Identifying amyotrophic lateral sclerosis through interactions with an internet search engine

Elad Yom-Tov, Indu Navar, Ernest Fraenkel, James D. Berry

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction/Aims: Amyotrophic lateral sclerosis (ALS), a motor neuron disease, remains a clinical diagnosis with an average time from onset of symptoms to diagnosis of about 1 year. Herein we examine the possibility that interactions with an internet search engine can identify people with ALS. Methods: We identified 285 anonymous Bing users whose queries indicated that they had been diagnosed with ALS and matched them to: (1) 3276 control users; and (2) 1814 users whose searches indicated they had ALS disease mimics. We tested whether the ALS group could be distinguished from controls and disease mimics based on search engine query data. Finally, we conducted a prospective validation from participants who provided access to their Bing search data. Results: The model distinguished between the ALS group and controls with an area under the curve (AUC) of 0.81. Model scores for the ALS group differed from the disease mimics group (rank sum test, p <.05 with Bonferroni correction). Mild cognitive impairment could not be distinguished from ALS (p >.05). In the prospective analysis, the model reached an AUC of 0.74. Discussion: Our results suggest that interactions with search engines should be further studied to understand the potential to act as a tool to assist in screening for ALS and to reduce diagnostic delay.

Original languageEnglish
Pages (from-to)40-47
Number of pages8
JournalMuscle and Nerve
Volume69
Issue number1
DOIs
StatePublished - Jan 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2023 The Authors. Muscle & Nerve published by Wiley Periodicals LLC.

Keywords

  • ALS
  • mild cognitive impairment
  • online data
  • screening
  • search engine

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