This application responds to RFA RR-03-008, Rare Diseases Clinical Research Network and proposes the investigation of 3 rare neurological channelopathies: periodic paralysis, non-dystrophic myotonic disorders and episodic ataxia. The research plan will exploit the strengths of 7 collaborating centers to link molecular scientists studying these disorders with clinical investigators with established expertise in the development of new treatments for neurological disease. It will extend a prototype NIH training program in experimental therapeutics to train a cadre of patient-oriented-researchers committed to rare disorders. Study investigators have strong links with the patient advocacy organizations focused on these rare disorders: the Periodic Paralysis Association, the National Ataxia Foundation and the Muscular Dystrophy Association. A particular strength of the collaborating institutions is an established nationwide infrastructure, including GCRCs and a biostatistician, for the implementation of multicenter clinical trials that will facilitate investigation of the efficacy of putative new treatments for rare diseases. Currently-supported studies of the pathophysiology of the 3 specific target diseases will provide resources for molecular characterization of subjects and make it possible to: (1) begin the characterization of the phenotype/natural history of each; (2) devise outcome measures for treatment trials; (3) assess quality of life -- all in preparation for pilot clinical trials of novel treatments. The focus of investigation is on: (1) Andersen's syndrome, a periodic paralysis with associated life-threatening cardiac arrhythmias for which no treatment has been identified; (2) the nondystrophic myotonias caused by sodium and chloride channel mutations for which there is no established treatment and there have been no well-designed clinical trials; (3) the episodic ataxias EA1 and EA2 for which treatment is not yet defined. Both cellular model systems and animal models, funded separately, are (or soon will be) available for each of these disorders and can provide pre- clinical data necessary for proposed phase 1 and 2 trials of novel treatments. These 3 disorders are prototypes for the development of treatment strategies for over 50 other rare neurological channelopathies. They may also offer a window for understanding common disorders likely to be caused by CNS channel mutations/dysfunction such as migraine and epilepsy.
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| Statland, Jeffrey M; Wang, Yunxia; Richesson, Rachel et al. (2011) An interactive voice response diary for patients with non-dystrophic myotonia. Muscle Nerve 44:30-5 |
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| Gooch, Clifton L; Amato, Anthony A (2010) Are anti-ganglioside antibodies of clinical value in multifocal motor neuropathy? Neurology 75:1950-1 |
| Cha, Yoon-Hee (2010) Migraine-associated vertigo: diagnosis and treatment. Semin Neurol 30:167-74 |
| Burns, Ted M; Conaway, Mark; Sanders, Donald B et al. (2010) The MG Composite: A valid and reliable outcome measure for myasthenia gravis. Neurology 74:1434-40 |
| Graves, T D; Rajakulendran, S; Zuberi, S M et al. (2010) Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins. Neurology 75:367-72 |
| Rajakulendran, Sanjeev; Graves, Tracey D; Labrum, Robyn W et al. (2010) Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy. J Physiol 588:1905-13 |
| Cha, Yoon-Hee (2009) Mal de debarquement. Semin Neurol 29:520-7 |
| Cha, Y-H; Lee, H; Santell, L S et al. (2009) Association of benign recurrent vertigo and migraine in 208 patients. Cephalalgia 29:550-5 |
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