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Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review

Background and Motivation: Diagnosis of Parkinson’s disease (PD) is often based on medical attention and clinical signs. It is subjective and does not have a good prognosis. Artificial Intelligence (AI) has played a promising role in the diagnosis of PD. However, it introduces bias due to lack of sa...

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Autores principales: Paul, Sudip, Maindarkar, Maheshrao, Saxena, Sanjay, Saba, Luca, Turk, Monika, Kalra, Manudeep, Krishnan, Padukode R., Suri, Jasjit S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774851/
https://www.ncbi.nlm.nih.gov/pubmed/35054333
http://dx.doi.org/10.3390/diagnostics12010166
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author Paul, Sudip
Maindarkar, Maheshrao
Saxena, Sanjay
Saba, Luca
Turk, Monika
Kalra, Manudeep
Krishnan, Padukode R.
Suri, Jasjit S.
author_facet Paul, Sudip
Maindarkar, Maheshrao
Saxena, Sanjay
Saba, Luca
Turk, Monika
Kalra, Manudeep
Krishnan, Padukode R.
Suri, Jasjit S.
author_sort Paul, Sudip
collection PubMed
description Background and Motivation: Diagnosis of Parkinson’s disease (PD) is often based on medical attention and clinical signs. It is subjective and does not have a good prognosis. Artificial Intelligence (AI) has played a promising role in the diagnosis of PD. However, it introduces bias due to lack of sample size, poor validation, clinical evaluation, and lack of big data configuration. The purpose of this study is to compute the risk of bias (RoB) automatically. Method: The PRISMA search strategy was adopted to select the best 39 AI studies out of 85 PD studies closely associated with early diagnosis PD. The studies were used to compute 30 AI attributes (based on 6 AI clusters), using AP(ai)Bias 1.0 (AtheroPoint(TM), Roseville, CA, USA), and the mean aggregate score was computed. The studies were ranked and two cutoffs (Moderate-Low (ML) and High-Moderate (MH)) were determined to segregate the studies into three bins: low-, moderate-, and high-bias. Result: The ML and HM cutoffs were 3.50 and 2.33, respectively, which constituted 7, 13, and 6 for low-, moderate-, and high-bias studies. The best and worst architectures were “deep learning with sketches as outcomes” and “machine learning with Electroencephalography,” respectively. We recommend (i) the usage of power analysis in big data framework, (ii) that it must undergo scientific validation using unseen AI models, and (iii) that it should be taken towards clinical evaluation for reliability and stability tests. Conclusion: The AI is a vital component for the diagnosis of early PD and the recommendations must be followed to lower the RoB.
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spelling pubmed-87748512022-01-21 Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review Paul, Sudip Maindarkar, Maheshrao Saxena, Sanjay Saba, Luca Turk, Monika Kalra, Manudeep Krishnan, Padukode R. Suri, Jasjit S. Diagnostics (Basel) Review Background and Motivation: Diagnosis of Parkinson’s disease (PD) is often based on medical attention and clinical signs. It is subjective and does not have a good prognosis. Artificial Intelligence (AI) has played a promising role in the diagnosis of PD. However, it introduces bias due to lack of sample size, poor validation, clinical evaluation, and lack of big data configuration. The purpose of this study is to compute the risk of bias (RoB) automatically. Method: The PRISMA search strategy was adopted to select the best 39 AI studies out of 85 PD studies closely associated with early diagnosis PD. The studies were used to compute 30 AI attributes (based on 6 AI clusters), using AP(ai)Bias 1.0 (AtheroPoint(TM), Roseville, CA, USA), and the mean aggregate score was computed. The studies were ranked and two cutoffs (Moderate-Low (ML) and High-Moderate (MH)) were determined to segregate the studies into three bins: low-, moderate-, and high-bias. Result: The ML and HM cutoffs were 3.50 and 2.33, respectively, which constituted 7, 13, and 6 for low-, moderate-, and high-bias studies. The best and worst architectures were “deep learning with sketches as outcomes” and “machine learning with Electroencephalography,” respectively. We recommend (i) the usage of power analysis in big data framework, (ii) that it must undergo scientific validation using unseen AI models, and (iii) that it should be taken towards clinical evaluation for reliability and stability tests. Conclusion: The AI is a vital component for the diagnosis of early PD and the recommendations must be followed to lower the RoB. MDPI 2022-01-11 /pmc/articles/PMC8774851/ /pubmed/35054333 http://dx.doi.org/10.3390/diagnostics12010166 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Paul, Sudip
Maindarkar, Maheshrao
Saxena, Sanjay
Saba, Luca
Turk, Monika
Kalra, Manudeep
Krishnan, Padukode R.
Suri, Jasjit S.
Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review
title Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review
title_full Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review
title_fullStr Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review
title_full_unstemmed Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review
title_short Bias Investigation in Artificial Intelligence Systems for Early Detection of Parkinson’s Disease: A Narrative Review
title_sort bias investigation in artificial intelligence systems for early detection of parkinson’s disease: a narrative review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774851/
https://www.ncbi.nlm.nih.gov/pubmed/35054333
http://dx.doi.org/10.3390/diagnostics12010166
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