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      Things to Consider When Automatically Detecting Parkinson’s Disease Using the Phonation of Sustained Vowels: Analysis of Methodological Issues

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      Applied Sciences
      MDPI AG

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          Abstract

          Diagnosing Parkinson’s Disease (PD) necessitates monitoring symptom progression. Unfortunately, diagnostic confirmation often occurs years after disease onset. A more sensitive and objective approach is paramount to the expedient diagnosis and treatment of persons with PD (PwPDs). Recent studies have shown that we can train accurate models to detect signs of PD from audio recordings of confirmed PwPDs. However, disparities exist between studies and may be caused, in part, by differences in employed corpora or methodologies. Our hypothesis is that unaccounted covariates in methodology, experimental design, and data preparation resulted in overly optimistic results in studies of PD automatic detection employing sustained vowels. These issues include record-wise fold creation rather than subject-wise; an imbalance of age between the PwPD and control classes; using too small of a corpus compared to the sizes of feature vectors; performing cross-validation without including development data; and the absence of cross-corpora testing to confirm results. In this paper, we evaluate the influence of these methodological issues in the automatic detection of PD employing sustained vowels. We perform several experiments isolating each issue to measure its influence employing three different corpora. Moreover, we analyze if the perceived dysphonia of the speakers could be causing differences in results between the corpora. Results suggest that each independent methodological issue analyzed has an effect on classification accuracy. Consequently, we recommend a list of methodological steps to be considered in future experiments to avoid overoptimistic or misleading results.

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          Most cited references46

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          Speaker Verification Using Adapted Gaussian Mixture Models

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              The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service.

              We have reviewed the clinical and pathological diagnoses of 143 cases of parkinsonism seen by neurologists associated with the movement disorders service at The National Hospital for Neurology and Neurosurgery in London who came to neuropathological examination at the United Kingdom Parkinson's Disease Society Brain Research Centre, over a 10-year period between 1990 and the end of 1999. Seventy-three (47 male, 26 female) cases were diagnosed as having idiopathic Parkinson's disease (IPD) and 70 (42 male, 28 female) as having another parkinsonian syndrome. The positive predictive value of the clinical diagnosis for the whole group was 85.3%, with 122 cases correctly clinically diagnosed. The positive predictive value of the clinical diagnosis of IPD was extremely high, at 98.6% (72 out of 73), while for the other parkinsonian syndromes it was 71.4% (50 out of 70). The positive predictive values of a clinical diagnosis of multiple system atrophy (MSA) and progressive supranuclear palsy (PSP) were 85.7 (30 out of 35) and 80% (16 out of 20), respectively. The sensitivity for IPD was 91.1%, due to seven false-negative cases, with 72 of the 79 pathologically established cases being diagnosed in life. For MSA, the sensitivity was 88.2% (30 out of 34), and for PSP it was 84.2% (16 out of 19). The diagnostic accuracy for IPD, MSA and PSP was higher than most previous prospective clinicopathological series and studies using the retrospective application of clinical diagnostic criteria. The seven false-negative cases of IPD suggest a broader clinical picture of disease than previously thought acceptable. This study implies that neurologists with particular expertise in the field of movement disorders may be using a method of pattern recognition for diagnosis which goes beyond that inherent in any formal set of diagnostic criteria.
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                Journal
                ASPCC7
                Applied Sciences
                Applied Sciences
                MDPI AG
                2076-3417
                February 2022
                January 19 2022
                : 12
                : 3
                : 991
                Article
                10.3390/app12030991
                caf1671a-b53f-4c19-a351-58c8caa7eb64
                © 2022

                https://creativecommons.org/licenses/by/4.0/

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