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Hi, I’m Nikita. Thanks for sparing a few minutes to read this post.
For most of us, a basic introduction like above is kindergarten stuff. But, for 36 million people worldwide wading through the tangles and plaques in the brain, recalling their name is an elusive challenge.
In fact, every four seconds, one person world over receives the cruel diagnosis of Alzheimer’s – memory evades them and they can’t trust what they remember. They are no longer there and yet they are.
The reach of Alzheimer’s is staggering.
Yet, after decades of research worth billions of dollars, Alzheimer’s drugs have a 99.6 percent fail rate in clinical trials.
There is absolutely no medicine, no treatment plan, no app, no game, no yoga in the market which can slow, cure or reverse this devastating neurological nightmare.
One of the biggest quandaries of neuroscience is grasping the depths of the ageing brain.
From 1988 to 2014, after billions of dollars and intense global research, 124 potential Alzheimer’s drug candidates reached advanced stages of clinical trials and only five got the US FDA’s approval to treat the underlying symptoms of the disease.
Their use is still controversial among doctors because many believe these drugs do not alter the disease progression at all. Despite exorbitantly expensive clinical trials, till date there are no drugs to actually slow down the memory fade. Not one drug has made the cut in market shelves in the last 15 years.
Alzheimer’s is a ticking time bomb. Tangles of amyloid plaques cover the grey matter in the brain, blocking the electrical signals and disrupting the flow of information. The sticky buildup is properly visible in brain scans, yet highly elusive to neurological investigations.
Timing is everything in Alzheimer’s research and treatment. The biggest hurdle is enrolling the right candidates for clinical trials.
In 2015, scientists in America found that people who have just been diagnosed with Alzheimer’s have had the disease eat away their brain at least 20 years before the symptoms started showing. So, the goal is to get volunteers even before they know they have the disease.
One way is to get high-risk genetically predisposed candidates and test their spinal fluid for two types of proteins – tau and amyloid, both found in the brains of people living with Alzheimer’s. If there is a tiny bit of these in the spinal fluid, it’s very likely the person will go on to develop the disease, but the problem is this test involves hospitalisation, local anesthesia, a needle puncture in the spine (ouch!) and is somewhat risky.
Lack of data sharing on clinical trial findings because of patents has largely been a pivotal reason for the blind alley in Alzheimer’s research.
Scientists across the world have been working solo, on independent tracks without any large-scale collaboration. Data sharing doesn’t serve the vested interests of big pharmas, the costs can run into millions of dollars.
Things have changed in the last couple of years.
Several European countries have taken giant leaps to make patient data open for access. Former UK Prime Minister David Cameron claims that with this collaboration, a research centre in England can now access eight times more data than previously available. UK has also seeded $100 million to change the trajectory of this deadly disease by 2025.
The deadline might be a tad unrealistic, but the thought of putting an end to a disease which robs people of their memory, sanity, relationships and life, is comforting, if not very hopeful.
Hi, I’m Nikita. Thanks for sparing a few minutes to read this post.
For most of us, a basic introduction like above is kindergarten stuff. But, for 36 million people worldwide wading through the tangles and plaques in the brain, recalling their name is an elusive challenge.
In fact, every four seconds, one person world over receives the cruel diagnosis of Alzheimer’s – memory evades them and they can’t trust what they remember. They are no longer there and yet they are.
The reach of Alzheimer’s is staggering.
Yet, after decades of research worth billions of dollars, Alzheimer’s drugs have a 99.6 percent fail rate in clinical trials.
There is absolutely no medicine, no treatment plan, no app, no game, no yoga in the market which can slow, cure or reverse this devastating neurological nightmare.
One of the biggest quandaries of neuroscience is grasping the depths of the ageing brain.
From 1988 to 2014, after billions of dollars and intense global research, 124 potential Alzheimer’s drug candidates reached advanced stages of clinical trials and only five got the US FDA’s approval to treat the underlying symptoms of the disease.
Their use is still controversial among doctors because many believe these drugs do not alter the disease progression at all. Despite exorbitantly expensive clinical trials, till date there are no drugs to actually slow down the memory fade. Not one drug has made the cut in market shelves in the last 15 years.
Alzheimer’s is a ticking time bomb. Tangles of amyloid plaques cover the grey matter in the brain, blocking the electrical signals and disrupting the flow of information. The sticky buildup is properly visible in brain scans, yet highly elusive to neurological investigations.
Timing is everything in Alzheimer’s research and treatment. The biggest hurdle is enrolling the right candidates for clinical trials.
In 2015, scientists in America found that people who have just been diagnosed with Alzheimer’s have had the disease eat away their brain at least 20 years before the symptoms started showing. So, the goal is to get volunteers even before they know they have the disease.
One way is to get high-risk genetically predisposed candidates and test their spinal fluid for two types of proteins – tau and amyloid, both found in the brains of people living with Alzheimer’s. If there is a tiny bit of these in the spinal fluid, it’s very likely the person will go on to develop the disease, but the problem is this test involves hospitalisation, local anesthesia, a needle puncture in the spine (ouch!) and is somewhat risky.
Lack of data sharing on clinical trial findings because of patents has largely been a pivotal reason for the blind alley in Alzheimer’s research.
Scientists across the world have been working solo, on independent tracks without any large-scale collaboration. Data sharing doesn’t serve the vested interests of big pharmas, the costs can run into millions of dollars.
Things have changed in the last couple of years.
Several European countries have taken giant leaps to make patient data open for access. Former UK Prime Minister David Cameron claims that with this collaboration, a research centre in England can now access eight times more data than previously available. UK has also seeded $100 million to change the trajectory of this deadly disease by 2025.
The deadline might be a tad unrealistic, but the thought of putting an end to a disease which robs people of their memory, sanity, relationships and life, is comforting, if not very hopeful.
(At The Quint, we question everything. Play an active role in shaping our journalism by becoming a member today.)
Published: 21 Sep 2017,07:52 AM IST