupil. This double-angle protocol ensures that acceptable Doppler angle is obtained on each retinal branch vessel in at least 1 scan. The CDCS scan data, a 3-dimensional volumetric OCT scan of the optic disc scan, and a color photograph of the optic disc are used together to obtain retinal blood flow measurement on an eye. We have developed a blood flow measurement software called "Doppler optical coherence tomography of retinal circulation" (DOCTORC). This semi-automated software is used to measure total retinal blood flow, vessel cross section area, and average blood velocity. The flow of each vessel is calculated from the Doppler shift in the vessel cross-sectional area and the Doppler angle between the vessel and the OCT beam. Total retinal blood flow measurement is summed from the veins around the optic disc. The results obtained at our Doppler OCT reading center showed good reproducibility between graders and methods (&lt;10%). Total retinal blood flow could be useful in the management of glaucoma, other retinal diseases, and retinal diseases. In glaucoma patients, OCT retinal blood flow measurement was highly correlated with visual field loss (R2&gt;0.57 with visual field pattern deviation). Doppler OCT is a new method to perform rapid, noncontact, and repeatable measurement of total retinal blood flow using widely available Fourier-domain OCT instrumentation. This new technology may improve the practicality of making these measurements in clinical studies and routine clinical practice.

Total retinal blood flow is measured by Doppler optical coherence tomography and semi-automated grading software.

Noncontact retinal blood flow measurements are performed with a Fourier domain optical coherence tomography (OCT) system using a circumpapillary double ...

Medicine

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy (oSLO) and Optical Coherence Tomography (OCT)

While fluorescence imaging is widely used in ophthalmology, a large field of view (FOV) three-dimensional (3D) fluorescence retinal image is still a big challenge with the state-of-the-art retinal imaging modalities because they would require z-stacking to compile a volumetric dataset. Newer optical coherence tomography (OCT) and OCT angiography (OCTA) systems overcome these restrictions to provide three-dimensional (3D) anatomical and vascular images, but the dye-free nature of OCT cannot visualize leakage indicative of vascular dysfunction. This protocol describes a novel oblique scanning laser ophthalmoscopy (oSLO) technique that provides 3D volumetric fluorescence retinal imaging. The setup of the imaging system generates the oblique scanning by a dove tail slider and aligns the final imaging system at an angle to detect fluorescent cross-sectional images. The system uses the laser scanning method, and therefore, allows an easy incorporation of OCT as a complementary volumetric structural imaging modality. In vivo imaging on rat retina is demonstrated here. Fluorescein solution is intravenously injected to produce volumetric fluorescein angiography (vFA).

Multimodal Volumetric Retinal Imaging by Oblique Scanning Laser Ophthalmoscopy oSLO and Optical Coherence Tomography OCT

Here, we present a protocol to get a large field of view (FOV) three-dimensional (3D) fluorescence and OCT retinal image by using a novel imaging multimodal platform. We will introduce the system setup, the method of alignment, and the operational protocols. In vivo imaging will be demonstrated, and representative results will be provided.

While fluorescence imaging is widely used in ophthalmology, a large field of view (FOV) three-dimensional (3D) fluorescence retinal image is still a big ...

Bioengineering

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo

Structural changes in the retina are common manifestations of ophthalmic diseases. Optical coherence tomography (OCT) enables their identification in vivo&#8212;rapidly, repetitively, and at a high resolution. This protocol describes OCT imaging in the mouse retina as a powerful tool to study optic neuropathies (OPN). The OCT system is an interferometry-based, non-invasive alternative to common post mortem histological assays. It provides a fast and accurate assessment of retinal thickness, allowing the possibility to track changes, such as retinal thinning or thickening. We present the imaging process and analysis with the example of the Opa1delTTAG mouse line. Three types of scans are proposed, with two quantification methods: standard and homemade calipers. The latter is best for use on the peripapillary retina during radial scans; being more precise, is preferable for analyzing thinner structures. All approaches described here are designed for retinal ganglion cells (RGC) but are easily adaptable to other cell populations. In conclusion, OCT is efficient in mouse model phenotyping and has the potential to be used for the reliable evaluation of therapeutic interventions.

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo

This manuscript describes a protocol for the in vivo imaging of the mouse retina with high-resolution spectral domain optical coherence tomography (SD-OCT). It focuses on retinal ganglion cells (RGC) in the peripapillary region, with several scanning and quantifying approaches described.

Structural changes in the retina are common manifestations of ophthalmic diseases. Optical coherence tomography (OCT) enables their identification in ...

In vivo Structural Assessments of Ocular Disease in Rodent Models using Optical Coherence Tomography

Spectral-domain optical coherence tomography (SD-OCT) is useful for visualizing retinal and ocular structures in vivo. In research, SD-OCT is a valuable tool to evaluate and characterize changes in a variety of retinal and ocular disease and injury models. In light induced retinal degeneration models, SD-OCT can be used to track thinning of the photoreceptor layer over time. In glaucoma models, SD-OCT can be used to monitor decreased retinal nerve fiber layer and total retinal thickness and to observe optic nerve cupping after inducing ocular hypertension. In diabetic rodents, SD-OCT has helped researchers observe decreased total retinal thickness as well as decreased thickness of specific retinal layers, particularly the retinal nerve fiber layer with disease progression. In mouse models of myopia, SD-OCT can be used to evaluate axial parameters, such as axial length changes. Advantages of SD-OCT include in vivo imaging of ocular structures, the ability to quantitatively track changes in ocular dimensions over time, and its rapid scanning speed and high resolution. Here, we detail the methods of SD-OCT and show examples of its use in our laboratory in models of retinal degeneration, glaucoma, diabetic retinopathy, and myopia. Methods include anesthesia, SD-OCT imaging, and processing of the images for thickness measurements.

Here, we describe the use of spectral-domain optical coherence tomography (SD-OCT) to visualize retinal and ocular structures in vivo in models of retinal degeneration, glaucoma, diabetic retinopathy, and myopia.

Spectral-domain optical coherence tomography (SD-OCT) is useful for visualizing retinal and ocular structures in vivo. In research, SD-OCT is a valuable ...

Using Optical Coherence Tomography and Optokinetic Response As Structural and Functional Visual System Readouts in Mice and Rats

Optical coherence tomography (OCT) is a fast, non-invasive, interferometric technique allowing high-resolution retinal imaging. It is an ideal tool for the investigation of processes of neurodegeneration, neuroprotection and neuro-repair involving the visual system, as these often correlate well with retinal changes. As a functional readout, visually evoked compensatory eye and head movements are commonly used in experimental models involving the visual function. Combining both techniques allows a quantitative in vivo investigation of structure and function, which can be used to investigate the pathological conditions or to evaluate the potential of novel therapeutics. A great benefit of the presented techniques is the possibility to perform longitudinal analyses allowing the investigation of dynamic processes, reducing variability and cuts down the number of animals needed for the experiments. The protocol described aims to provide a manual for acquisition and analysis of high quality retinal scans of mice and rats using a low cost customized holder with an option to deliver inhalational anesthesia. Additionally, the proposed guide is intended as an instructional manual for researchers using optokinetic response (OKR) analysis in rodents, which can be adapted to their specific needs and interests.

A detailed protocol for the assessment of structural and visual readouts in rodents by optical coherence tomography and optokinetic response is presented. The results provide valuable insights for ophthalmologic as well as neurologic research.

Optical coherence tomography (OCT) is a fast, non-invasive, interferometric technique allowing high-resolution retinal imaging. It is an ideal tool for ...

Oxygen-Induced Retinopathy Model for Ischemic Retinal Diseases in Rodents

One of the commonly used models for ischemic retinopathies is the oxygen-induced retinopathy (OIR) model. Here we describe detailed protocols for the OIR model induction and its readouts in both mice and rats. Retinal neovascularization is induced in OIR by exposing rodent pups either to hyperoxia (mice) or alternating levels of hyperoxia and hypoxia (rats). The primary readouts of these models are the size of neovascular (NV) and avascular (AVA) areas in the retina. This preclinical in vivo model can be used to evaluate the efficacy of potential anti-angiogenic drugs or to address the role of specific genes in the retinal angiogenesis by using genetically manipulated animals. The model has some strain and vendor specific variation in the OIR induction which should be taken into consideration when designing the experiments.

Oxygen-induced retinopathy (OIR) can be used to model ischemic retinal diseases such as retinopathy of prematurity and proliferative diabetic retinopathy and to serve as a model for proof-of-concept studies in evaluating antiangiogenic drugs for neovascular diseases. OIR induces robust and reproducible neovascularization in the retina that can be quantified.

One of the commonly used models for ischemic retinopathies is the oxygen-induced retinopathy (OIR) model. Here we describe detailed protocols for the OIR ...

In Vivo Vascular Injury Readouts in Mouse Retina to Promote Reproducibility

Advancements in ophthalmic imaging tools offer an unprecedented level of access to researchers working with animal models of neurovascular injury. To properly leverage this greater translatability, there is a need to devise reproducible methods of drawing quantitative data from these images. Optical coherence tomography (OCT) imaging can resolve retinal histology at micrometer resolution and reveal functional differences in vascular blood flow. Here, we delineate noninvasive vascular readouts that we use to characterize pathological damage post vascular insult in an optimized mouse model of retinal vein occlusion (RVO). These readouts include live imaging analysis of retinal morphology, disorganization of retinal inner layers (DRIL) measure of capillary ischemia, and fluorescein angiography measures of retinal edema and vascular density. These techniques correspond directly to those used to examine patients with retinal disease in the clinic. Standardizing these methods enables direct and reproducible comparison of animal models with clinical phenotypes of ophthalmic disease, increasing the translational power of vascular injury models.

In Vivo Vascular Injury Readouts in Mouse Retina to Promote Reproducibility

Here, we present three data analysis protocols for fluorescein angiography (FA) and optical coherence tomography (OCT) images in the study of Retinal Vein Occlusion (RVO).

Advancements in ophthalmic imaging tools offer an unprecedented level of access to researchers working with animal models of neurovascular injury. To ...

Evaluation of Capillary and Other Vessel Contribution to Macular Perfusion Density Measured with Optical Coherence Tomography Angiography

Parafoveal circulation of the superficial retinal capillary plexus is usually measured with vessel density, which determines the length of capillaries with circulation, and perfusion density, which calculates the percentage of the evaluated area that has circulation. Perfusion density also considers the circulation of vessels larger than capillaries, although the contribution of these vessels to the first is not usually evaluated. As both measurements are automatically generated by optical coherence tomography angiography devices, this paper proposes a method for estimating the contribution of vessels larger than capillaries by using a coefficient of determination between vessel and perfusion densities. This method can reveal a change in the proportion of perfusion density from vessels larger than capillaries, even when mean values do not differ. This change could reflect compensatory arterial vasodilatation as a response to capillary dropout in the initial stages of retinal vascular diseases before clinical retinopathy appears. The proposed method would allow the estimation of the changes in the composition of perfusion density without the need for other devices.

We describe the evaluation of a coefficient of determination between vessel and perfusion density of the parafoveal superficial capillary plexus to identify the contribution of vessels larger than capillaries to perfusion density.

Parafoveal circulation of the superficial retinal capillary plexus is usually measured with vessel density, which determines the length of capillaries ...

Application of Optical Coherence Tomography to a Mouse Model of Retinopathy

Optical coherence tomography (OCT) offers a noninvasive method for the diagnosis of retinopathy. The OCT machine can capture retinal crosssectional images from which the retinal thickness can be calculated. Although OCT is widely used in clinical practice, its application in basic research is not as prevalent, especially in small animals such as mice. Because of the small size of their eyeballs, it is challenging to conduct fundus imaging examinations in mice. Therefore, a specialized retinal imaging system is required to accommodate OCT imaging on small animals. This article demonstrates a small-animal-specific system for OCT examination procedures and a detailed method for image analysis. The results of retinal OCT examination of very-low-density lipoprotein receptor (Vldlr) knockout mice and C57BL/6J mice are presented. The OCT images of C57BL/6J mice showed retinal layers, while those of Vldlr knockout mice showed subretinal neovascularization and retinal thinning. In summary, OCT examination could facilitate the noninvasive detection and measurement of retinopathy in mouse models.

Here, we describe an in vivo imaging technique using optical coherence tomography to facilitate the diagnosis and quantitative measurement of retinopathy in mice.

Optical coherence tomography (OCT) offers a noninvasive method for the diagnosis of retinopathy. The OCT machine can capture retinal crosssectional images ...

Image-Guided Optical Coherence Tomography to Assess Structural Changes in Rodent Retinas

Ocular diseases, such as age-related macular degeneration, glaucoma, retinitis pigmentosa, and uveitis, are always accompanied by retinal structural changes. These diseases affecting the fundus always exhibit typical abnormalities in certain cell types in the retina, including photoreceptor cells, retinal ganglion cells, cells in the retinal blood vessels, and cells in the choroidal vascular cells. Noninvasive, highly efficient, and adaptable imaging techniques are required for both clinical practice and basic research. Image-guided optical coherence tomography (OCT) satisfies these requirements because it combines fundus photography and high-resolution OCT, providing an accurate diagnosis of tiny lesions as well as important changes in the retinal architecture. This study details the procedures of data collection and data analysis for image-guided OCT and demonstrates its application in rodent models of choroidal neovascularization (CNV), optic nerve crush (ONC), light-induced retinal degeneration, and experimental autoimmune uveitis (EAU). This technique helps researchers in the eye field to identify rodent retinal structural changes conveniently, reliably, and tractably.

The protocol presented here details the procedures of data collection and data analysis for image-guided optical coherence tomography (OCT) and demonstrates its application in multiple rodent models of ocular diseases.

Ocular diseases, such as age-related macular degeneration, glaucoma, retinitis pigmentosa, and uveitis, are always accompanied by retinal structural ...

Retinal Vascular Reactivity as Assessed by Optical Coherence Tomography Angiography

Samenvatting

Meer video's verkennen