Technology that translates neural activity into speech would be transformative for people who are unable to communicate as a result of neurological impairments. Decoding speech from neural activity is challenging because speaking requires very precise and rapid multi-dimensional control of vocal tract articulators. Here we designed a neural decoder that explicitly leverages kinematic and sound representations encoded in human cortical activity to synthesize audible speech. Recurrent neural networks first decoded directly recorded cortical activity into representations of articulatory movement, and then transformed these representations into speech acoustics. In closed vocabulary tests, listeners could readily identify and transcribe speech synthesized from cortical activity. Intermediate articulatory dynamics enhanced performance even with limited data. Decoded articulatory representations were highly conserved across speakers, enabling a component of the decoder to be transferrable across participants. Furthermore, the decoder could synthesize speech when a participant silently mimed sentences. These findings advance the clinical viability of using speech neuroprosthetic technology to restore spoken communication.
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The data that support the findings of this study are available from the corresponding author upon request.
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We thank M. Leonard, N. Fox and D. Moses for comments on the manuscript and B. Speidel for his help reconstructing MRI images. This work was supported by grants from the NIH (DP2 OD008627 and U01 NS098971-01). E.F.C. is a New York Stem Cell Foundation-Robertson Investigator. This research was also supported by The William K. Bowes Foundation, the Howard Hughes Medical Institute, The New York Stem Cell Foundation and The Shurl and Kay Curci Foundation.
Nature thanks David Poeppel and the other anonymous reviewer(s) for their contribution to the peer review of this work.
The authors declare no competing interests.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
a, b, Median spectrograms, time-locked to the acoustic onset of phonemes from original (a) and decoded (b) audio (/i/, n = 112; /z/, n = 115; /p/, n = 69, /ae/, n = 86). These phonemes represent the diversity of spectral features. Original and decoded median phoneme spectrograms were well-correlated (Pearson’s r > 0.9 for all phonemes, P = 1 × 10−18).
a, b, WERs for individually transcribed trials for pools with a size of 25 (a) or 50 (b) words. Listeners transcribed synthesized sentences by selecting words from a defined pool of words. Word pools included correct words found in the synthesized sentence and random words from the test set. One trial is one transcription of one listener of one synthesized sentence.
MRI reconstructions of participants’ brains with overlay of electrocorticographic electrode (ECoG) array locations. P1–5, participants 1–5.
Data from participant 1. a, Correlations of all 33 decoded articulatory kinematic features with ground-truth (n = 101 sentences). EMA features represent x and y coordinate traces of articulators (lips, jaw and three points of the tongue) along the midsagittal plane of the vocal tract. Manner features represent complementary kinematic features to EMA that further describe acoustically consequential movements. b, Correlations of all 32 decoded spectral features with ground-truth (n = 101 sentences). MFCC features are 25 mel-frequency cepstral coefficients that describe power in perceptually relevant frequency bands. Synthesis features describe glottal excitation weights necessary for speech synthesis. Box plots as described in Fig. 2.
Extended Data Fig. 5 Comparison of cumulative variance explained in kinematic and acoustic state–spaces.
For each representation of speech—kinematics and acoustics—a principal components analysis was computed and the explained variance for each additional principal component was cumulatively summed. Kinematic and acoustic representations had 33 and 32 features, respectively.
Acoustic similarity matrix compares acoustic properties of decoded phonemes and originally spoken phonemes. Similarity is computed by first estimating a Gaussian kernel density for each phoneme (both decoded and original) and then computing the Kullback–Leibler (KL) divergence between a pair of decoded and original phoneme distributions. Each row compares the acoustic properties of a decoded phoneme with originally spoken phonemes (columns). Hierarchical clustering was performed on the resulting similarity matrix. Data from participant 1.
The acoustic properties of ground-truth spoken phonemes are compared with one another. Similarity is computed by first estimating a Gaussian kernel density for each phoneme and then computing the Kullback–Leibler divergence between a pair of a phoneme distributions. Each row compares the acoustic properties of two ground-truth spoken phonemes. Hierarchical clustering was performed on the resulting similarity matrix. Data from participant 1.
a, b, Comparison metrics included spectral distortion (a) and the correlation between decoded and original spectral features (b). Decoder performance for these two types of sentences was compared and no significant difference was found (P = 0.36 (a) and P = 0.75 (b), n = 51 sentences, Wilcoxon signed-rank test). A novel sentence consists of words and/or a word sequence not present in the training data. A repeated sentence is a sentence that has at least one matching word sequence in the training data, although with a unique production. Comparison was performed on participant 1 and the evaluated sentences were the same across both cases with two decoders trained on differing datasets to either exclude or include unique repeats of sentences in the test set. ns, not significant; P > 0.05. Box plots as described in Fig. 2.
Extended Data Fig. 9 Kinematic state–space trajectories for phoneme-specific vowel–consonant transitions.
Average trajectories of principal components 1 (PC1) and 2 (PC2) for transitions from either a consonant or a vowel to specific phonemes. Trajectories are 500 ms and centred at transition between phonemes. a, Consonant to corner vowels (n = 1,387, 1,964, 2,259, 894, respectively, for aa, ae, iy and uw). PC1 shows separation of all corner vowels and PC2 delineates between front vowels (iy, ae) and back vowels (uw, aa). b, Vowel to unvoiced plosives (n = 2,071, 4,107 and 1,441, respectively, for k, p and t). PC1 was more selective for velar constriction (k) and PC2 for bilabial constriction (p). c, Vowel to alveolars (n = 3,919, 3,010 and 4,107, respectively, for n, s and t). PC1 shows separation by manner of articulation (nasal, plosive or fricative) whereas PC2 is less discriminative. d, PC1 and PC2 show little, if any, delineation between voiced and unvoiced alveolar fricatives (n = 3,010 and 1,855, respectively, for s and z).
This file contains: a) Place-manner tuples used to augment EMA trajectories; b) Sentences used in listening tests Original Source: MOCHA-TIMIT20 dataset; c) Class sizes for the listening tests; d) Transcription interface for the intelligibility assessment; and e) Number of listeners used for intelligibility assessments.
The video presents examples of synthesized audio from neural recordings of spoken sentences. In each example, electrode activity corresponding to a sentence is displayed (top). Next, simultaneous decoding of kinematics and acoustics are visually and audible presented. Decoded articulatory movements are displayed (middle left) as the synthesized speech spectrogram unfolds. Following the decoding, the original audio, as spoken by the patient during neural recording, is played. Lastly, the decoded movements and synthesized speech is once again presented. This format is repeated for a total of five examples (from participants P1 and P2). On the last example, kinematics and audio are also decoded and synthesized for silently mimed speech.
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Anumanchipalli, G.K., Chartier, J. & Chang, E.F. Speech synthesis from neural decoding of spoken sentences. Nature 568, 493–498 (2019). https://doi.org/10.1038/s41586-019-1119-1
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