Electrophysiological biomarkers for spatial hearing impairments resulting from ea
Electrophysiological biomarkers for spatial hearing impairments resulting from ea
批准号:
9013467
负责人:
Alexander T Ferber
金额:
$3.16万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-03-01 至 2017-02-28
关键词:
AcousticsAdultAffectAnatomyAnimal ExperimentsAnimalsAuditoryAuditory Brainstem ResponsesAuditory systemBasic ScienceBehaviorBehavioralBehavioral AssayBilateralBinauralBiological MarkersBrain StemCalibrationCaviaCell NucleusCentral Auditory Processing DisorderChildChildhoodChronicClinicalClinical ResearchComplexConductive hearing lossCuesDependenceDetectionDevelopmentDiagnosisDiagnosticEarElectrophysiology (science)EnvironmentExposure toFunctional disorderHearingHumanImpairmentIndividualInferior ColliculusLanguageLeadLearningLifeLinkLocationMeasuresMethodsMissionNational Institute on Deafness and Other Communication DisordersNatureNeuronsOtitis MediaOtitis Media with EffusionPerceptionPerformancePhysiologyProcessRecoveryResearchResidual stateResolutionSignal TransductionSiteSound LocalizationSourceSpeechSumSystems DevelopmentTechnologyTestingTimeTrainingVisitWorkbehavior measurementbinaural hearingclinical applicationclinically relevantclinically significantdesignear infectionexperiencehearing impairmentinfancyinsightlanguage impairmentmiddle earnovelpublic health relevanceresponsesoundsuperior olivary nucleussymptom clustertargeted treatmenttool
中文摘要
描述(由申请人提供):传导性听力损失(CHL)-例如由中耳感染和其他耳部疾病引起的-可以以深刻和有害的方式影响听觉系统。CHL造成的干扰通常是双耳听力任务的损伤,这些任务需要整合来自双耳的信息,例如声音的“过滤”。
在嘈杂和混响的环境中。长期的言语和语言障碍可能由CHL引起。直到今天,长期CHL影响中枢听觉系统的确切方式还不完全清楚,但很明显,这种影响可能是严重和持久的。这一系列症状被称为中枢听觉处理障碍(或(C)APD)。目前,(C)APD的诊断很困难,需要一系列测试和数月的时间。这是有问题的,因为研究表明尽早治疗(C)APD是有益的。可用于评估双耳听力功能和诊断(C)APD的一个潜在度量是听觉脑干反应(ABR)的双耳交互分量(BIC)。声诱发双耳相互作用分量(BIC)是从单耳诱发的ABR之和中减去双耳诱发的ABR后剩余的残余听觉脑干反应(ABR)。峰是BIC中的第一个负峰,其与双耳处理有关。在人类和动物研究中的Lavonof表明它在下丘及其输入水平具有脑干起源。下丘伊萨所有脑干核团输入的汇聚点,包括上级橄榄复合体的核团,其计算双耳声学线索以定位(耳间时间(ITD)和水平(ILD)差异)。BIC可能具有重要的诊断价值;例如,儿童和成人的峰的波幅和振幅的改变与慢性CHL相关的双耳处理中相同的长期行为缺陷相关并预测。在这个提议中,我们研究了CHL对BIC峰的影响,并将BIC与声音定位能力的行为测量(声学惊吓反应)相关联。在诱导的单侧CHL过程中,将在一系列ITD和ILD线索中评估BIC峰的振幅和潜伏期,并在相应的时间点评估声音定位行为。我们假设CHL以可预测的方式改变声音定位线索的整合,这将增强我们对CHL对双耳听力影响的理解。此外,我们预计行为和BIC都将随着时间的推移而恢复,BIC预测声音定位能力的水平。了解声音定位和BIC之间的相互作用有望产生一个临床上有用的工具,用于评估中耳炎儿童的双耳听力和CHL。这项建议是专门为提供培训,在基础科学和临床方面的听觉研究,促进使命的NIDCD。
英文摘要
DESCRIPTION (provided by applicant): Conductive hearing loss (CHL)-such as is caused by middle ear infections and other ear conditions-can affect the auditory system in a profound and detrimental manner. The disruptions caused by CHL are often impairments of binaural hearing tasks that require the integration of information from both ears, such as the "filtering" of sounds
in noisy and reverberant environments. Long-term speech and language impairments can result from CHL. Still today, the exact manner in which long-term CHL affects the central auditory system is not entirely known, but it is clear that the effects can be severe and long lasting. The cluster of symptoms that result are termed Central Auditory Processing Disorder (or (C)APD). Currently, diagnosis of (C)APD is difficult, requiring a battery of tests and months of time. This s problematic, since studies have shown that it is beneficial to treat (C)APD as early as possible. One potential metric that could be used to assess binaural hearing function and diagnose (C)APD is the binaural interaction component (BIC) of the auditory brainstem response (ABR). The sound-evoked binaural interaction component (BIC) is the residual auditory brainstem response (ABR) remaining after subtracting the binaurally evoked ABR from the sum of the monaurally evoked ABRs. The ¿ peak is the first negative peak in the BIC, which is related to binaural processing. Latencies of ¿ in both human and animal studies indicate it has a brainstem origin at the level of the inferior colliculus and its inputs. The inferior colliculus isa site of convergence of inputs from all brainstem nuclei, including nuclei of the superior olivary complex, which computes binaural acoustical cues to location (interaural time (ITD) and level (ILD) differences). The BIC may have important diagnostic value; for example, altered latencies and amplitudes of the ¿ peak in children and adults are correlated with and predictive of the same long-term behavioral deficits in binaural processing associated with chronic CHL. In this proposal, we investigate the effect of CHL on the BIC ¿ peak and correlate the BIC with a behavioral measure of sound localization ability, the acoustic startle response. The amplitude of and latency of the BIC ¿ peak will be assessed across a range of ITD and ILD cues to location during the course of an induced unilateral CHL, and sound localization behavior will be assessed at corresponding time points. We hypothesize that CHL alters the integration of sound localization cues in a predictable way, which will enhance our understanding of the effect of CHL on binaural hearing. Furthermore, we expect that both behavior and BIC will recover with time, with BIC predicting the level of sound localization ability. Understanding the interaction between sound localization and the BIC promises to yield a clinically useful tool for assessing binaural hearing ability and CHL in children with otitis media. This proposal is specifically designed to provide training in both basic science and clinical aspects of auditory research, furthering the mission of the NIDCD.
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Electrophysiological biomarkers for spatial hearing impairments resulting from ea
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批准号:8715451
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项目类别:
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资助金额:$3.07万
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财政年份:2014
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负责人:Alexander T Ferber
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依托单位:
海外基金