# Overcoming Data Loss in Wearable Disease Detection with GAN-Based Imputation

**Authors:** Jürgen Wallner, Sarah Berbuir, Lukas Birner, Adrian Dendorfer, Bivek Panthi, Beatrix Rahnsch, Julius Muma, Stephen Munga, David Obor, Till Bärnighausen, Sandra Barteit

PMC · DOI: 10.1038/s41746-026-02518-4 · 2026-03-27

## TL;DR

A GAN-based system improves early detection of infectious diseases by imputing missing wearable sensor data, even in low-resource settings.

## Contribution

A lightweight GAN framework that imputes missing heart rate data and enables early infection detection using rule-based anomaly detection.

## Key findings

- The system triggered early alerts in 100 malaria cases, including 42 solely through imputation.
- Alerts occurred 11.9 days before symptom onset, matching the parasitemia window.
- The GAN reduced reconstruction error by 58% when generalizing from COVID-19 data to malaria.

## Abstract

High rates of missing data in wearable sensor streams hinder early detection of infectious diseases, especially in low-resource settings with inconsistent device adherence and connectivity. We developed a lightweight generative adversarial network (GAN) framework that imputes missing heart rate data and integrates with a rule-based anomaly detection algorithm to identify early signs of infection. In a cohort from rural Kenya (n = 300, 161 malaria-positives), our system triggered early alerts in 100 cases, including 42 solely with imputation. Alerts preceded symptom onset by 11.9 days, aligning with the 11.7-day parasitemia window from controlled trials. Despite 50% data coverage, alerts occurred on 3.5 consecutive days during the infection window, improving early detection by 35%. The GAN, trained only on external COVID-19 data (n = 3318), generalized to malaria, reducing reconstruction error by 58%. This approach demonstrates scalable, cross-pathogen physiological monitoring and offers a robust tool for disease surveillance in settings challenged by high wearable data loss.

## Linked entities

- **Diseases:** malaria (MONDO:0005136), COVID-19 (MONDO:0100096)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** NCDs (MESH:D000073296), inactivity (MESH:C564765), GAN (MESH:D004829), fatigue (MESH:D005221), autonomic (MESH:D001342), cardiovascular or metabolic disorders (MESH:D024821), infectious disease (MESH:D003141), febrile illnesses (MESH:D005334), parasitemia (MESH:D018512), inflammatory (MESH:D007249), COVID-19 (MESH:D000086382), infected (MESH:D007239), CHMI (MESH:D008288), sleep disorders (MESH:D012893), cardiovascular disease (MESH:D002318), febrile (MESH:D000071072), diabetes (MESH:D003920), headache (MESH:D006261), tachycardia (MESH:D013610)
- **Chemicals:** glucose (MESH:D005947), FSM (-), cortisol (MESH:D006854), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13043753/full.md

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Source: https://tomesphere.com/paper/PMC13043753