7 posts from September, 2017

MS and Biotin: Is there a link?

Posted September 29th, 2017 by

You’ve probably heard about biotin and reports that it might improve health. Like most things on the internet, the truth isn’t always clear. To clear up some of the swirl, our Health Data Integrity team took a deep dive into the current research. So, what’s biotin and how can it impact health and MS? Take a look.

What is Biotin?

Biotin is a water soluble type of vitamin B, or more specifically vitamin B7 that can be found in a variety of plants but mostly found in liver, egg yolk, soybean products, yeast, and many other foods. While the primary function of biotin is still unclear, it helps the body produce and use certain nutrients and it can be used to improve biotin deficiency associated with pregnancy, malnutrition, rapid weight loss, and long-term tube feeding. Although there is insufficient evidence, biotin also has been used as a supplement to help treat hair loss, brittle nails, diabetes, and certain types of rash in infants.

(source: https://medlineplus.gov/druginfo/natural/313.html)

Biotin and MS?

The exact role of biotin in the progression of multiple sclerosis (MS) is still unclear. MS develops when myelin, a substance that protects the nerve cells, is damaged. Having the proper amount of myelin protecting the nerve cells allows these cells to communicate with each other more easily. Biotin is believed to help the body produce more myelin which could mean it may be helpful for patients with MS.

small study was done with 11 secondary progressive MS, 4 primary progressive MS, and 6 patients with relapsing-remitting MS taking 300 mg of biotin daily. After evaluating at 3 months, 1 patient showed signs of improvement in arthritic pain. Another patient noted great improvement in energy. The main result noted that none of the patients experienced any adverse outcomes with biotin.

Another study involving 14 patients with primary progressive MS and 9 patients with secondary progressive MS looked at treatment with 100-600 mg of biotin daily. After 3 months of treatment, the 4 patients in the study with chronic visual loss showed improvement in their vision. Additionally, 16 out of 18 patients with spinal cord involvement displayed clinical improvement after 2 to 8 months of treatment.

These results have also been supported by the findings of a study of 154 patients with progressive MS. In this study, it was found that treatment with a specific high-dose formulation of biotin was able to improve certain measures of disability.

It’s important to keep in mind that this data has come from a selection of relatively small studies so it will be important to see if these findings can be confirmed in larger studies. Currently, there are a handful of studies being conducted to evaluate the use of biotin to treat MS. These include three different phase III studies evaluating the use of a specific formulation of high-dose biotin in patients with:

  • spinal progressive MS (click here for more information)
  • chronic visual loss related to optic neuritis in MS (click here for more information)
  • progressive MS (click here for more information; this trial is currently in the process of recruiting participants)

(sources: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098693/http://www.neurology.org/content/86/16_Supplement/P3.039http://www.sciencedirect.com/science/article/pii/S2211034815000061)

Currently, there isn’t a specific recommended dietary allowance for biotin as the appropriate dose will depend on several factors like the patient’s age and health. However, the adequate intake for biotin is 30 mcg daily for adults and many individuals are able to get this amount from eating a healthy diet.

There is no toxicity reported as being associated with excess biotin intake. However, biotin can interfere with certain laboratory tests such as thyroid function. Make sure to tell your doctor if you start taking biotin.

So, what’s the takeaway?

While preliminary research shows that biotin may improve symptoms in patients with MS, more extensive clinical trials are in progress to evaluate the efficacy and safety of a specific high-dose formulation of biotin in patients with MS.

As mentioned above, one of these studies is currently recruiting participants who are diagnosed with primary or secondary progressive MS. To find out if you qualify and the locations of the studies, you can click here for more information.

Even with the current studies, the role of biotin in the treatment of MS is not completely known. Talk to your doctor if you want to start taking biotin supplements and decide if this treatment is right for you.

Share this post on Twitter and help spread the word.











The ALS battle forces changes: A guest blog by member Jim Burton, the ALS Warrior

Posted September 25th, 2017 by

Jim Burton, January’15

A harsh reality of progressive diseases like ALS is that your body is constantly changing. After my ALS diagnosis in January 2013, I noticed that the progression seemed to happen in stages. After losing some degree of capacity, I’d settle on a new plateau, which became my norm for a while. The plateaus have become shorter, and the declines have become more pronounced.

Neurologists call ALS a progressive disease, but to my family and me it’s digressive as my health declines. In turn, the digression forces change as today I can’t do what I did yesterday.

The biggest changes happened early on as I lost the ability to walk and began using a motorized wheelchair. As dramatic as the change appeared when I became a de facto paraplegic, the new plateau felt manageable. With a handicap-equipped van and hand controls for driving, I maintained most of my independence.

For several years after the diagnosis, I worked as a freelance journalist not only writing stories, which I could do from my home, but also going on location for the photographs. In one week, I traveled alone about 900 miles throughout Georgia and stayed in several hotels. Two years later, I had digressed to yet another plateau, and that independence became history.

Transitioning to a motorized wheelchair represented a radical lifestyle change. Now the disease has reached my shoulders, arms, and hands, creating new and different challenges.

Jim Burton in Dalton, Ga., in January 2015 while on a freelance assignment for a statewide newspaper. Photograph by Gibbs Frazeur.

Recently, I’ve made another major adjustment. Practicing journalism and doing location photography has become impractical. Just this year, I’ve lost the capacity to type, which I’ve done since the ninth grade. I now produce copy like this blog with talk-to-type software, and I’ve written four novels. The capacity to continue writing has kept me “in the game.” Though fiction is a new genre for me, I’m growing as a writer and continuing to exercise my creative capacity as a communicator. This new discipline keeps my mind sharp and my motivation high to press on and live as fully as possible even with my digression. Still, new challenges arise daily.

Jim Burton speaks with M.B. Howard, a former colleague, during the twenty-year reunion July 29, 2017, of a former Memphis-based nonprofit where they both worked. The trip from Atlanta to Memphis would have been impractical for Burton, so the organizers recommended an adjustment that allowed him to participate via Skype. Photograph by Bill Bangham.

In my home office, I have a workstation with a desktop computer and printer. When first diagnosed, I worked daily on my final doctoral writing project and used the printer constantly. Normal functions included loading paper, changing ink cartridges, loading documents into the feeder, and of course retrieving the printed pages. Each of those seemingly simple tasks now exceeds my physical capacity. The most frustrating challenge has been the inability to retrieve a printed piece of paper that lays on a shelf about four inches off the table. Unable to raise my hand that high, I discovered a way to work around that challenge. By placing my stapler beneath the shelf, I can put my hand there and then reach the printed paper. Another problem solved. These incremental changes that allow me to solve new challenges, create hope. And with every accomplishment, ALS loses.

Several years ago, I determined that I would not see myself as an ALS patient or victim. I’ve chosen to be an ALS warrior because I fight this disease every day along with thirty thousand other Americans and their families. Whether large or small, each victory matters.

I encourage you to remain determined each day in your battle to defeat ALS.

Jim Burton is a writer based in Atlanta who frequently writes about his ALS journey at http://life-bluezone.com/blog.html.

Share this post on Twitter and help spread the word.