CMT Research Foundation Invests in Test if Known Drug is Effective Treatment for X-linked Charcot-Marie-Tooth Disease
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Dr. Abrams' work is consistently productive and key to helping us find cures for ALL forms of CMT.”
ATLANTA, GA, USA, April 23, 2024 /EINPresswire.com/ -- The CMT Research Foundation1, a non-profit focused solely on delivering treatments and cures for Charcot-Marie-Tooth disease (CMT)*, has invested in a project led by Dr. Charles Abrams, a Professor in the Department of Neurology and Rehabilitation at the University of Illinois at Chicago. The study will determine if a commercially available drug can improve symptoms in mouse models of Charcot-Marie-Tooth disease type 1X-which is the second most common form of CMT. If successful, these studies will provide a strong basis for working to quickly advance this already commercially available drug as a potential clinical treatment for CMT1X patients.— Cleary Simpson, CEO of CMTRF
CMT1X is caused by mutations in the gene that encodes for the connexin 32 gap junction protein. CMT1X is known to be associated with inflammation, which is thought to contribute to damage of the protective covering of nerve cells, a process known as demyelination, which leads to disease symptoms.
Previous work done by Dr. Abrams demonstrated that nerves of a mouse model of CMT1X have reduced levels of adenosine, a naturally occurring molecule with anti-inflammatory properties, which provides a potential explanation for the nerve inflammation observed in CMT1X. Dr. Abrams and his team will perform a series of experiments to test whether a commercially available immunosuppressive drug can reduce the severity of the neuropathy in two mouse models of CMT1X by increasing the levels of adenosine and reducing nerve inflammation.
Dr. Abrams, a member of the CMTRF Scientific Advisory Board, will collaborate on this project with Mona Freidin, an Assistant Professor at the University of Illinois at Chicago, whose expertise lies in connexin biology; and Dr. Benayahu Elbaz, an Assistant Professor of Neurology at Northwestern University, whose research focuses on myelin and myelin-forming cells in both the central and peripheral nervous systems.
“Dr. Abrams specializes in studying the roles of connexins, or gap junction proteins, in myelination in both the central and peripheral nervous systems,” says Cleary Simpson, CEO of CMTRF. “His work is consistently productive and key to helping us find cures for ALL forms of CMT.”
CMT Research Foundation (CMTRF) is a patient-led, non-profit focused on delivering treatments and cures for CMT. The foundation identifies significant obstacles or deficiencies impeding progress toward a cure and seeks out collaborators to address these issues. To date, CMTRF has funded 21 projects, of which 6 are completed. Of those 6 completed projects, 5 have clinical candidates. CMTRF's mission to invest in promising science with high potential of leading to treatments and cures was proven effective and ground-breaking when DTx Pharma with a CMTRF- backed program as its lead candidate was acquired by Novartis for $1 billion. Founded by two patients who are driven to expedite drug delivery to people who live with CMT, the 501(c)(3) federal tax-exempt organization is supported by personal and corporate financial gifts.
*Charcot-Marie-Tooth encompasses2 a group of inherited, chronic peripheral neuropathies that result in nerve degradation. CMT patients suffer from progressive muscle atrophy of legs and arms, causing walking, running and balance problems as well as abnormal functioning of hands and feet. CMT affects one in 2,500 people (about the same prevalence as cystic fibrosis), including 150,000 Americans and nearly 3 million people worldwide. At the moment, there is no treatment or cure for CMT.
George Simpson
CMT Research Foundation
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1 https://cmtrf.org/
2 https://cmtrf.org/what-is-cmt-disease/types-of-cmt/
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