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MiloMcgrath4 (トーク | 投稿記録) (ページの作成:「<br>Quantitatively figuring out physiological parameters at a microscopic level in the retina furthers the understanding of the molecular pathways of blinding diseases, e…」) |
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2025年9月12日 (金) 06:57時点における版
Quantitatively figuring out physiological parameters at a microscopic level in the retina furthers the understanding of the molecular pathways of blinding diseases, equivalent to diabetic retinopathy and glaucoma. An essential parameter, which has yet to be quantified noninvasively, is the retinal oxygen metabolic fee (rMRO 2). Quantifying rMRO 2 is difficult because two parameters, the blood flow rate and hemoglobin oxygen saturation (sO 2), must be measured collectively. We combined photoacoustic ophthalmoscopy (PAOM) with spectral area-optical coherence tomography (SD-OCT) to sort out this challenge, during which PAOM measured the sO 2 and SD-OCT mapped the blood movement fee. This quantitative methodology might shed new light on each elementary analysis and clinical care in ophthalmology in the future. T he demand for treating blindness and low imaginative and prescient continue to escalate as human longevity will increase worldwide. By 2004 1 , for example, blindness and low vision had affected greater than three million Americans aged 40 years and older; by 2010 2 , 285 million people globally had been affected.
Greater than 80% of such visible impairments had been caused by eye diseases 1 , BloodVitals SPO2 which include glaucoma, diabetic retinopathy (DR), age-related macular degeneration (AMD), and cataracts 1,2. Alterations in oxygen metabolism are believed to be involved in most of these diseases 3,4. For instance, hypoxia within the glaucomatous retina can harm the optic nerve head, partially resulting from insufficient vascular perfusion 5. In DR, the lack of pericytes is commonly related to poorly regulated blood flow 6 , which might additional result in retinal vascular occlusion and retinal hypoxia 7. In AMD, abnormalities in retinal perfusion have also been reported 8. Perturbations in retinal oxygenation can prompt, for BloodVitals wearable instance, degeneration of retinal neurons, lack of photoreceptors, and onset of neovascularization, finally inflicting visual impairment. Therefore, the exact measurement of retinal oxygen metabolic fee (rMRO 2) will be important in investigating these blinding diseases. Non-invasive rMRO 2 quantification has been proposed for many years 9,10 without being efficiently demonstrated. Obtaining rMRO 2 measurements is challenging as a result of it requires measuring retinal blood movement and oxygen saturation (sO 2) collectively. Advances in Doppler spectral domain optical coherence tomography (SD-OCT) makes it attainable to precisely detect retinal blood flow 11. The main impediment is precisely measuring retinal sO 2. To measure retinal sO 2 , researchers have used oxygen-sensitive electrodes and magnetic resonance imaging 12-15 , however these efforts are usually restricted to terminal experiments and/or limited by low spatial resolution.
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