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Blood Test Could Predict Progression of Multiple Sclerosis Disability Symptoms
News

Blood Test Could Predict Progression of Multiple Sclerosis Disability Symptoms

Blood Test Could Predict Progression of Multiple Sclerosis Disability Symptoms
News

Blood Test Could Predict Progression of Multiple Sclerosis Disability Symptoms

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A blood test may help predict which people with multiple sclerosis (MS) will get worse during the following year, according to a study published in the May 20, 2020, online issue of Neurology®, the medical journal of the American Academy of Neurology.

"In a disease like MS that is so unpredictable and varies so much from one person to the next, having a noninvasive blood test like this could be very valuable, especially since treatments are most effective in the earliest stages of the disease," said study author Ali Manouchehrinia, PhD, of the Karolinska Institutet in Stockholm, Sweden.

The blood test looks for a biomarker called neurofilament light chain, a nerve protein that can be detected in the blood when nerve cells die.

The study involved 4,385 people with MS and 1,026 people matched for age and sex who did not have MS. The level of the biomarker in the blood was tested in all of the participants. The participants were followed to see which people with MS got worse during the following year and then which reached continued, increased levels of disability over a total of five years. They also looked at whether people with high levels of the protein were more likely to develop worsening of disability during the following years, and later a more serious stage of the disease, called secondary progressive MS.

The people with MS had an average of 11.4 picograms per milliliter (pg/ml) of the nerve protein in their blood compared to an average of 7.5 pg/ml for the people who did not have MS.

The people with MS with high levels of the protein were 40% to 70% more likely to have worsening disability during the next year than those with low levels of the protein. These results took into account other factors that could affect their risk of worsening disability, such as how long they had the disease and how often they were having relapses at the start of the study.

The people with high protein levels were also 50% more likely to reach either a level of moderate disability that affected daily activities but not walking ability, or significant disability that impaired walking but still meant people were able to walk without help or rest for 500 meters. A total of 525 people reached the moderate level of disability, or 16%, and 352 people, or 9% reached significant disability.

The researchers found that high protein levels were not consistently associated with a greater risk of more significant disability, defined as needing a cane or crutch to walk 100 meters, or with the risk of developing secondary progressive MS.

"These results suggest that elevated levels of these proteins measured early on in the course of the disease may help us to predict how the disease will develop and monitor how treatment is working," Manouchehrinia said. "More research is needed before a blood test could be used routinely in the clinical setting, but our results are encouraging."

He said that a limitation of the study was that the level of the nerve protein varied significantly and overlapped between the people with MS and the people without the disease, and it is likely that the levels are influenced by other factors, such as other medical conditions, that were not analyzed in the study.

Reference: Manouchehrinia, A., Stridh, P., Khademi, M., Leppert, D., Barro, C., Michalak, Z., Benkert, P., Lycke, J., Alfredsson, L., Kappos, L., Piehl, F., Olsson, T., Kuhle, J., & Kockum, I. (2020). Plasma neurofilament light levels are associated with the risk of disability in multiple sclerosis. Neurology, 10.1212/WNL.0000000000009571. https://doi.org/10.1212/WNL.0000000000009571

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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