MS Research: Decoding Hype, Finding Hope in Science Communication

Between Hype and Hope: The Language of MS Research

How researchers say (or don’t say) what they say in research papers says a lot … or does it?
Between Hype and Hope: The Language of MS Research
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Have you ever listened — really listened — to a broadcast weather forecaster’s use of ambiguous language?

“Mostly sunny with a chance of scattered rain showers.”

“Morning clouds and fog clearing as the morning progresses, except in areas where it will persist.”

What the hell does any of that even mean to the guy who wants to wash his car, or the woman thinking about setting some flowers in the raised beds?

Perplexing Word Choices

I feel that way, sometimes, when I read or report on multiple sclerosis medical research. The analogy of forecasting the weather is strong when it comes to “possible long-term outcomes,” “more research required,” and “standard deviation of residuals.”

The same can be said of reporting on such research. I recently read reports about a study published in JAMA on the effects of high-dose vitamin D therapy on early-stage MS.

The reporting on the study used two terms I’d not seen before in this vein — “tames” and “curbs” — in reference to successful use of high doses of vitamin D administered early on in the course of MS (specifically, at the stage of clinically isolated syndrome).

The research showed that only 60 percent of patients exhibited an occurrence of a relapse or magnetic resonance imaging activity (new or contrast-enhancing lesions) over 24 months when they were given high-dose cholecalciferol (a dietary supplement that is used to treat vitamin D deficiency), while 74 percent of patients with CIS who were given placebo showed disease activity or progression.

Great news for the next generation of MS, but nowhere in the research was “tame” or “curb” ever mentioned.

What researchers did write was an old favorite of mine: “These results warrant further investigation.”

I know that science means that our understanding changes as new data is presented and tested. We all know that some things work better for one person than another. I just wish that we could find common ground in between the hype and the hope of media and research.

Causation vs. Correlation

Another concept those of us living with MS have to learn is the difference (and similarity) between correlation and causation. Just because two things happen in correlation doesn’t necessarily mean that one causes the other.

This can be particularly important to keep in mind when we look at natural history studies — observational studies intended to track the course of the disease — which can mine existing data to ascertain possible contributing factors of a disease.

One such study, recently published in the Journal of Neurology, Neurosurgery & Psychiatry, linked the use of oral contraceptives by women before their diagnosis with MS to a lower risk of progression independent of relapse activity (PIRA), or disability that accumulates in the absence of MS relapses.

Those researchers found that “[p]atients who used oral contraceptives before MS diagnosis had a 26 percent lower risk of PIRA and a delayed median time to the first PIRA event (9.94 vs. 7.5 years).”

Even with what seems like fairly conclusive evidence, the researchers concluded, “This study suggests that early oral contraceptives may delay future disability progression, supporting the importance of sex hormones in MS and prompting further prospective investigations on oral contraceptives to slow disease progression.”

The italics are mine to emphasize my point.

The Importance of Educating Ourselves

To me this is another excellent example of the importance of educating ourselves to be good (if not “professional”) patients. I have found it helpful to understand (or partly understand) the science that is reported in these studies rather than relying on the editorializing and reporting or even on the conclusions that researchers draw, because even those must be tempered.

So, here’s to educating ourselves, learning how to read what is and isn’t being written, and to finding that fine line between hype and hope.

Wishing you and your family the best of health.

Cheers,

Trevis

Important: The views and opinions expressed in this article are those of the author and not Everyday Health.

Ingrid Strauch

Fact-Checker

Ingrid Strauch joined the Everyday Health editorial team in May 2015 and oversees the coverage of multiple sclerosis, migraine, macular degeneration, diabetic retinopathy, other neurological and ophthalmological diseases, and inflammatory arthritis. She is inspired by Everyday Health’s commitment to telling not just the facts about medical conditions, but also the personal stories of people living with them. She was previously the editor of Diabetes Self-Management and Arthritis Self-Management magazines.

Strauch has a bachelor’s degree in English composition and French from Beloit College in Wisconsin. In her free time, she is a literal trailblazer for Harriman State Park and leads small group hikes in the New York area.

Trevis Gleason

Author

Trevis L. Gleason is an award-winning chef, writer, consultant, and instructor who was diagnosed with secondary progressive multiple sclerosis in 2001. He is an active volunteer and ambassador for the National Multiple Sclerosis Society and speaks to groups, both large and small, about living life fully with or without a chronic illness. He writes for a number of MS organizations, like The Multiple Sclerosis Society of Ireland, and has been published in The Irish Times, Irish Examiner, Irish Independent, The Lancet, and The New England Journal of Medicine.

His memoir, Chef Interrupted, won the Prestige Award of the International Jury at the Gourmand International World Cookbook Awards, and his book, Dingle Dinners, represented Ireland in the 2018 World Cookbook Awards. Apart from being an ambassador MS Ireland and the Blas na hÉireann Irish Food Awards, Gleason is a former U.S. Coast Guard navigator. Gleason lives in Seattle, Washington and County Kerry, Ireland with his wife, Caryn, and their two wheaten terriers, Sadie and Maggie.

EDITORIAL SOURCES
Everyday Health follows strict sourcing guidelines to ensure the accuracy of its content, outlined in our editorial policy. We use only trustworthy sources, including peer-reviewed studies, board-certified medical experts, patients with lived experience, and information from top institutions.