Everyday Driving and Plasma Biomarkers in Alzheimer's Disease: Leveraging Artificial Intelligence to Expand Our Diagnostic Toolkit.


Journal

Journal of Alzheimer's disease : JAD
ISSN: 1875-8908
Titre abrégé: J Alzheimers Dis
Pays: Netherlands
ID NLM: 9814863

Informations de publication

Date de publication:
2023
Historique:
pmc-release: 01 01 2024
medline: 25 4 2023
pubmed: 21 3 2023
entrez: 20 3 2023
Statut: ppublish

Résumé

Driving behavior as a digital marker and recent developments in blood-based biomarkers show promise as a widespread solution for the early identification of Alzheimer's disease (AD). This study used artificial intelligence methods to evaluate the association between naturalistic driving behavior and blood-based biomarkers of AD. We employed an artificial neural network (ANN) to examine the relationship between everyday driving behavior and plasma biomarker of AD. The primary outcome was plasma Aβ42/Aβ40, where Aβ42/Aβ40 < 0.1013 was used to define amyloid positivity. Two ANN models were trained and tested for predicting the outcome. The first model architecture only includes driving variables as input, whereas the second architecture includes the combination of age, APOE ɛ4 status, and driving variables. All 142 participants (mean [SD] age 73.9 [5.2] years; 76 [53.5%] men; 80 participants [56.3% ] with amyloid positivity based on plasma Aβ42/Aβ40) were cognitively normal. The six driving features, included in the ANN models, were the number of trips during rush hour, the median and standard deviation of jerk, the number of hard braking incidents and night trips, and the standard deviation of speed. The F1 score of the model with driving variables alone was 0.75 [0.023] for predicting plasma Aβ42/Aβ40. Incorporating age and APOE ɛ4 carrier status improved the diagnostic performance of the model to 0.80 [>0.051]. Blood-based AD biomarkers offer a novel opportunity to establish the efficacy of naturalistic driving as an accessible digital marker for AD pathology in driving research.

Sections du résumé

BACKGROUND
Driving behavior as a digital marker and recent developments in blood-based biomarkers show promise as a widespread solution for the early identification of Alzheimer's disease (AD).
OBJECTIVE
This study used artificial intelligence methods to evaluate the association between naturalistic driving behavior and blood-based biomarkers of AD.
METHODS
We employed an artificial neural network (ANN) to examine the relationship between everyday driving behavior and plasma biomarker of AD. The primary outcome was plasma Aβ42/Aβ40, where Aβ42/Aβ40 < 0.1013 was used to define amyloid positivity. Two ANN models were trained and tested for predicting the outcome. The first model architecture only includes driving variables as input, whereas the second architecture includes the combination of age, APOE ɛ4 status, and driving variables.
RESULTS
All 142 participants (mean [SD] age 73.9 [5.2] years; 76 [53.5%] men; 80 participants [56.3% ] with amyloid positivity based on plasma Aβ42/Aβ40) were cognitively normal. The six driving features, included in the ANN models, were the number of trips during rush hour, the median and standard deviation of jerk, the number of hard braking incidents and night trips, and the standard deviation of speed. The F1 score of the model with driving variables alone was 0.75 [0.023] for predicting plasma Aβ42/Aβ40. Incorporating age and APOE ɛ4 carrier status improved the diagnostic performance of the model to 0.80 [>0.051].
CONCLUSION
Blood-based AD biomarkers offer a novel opportunity to establish the efficacy of naturalistic driving as an accessible digital marker for AD pathology in driving research.

Identifiants

pubmed: 36938737
pii: JAD221268
doi: 10.3233/JAD-221268
pmc: PMC10133181
mid: NIHMS1885774
doi:

Substances chimiques

Amyloid beta-Peptides 0
Biomarkers 0
Peptide Fragments 0
Apolipoproteins E 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1487-1497

Subventions

Organisme : NIA NIH HHS
ID : R01 AG056466
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG067428
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG068183
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG066444
Pays : United States

Références

Neurology. 2019 Oct 22;93(17):e1647-e1659
pubmed: 31371569
NPJ Digit Med. 2019;2:
pubmed: 31119198
Expert Rev Neurother. 2017 Jan;17(1):7-16
pubmed: 27223100
J Alzheimers Dis. 2021;79(3):1009-1014
pubmed: 33361605
Alzheimers Dement. 2017 Jan;13(1):45-58
pubmed: 27870940
J Alzheimers Dis. 2019;70(2):323-341
pubmed: 31256142
J Alzheimers Dis. 2016 Feb 9;52(1):77-90
pubmed: 26967209
Clin Chim Acta. 2021 Aug;519:267-275
pubmed: 34015303
Alzheimers Res Ther. 2021 Jun 14;13(1):115
pubmed: 34127064
Alzheimers Dement. 2018 May;14(5):610-616
pubmed: 29328928
Alzheimers Dement. 2018 Feb;14(2):121-129
pubmed: 29233480
Aging health. 2010 Feb 1;6(1):77-85
pubmed: 20368745
J Biomed Inform. 2018 Sep;85:189-203
pubmed: 30031057
Alzheimers Dement (Amst). 2021 May 13;13(1):e12187
pubmed: 34027017
Geriatrics (Basel). 2018 Jun;3(2):
pubmed: 29805967
J Appl Gerontol. 2019 Feb;38(2):277-289
pubmed: 28380718
F1000Res. 2016 Sep 26;5:2376
pubmed: 27990264
JAMA Netw Open. 2022 Apr 1;5(4):e228392
pubmed: 35446396
Alzheimers Dement (N Y). 2017 Jan;3(1):74-82
pubmed: 28435853
PLoS Genet. 2010 Sep 16;6(9):e1001101
pubmed: 20862329
Arch Gen Psychiatry. 1983 Jul;40(7):812
pubmed: 6860082
Gerontology. 2022;68(1):106-120
pubmed: 33895746
J Alzheimers Dis. 2019;68(4):1625-1633
pubmed: 30958365
J Alzheimers Dis. 2017;60(4):1477-1487
pubmed: 29081416
Degener Neurol Neuromuscul Dis. 2019 Dec 24;9:123-130
pubmed: 31920420
Brain. 2021 Oct 22;144(9):2826-2836
pubmed: 34077494
Nat Rev Neurol. 2013 Dec;9(12):677-86
pubmed: 24217510
Nature. 2018 Feb 8;554(7691):249-254
pubmed: 29420472
Acta Neuropathol Commun. 2014 Sep 18;2:135
pubmed: 25231068
Can Fam Physician. 2017 Jan;63(1):27-31
pubmed: 28115437
J Geriatr Psychiatry Neurol. 2004 Dec;17(4):232-40
pubmed: 15533995
JAMA Neurol. 2019 Sep 01;76(9):1060-1069
pubmed: 31233127
Neurology. 1993 Nov;43(11):2412-4
pubmed: 8232972
J Steroid Biochem Mol Biol. 2016 Jun;160:134-47
pubmed: 26969397
F1000Res. 2016 Jul 15;5:1716
pubmed: 27785360
Alzheimers Dement. 2011 May;7(3):280-92
pubmed: 21514248
J Alzheimers Dis. 2018;61(2):509-513
pubmed: 29171997
Alzheimer Dis Assoc Disord. 2017 Jan-Mar;31(1):69-72
pubmed: 27128959

Auteurs

Sayeh Bayat (S)

Department of Biomedical Engineering, University of Calgary, Calgary, AB, Canada.
Department of Geomatics Engineering, University of Calgary, Calgary, AB, Canada.
Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.

Catherine M Roe (CM)

Roe Consulting LLC, St. Louis, MO, USA.

Suzanne Schindler (S)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

Samantha A Murphy (SA)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

Jason M Doherty (JM)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

Ann M Johnson (AM)

Center for Clinical Studies, Washington University School of Medicine, St. Louis, MO, USA.

Alexis Walker (A)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

Beau M Ances (BM)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

John C Morris (JC)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.

Ganesh M Babulal (GM)

Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Institute of Public Health, Washington University School of Medicine, St. Louis, MO, USA.
Department of Psychology, Faculty of Humanities, University of Johannesburg, Johannesburg, South Africa.
Department of Clinical Research and Leadership, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.

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