Photobiomodulation & Dry AMD Treatment

Age‐related macular degeneration (AMD) is a retinal degenerative disease that causes irreversible and profound vision loss in people over the age of 60 years with estimates of AMD patients nearing 70 million worldwide.

It is emerging as one of the primary causes of vision impairment in the developed world.

Age‐related macular degeneration (AMD) occurs in two major forms: exudative (wet) and atrophic (dry) AMD. Dry AMD is characterized by drusen, retinal pigment epithelial (RPE) cell atrophy and subjacent photoreceptor degeneration.

Factors involved in causing RPE cell injury and dysfunction have been shown to include mitochondrial dysfunction, oxidative stress, inflammation and genetic disposition.

The vast majority of AMD patients suffering from dry AMD, marked by RPE dysfunction with drusen formation and eventual retinal atrophy, have no effective treatment options other than lifestyle modification and the use of vitamins.

A safe and globally expanding medical intervention is the use of low‐level laser (light) therapy (LLLT) that now includes diabetic wound repair, arthritis, cancer radiation protection (oral mucositis), dental, sports medicine and skeletal muscle disorders (trauma and pain).

In the last couple of decades, Photobiomodulation (PBM) therapy – a light-based treatment approach used widely for tissue repair and reducing pain and inflammation – has gained recognition among biomedical researchers and healthcare professionals.

Low‐level laser therapy exerts its beneficial effects through increased blood flow and stimulation of cellular functions, a process called photobiomodulation (PBM).

Photobiomodulation (PBM) involves the use of visible to near‐infrared (NIR) light (500–1000 nm) produced by a laser or non‐coherent light sources such as light emitting diodes (LEDs) applied to the body to produce beneficial cellular effects.

Light in this range penetrates tissue depending on the wavelength and stimulates cellular function via activation of photoacceptors.

How PBM Works

PBM works by activating mitochondrial respiratory chain components and stabilizing their metabolic function. It is applicable to a broad spectrum of retinal and optic nerve disorders – from inherited retinal disorders, AMD, diabetic eye diseases, and glaucoma, to trauma and wound healing.

Current treatments for ocular disease work on symptoms, rather than targeting the underlying pathology of the disease. In retinal disease and/or damage, there is an increase in mitochondrial dysfunction and oxidative damage.

The effects of PBM at the cellular level include increasing ATP generation, modulation of intracellular signaling molecules, including reactiveoxygen species (ROS) and nitric oxide (NO) and secondary effects that culminate in sustained changes in cell function and viability. Improvement in these cellular outcomes leads to benefits at the clinical level.

The photobiomodulatory effects of PBM at the molecular level begin with the absorption of specific wavelengths of light by a key mitochondrial enzyme, cytochrome c oxidase (CcO). The interaction of light with CcO creates a biochemical response.

Just as the chlorophyll molecules in plants absorb light and turn it into energy stimulating growth, the mitochondria in animal cells can use light to stimulate cell function and activate protective intracellular pathways.

The process only works when the mitochondria are not functioning properly – if the cells is healthy, the light will not improve its function, and no beneficial effect is observed.

In a malfunctioning cell, mitochondrial output becomes impaired and energy production can become reduced resulting in cellular dysfunction and subsequent clinical complications.

Treatment with PBM can stimulate CcO to optimize its output and thereby improve mitochondrial function. PBM also activates transcription factors in the nucleus resulting in changes at the molecular level which aid in cellular response and resets the metabolic environment in the cell.

It’s important to note that the dose or fluence has to be just right; too little light will not have the desired effect, and if there is too much, the beneficial effect is turned off. This “just right” does can be very difficult to determine in the case of more traditional pharmacological treatments.

Research efforts in the PBM field will allow for further optimization of light dosing to treat different indications.

Many applications of PBM, from heart disease, diabetic wound healing, skeletal muscle injuries, spinal cord healing to neurodegenerative diseases such as Alzheimer’s, traumatic brain injuries, and many more are being investigated. PBM has a tremendous potential in preventive medicine as well.

One of the important aspects of PBM is that different wavelengths produce different effects. When designing Valeda, we had to choose the right targets and select the appropriate PBM wavelengths – from the visible to near infrared light.

The enzyme Cytochrome c Oxidase (CcO) absorbs light at two different wavelengths, which are critical for the optimal PBM functioning by the Valeda system. These wavelengths are 660 nm – far red – and 850 nm – infrared.

We could have developed a system that would use only one of those wavelengths, but when assessing the targets, we found that they were both critical for the enzyme to work. Each wavelength targets a different, but critical site of CcO function.

Next, we decided to add a third wavelength based on different literature publications. We knew that the disease progresses to Geographic Atrophy and 10-15 percent of dry AMD patients’ disease convert to wet AMD.

In the literature, the 590 nm wavelength – yellow – improves nitric oxide generation in ischemia conditions potentially improving local blood flow, and we also saw that it inhibits VEGF expression in RPE cells.

We felt that we might be able to slow disease progression and reduce the number of patients converting to wet AMD, and/or allow us to treat wet AMD patients.

Given that each one of these wavelengths had specific and unique targets, by putting them together we knew we could get the most benefit out of the Valeda system.

We created a delivery system in Valeda that allows us to optimize each wavelength individually and provides us with an adaptable therapy. We are now beginning to investigate the use of Valeda in diabetic macular edema and other ocular areas.

Each disease may require further study, but we have a good starting place from our studies in dry AMD. It is an evolving project; our ultimate aim is to create a system that can be optimized for different treatments.

We believe the use of PBM in ophthalmology is just beginning. We are excited to get the PBM technology platform into the hands of physicians to work with us and provide new treatments for their patients.

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