21st SMA Researcher Meeting
21st SMA Researcher Meeting
批准号:
9397501
负责人:
Jacqueline J. Glascock
金额:
$2.5万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-06-15 至 2018-05-31
关键词:
2 year oldAffectAreaBackBasic ScienceBiologicalBiotechnologyCessation of lifeChestChildClinicalClinical ResearchCollaborationsCommunicationCommunitiesCountryDataDefectDevelopmentDisciplineDiseaseDrug TargetingEarly treatmentEventFamilyFatigueFeesFinancial SupportFloridaFundingFutureGenesGeneticGoalsIndustrializationIndustryInheritedInstitutionInterventionLimb structureLive BirthMedicalMolecularMotorMotor NeuronsMuscle WeaknessMuscle functionMuscular AtrophyMutationNeckNeuromuscular DiseasesPatientsPharmaceutical PreparationsPharmacologic SubstancePharmacotherapyProductionProteinsResearchResearch PersonnelRoleRouteSMN protein (spinal muscular atrophy)SMN1 geneSMN2 geneScientistSpinal Muscular AtrophyStudentsTherapeuticTimeTrainingTranslational Researchdemographicsdrug developmentmeetingsmotor disordermotor neuron functionnervous system disorderneuron lossnovelpostersresearch and developmentsymposiumtherapy development
中文摘要
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英文摘要
Project Summary
Spinal Muscular Atrophy (SMA) is an inherited neuromuscular disease that leads to motor dysfunction and
death. Affecting one in 6,000 to 10,000 babies born, it is the leading genetic killer of children under two years
of age. The molecular basis of the disease is a deficiency in the production of a specific protein – Survival of
Motor Neuron (SMN) protein. Motor neuron function is sensitive to reduced SMN protein levels, and this
cellular defect leads to the loss of muscle function in the limbs, neck, and chest. Currently there is no treatment
for SMA. However, researchers have suggested that it is one of the neurological diseases closest to
treatment, due to the unique presence of a back-up gene called SMN2. In fact, this past September Biogen
submitted the first ever NDA for SMA to the FDA for a drug targeting the SMN2 back-up gene.
Cure SMA has sponsored the SMA Researcher Meeting for 21 years. In 2017, the conference will be held
June 29 to July 2 in Orlando, Florida at the Contemporary Hotel. It is now the largest SMA research conference
worldwide with more than 330 attendees each year. Basic researchers, clinicians, and industrial researchers all
attend the conference, allowing for cross-disciplinary dialogue crucial to therapy development. The meeting is
held simultaneously with the Annual SMA Conference, with 1,200 people affected by SMA attending.
The major meeting goal is to provide a venue for SMA experts to share unpublished data and develop scientific
collaborations to hasten the development of a cure for SMA. Conference presentations are organized into 3
major areas: clinical research, basic research, and translational research. This allows researchers from
different scientific disciplines to communicate about SMA. Another important meeting goal is to introduce new
scientists to SMA research. This includes researchers in training to build the future of our research community
and industrial researchers to integrate them quickly into our research community. Finally, a major focus of the
2017 meeting will be a special session on “The Role of Fatigue and Muscle Weakness in SMA with
Therapeutic Implications”. As mentioned above, the SMA field has made major advances with SMN enhancing
approaches, but to achieve the greatest impact from this therapeutic approach, early treatment will likely be
required. Therefore, the goal of this session is to discuss novel mechanisms that could result in greater motor
and muscle function at advanced stages of SMA. Many older SMA patients cite fatigue and endurance as a
significant concern, yet the biological origin, as well as the treatment options are poorly understood. The
session will discuss these concerns from a clinical and biological perspective, breaking down the potential role
of the different components of the motor unit and possible ways to intervene therapeutically.
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