Auditory processing disorder | EPFL Graph Search

Auditory processing disorder (APD), rarely known as King-Kopetzky syndrome or auditory disability with normal hearing (ADN), is a neurodevelopmental disorder affecting the way the brain processes sounds. Individuals with APD usually have normal structure and function of the outer, middle, and inner ear (peripheral hearing). However, they cannot process the information they hear in the same way as others do, which leads to difficulties in recognizing and interpreting sounds, especially the sounds composing speech. It is thought that these difficulties arise from dysfunction in the central nervous system. The American Academy of Audiology notes that APD is diagnosed by difficulties in one or more auditory processes known to reflect the function of the central auditory nervous system. It can affect both children and adults. Although the actual prevalence is currently unknown, it has been estimated to impact 2–7% in children in US and UK populations.

Prenatal auditory experience and its sequelae

Marin Vogelsang, Lukas Vogelsang

Towards the end of the second trimester of gestation, a human fetus is able to register environmental sounds. This in utero auditory experience is characterized by comprising strongly low-pass-filtered versions of sounds from the external world. Here, we present computational tests of the hypothesis that this early exposure to severely degraded auditory inputs serves an adaptive purpose-it may induce the neural development of extended temporal integration. Such integration can facilitate the detection of information carried by low-frequency variations in the auditory signal, including emotional or other prosodic content. To test this prediction, we characterized the impact of several training regimens, biomimetic and otherwise, on a computational model system trained and tested on the task of emotion recognition. We find that training with an auditory trajectory recapitulating that of a neurotypical infant in the pre-to-postnatal period results in temporally extended receptive field structures and yields the best subsequent accuracy and generalization performance on the task of emotion recognition. This strongly suggests that the progression from low-pass-filtered to full-frequency inputs is likely to be an adaptive feature of our development, conferring significant benefits to later auditory processing abilities relying on temporally extended analyses. Additionally, this finding can help explain some of the auditory impairments associated with preterm births, suggests guidelines for the design of auditory environments in neonatal care units, and points to enhanced training procedures for computational models.

WILEY2022

An insular cortex - lateral amygdala network in fear learning

Shriya Palchaudhuri

Animals are capable of evaluating sensory cues for possible threats and adapting their behaviours accordingly. Fear learning is an evolutionarily conserved behaviour crucial for animal survival, during which sensory percepts with a negative reinforcing quality, also called unconditioned stimuli (US), influence the valence of initially neutral sensory cues (conditioned stimulus, CS). The lateral amygdala (LA) is thought to integrate information about sensory cues like tones (the CS), and information about primary reinforcers like painful stimuli (the US). Nevertheless, synaptic afferents to the LA and upstream brain areas remain understudied in fear learning. The posterior insular cortex (pInsCx) has been shown to project to the LA and is known to be a multimodal sensory area which processes auditory, somatosensory-nociceptive, and interoceptive information, making it an interesting brain area with a putative role in fear learning. My PhD thesis therefore aimed to investigate a possible connection from the pInsCx to the LA, and the role of this pathway in the fear learning circuitry. I first used anatomical anterograde and retrograde tracing strategies in the mouse to study the afferents to the LA. Besides previously known inputs, I found that the granular (GI) and the dysgranular (DI) areas of the pInsCx strongly project to the anterior LA. With optogenetically-assisted circuit mapping (OACM), I found a glutamatergic monosynaptic connection from the pInsCx to LA principal neurons that, in agreement with the anatomical findings, was localized more to the anterior LA. In comparison, a well-studied auditory thalamic (MGm/PIN) input was localized more to the posterior LA. Despite this regional input specificity, ~30% LA principal neurons received projections from both areas. Thus, in the first part, using anatomical tracing and OACM, I have unambiguously shown a robust functional excitatory connection from the pInsCx (GI/DI) to the LA.In the second part of my thesis, I aimed to characterize the role of the pInsCx and the pInsCx-LA pathway in fear learning. Using archaerhodopsin-mediated optogenetic inhibition, I found that silencing of footshock-driven activity of pInsCx neurons in-vivo, partially blocks auditory-cued fear memory. These results were also supported by chemogenetic silencing of the pInsCx during the training day, which led to a modest impairment of fear retrieval a day later. Next, to investigate the role of the pInsCx-LA projection more specifically, I used a retrograde expression approach to silence LA-projectors during the footshock, which again, suppressed fear memory one day later. In further ex-vivo experiments, I found that EPSCs at the pInsCx-LA connection exhibited an increased AMPA/NMDA ratio following fear learning, indicating that plasticity occurs at this pathway during fear learning. Finally, miniature microscopic Ca2+ imaging of LA neurons combined with halorhodopsin-mediated axon inhibition, showed that the pInsCx-LA excitatory synapse contributes to transmitting footshock information to a sub-population of LA neurons. This study unravels the relationship between two serial nodes, the pInsCx and the LA, in the fear learning network. Thus, the pInsCx-LA connection is a novel pathway in auditory-cued fear memory that is strengthened with learning and that partly provides aversive information to the amygdala.

EPFL2022

Individual Differences in the Discrimination of Novel Speech Sounds: Effects of Sex, Temporal Processing, Musical and Cognitive Abilities

John Christian Thoresen

This study examined whether rapid temporal auditory processing, verbal working memory capacity, non-verbal intelligence, executive functioning, musical ability and prior foreign language experience predicted how well native English speakers (N = 120) discriminated Norwegian tonal and vowel contrasts as well as a non-speech analogue of the tonal contrast and a native vowel contrast presented over noise. Results confirmed a male advantage for temporal and tonal processing, and also revealed that temporal processing was associated with both non-verbal intelligence and speech processing. In contrast, effects of musical ability on non-native speech-sound processing and of inhibitory control on vowel discrimination were not mediated by temporal processing. These results suggest that individual differences in non-native speech-sound processing are to some extent determined by temporal auditory processing ability, in which males perform better, but are also determined by a host of other abilities that are deployed flexibly depending on the characteristics of the target sounds.

Public Library of Science2012

An insular cortex - lateral amygdala network in fear learning

Shriya Palchaudhuri

EPFL2022