propidium has been researched along with Neuromyelitis Optica in 1 studies
Propidium: Quaternary ammonium analog of ethidium; an intercalating dye with a specific affinity to certain forms of DNA and, used as diiodide, to separate them in density gradients; also forms fluorescent complexes with cholinesterase which it inhibits.
Neuromyelitis Optica: A syndrome characterized by acute OPTIC NEURITIS; MYELITIS, TRANSVERSE; demyelinating and/or necrotizing lesions in the OPTIC NERVES and SPINAL CORD; and presence of specific autoantibodies to AQUAPORIN 4.
Excerpt | Relevance | Reference |
---|---|---|
"Neuromyelitis optica is an inflammatory demyelinating central nervous system disease, usually relapsing, that causes variable degrees of attack-related disability." | 1.35 | Prediction of neuromyelitis optica attack severity by quantitation of complement-mediated injury to aquaporin-4-expressing cells. ( Apiwattanakul, M; Fryer, JP; Hinson, SR; Lennon, VA; McKeon, A; Pittock, SJ, 2009) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hinson, SR | 1 |
McKeon, A | 1 |
Fryer, JP | 1 |
Apiwattanakul, M | 1 |
Lennon, VA | 1 |
Pittock, SJ | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
An Open Label Study of the Effects of Eculizumab in Neuromyelitis Optica[NCT00904826] | Phase 1/Phase 2 | 14 participants (Actual) | Interventional | 2009-04-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
The EDSS is an ordinal clinical rating scale ranging from 0 (normal neurologic examination) to 10 (death) in half-point increments. (NCT00904826)
Timeframe: baseline, 12 months
Intervention | units on a scale (Mean) |
---|---|
Eculizumab | -0.7 |
(NCT00904826)
Timeframe: 3 months
Intervention | ng/mL (Mean) |
---|---|
Eculizumab | 34.7 |
Ambulation was measured by the Hauser Ambulation Index, which ranges from 0 (asymptomatic; fully active) to 9 (restricted to wheelchair; unable to transfer self independently.) (NCT00904826)
Timeframe: 12 months
Intervention | participants (Number) |
---|---|
Eculizumab | 3 |
Visual acuity was measured using the the Visual Acuity subscale of the Opticospinal Impairment Score (OSIS) for Exacerbations. This subscale ranges from 0 (normal) to 8 (no light perception). (NCT00904826)
Timeframe: 12 months
Intervention | participants (Number) |
---|---|
Eculizumab | 5 |
(NCT00904826)
Timeframe: 12 months
Intervention | participants (Number) |
---|---|
Eculizumab | 2 |
(NCT00904826)
Timeframe: baseline, 3 months
Intervention | ng/mL (Mean) | |
---|---|---|
Baseline | 3 months | |
Eculizumab | 144 | 60.8 |
(NCT00904826)
Timeframe: 6 weeks, 3 months, 6 months, 9 months, 12 months
Intervention | micrograms/mL (Mean) | |||
---|---|---|---|---|
6 weeks | 3 months | 9 months | 12 months | |
Eculizumab | 206 | 187 | 230 | 246 |
(NCT00904826)
Timeframe: baseline, after 12 months of treatment
Intervention | attacks per year (Median) | |
---|---|---|
Baseline | After 12 months of treatment | |
Eculizumab | 3 | 0 |
Percentage of hemolysis is a measure of complement activity. Less than 20% lysis is deemed to be complete complement inhibition. (NCT00904826)
Timeframe: baseline, 6 weeks, 3 months, 6 months, 9 months, 12 months
Intervention | percentage of hemolysis (Mean) | |||||
---|---|---|---|---|---|---|
Baseline | 6 weeks | 3 months | 6 months | 9 months | 12 months | |
Eculizumab | 88.5 | 0.4 | 0 | 0.2 | 0.4 | 0.9 |
1 other study available for propidium and Neuromyelitis Optica
Article | Year |
---|---|
Prediction of neuromyelitis optica attack severity by quantitation of complement-mediated injury to aquaporin-4-expressing cells.
Topics: Adolescent; Adult; Aged; Aquaporin 4; Astrocytes; Biomarkers; Cell Line; Child; Complement Activatio | 2009 |