Deep phenotyping in blepharospasm
眼睑痉挛的深层表型分析
基本信息
- 批准号:10677839
- 负责人:
- 金额:$ 37.67万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-09-29 至 2025-06-30
- 项目状态:未结题
- 来源:
- 关键词:AddressAffectAlgorithmsApraxiasAssessment toolBiologicalBiological MarkersBlepharospasmBlinkingBody RegionsClinicClinicalClinical TrialsCluster AnalysisDetectionDevelopmentDevicesDiagnosisDiscriminationDiseaseDyskinetic syndromeDystoniaElementsEtiologyEyeEyelid structureFaceFutureGoalsHeterogeneityImpairmentInterventionJawMeasurementMeasuresMonitorMovementMuscleMuscle ContractionNeurologicOutcomePathogenicityPatientsPhenotypePopulationPropertyProteomicsPublishingResearchSerumSeveritiesSeverity of illnessSmooth MuscleSpasmSubgroupSymptomsTestingTimeTrainingblood-based biomarkerclinical applicationclinical phenotypecohortexperienceimprovedinsightnervous system disordernovelphenotypic datapilot testpotential biomarkerrecruitsensortoolwearable device
项目摘要
PROJECT SUMMARY
The dystonias are a group of disorders characterized by excessive involuntary muscle contractions leading to
spasms and abnormal movements. Any region of the body may be affected. One of the most commonly affected
regions is the upper face, leading to blepharospasm (BL). Patients experience a number of distinct but
overlapping problems that include spasms of the muscles around the eyes, excessive blinking, eyelid fluttering,
impaired eyelid opening, and spread to the lower face or jaw. Traditionally, BL has been viewed as a relatively
homogeneous disorder, differing only in grades of severity. However, there is increasing evidence that BL is not
a homogeneous disorder. For example, recent cluster analyses including large numbers of patients have
provided evidence for phenotypically distinct subgroups. Clinically, it has been recognized for some time that
some subtypes of BL are more difficult to treat than others. There also is evidence that the core symptoms of
BL have different pathogenic mechanisms. Thus, there already is strong evidence for etiological heterogeneity.
Despite the importance of these different clinical manifestations, there are no tools for distinguishing and
measuring them. Future clinical and scientific studies of BL require more sophisticated tools to discriminate the
distinct phenotypic elements of BL. These tools are fundamental needs to improve diagnosis and treatment of
the different subtypes of BL, to monitor outcomes of clinical trials for BL, and to provide richer and more
meaningful phenotypic data in in support of studies of the pathophysiologic underpinnings of BL. The studies of
this proposal describe the development of a novel simple clinical rating scale to separately quantify the distinct
features of BL in the clinic, a novel an unobtrusive wearable device for rigorous discrimination and quantification
of these features, and preliminary characterization of potential blood-based biomarkers for the disorder.
项目摘要
肌张力障碍是一组以过度的不随意肌肉收缩为特征的疾病,
痉挛和异常运动。身体的任何部位都可能受到影响。其中最常见的影响
区域是上面部,导致眼睑痉挛(BL)。患者经历了许多不同的,但
重叠的问题,包括眼睛周围的肌肉痉挛,过度眨眼,眼睑颤动,
眼睑张开受损,并扩散到下面部或下颌。传统上,BL被视为相对
同质性疾病,仅严重程度不同。然而,越来越多的证据表明,BL不是
一种同质的紊乱例如,最近的聚类分析包括大量的患者,
为表型不同的亚组提供了证据。在临床上,一段时间以来人们已经认识到,
BL的某些亚型比其它亚型更难治疗。也有证据表明,
BL具有不同的致病机制。因此,已经有强有力的证据表明病因异质性。
尽管这些不同的临床表现的重要性,有没有工具来区分和
测量它们。未来BL的临床和科学研究需要更复杂的工具来区分
BL的不同表型元件。这些工具是改善疾病诊断和治疗的基本需求。
BL的不同亚型,以监测BL临床试验的结果,并提供更丰富和更
有意义的表型数据支持BL的病理生理基础的研究。的研究
该提案描述了一种新的简单临床评定量表的开发,
BL在临床上的特点,一种新颖的不显眼的可穿戴设备,用于严格的区分和量化
这些特征,以及对该疾病的潜在血液生物标志物的初步表征。
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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HYDER A JINNAH其他文献
HYDER A JINNAH的其他文献
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{{ truncateString('HYDER A JINNAH', 18)}}的其他基金
Modeling Inherited Neurodevelopmental Disorders with Human Induced Pluripotent Stem Cells
用人类诱导多能干细胞模拟遗传性神经发育障碍
- 批准号:
10397399 - 财政年份:2019
- 资助金额:
$ 37.67万 - 项目类别:
Human Induced Pluripotent Stem Cells As Models for Inherited Developmental Disorders
人类诱导多能干细胞作为遗传性发育障碍的模型
- 批准号:
9512060 - 财政年份:2017
- 资助金额:
$ 37.67万 - 项目类别:
Identification of genetic and metabolomic markers influencing dystonia
鉴定影响肌张力障碍的遗传和代谢组学标记
- 批准号:
9091024 - 财政年份:2016
- 资助金额:
$ 37.67万 - 项目类别:
Identification of genetic and metabolomic markers influencing dystonia
鉴定影响肌张力障碍的遗传和代谢组学标记
- 批准号:
9262303 - 财政年份:2016
- 资助金额:
$ 37.67万 - 项目类别:
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