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Response to beta interferon 1b among Saudi patients with multiple sclerosis
Haga Kargwell1, Basim A Yaqub, Saleh M Al-Deeb
1Department of Neurosciences, Armed Forces Hospital, PO Box 7897, Riyadh 11159, Kingdom of Saudi Arabia. rkhnsksa@zajil.net, hkargwell@hotmail.com
Saudi Medical Journal
|February 19, 2003
Summary
Subcutaneous beta interferon 1b (B1F1b) effectively reduced relapse rates and disability progression in Saudi patients with relapsing-remitting multiple sclerosis (R-R MS). The treatment was well-tolerated, though longer follow-up is needed to confirm long-term disability prevention.
Area of Science:
- Neurology
- Immunology
Background:
- Multiple Sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system.
- Relapsing-remitting MS (R-R MS) is the most common form, characterized by unpredictable relapses.
- Beta interferons are disease-modifying therapies used in MS treatment.
Purpose of the Study:
- To evaluate the efficacy and tolerability of subcutaneous beta interferon 1b (B1F1b) in Saudi patients diagnosed with R-R MS.
- To assess the impact of B1F1b on relapse rates, disability progression, and patient safety.
Main Methods:
- An open-label study conducted in Riyadh, Saudi Arabia, from 1997 to 2001.
- Thirty-two R-R MS patients under 50 years old with mild to moderate disability received subcutaneous B1F1b (8 million IU) three times weekly.
- Primary outcomes included relapse rate reduction and time to first relapse; secondary outcomes assessed disability progression, tolerability, and safety.
Main Results:
- Twenty-eight patients completed the study; 32.5% were relapse-free, and 37.5% experienced a reduction in relapses.
- No patients showed progression of disability (P<0.0249).
- Adverse reactions were generally mild, with influenza-like symptoms (53.6%) and injection-site reactions (35.7%) being most common.
Conclusions:
- Subcutaneous B1F1b demonstrates efficacy in Saudi R-R MS patients, notably in reducing relapse rates and potentially preventing disability.
- The treatment is well-tolerated, with manageable side effects.
- Further long-term studies are warranted to fully ascertain B1F1b's role in preventing long-term disability progression.