Tools
Tools
Idro, Richard, Anguzu, Ronald, Ogwang, Rodney, Akun, Pamela, Abbo, Catherine, Mwaka, Amos Deogratius, Opar, Bernard, Nakamya, Phyellister, Taylor, Mark 
ORCID: https://orcid.org/0000-0003-3396-9275, Elliott, Alison, Vincent, Angela, Newton, Charles and Marsh, Kevin
(2019)
'Doxycycline for the treatment of nodding syndrome (DONS); the study protocol of a phase II randomised controlled trial'. BMC Neurology, Vol 19, Issue 35.
|
Text
Mark Taylor.pdf - Published Version Available under License Creative Commons Attribution. Download (1MB) | Preview |
Abstract
Background: Nodding syndrome is a poorly understood neurological disorder of unknown aetiology, affectingseveral thousand children in Africa. There has been a consistent epidemiological association with infection by the filarial parasite, Onchocerca volvulus and antibodies to leiomodin and DJ-1, cross-reacting with O.volvulus proteins, have been reported. We hypothesized that nodding syndrome is a neuro-inflammatory disorder, induced by antibodies to O.volvulus or its symbiont, Wolbachia, cross-reacting with human neuron proteins and that doxycycline, which kills Onchocerca through effects on Wolbachia, may be used as treatment.
Methods: This will be a two-arm, double-blind, placebo-controlled, randomised phase II trial of doxycycline 100 mg daily for six weeks in 230 participants. Participants will be patients’ ages≥8 years with nodding syndrome. They will receive standard of care supportive treatment. All will be hospitalised for 1–2 weeks during which time baseline measurements including clinical assessments, EEG, cognitive and laboratory testing will be performed and antiepileptic drug doses rationalised. Participants will then be randomised to either oral doxycycline (Azudox®, Kampala Pharmaceutical Industries) 100 mg daily or placebo. Treatment will be initiated in hospital and continued
at home. Participants will be visited at home at 2, 4 and 6 weeks for adherence monitoring. Study outcomes will be assessed at 6, 12, 18 and 24-month visits. Analysis will be by intention to treat. The primary efficacy outcome measure will be the proportion of patients testing positive and the levels or titires of antibodies to host neuron proteins (HNPs) and/or leiomodin at 24 months. Secondary outcome measures will include effect of the intervention on seizure control, inflammatory markers, cognitive function, disease severity and quality of life.
Discussion: This trial postulates that targeting O.volvulus through drugs which kill Wolbachia can modify the pathogenic processes in nodding syndrome and improve outcomes. Findings from this study are expected to substantially improve the understanding and treatment of nodding syndrome.
Trial registration: Registered with clinicaltrials.gov ID: NCT02850913 on 1st August, 2016.
Keywords: Nodding syndrome, Doxycycline, Onchocerca volvulus, Randomized controlled trial
| Item Type: | Article |
|---|---|
| Subjects: | QW Microbiology and Immunology > Bacteria > QW 131 Gram-negative bacteria. QX Parasitology > QX 4 General works WC Communicable Diseases > Tropical and Parasitic Diseases > WC 680 Tropical diseases (General) WC Communicable Diseases > Tropical and Parasitic Diseases > WC 695 Parasitic diseases (General) WC Communicable Diseases > Tropical and Parasitic Diseases > WC 850 Nematode infections (General) |
| Faculty: Department: | Biological Sciences > Department of Tropical Disease Biology |
| Digital Object Identifer (DOI): | https://doi.org/10.1186/s12883-019-1256-z |
| Depositing User: | Stacy Murtagh |
| Date Deposited: | 15 Apr 2019 09:12 |
| Last Modified: | 16 Sep 2019 09:02 |
| URI: | https://archive.lstmed.ac.uk/id/eprint/10649 |
Statistics
Actions (login required)
 |
Edit Item |