Neural encoding of speech envelopes during development: A frequency-specific investigation
发育过程中语音包络的神经编码:特定频率的研究
基本信息
- 批准号:10190883
- 负责人:
- 金额:$ 5.68万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-06-12 至 2022-03-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAgeAge of OnsetAuditory systemBehavioralBindingBrain StemCalibrationChildChildhoodCochleaCochlear Hearing LossComplexCueing for speechCuesDevelopmentDevicesDimensionsDiseaseEarEarly InterventionElectroencephalogramElectroencephalographyFrequenciesGenderGoalsHeadHearing AidsHearing TestsHumanInterest GroupInvestigationKnowledgeMeasuresMethodsNatureNeural PathwaysNoiseOutcomeParticipantPathway interactionsPerceptionPeriodicityPhaseProcessResearchScalp structureSignal TransductionSpeechSpeech DiscriminationSpeech SoundStimulusTestingTimeVoiceWorkage groupage relatedauditory processingbasechildhood hearing losscomparison groupexperiencehearing impairmentinfancyneurodevelopmentnormal hearingnovelrelating to nervous systemresponsesignal processingsoundtool
项目摘要
Project Summary
An important time-based cue for understanding speech in quiet and in the presence of noise is the periodicity in
voicing at the fundamental frequency (f0). The ability of children to use f0-rate information for speech understand-
ing depends on how well their auditory system extracts this information in each frequency region. The ability
to extract such information could be influenced by the cochlear-place-specific development of neural pathways
and the tendency for auditory processing to develop earlier in pathways innervating the cochlear base. f0 encod-
ing can be evaluated using envelope following response (EFRs)—an electroencephalogram-based method that
reflects neural activity phase-locked to the periodic f0 envelope. However, little is known about the frequency-
specific development of f0 encoding because of the predominant use of broadband vowels to elicit EFRs. To this
end, our goal is to systematically evaluate the frequency-specific developmental time course of f0 encoding.
The proposed studies will use novel band-limited speech stimuli to investigate the developmental time course of
f0 encoding initiated in different cochlear regions corresponding to low, mid and high frequencies. In addition to
using a frequency-specific approach, f0 encoding will be assessed as a function of (i) f0 rate—a parameter that
changes by talker age and gender, (ii) decreasing signal-to-noise ratio—a parameter that simulates challenging
listening conditions especially for children, and (iii) behavioral relevance of the stimulus—a parameter that can
disambiguate the impact of everyday listening experience. The two pediatric age groups of interest with immature
perception of f0-rate envelope periodicity are, 0.3-1 years and 5-8 years, as they align with mature cochlear, and
cochlear and brainstem function, respectively. For rigorous adult-child comparisons of f0 encoding in the presence
of age-dependent ear and head sizes, the approach will entail: (i) stimulus calibration in each test ear to equalize
stimulus level across all test ears, (ii) use of phase coherence—a normalized response measure independent of
absolute response strength and latency—as the maturity metric, and (iii) between-group comparisons of stimulus-
induced changes rather than raw EFR measures. Findings will reveal if f0 encoding at low frequencies is the last
to achieve adult-like processing and if such a developmental trajectory is specific to speech.
The proposed research has important implications for children with cochlear hearing loss who may experience
frequency-specific abnormal f0 encoding as a function of hearing loss degree. The age-, frequency-, rate-, signal-
to-noise ratio-, and stimulus-specific development of f0 encoding from the proposed work will advance our ability
to detect and assess the nature and extent of abnormal f0 encoding due to cochlear hearing loss and/or signal
processing in devices like hearing aids. The use of EFRs will enable assessment of f0 encoding in children too
young to participate in behavioral hearing tests and in turn, offer the opportunity to inform changes in intervention
earlier than behavioral hearing tests can.
项目概要
在安静和有噪音的情况下理解语音的一个重要的基于时间的线索是周期性
以基频 (f0) 发声。儿童使用 f0 速率信息进行语音理解的能力
听力取决于他们的听觉系统在每个频率区域提取此信息的能力。能力
提取此类信息可能会受到耳蜗位置特定的神经通路发育的影响
听觉处理在支配耳蜗基底的通路中较早发展的趋势。 f0 编码-
可以使用包络跟踪响应 (EFR) 进行评估,这是一种基于脑电图的方法,
反映锁相到周期性 f0 包络的神经活动。然而,人们对频率知之甚少——
由于主要使用宽带元音来引出 EFR,因此 f0 编码的具体开发。对此
最后,我们的目标是系统地评估 f0 编码的特定频率发展时间过程。
拟议的研究将使用新颖的限带语音刺激来研究发育时间过程
f0 编码在对应低、中、高频的不同耳蜗区域启动。此外
使用特定于频率的方法,f0 编码将被评估为 (i) f0 速率的函数——该参数
随说话者年龄和性别的变化,(ii) 降低信噪比——模拟挑战性的参数
听力条件,尤其是儿童的听力条件,以及(iii)刺激的行为相关性——一个可以
消除日常聆听体验的影响。两个感兴趣的儿童年龄组
f0 速率包络周期的感知为 0.3-1 年和 5-8 年,因为它们与成熟的耳蜗一致,并且
分别是耳蜗和脑干功能。用于在存在 f0 编码的情况下进行严格的成人与儿童比较
根据年龄相关的耳朵和头部尺寸,该方法将需要:(i)每个测试耳的刺激校准以均衡
所有测试耳的刺激水平,(ii) 使用相位相干性——一种独立于
绝对反应强度和潜伏期——作为成熟度指标,以及(iii)刺激的组间比较——
诱发的变化而不是原始的 EFR 措施。研究结果将揭示低频 f0 编码是否是最后一个
实现类似成人的处理能力,并且这种发展轨迹是否特定于言语。
拟议的研究对于患有耳蜗听力损失的儿童具有重要意义,他们可能会经历
频率特定的异常 f0 编码作为听力损失程度的函数。年龄-、频率-、速率-、信号-
根据提议的工作对 f0 编码进行信噪比和特定刺激的开发将提高我们的能力
检测和评估由于耳蜗听力损失和/或信号导致的异常 f0 编码的性质和程度
助听器等设备中的处理。 EFR 的使用也将能够评估儿童的 f0 编码
年轻人参加行为听力测试,从而提供了解干预措施变化的机会
比行为听力测试更早。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
VIJAYALAKSHMI EASWAR其他文献
VIJAYALAKSHMI EASWAR的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('VIJAYALAKSHMI EASWAR', 18)}}的其他基金
Neural encoding of speech envelopes during development: A frequency-specific investigation
发育过程中语音包络的神经编码:特定频率的研究
- 批准号:
10046949 - 财政年份:2020
- 资助金额:
$ 5.68万 - 项目类别:
Longitudinal outcomes of hearing-impaired children: early vs later intervention
听力障碍儿童的纵向结果:早期干预与后期干预
- 批准号:
10188485 - 财政年份:2007
- 资助金额:
$ 5.68万 - 项目类别:
Longitudinal outcomes of hearing-impaired children: early vs later intervention
听力障碍儿童的纵向结果:早期干预与后期干预
- 批准号:
10451520 - 财政年份:2007
- 资助金额:
$ 5.68万 - 项目类别:
Longitudinal outcomes of hearing-impaired children: early vs later intervention
听力障碍儿童的纵向结果:早期干预与后期干预
- 批准号:
10645047 - 财政年份:2007
- 资助金额:
$ 5.68万 - 项目类别:
相似国自然基金
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
- 批准号:JCZRQN202500010
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
- 批准号:2025JJ70209
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
- 批准号:
- 批准年份:2024
- 资助金额:0 万元
- 项目类别:面上项目
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
- 批准号:2023JJ50274
- 批准年份:2023
- 资助金额:0.0 万元
- 项目类别:省市级项目
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
- 批准号:
- 批准年份:2022
- 资助金额:33 万元
- 项目类别:地区科学基金项目
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
- 批准号:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
- 批准号:
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
- 批准号:81973577
- 批准年份:2019
- 资助金额:55.0 万元
- 项目类别:面上项目
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
- 批准号:81602908
- 批准年份:2016
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
- 批准号:81501928
- 批准年份:2015
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
相似海外基金
Determining the mechanism of action of cis-acting modifiers on the age of onset of Huntington Disease
确定顺式作用修饰剂对亨廷顿病发病年龄的作用机制
- 批准号:
417256 - 财政年份:2019
- 资助金额:
$ 5.68万 - 项目类别:
Studentship Programs
Effect of age of onset of contraception use on brain functioning.
避孕开始年龄对大脑功能的影响。
- 批准号:
511267-2017 - 财政年份:2017
- 资助金额:
$ 5.68万 - 项目类别:
University Undergraduate Student Research Awards
Non-random occurrence and early age of onset of diverse lymphoid cancers in families supports the existence of genetic risk factors for multiple lymphoid cancers.
家族中多种淋巴癌的非随机发生和发病年龄较早,支持多种淋巴癌存在遗传危险因素。
- 批准号:
347105 - 财政年份:2016
- 资助金额:
$ 5.68万 - 项目类别:
Polish-German Child Bilingualism: The Role of Age of Onset for Long-Term Achievement
波兰-德国儿童双语:发病年龄对长期成就的作用
- 批准号:
277135691 - 财政年份:2015
- 资助金额:
$ 5.68万 - 项目类别:
Research Grants
Bioinformatics strategies to relate age of onset with gene-gene interaction
将发病年龄与基因间相互作用联系起来的生物信息学策略
- 批准号:
9097781 - 财政年份:2015
- 资助金额:
$ 5.68万 - 项目类别:
Early Age-of-Onset AD: Clinical Heterogeneity and Network Degeneration
早期 AD 发病年龄:临床异质性和网络退化
- 批准号:
9212684 - 财政年份:2014
- 资助金额:
$ 5.68万 - 项目类别:
Early Age-of-Onset AD: Clinical Heterogeneity and Network Degeneration
早期 AD 发病年龄:临床异质性和网络退化
- 批准号:
8696557 - 财政年份:2014
- 资助金额:
$ 5.68万 - 项目类别:
Effects of delaying age of onset of binge drinking on adolescent brain development: A proposal to add neuroimaing measures to the CO-Venture Trial.
延迟酗酒的发病年龄对青少年大脑发育的影响:在 CO-Venture 试验中添加神经影像测量的建议。
- 批准号:
267251 - 财政年份:2012
- 资助金额:
$ 5.68万 - 项目类别:
Operating Grants
Stress Effects on Alcohol Consumption: Age of onset and genes in heavy drinkers
压力对饮酒的影响:酗酒者的发病年龄和基因
- 批准号:
8606722 - 财政年份:2012
- 资助金额:
$ 5.68万 - 项目类别:
Marijuana: Neurobiologic Correlates of Age of Onset
大麻:发病年龄的神经生物学相关性
- 批准号:
8644793 - 财政年份:2012
- 资助金额:
$ 5.68万 - 项目类别:














{{item.name}}会员




