Yeah, sure there are many things we don't know about all these brain conditions. In fact, I don't know if there are people with Meniere's, otosclerosis, etc. that never develop tinnitus, because a good gating system protects them by holding off those signals. You would think that that would be possible for a few of those people at least. Someone must have that gating system. But if this isn't happening and in those cases we know that the problem is in their cochlea, then one could say that the gating system doesn't exist or plays no role whatsoever.Agreed. Again, just hypothesising, but if those diseases cause a symptomatic increase in subconscious neural activity, say as a result of inflammation or various misfirings, then these raised levels of activity leaking across the faulty gate to be perceived as tinnitus sounds plausible. This is the thing I like about the gating theory; it doesn't really care much for where the signals originate, just that they reach the gate and leak over it.
Regarding other non-related conditions as an example, this is where I could believe something like schizophrenia originates. I get a sense that there we have 'satellite' personalities, or fragments thereof, orbiting our central-self that for a healthy person cause no issue because of a functioning related gating system. However, if that system were to fail then it seems plausible that just like tinnitus, aspects of 'other' self/personalities could leak over into our main one and cause those horrible symptoms.
Ultimately, if this gating thing holds up, I do believe there'll be a biomarker for it.
Looks like electrical stimulation is a new avenue to explore. Great that someone is thinking outside the box.Having said that, what is incredibly encouraging about the Mayo Clinic's early results is the four-fold decrease on standard THI. I reckon with figures like that there can be no mistake that the device is really doing something.
Explore? Why can't I personally explore this now at some European clinic willing to take my money? There's plenty of clinics willing to inflict all kinds of unproven but relatively harmless things on you for any affliction you might think of.Looks like electrical stimulation is a new avenue to explore. Great that someone is thinking outside the box.
Totally false. Medical University of Łódź, Poland, where @Mentos was treated, started testing this shit in early 1970s. Basically it is a very old method.Looks like electrical stimulation is a new avenue to explore. Great that someone is thinking outside the box.
I stand corrected. Thank you for putting me straight. When I think about it, I seem to recall some proponent of acupuncture at some time using electrical stimulation of his needles on the meridian points to up the potential (or something similar). How that worked out I've got no idea but I've read quite a few articles over the years that acupuncture is not much use for chronic tinnitus (It didn't help mine)...Totally false. Medical University of Łódź, Poland, where @Mentos was treated, started testing this shit in early 1970s. Basically it is a very old method.
Where are these studies you speak of?Totally false. Medical University of Łódź, Poland, where @Mentos was treated, started testing this shit in early 1970s. Basically it is a very old method.
Isn't this a bit contradictory, or am I missing something?- According to the theory of Dr. Susan Shore, tinnitus is the brain's reaction to the hearing loss.
First thing is those phenomena are two separate issues. Second thing is the fact that you don't need to have major hearing loss to get tinnitus.
When you are analyzing the above statements, the logical conclusion is that the statement of tinnitus originating in the cochlea is totally wrong.
There's gating areas in the brain that shut down the tinnitus for some people. In people who have tinnitus, those gating areas don't work for some reason. I believe Dr. Rauschecker talks about this in his TED talk.Isn't this a bit contradictory, or am I missing something?
The brain reacts to the hearing loss (but not for everyone with hearing loss) by producing a phantom sound. Hearing loss often originates in the cochlea, right? Then how is the tinnitus not related to the cochlea?
Hearing loss leads to reduced electrical activity down the auditory nerve. This causes changes in the DCN, where cells fire spontaneously, and this is then transmitted further through the auditory parts of the brain. Sounds are then processed in the auditory cortex. By stimulating the cochlea, you are increasing that electrical activity again and this causes adaptive changes in the brain, much in the same way a cochlear implant does.The brain reacts to the hearing loss (but not for everyone with hearing loss) by producing a phantom sound. Hearing loss often originates in the cochlea, right? Then how is the tinnitus not related to the cochlea?
This is what this technique does:I think it's safe to say that the cochlea isn't the root cause of tinnitus, for the most part. What should be targeted is the brain stem (DCN), which has been shown in numerous studies, to be the epicenter of tinnitus generation (at least in noise-induced tinnitus cases), like in Susan Shore's papers.
I am super curious how this whole electrical stimulation to the cochlea method would affect reactivity and/or hyperacusis. A part of me thinks it would drive my reactivity crazy! But I could be wrong. Although reactivity very much feels like it is in the inner ear, anything I have read on it more mentions neural networks in the brain gone awry. I just need my reactivity to STOP. I so envy those with "normal" tinnitus that does not spike or change to external sound stimuli.
Good point. One approach can't address every cause or form of it. Similarly, when I read posts saying "there is no cure, nothing works" I think "...except for everyone who's cured."All tinnitus will be cured, or tinnitus from loud noises, or tinnitus from neck/jaw, etc?
Tinnitus setting in the brain is BS. I had had tinnitus for 5 years. I got a cochlear implant and my tinnitus is much better as a result. It takes time for the brain to adjust but it filters and adjusts to hearing sound again.I think those theories are BS. Chronic tinnitus usually fluctuates and we have moderate and severe days, so it can change.
Seems to indicate that -- in your case -- the tinnitus and the remedy are situated in the ear/cochlea.Tinnitus setting in the brain is BS. I had had tinnitus for 5 years. I got a cochlear implant and my tinnitus is much better as a result. It takes time for the brain to adjust but it filters and adjusts to hearing sound again.
No, the extra electrical input modifies the brain plasticity.Seems to indicate that -- in your case -- the tinnitus and the remedy are situated in the ear/cochlea.
I agree.No, the extra electrical input modifies the brain plasticity.
It's so frustrating for sure. I'm not sure why they always stop short during these experiments. I don't know if they just want to do the bare minimum, or they just end up running out of money so they can only do so much, I'm not really sure.My God, I can't wait until they figure this out. I'm so tired of this back and forth. Why can't they just keep tinkering with it until they get the right results?
Nice find @ErikaS.Dr. Carlson's trial at Mayo Clinic in Rochester, MN is active/no longer taking participants and they updated the estimated study completion time to December 2023. Sample size of 9, but given the strict "rules" around the study and also people being willing to have the device implanted in mastoid bone, I'm not surprised at the low sample size. In any case, I will be very interested to see these outcomes.
→ Novel Tinnitus Implant System for the Treatment of Chronic Severe Tinnitus
I guess not, @Nick47? Good question.Nice find @ErikaS.
Does this mean they don't exclude severe-profound hearing loss at 4 kHz and above?
Inclusion criteria:
- Normal to moderate SNHL (≤70 dB HL; based on PTA of 0.5, 1 and 2 kHz) and WRS ≥ 75%.
I've had a rethink on this, after reviewing the evidence, the highly significant pilot studies on these extracochlear implants, cochlear implants, and a conversation with Prof. Peter McNaughton.I think it's safe to say that the cochlea isn't the root cause of tinnitus, for the most part. What should be targeted is the brain stem (DCN), which has been shown in numerous studies, to be the epicenter of tinnitus generation (at least in noise-induced tinnitus cases), like in Susan Shore's papers.
What do you think so far?Prof. McNaughton said:The cochlear nucleus is the first stop for signals originating in the auditory nerve. The increased activity that the Shore group have identified in cochlear neurons lines up nicely with our views that in fact abnormal activity originates in the auditory nerve itself. The auditory nerve is a more promising place to look for pharmacological targets because it is in the peripheral nervous system – targets in the CNS almost inevitably involve psychotropic effects which may be very undesirable. We are trying to develop peripherally restricted drugs which will not have CNS effects.
Honestly it's all speculation. We can't know for sure unless more research is done. I never thought that tinnitus is solely DCN, just that, possibly, catastrophic tinnitus has significantly more somatic crossfire which causes insanely more hyperactivity specifically in the DCN.I've had a rethink on this, after reviewing the evidence, the highly significant pilot studies on these extracochlear implants, cochlear implants, and a conversation with Prof. Peter McNaughton.
Currently it points to aberrant activity in the DCN as the first part of the tinnitus brain network, but that the activity starts peripherally in the auditory nerve as tinnitus can, without doubt, be modulated by extra and intra implants. Add this to the elimination of tinnitus in guinea pigs with the HCN2 blocking drugs, which according to Prof. McNaughton, cannot penetrate the BBB, supporting the hypothesis of a peripherally driven phenomenon. He did say he has been wrong before and will be wrong again, and was very modest and humble, but that he now had some evidence to support his hypothesis. He also said if his hypothesis was right, it would be much easier to treat, rather than designing a drug that crosses the BBB and causes side effects.
He said his hypothesis and early findings support the role of the DCN being involved.
What do you think so far?
In which category does Lenire and Dr. Shore's device lie?Here is a really good review of different types of electrical stimulus techniques and related tinnitus reductions (or not). Some side effects were noted in some people.
→ Tinnitus Treatment Using Noninvasive and Minimally Invasive Electric Stimulation: Experimental Design and Feasibility
None. They do not apply electrical stimulation to the cochlea nor count as electrical stimulation generally, because they are bimodal (electric and audio).In which category does Lenire and Dr. Shore's device lie?