Wednesday 31 January 2024

Headlines from research papers

There has been quite a bit of excitement from the EuroHSP project, investigating a potential candidate drug for SPG4. This work develops on from work recently partially funded by the HSP Support Group. The drugs target is recovering levels of spastin in people with SPG4. There are more details here: https://www.eurohsp.eu/eurospg4 

I decided I would have a look and see what else I could find which has been going on recently. I found three different studies looking at gene therapy treatment for HSP, and an article summarising the non-pharmacological treatments for HSP.

Non-pharmacological HSP Treatments

This is the type of article I like. A team in Italy present a review of the different non-medicinal treatments for HSP, and I summarise the article in this post. My overall conclusion is that there are not many papers reporting the benefits of the different types of treatment that people with HSP use.

You can read the full article here: Macorra et al: https://link.springer.com/article/10.1007/s10072-023-07200-1

They undertook a literature review of relevant articles, and focussed their review on studies which met certain criteria. 117 papers/studies were identified, of which 39 were selected for a more detailed examination. From these 13 studies were included for the review.

Physical therapy

Most studies were uncontrolled, and did not report details of timings and details of the types of therapy tested. However the following is noted:

One study reported Functional Electrical Stimulation (FES) on 11 people with HSP and 11 controls. The FES was reported to improve toe clearance during walking and speed of walking. https://www.neuromodulationjournal.org/article/S1094-7159(13)60046-X/fulltext

Another study reports robotic gait training used over 6 weeks. Whilst the study did not report a change in spasticity, the participants had an improved quality of life. https://content.iospress.com/articles/neurorehabilitation/nre1196

Nine people with HSP took part in a 10 week hydrotherapy programme. This improved step length and walking speed, and other gait changes. https://www.sciencedirect.com/science/article/abs/pii/S0966636214000290?via%3Dihub

One study showed that warming legs up for 30 minutes could decrease spasticity and a parallel study showed that 30-60 minutes of warming could increase walking speeds. https://www.sciencedirect.com/science/article/pii/S1877065716300380?via%3Dihub and https://www.sciencedirect.com/science/article/pii/S1877065717304530?via%3Dihub.

A small study showed that an 8 week intensive physiotherapy programme saw improvements in all parameters measured. https://www.ijmhr.org/ijpr_articles_vol1_03/320.pdf

Surgery

Four people with severe spasticity underwent selective dorsal rhizotomy (SDR) surgery. After a 2 year follow up there was a good reduction in spasticity. Another study identified similar benefits in 2 children with HSP, but not in 2 people who's HSP diagnosis became ALS. https://www.jocn-journal.com/article/S0967-5868(13)00322-6/fulltext and https://link.springer.com/article/10.1007/s00381-016-3122-2.

Non-invasive stimulation

A range of studies report using transcranial magnetic stimulation to treat different neurological and/or similar conditions, including reducing spasticity in Parkinson's. Other types of stimulation are noted, 

Transcranial magnetic stimulation of the motor cortex is reported for HSP, with 14 people with HSP getting the stimulation over 5 days. Results showed a reduction in spasticity and an improvement in muscle strength. https://www.hindawi.com/journals/np/2019/7638675/ 

Another similar study of 8 people with HSP showed a reduction in spasticity a month after stimulation, but no change in quality of life. https://journals.lww.com/clinicalneurophys/abstract/2023/02000/a_randomized_controlled_trial_of_the_effect_of.13.aspx

A small study looked at transspinal magnetic stimulation in HSP, but didnt assess outcomes on walking speed etc. Another study looked at 15 people, of which 2 had HSP, testing magnetic root stimulation, with some improvement in spasticity. 

Lastly, 11 people with HSP had spinal direct current stimulation for short sessions over 5 days. This showed improvements in spasticity and joint movement. https://www.tandfonline.com/doi/full/10.1080/10790268.2018.1543926

Gene Therapy

Gene Therapy for SPG50

In the USA one team are working on a gene therapy treatment for SPG50. Their trial tests this in mice, showing some positive results, and testing the safety in a range of animals. They suggest that this approach could proceed to further trials. SPG50 is a childhood onset type of HSP, with additional symptoms beyond spasticity, making it a 'complex' form. There are two articles in the same journal about this:

Chen, et al: https://www.jci.org/articles/view/164575

Brent and Deng: https://www.jci.org/articles/view/170226 

Gene Therapy for SPG56

Similarly, another team are working on a gene therapy treatment for SPG56. This research appears to be at an earlier stage, as the announcement I saw reported a contract for two parties to collaborate on this. SPG56 is also a childhood onset type of HSP, with additional symptoms beyond spasticity for some.

Report: https://ir.criver.com/news-releases/news-release-details/charles-river-and-genetic-cures-kids-announce-gene-therapy 

You can read more about the wider project here: https://ourmoonsmission.org/

Gene Therapy for SPG61

Finally, another gene therapy target has been identified by a team in Korea. This article reports that the gene ARL6IP1 could be a good gene therapy target for HSP. A quick bit of searching identifies that this gene is associated with SPG61. 

https://rupress.org/jem/article/221/1/e20230367/276392/ARL6IP1-gene-delivery-reduces-neuroinflammation

Saturday 20 January 2024

2023 Blog Data and Health Review

As noted last year, and thereby setting a new trend, the passing of the year means its time to update the pages of this blog, and to take the opportunity to review my health data.

In terms of the blog update, I've updated the four pages as follows:

  • Index - easy!
  • Survey summary (my on-line research page) - easy!

Blog statistics

There have been fewer sessions on the blog in 2023 compared with previous recent years, about half the number of 2022. The more popular posts are following the general pattern established in recent years, so its unlikely to be any differences in the content that I'm creating. There are several potential reasons for this, and I think its unlikely to be just one.
  • Compared with previous years, I didnt plug the results of my 2022 survey when I published it on rare disease day 2023. This means there are likely to be fewer people looking at other pages after looking at that.
  • In 2023 Twitter became X, and that might mean that my tweets about each blog post are now seen by fewer people than previously - although on the opposite side, I'm now posting about each post on Facebook as well as X.
  • My mental health has been a bit lower in 2023, with a bit less enthusiasm for writing the blog, and feeling that I'm very busy with the rest of life. This may have filtered into my writing style.

Health data (Symptoms timeline page)

The health data for 2023 shows a few interesting patterns:
  • My weight has gone up
  • My alcohol level has gone up
  • My sleep duration is similar to 2022 
  • The number of active minutes is lower in 2022 and 2023
  • My total number of steps is similar to 2022
  • I didnt get on my bike at all during 2023
The consequence of this is for me to be aspirational in 2024 - seeking to get my weight down, and to improve my cardiovascular health. Essentially I need to do more exercise and pay more attention to what I'm eating and drinking.

Taking a broader look at health, earlier this year (as noted in August) I started using a muscle roller to try and help my spasticity a bit. I think my muscles feel a bit less tight, but its difficult to say. However, it is only taking a few minutes at the end of each day, and I'm carrying on with this.

Considering Pilates, I note that there are various movements that I'm finding less easy to do, and I'm having to improvise a few adaptions during classes. Some of these are about making sure that I have a chair/wall/table near where I'm doing my Pilates to allow me to keep my balance more. By having a light touch on something else with my hand I'm able to focus on the movement that we're working on, and not also having to focus on co-ordinating several different element together.

Disclosure

I think that 2024 is going to be the year when I decide that I am now a disabled person, or should that be a person with a disability? On the balance of things, I'm heading towards where the overall balance of impacts are significant, which is the switchover point from "not disabled" to "disabled". It means that I'm going to have to start thinking about the various things I might be entitled to, and to make sure that I'm updating work accordingly.