| Literature DB >> 35145758 |
Ben Alderson-Day, Jamie Moffatt, César F Lima, Saloni Krishnan, Charles Fernyhough, Sophie K Scott, Sophie Denton, Ivy Yi Ting Leong, Alena D Oncel, Yu-Lin Wu, Zehra Gurbuz, Samuel Evans.
Abstract
Auditory verbal hallucinations (AVHs)-or hearing voices-occur in clinical and non-clinical populations, but their mechanisms remain unclear. Predictive processing models of psychosis have proposed that hallucinations arise from an over-weighting of prior expectations in perception. It is unknown, however, whether this reflects (i) a sensitivity to explicit modulation of prior knowledge or (ii) a pre-existing tendency to spontaneously use such knowledge in ambiguous contexts. Four experiments were conducted to examine this question in healthy participants listening to ambiguous speech stimuli. In experiments 1a (n = 60) and 1b (n = 60), participants discriminated intelligible and unintelligible sine-wave speech before and after exposure to the original language templates (i.e. a modulation of expectation). No relationship was observed between top-down modulation and two common measures of hallucination-proneness. Experiment 2 (n = 99) confirmed this pattern with a different stimulus-sine-vocoded speech (SVS)-that was designed to minimize ceiling effects in discrimination and more closely model previous top-down effects reported in psychosis. In Experiment 3 (n = 134), participants were exposed to SVS without prior knowledge that it contained speech (i.e. naïve listening). AVH-proneness significantly predicted both pre-exposure identification of speech and successful recall for words hidden in SVS, indicating that participants could actually decode the hidden signal spontaneously. Altogether, these findings support a pre-existing tendency to spontaneously draw upon prior knowledge in healthy people prone to AVH, rather than a sensitivity to temporary modulations of expectation. We propose a model of clinical and non-clinical hallucinations, across auditory and visual modalities, with testable predictions for future research.Entities:
Keywords: audition; predictive coding; psychosis; speech perception; speech-in-noise
Year: 2022 PMID: 35145758 PMCID: PMC8824703 DOI: 10.1093/nc/niac002
Source DB: PubMed Journal: Neurosci Conscious ISSN: 2057-2107
Figure 1.Overview of experiments. (A) Experiment 1a: Participants heard 90 trials comprised of potentially intelligible and unintelligible sounds and judged whether each sound contained speech (pre-exposure). They were then exposed to the target clear speech exemplars from which the intelligible trials were made (exposure) and then asked again to judge which trials contained speech (post-exposure). (B) Experiment 1b: Participants took part in the same paradigm as Experiment 1a but half the participants were primed by listening to a busy auditory scene and the other half were not. (C) Experiment 2: Participants heard blocks of 10 trials using the same pre-exposure, exposure, post-exposure cycles in Study 1. (D) Experiment 3: Participants took part in a naïve listening experiment in which they were tasked with identifying sounds with a specific acoustic quality (noise-vocoded sounds). They were not informed that some sounds contained speech. They were then asked whether they had heard any speech in the naïve listening task and took part in a memory recognition test to see if they remembered the intelligible trials. They were then exposed to the clear speech targets and tested on their identification of speech
Signal detection outcomes for the SWS discrimination task in experiment 1a
| Before | After | ||||||
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| 1.47 | 0.77 | 2.17 | 0.81 | −8.63 | 4.809e−12 | −0.90 |
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| 0.19 | 0.45 | −0.37 | 0.44 | −6.25 | 4.212e−10 | 0.81 |
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| 1.63 | 1.87 | 0.60 | 0.51 | −5.74 | 9.202e−09 | 0.74 |
Note: Higher values of dʹ indicate increased sensitivity to detect speech. Scores below 0 for C and 1 for beta indicate a bias to indicate speech is present. Wilcoxon tests were used for C and beta due to non-parametric data.
Figure 2.Comparing discrimination pre- and post-template exposure (A) and the relation of performance change to hallucination-proneness (B)
Figure 3.Change in discrimination pre- and post-exposure divided by priming group (A) and relation to hallucination-proneness (B)
Signal detection outcomes for the SWS discrimination task in experiment 1b
| Before | After | ||||||
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| 1.56 | 0.76 | 2.34 | 0.72 | −9.05 | 9.298e-13 | −1.05 |
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| 0.29 | 0.63 | −0.42 | 0.52 | 9.65 | 9.59e-14 | 1.22 |
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| 2.58 | 3.04 | 0.88 | 1.62 | −5.79 | 6.741e-09 | 0.75 |
Note: higher values of d′ indicate increased sensitivity to detect speech. Scores below 0 for C and 1 for beta indicate a bias to indicate speech is present. Wilcoxon tests were used for beta due to non-parametric data.
Figure 4.(A) d′ (left) and C change (right panel) with prior knowledge exposure, (B) d′ change over time in the common 8 band, +6 dB condition. Note that the grand mean for d′ values for the by block analyses differs to the main analysis because the adjustment for extreme values was conducted by block in this instance rather than across the whole experiment (Macmillan and Kaplan 1985), (C) showing the lack of evidence in support of a relationship between d′ change and the CAPS (left) and PDI measures (right panel)
Signal detection outcomes for the SVS speech detection task for the 8 band, +6 dB condition. Wilcoxon tests were used beta due to non-parametric data
| Before | After | ||||||
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| d’ | 1.20 | 1.09 | 1.72 | 1.25 | 9.34 | 3.217e-15 | 0.44 |
| C | 0.04 | 0.48 | −0.06 | 0.45 | 2.99 | 0.004 | 0.22 |
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| 1.28 | 1.23 | 1.14 | 0.98 | 1.59 | 0.113 | 0.16 |