Evidence map›Paper›PMID 38798505›Full record

ArticlemedRxiv : the preprint server for health sciences2024

A Novel Explainable AI Method to Assess Associations between Temporal Patterns in Patient Trajectories and Adverse Outcome Risks: Analyzing Fitness as a Risk Factor of ADRD.

Yijun Shao, Edward Y Zamrini, Ali Ahmed, Yan Cheng, Stuart J Nelson, Peter Kokkinos, Qing Zeng-Treitler

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Yijun ShaoGeorge Washington University, Washington, DC, USA.
Edward Y ZamriniGeorge Washington University, Washington, DC, USA.
Ali AhmedGeorge Washington University, Washington, DC, USA.
Yan ChengGeorge Washington University, Washington, DC, USA.
Stuart J NelsonGeorge Washington University, Washington, DC, USA.
Peter KokkinosGeorge Washington University, Washington, DC, USA.
Qing Zeng-TreitlerGeorge Washington University, Washington, DC, USA.

Funding

MWAS+ – A Novel Drug Repurposing Strategy for ADRD PreventionR01AG073474 · NIA · GEORGE WASHINGTON UNIVERSITY · PI ALI AHMED, QING ZENG · 2022 to 2026
$3.4M
Use Explainable AI to Improve the Trust of and Detect the Bias of AI ModelsRF1AG069121 · NIA · GEORGE WASHINGTON UNIVERSITY · PI KOKKINOS, PETER F., ZAMRINI, EDWARD Y · 2020 to 2022
$2.3M
NIA NIH HHS R01 AG073474NIA NIH HHS RF1 AG069121
6 · The paper itself

Abstract

We present a novel explainable artificial intelligence (XAI) method to assess the associations between the temporal patterns in the patient trajectories recorded in longitudinal clinical data and the adverse outcome risks, through explanations for a type of deep neural network model called Hybrid Value-Aware Transformer (HVAT) model. The HVAT models can learn jointly from longitudinal and non-longitudinal clinical data, and in particular can leverage the time-varying numerical values associated with the clinical codes or concepts within the longitudinal data for outcome prediction. The key component of the XAI method is the definitions of two derived variables, the temporal mean and the temporal slope, which are defined for the clinical concepts with associated time-varying numerical values. The two variables represent the overall level and the rate of change over time, respectively, in the trajectory formed by the values associated with the clinical concept. Two operations on the original values are designed for changing the values of the two derived variables separately. The effects of the two variables on the outcome risks learned by the HVAT model are calculated in terms of impact scores and impacts. Interpretations of the impact scores and impacts as being similar to those of odds ratios are also provided. We applied the XAI method to the study of cardiorespiratory fitness (CRF) as a risk factor of Alzheimer's disease and related dementias (ADRD). Using a retrospective case-control study design, we found that each one-unit increase in the overall CRF level is associated with a 5% reduction in ADRD risk, while each one-unit increase in the changing rate of CRF over time is associated with a 1% reduction. A closer investigation revealed that the association between the changing rate of CRF level and the ADRD risk is nonlinear, or more specifically, approximately piecewise linear along the axis of the changing rate on two pieces: the piece of negative changing rates and the piece of positive changing rates.

Identifiers

PMID38798505
PMCPMC11118636

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.