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Stem cells Treatment for Atrophic Optic Nerve

Optic Nerve Atrophy is damage to the optic nerve causing visual loss. Medically, optic nerve atrophy can be linked with the sudden degeneration of retinal ganglion cells, which have been structured to form an optic nerve. The condition can as well be referred to as Atrophic Optic Nerve, and/or optic neuropathy.

Optic nerve atrophy can be an indication of end stage neural damage, anywhere along the path of a visual function. As a matter of fact, optic nerve plays a very pivotal role in transmitting nerve signals that have been received through the eye and pass it on to the central nervous system; in order to visualize an image.  Since, optic nerve is damaged in optic nerve atrophy; transmission of important information to the brain can be halted severely, thus causing visual damage. Moreover, optic nerve atrophy can indicate different complicated conditions, such as neurodegenerative disorders. Some of the common predisposing factors, associated with the conditions can be:

  • Physical damage to the eye
  • Genetic Predisposition
  • History of neurological disorders
  • Increased Blood pressure
  • Environmental triggers

Apparently, above mentioned parameters are only risk factors; whereas causes can be altogether different and can be noted as:

  • Decreased blood supply (ischemia) or oxygen supply (hypoxia) causing swelling/ Stroke
  • Tumor
  • Trauma/Shock/Radiation
  • Heredity
  • Hydrocephalus
  • Toxins (Alcohol/tobacco/ other poisons)
  • Infection
  • Degenerative disorders
  • Glaucoma
  • Diabetes
  • Temporal arteritis
  • Autoimmune disorders (multiple sclerosis/ SLE/Sarcoidosis)
  • Medicines

Some of the common symptoms and signs are:

  • Complete loss of vision
  • Reduced vision- central/periphery
  • Reduced colour vision/ colour seems faded
  • Ability to see fine details is lost
  • Bulging of the eyes
  • Dimming or blurring of vision
  • Double vision
  • Eye redness
  • Involuntary movement of the eyes
  • Seeing blind spots in your peripheral vision
  • Seeing rainbows or halos
  • Severe eye or brow pain or pain when moving the eye


  • Pallor of optic nerve
  • Pupil- reaction to light sluggish
  • Pupil- reaction to light absent
  • Visual acuity
  • Eye pressure
  • Papilloedema

Conventional treatment regimen for atrophic optic nerve include, generalized physiotherapy related to eye and steroidal medications. Damage from optic nerve atrophy cannot be reversed. The underlying disease must be diagnosed and treated. Else, vision loss continues. Rarely, conditions that lead to optic atrophy may be treatable.

Outlook (Prognosis): Vision lost to optic nerve atrophy cannot be recovered. It is essential to protect the other eye.

Alternative treatment with Stem cells has shown promising results in visual recovery after optic nerve atrophy. Stem Cells are the unique core cells of the body, with the potential ability to differentiate into cells of different lineages. The technology has now enabled isolation of Mesenchymal Stem Cells (MSC) from umbilical cord tissue, which is generally being discarded immediately after child birth. These cells have been proven to be immunoprivileged and hence can be exploited without any hurdles of HLA matching. Thus, allogenic application of these MSCs can effectively restore back function through generation of micro environment, regenerating lost cells and secreting important growth factors promoting recovery.

Thus, allogenic application of MSCs can be deployed as the best investigational treatment regimen to help patients suffering from optic nerve atrophy to achieve better visual recovery.

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Stem Cell Treatment for Optic Neuritis

Optic neuritis is a demyelinating inflammation of the optic nerve; that is generally triggered by the immune destruction of surrounding myelin sheath. This demyelination can contribute to the visual disturbances, color blindness and pain in the eyes especially associated with eye movement or dull aching pain behind the eyes. Apparently in more advanced cases, it may indicate optic nerve abnormalities, neural damage, increased neural pressure and neurodegenerative disorders, such as multiple sclerosis. Thus, in fact the optic neuritis may lead to total visual loss, if not treated well in time.

The condition is mostly common in younger adults below 45 years; with suggestive altogether higher incidences in women than in men. In majority of patients, it is either associated with multiple sclerosis (MS) or ischemic optic neuropathy (Blood Clot). Thus besides deliberately promoting visual damage; it can often be related to the neural damage in MS that may be associated with locomotary and sensory functional loss.

As a matter of fact, some of the less common causes of optic neuritis may include:

  • Viral (measles, mumps and herpes) or bacterial infections (Lyme disease, cat-scratch fever and syphilis etc)
  • Sarcoidosis and Lupus
  • Drugs such as Quinine
  • Sinusitis
  • Genetic Predisposition
  • Nutritional deficiency
  • Environmental exposure to toxins

Diagnosis is confirmed by signs which include reduced visual acuity, substantial decrease in the peripheral vision of the patient, reduced sense of colour discrimination and identification of physical abnormality in the pupil of the affected eye confirmed by Slit lamp examination or ophthalmoscope. Visible swelling, blood vessel enlargement and retro bulbar inflammation around the optic nerve are other associated symptoms.
Conventionally, the treatment of MS associated optic neuritis includes intravenous administration of steroidal medications with the notion to reduce optic nerve inflammation; however studies have reported various possible side effects, such as weight gain, mood swings, facial flushing, stomach upset, and sleep apnea. Moreover, long term exposure may dangerously promote organ damage or hormonal disturbances.
Conventional treatment with steroidal medications is associated with numerous side effects. A science of stem cells has a precise solution to limit those challenges; by maximizing neural regeneration, reduction in the inflammation causing glial cell damage and promoting the production of oligodendrocytes.
Stem cells are the naive cells in the body with the potential to differentiate into multiple cells of different lineages or origin. Accordingly, mesenchymal stem cells isolated from human umbilical cord have been reported to be the most potent cells, exhibiting anti inflammatory, immunomodulatory and angiogenic ability. The vast database generated from worldwide clinical studies have raised hope of millions of people, that stem cells therapy can be employed successfully to treat patients with optic neuritis and associated conditions. These cells are reportedly contributing to the stimulation of endogenous stem cells, once infused inside the body; in order to enforce prompt repair and regeneration of lost cells to restore back the function.
Thus, a unique approach of treating degenerative disorders like Optic Neuritis with the help of allogenic administration of mesenchymal stem cells have definitely proven to be very critical in transforming bench side discovery into beneficial therapy.

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Optic Nerve Atrophy: The Symptoms

Optic Nerve Atrophy: The Symptoms

Optic Nerve Atrophy, also known as optic neuropathy, is a common form of neurodegenerative disorder. Optic nerves are the important connecting link between eye and the brain; which is associated with overall visual performance.

The human eye, is nothing but an orbit of the bony cavity, that contains muscles, nerves, blood vessels as well as some important structures that produce and drain tears and the eye ball,. All the cellular structures are networked with each other with the help of nerves; which have come together towards the small circular area of the retina, known as the optic disc. The most sensitive part of the retina is known to be “Macula”; which is made up of millions of light sensitive cells termed as “Rods” and “Cones”. Cones are mainly responsible for detailed, acute, central vision as well as colour perception; whereas rods are responsible for peripheral and night vision.

Information, regarding the object is passed on to the brain, in the form of nerve signals from each eye, through optic nerve and other nerve fibers; where the vision is anticipated and interpreted. When there is steady degeneration of optic nerve as an end result of some of the diseased conditions; it can give rise to Optic Nerve Atrophy.

Symptoms of the Atrophy

Symptoms associated with optic atrophy are variable, on the basis of its general classification; based on some of the parameters such as morphology and pathogenesis. However, some of the common symptoms, associated with change in visual performances of an individual are:

  • Blurry vision
  • Difficulty in discrimination between colorful objects
  • Reduced visual acuity and side vision
  • Decreased brightness in one eye relative to the other

Further to these commonly expressed symptoms; some of the other symptoms, associated with specific conditions, can be explained on the basis of further classification of the atrophy.

With the help of ophthalmoscopic observation; optic atrophy can be classified as Primary Atrophy, Secondary Atrophy and Glaucomatous Atrophy of the optic nerve.

Primary Atrophy of the Optic Nerve: –

Primary Atrophy can be further subcategorized as:

  • Ascending Atrophy; which is associated with ischemic occlusion of the central part of the retina. Some of the symptoms associated with the condition, can be listed out as; transient visual loss, temporal pain, pain in the jaw or ears, fatigue, sudden weight loss and unexplained muscular pain.
  • Descending Atrophy; is associated with optic nerve compression due to hydrocephalous, traumatic fracture, hematoma formation, in surrounding area like optic sheath and/or inflammatory compression due to arachnoiditis or syphilis. The clinical hallmarks of compressive descending optic neuropathy include slow, progressive visual loss, inability to differentiate colored vision, afferent papillary defect, visual field defect as well as edema or inflammation. There can as well be a detection of compressive lesion on the eye surface.
  • Toxic Atrophy takes place due to long term abuse of optic nerve, because of low grade tobacco, alcohol consumption and/or long term exposure to harmful chemicals, etc. The vision loss associated with toxic atrophy is bilateral, symmetric and/or progressive degeneration of optic nerve. The symptoms associated with the clinical condition can often be described as reduced brightness of a particular color, generally red; or in general loss of color perception. Some people can as well notice, progressive decline of visual acuity. Upon physical observation, some pupils usually reflect normal response to light as well as visual stimulus. There can as well be rare observation of optic disc hemorrhages, leading to the continuous damage of optic nerve.
  • Congenital or Hereditary Atrophy; is often a result of infantile hereditary defect. The affected eye can display swollen appearance of the nerve fibers; upon fundus examination papillary defect may be visible.

Secondary Atrophy of the Optic Nerve: –

It is often associated with some primary disease conditions such as papilledema, papillitis, , etc. The main symptoms associated with clinical conditions are progressive visual damage, difficulty in colored objects discrimination, reduced peripheral vision, etc.

Glaucomatous Atrophy of the Optic Nerve: –

It is the most commonly occurring optic nerve atrophy, encountered in clinical practice; characteristically associated with increase in intraocular pressure causing gradual loss of vision. Glaucomatous optic nerve damage without elevation of intraocular pressure is sometimes referred to as “low tension glaucoma” or “normal pressure glaucoma.”.

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Optic Nerve Atrophy: A Detailed Pathophysiology!

Optic Nerve Atrophy: A Detailed Pathophysiology!

Optic Nerve Atrophy (ONA) is mild to severe damage to the optic nerve resulting in loss of some or most of the nerve fibers. This progressive degeneration is in turn associated with variable degree of visual dysfunction.

Optic nerve also known as the second cranial nerve, is a bundle of millions of nerve fibers, conveying the visual information, from retina of the eye to the specific optic centers of the brain. When some of these nerve fibers are severely damaged due to diseased condition; the passage of information from eye to the brain and vice versa is blocked, this in turn can reduce person’s visual acuity. If ignored for a long term; it leads to the permanent blindness.

Thus, optic atrophy itself is not a disease, but an end result of the destruction to the optic nerve, due to several diseased conditions; which may also be progressive, depending upon its Pathophysiology. Common symptoms associated with optic atrophy include visual loss, reduced ability to distinguish colors, blurring of vision , double vision , etc. Clinically pallor of the optic disc/nerve, abnormal reaction of the pupil to light along with reduced visual acuity firmly establishes the diagnosis.With conventional treatment approach, medical fraternity is unable to restore the lost function of an atrophic optic nerve; however the primary focus would always be to pinpoint the possible cause of damage and to stabilize further progression.

Although there are diverse causes ranging from trauma to hereditary causes, that can cause injury to the optic nerve; by far some of the most common causes are Ischemic Optic Neuropathy, Optic Neuritis and Glaucoma.

Ischemic Optic Neuropathy

It is the most common cause of acute optic neuropathy, especially in older adults above 50. Also It is often referred to as the stroke of the optic nerve, occurring due to reduced or blocked blood circulation to the vessels supplying the front or the anterior side of the optic nerve (Anterior optic nerve atrophy or AION).There are two different mechanisms responsible for causing the vision loss from AION, the “arteritic”  and the ‘non arteritic forms.

The “arteritic” form caused by a disease called Giant Cell Arteritis (GCA) predominantly affects those over the age of 55 and it is estimated that women are three times more vulnerable to the condition, than men. In about 80 % of the reported cases, patients exhibit symptoms such as general fatigue, weight loss, fever, pain in neck, difficulty in chewing, headache, anemia and achy joints; which can proceed towards the blurry vision or total vision loss.

The “Non-Arteritic” form is the most common form of AION with a better visual outcome than the arteritic form. It generally affects a patient at any age with about 10% of patients being under the age of 45. Both males and females have equal predilection. It is caused by an acute impairment to the circulation of the arteries supplying the optic nerve due to a temporary fall in blood pressure. Some of the common diseases which can put a patient at higher risk for ‘Non arteritic’ form are Diabetes mellitus, Rheumatoid Arthritis, Herpes Zoster, Anemia, Sickle Cell Trait, Syphilis, and Polyarteritis nodosa.

Optic Neuritis

Optic neuritis is an inflammation of the optic nerve, as a result of damage to its myelin sheath; causing it to pain and leading to the temporary visual loss. The condition often precedes the onset of neurodegenerative autoimmune diseases, such as multiple sclerosis, neuromyelitis optica.

A gradual restoration of vision, back to normal is a characteristic of optic neuritis; althoughvision loss is permanent in some cases., with color vision and high sensitivity to contrast and brightness. Some of the common symptoms of optic neuritis include pain, temporary vision loss in one or both the eyes, loss of ability to discriminate colors, etc. Some people with optic neuritis report seeing flashes or flickers of lights.


Glaucoma is a condition associated with gradually progressive optic nerve damage. It usually occurs due to increased pressure as a result of fluid accumulation on the front walls of the eye. The studies have indicated that eye pressure is the primary factor for glaucoma and eventually optic nerve damage. According to the recent survey, Glaucoma is the second leading cause of visual damage in the developed countries. As there are no significantly reported early symptoms for glaucoma; more than 60% of cases go unnoticed in their initial stages.

Apart from these common causes, other less noted causes are, inherent underdevelopment of the optic nerve affecting children and young adults; diseased conditions such as brain tumor, cranial arteritis, pituitary gland tumors and swelling of the blood vessels known as cerebral aneurysm can as well pressurize optic nerve; leading to its damage.

Other direct reasons that are responsible for optic nerve damage are trauma, shock, long term exposure to radiations, etc.

Conclusively it has been widely accepted that Optic Nerve Atrophy is relatively very easy to diagnose; but the cause for the same is quite difficult to ascertain. It is thus very important to keep a check on some of the related symptoms and physical presentations for patients complaining sudden visual issues.