Analysis of Retinochoroidal Vasculature in Underweight Women Using Optical Coherence Tomography Angiography
Study Details
Study Description
Brief Summary
Cachectic patients and controls undergoing a comprehensive ophthalmologic examination. The imaging of all subjects is undertaken using a commercial OCTA device with a scan rate of 70,000 A-scans/s, scan beam wavelength of 840 ± 10 nm and bandwidth of 45 nm. All measurements are performed between 10:00 and 12:00 on the same day. The OCTA images are independently graded and assessed by two retinal specialists. The software automatically segmented these full-thickness retinal scans into the superficial and deep inner retinal vascular plexuses, outer retina, and choriocapillaris (CC). The vascular density in the superficial and deep retinal vascular zones is calculated automatically by the software, and the foveal avascular zone (FAZ) and foveal density (FD) are also automatically determined. Choroidal thickness is calculated manually by two retinal specialists, and the average value was used.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Cachectic patients and controls undergoing a comprehensive ophthalmologic examination, including the measurements of best-corrected visual acuity (BCVA), refractive error (KR-8900; Topcon, Tokyo, Japan), intraocular pressure (IOP, Full Auto Tonometer TX-F; Topcon), axial length (AL, Lenstar LS 900, Haag-Streit AG, Switzerland), slit lamp examination of the anterior segment, dilated fundus examination, and OCTA imaging (Optovue RTVue XR 100 Avanti, Freemont, California, USA) are included in the study. To calculate BMI, height is measured using a standard anthropometric tape (Bioplus Stature Meter, model number IND/09/2005/815), and a certified electronic weighing scale (model number Omron HN-283) is used to measure weight.
According to the national guidelines, the patients are classified into two underweight groups: Group 1 consisting of those with a BMI of <17.00 kg/m2 and Group 2 comprising those with a BMI of 17.00 to 18.49 kg/m2. The control group is formed with individuals with a normal BMI (18.50 to 24.99 kg/m2).
The right eye of each participant is included in the study. If the right eye meets any of the exclusion criteria, then the left eye is selected for the sample. The inclusion criteria for the patient group is being underweight (BMI < 18.50 kg/m2). The exclusion criteria for all groups are as follows: refractive error >+3.0 diopters (D) or <-3.0 D spherical equivalent; poor image quality <60 due to unstable fixation; IOP > 21 mm Hg; longer AL (>25 mm); pre-existing ophthalmic pathologies; prior ocular surgery; and a systemic chronic disease that can cause underweight or retinopathy, such as cancer, malnutrition, and diabetes mellitus.
OCTA
The imaging of all subjects is undertaken using a commercial OCTA device with a scan rate of 70,000 A-scans/s, scan beam wavelength of 840 ± 10 nm and bandwidth of 45 nm. This device can perform 70 000 A-scans/s per second to acquire volumes of 304 × 304 A-scans. All measurements are performed between 10:00 and 12:00 on the same day.
To evaluate the vascular structures, 6×6 mm OCTA software is used. The split-spectrum amplitude decorrelation angiography (SSADA) algorithm is performed in all participants. The images of poor quality (signal strength index (SSI) < 8) with either significant motion artifact or incorrect segmentation are excluded. The OCTA images are independently graded and assessed by two retinal specialists. The software automatically segmented these full-thickness retinal scans into the superficial and deep inner retinal vascular plexuses, outer retina, and choriocapillaris (CC). The vascular density in the superficial and deep retinal vascular zones is calculated automatically by the software, and the foveal avascular zone (FAZ) and foveal density (FD) are also automatically determined. The same software also calculates the flow index rates in a central circular zone of 3.144 mm² in the outer retina and CC segments. Choroidal thickness is calculated manually by two retinal specialists, and the average value was used.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Underweight Comprehensive ophthalmologic examination |
Diagnostic Test: Comprehensive ophthalmologic examination
Measurements of best-corrected visual acuity, refractive error, intraocular pressure, axial length, slit lamp examination of the anterior segment, dilated fundus examination, and optical coherence tomography angiography imaging.
|
| Control Comprehensive ophthalmologic examination |
Diagnostic Test: Comprehensive ophthalmologic examination
Measurements of best-corrected visual acuity, refractive error, intraocular pressure, axial length, slit lamp examination of the anterior segment, dilated fundus examination, and optical coherence tomography angiography imaging.
|
Outcome Measures
Primary Outcome Measures
- Choriocapillaris flow area [10 minutes]
Choriocapillaris flow area assessed with optical coherence tomography angiography
Secondary Outcome Measures
- Subfoveal choroidal thickness [10 minutes]
Subfoveal choroidal thickness assessed with optical coherence tomography angiography
- Vessel density [10 minutes]
Vessel density assessed with optical coherence tomography angiography
- Foveal avascular zone [10 minutes]
Foveal avascular zone assessed with optical coherence tomography angiography
- Subfoveal central macular thickness [10 minutes]
Subfoveal central macular thickness assessed with optical coherence tomography angiography
Eligibility Criteria
Criteria
Inclusion Criteria:
- Underweight (BMI < 18.50 kg/m2).
Exclusion Criteria:
-
refractive error >+3.0 diopters (D) or <-3.0 D spherical equivalent;
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poor image quality <60 due to unstable fixation
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IOP > 21 mm Hg
-
longer AL (>25 mm)
-
pre-existing ophthalmic pathologies
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prior ocular surgery
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a systemic chronic disease that can cause underweight or retinopathy, such as cancer, malnutrition, and diabetes mellitus.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Aslı Çentinkaya Yaprak | Antalya | Turkey | 070059 |
Sponsors and Collaborators
- Akdeniz University
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 19102017-15/4-184