Stem cells ‘reverse’ Multiple Sclerosis?

Stem cells and multiple sclerosis

Stem cells and multiple sclerosis

“Stem cell transplants could provide a cure for multiple sclerosis”, The Sun reported. It said that in a recent trial of 21 patients with MS, 17 had shown improvement three years after being injected with cells from their own bone marrow. The newspaper said the stem cells appear to reduce the inflammation that can worsen the disease. The study leader was quoted as saying: “It seems to prevent neurological progression and reverse disability.”

The news story is based on an early phase trial, which found that stem cell transplants reversed neurological deficits in people with relapsing-remitting MS, the most common form of the disease. It did not look at other forms of the condition, such as secondary progressive MS. Patients were compared before and after the transplant, and the results were promising, with sustained improvements in disability in 81% of patients.

As is usual when testing treatments, the intervention will go on to be tested in larger, controlled trials, probably randomised controlled trials across different centres. Until then, the researchers emphasize that it’s not possible to determine whether this treatment is better than existing treatments for relapsing-remitting MS.

Where did the story come from?

The research was carried out by Dr Richard K. Burt and colleagues from the Northwestern University Feinberg School of Medicine and Department of Neurological Sciences, Rush University Medical Centre in Chicago, Imperial College London, the University of Utah and other international academic and medical institutions. The study was published in the (peer-reviewed) medical journal: the Lancet.

What kind of scientific study was this?

The researchers say that when most people are first diagnosed with MS, they have only intermittent symptoms; a form of the disease called relapsing-remitting MS. Although many go on to develop irreversible progressive MS, which results in gradual reduction in neurological function, MS may be at least partially reversible while in this initial phase.

During its early stages, the immune system limits the damage that MS has on nerve cells. Treatments at this time include immune therapies aimed at improving this response. This early phase I/II study investigated if the transplantation of certain blood stem cells during the relapsing-remitting phase of MS could reverse neurological disability. The process of transplanting blood stem cells back into bone marrow is known as haemopoietic stem cell transplation.

The study involved 21 MS patients aged between 18 and 55 years who had not responded to at least six months of therapy with interferon alpha (an immune therapy). All patients had a minimal to severe disability (according to a well-known disability scale) and had normal lung, kidney, heart and liver function and no history of cancer (except skin cancer).

Before their stem cell transplantations, the patients’ immune systems were prepared for the donor cells by a non-myeloablative pre-treatment. This means that their body’s ability to make blood cells was only weakened rather than destroyed. The patients’ physical and neurological abilities were tested by several assessments including a timed 25ft walk and a nine-hole peg test. These were repeated six and 12 months after the transplantation, and annually after that. The patients were also asked to report any new symptoms or worsening between visits, at which point they would be immediately reassessed.

Disability and function was assessed using the expanded disability status scale (EDSS), the neurological rating scale (NRS) and the paced auditory serial addition test (PASAT). Blood transfusions and antifungal and antiviral treatment were given as necessary during the procedure, and adverse events were dealt with.

The patients were followed up for an average of 37 months and their neurological functioning, progression free survival (the length of time that symptoms do not worsen) and performance on different tests were compared with measures taken before treatment.

What were the results of the study?

The study found that the patients’ average score on the EDSS had significantly improved by 0.8 points six months after the stem cells were transplanted, and had improved by 1.7 points by the fourth year of follow-up. Other measures of neurological function also significantly improved after the transplant for the majority of patients, including assessments on the NRS, the timed 25ft walk and the PASAT. Although there was an improvement in scores on the nine-hole peg tests, these were not significantly different between the time before and after transplantation. The patients also reported that their general health status improved.

Despite showing early neurological improvements, five patients relapsed an average of 11 months after transplantation.

What interpretations did the researchers draw from these results?

The researchers conclude that 81% of patients showed a reversal of neurological disability. They also had sustained improvements in function as demonstrated by improvements of one point or more in EDSS scores. They say that stem cell transplantation reverses neurological deficits in people with relapsing-remitting MS, but caution that these results need to be confirmed in a randomised trial.

What does the NHS Knowledge Service make of this study?

This study focuses on relapsing-remitting MS, which is the most common of the four types of multiple sclerosis. Many people with this type go on to develop secondary progressive MS (a steady worsening in symptoms and disability). It is important to highlight that the findings only apply to people who have relapsing-remitting MS. The researchers state that studies have found no improvement in neurological disability with transplantation in secondary progressive MS.

When new treatments are being tested, they usually go through a three-stage study process before being licensed for use. Early studies – phase I and II trials such as this one – are smaller and often do not have a comparison group with which to compare an intervention. If efficacy (the power to produce an effect) and safety are demonstrated in such studies, the intervention is then assessed in larger studies; the largest being phase III trials which are randomised, controlled studies which can have thousands of patients. Given the promising results in this preliminary study, stem cell transplantation for relapsing-remitting MS patients will probably be studied further in larger trials.

The researchers draw attention to the fact that this study does not compare stem cell treatment with current management of relapsing-remitting MS. Only a randomised controlled trial will provide this answer.

Orkney’s world-record MS rates – Vikings to blame?

Orkney's world-record MS rates – Vikings to blame?

Orkney’s world-record MS rates – Vikings to blame?

‘Vikings could be to blame for why Scots have highest levels of multiple sclerosis’ is the somewhat imaginative leap taken by the Daily Mail as it reports on multiple sclerosis (MS) rates in Aberdeen, Orkney and Shetland.

The headline is based on a study that tried to find out if numbers of people with the disease in these areas had changed over the last 30 years. Researchers were specifically looking at the prevalence of MS, which affects muscle movement, balance and vision.

The study found that over the combined area, 248 per 100,000 inhabitants had MS (approximately 0.25%), while in Orkney the figure was over 400 per 100,000 (approximately 0.4%), the highest recorded rate worldwide. Women were more affected than men, with about 1 in 170 women in Orkney (approximately 0.59%) affected. These figures are a marked increase compared with earlier research carried out in the 1980s.

Despite the Mail’s headline, the researchers provide no firm conclusions about what could explain the high rates. They speculate the following two factors may be involved:

genetics – Orkney is an island community that was settled by the Vikings

the environment – such as lower levels of vitamin D exposure

Vitamin D production is stimulated by sunlight, so the further away from the equator you get, the lower levels of vitamin D in the general population tend to be. Other geographical studies have found countries on the same latitude as Northern Scotland also have higher than average rates of MS.

This well-conducted study builds on previous work and could offer some important clues as to the origins of this disease and whether any genetic or environmental factors play a role.

Where did the story come from?

The study was published in the peer-reviewed Journal of Neurology, Neurosurgery and Psychiatry. It was funded by the Scottish government.

It was covered fairly by the papers, although the Daily Mail’s link between the origins of MS and the Vikings, accompanied by a comic photo, was a little over the top. The study does not mention Vikings, and in fact, the paper seems to imply that the rise in prevalence is more likely due to environmental factors than genetics.

However, it does suggest that a ‘gene-environment’ interaction may be the cause, while comments by the authors have reportedly linked the Orkney Islands’ high multiple sclerosis rates it to its Scandinavian history.

While the media coverage of the study does discuss vitamin D exposure as a possible environmental risk factor, other factors that are discussed in the study include exposure to a viral infection, such as the Epstein-Barr virus (the virus that causes glandular fever).

Finally, and somewhat oddly, the study has made today’s news sources despite being published in May 2012. It is unclear why it has taken seven months for the study to hit the headlines.

What kind of research was this?

This was a study of the prevalence of multiple sclerosis in three areas of northern Scotland: Orkney, Shetland and Aberdeen. The prevalence of a disease is the proportion of people who have it within a given population at any given time. This is different from the incidence, which is the number of newly diagnosed cases of a disease within a specific period – normally a year.

Multiple sclerosis is a progressive disease affecting nerves in the brain and spinal cord, causing problems with muscle movement, balance and vision. The cause is unknown.

The current thinking is that MS is likely to arise from a complex interaction of both environmental and genetic factors.

There is currently no cure, although treatment can delay symptoms.

The researchers say that very high multiple sclerosis prevalence rates were recorded in northern Scotland 30 years ago. In particular, between the 1950s and 1980s, studies in Orkney and Shetland showed a steady rise in prevalence to about 190 per 100,000 (about 0.19%), while similar increases were found in Aberdeen and north east Scotland. These were age and gender specific rates and standardised to the Scottish population, meaning that there were minor adjustments to the numbers to allow for direct comparison between the three areas.

There have been no prevalence studies of MS in northern Scotland since the early 1980s, despite this area having one of the highest rates of MS in the world.

This new study aimed to measure current prevalence rates in Aberdeen, Orkney and Shetland, among men and women and among different age groups. The researchers aimed to assess whether the rates had changed over time and to determine which factors might be an influence.

What did the research involve?

In 2009, the researchers searched the records of hospitals, general practices and laboratories in the relevant areas to identify MS patients who were alive, residing in the study area and registered with a participating general practice.

All GPs in Aberdeen, Orkney and Shetland were approached. All appropriate doctors involved in the care or diagnosis of patients with MS were informed of the project by letter. The number in each area’s general population was calculated using GP data.

Researchers identified MS patients by a number of methods. They searched GP databases for patients registered on the relevant day (September 24 2009) with a specific MS diagnostic code. They also searched hospital discharge data using a diagnostic code, MS specialist nurse databases and relevant hospital laboratory results. The project was supported and advertised by MS patient organisations.

A neurology specialist reviewed all hospital and GP records and laboratory data of all patients identified by the searches to confirm the diagnosis according to internationally accepted criteria.

Patients were included if they satisfied one set of established criteria for clinically ‘definite’ or ‘probable’ and laboratory supported ‘definite’ or ‘probable’ MS. In cases of doubt, a senior neurologist made the final decision.

Researchers also recorded different MS subtypes and whether and how patients were disabled, using established disability scales. They also used a national index of multiple deprivation to analyse patients’ economic status.

They sent out a subsequent postal questionnaire to those MS patients considered suitable, asking further about:

levels of disability

place and date of diagnosis (to identify those who migrated into the area after diagnosis)

employment status

The researchers calculated age-gender specific prevalence rates and standardised these to the Scottish population. This allows them to directly compare populations with different age structures with each other and gives an overall expected rate as if the population in these cities and islands were the same as those in Scotland as a whole.

Researchers say they expected to find 480 MS patients in the areas studied, based on previous prevalence of about 190 per 100,000. This would give sufficient statistical power to detect any increase in prevalence over time (that is, any increase detected would be highly unlikely to be the result of pure chance).

 

What were the basic results?

The researchers identified 590 patients (420 women and 170 men) who satisfied diagnostic criteria for MS. There were 442 patients from Aberdeen, 82 from Orkney and 66 from Shetland.

The average age was 53 years and on average, they had had the disease for 19.4 years.

Using one set of diagnostic criteria, the researchers found that prevalence rates for probable or definite MS per 100,000 were:

Combined area – 248 (95% confidence interval (CI) 229 to 269)

Orkney – 402 (95% CI 319 to 500),

Shetland – 295 (95% CI 229 to 375)

Aberdeen – 229 (95% CI 208 to 250).

Another set of diagnostic criteria, that made use of a more stringent set of criteria, gave a lower prevalence of 202 (95% CI 198 to 206). The researchers also found that:

prevalence of MS was highest in women (female:male ratio of 2.55:1, 95% CI 2.26 to 2.89) with about 1 in 170 women in Orkney affected

prevalence was lowest in the most deprived socioeconomic group

45% of the patients had significant disability

To put these figures in some sort of context, the prevalence of MS of the United States (at the upper limit of the range of estimation) is 95 per 100,000 – so rates in Orkney are four times higher.

 

How did the researchers interpret the results?

The researchers say that the prevalence of MS has increased in the overall area, most markedly in Orkney, then Shetland, over the past 30 years. For example, the difference in prevalence between the 1980s and the year of the study was 37 per 100,000 for the whole area and 186 per 100,000 for Orkney.

They say the increase could be due to a number of factors, but the most likely cause is rising incidence (the number of new cases being diagnosed each year), influenced by gene-environment interaction.

They point out that Orkney has the highest prevalence rate recorded worldwide. However, the disproportionate rise in the northern islands may be the result of random fluctuation in small populations. The smaller a sample is, the more likely it is to give a skewed result – toss a coin five times in a row and you might get four heads – toss it 500,000 times in a row and you’re likely to get a 50/50 split between heads and tails.

In their discussion, the researchers say that a rise in incidence over such a short period cannot be accounted for by genetic factors alone and that an environmental factor is likely to be involved.

They point out that recent evidence has suggested a significant role for vitamin D in the development of MS and changes in vitamin D levels may play a role, although the study did not measure vitamin D levels.

They also mention other theories, suggesting the higher MS prevalence among higher socioeconomic groups may be due to:

these groups having less immunity to viruses implicated in the development of MS (the hygiene hypothesis)

less exposure to sunlight, which is needed for the skin to make vitamin D and linked to a vitamin D theory of MS causation

Conclusion

This was a well-conducted study which carried out a thorough review of medical and laboratory records to verify each diagnosis of MS, and used internationally accepted criteria to establish the prevalence of MS (although prevalence rates for the study did vary according to different diagnostic criteria).

However, as the authors point out, most patients were not reviewed in person by the study team, so it is possible there were some inaccuracies. In particular, a number of older people who were diagnosed with MS before the widespread introduction of MRI scans to help diagnose the disease more accurately, may have had other nervous system diseases.

Further research is required to find out the reasons for high rates of MS in northern Scotland and the recent increase in prevalence indicated by this study.

The researchers are now working on ongoing research looking at vitamin D levels in people living in Orkney. We look forward to reading their results with interest.

Montel Williams Opens Up About Living With Multiple Sclerosis

Montel Williams Opens Up About Living With MS

Montel Williams Opens Up About Living With MS

Montel Williams Opens Up About Living With MS

Montel is one of the most famous people who have gone public with their diagnosis of multiple sclerosis. We have covered this a few times in the past. Please have a look here and here.

But we felt that this interview is well worth watching!

Heat and Fatigue in Multiple Sclerosis – Great MS Life Hacks from National MS Society

Heat and Fatigue in Multiple Sclerosis - National MS Society

Heat and Fatigue in Multiple Sclerosis – National MS Society

Heat and Fatigue in Multiple Sclerosis from National MS Society.

This excellent video gives us some great tips for dealing with MS related heat intolerance and fatigue.