Measurement-Error-Aware Causal Distributed-Lag Quantile Modeling of Indoor Air Pollution and Short-Term Lung-Function Deterioration
Abstract
Low-cost indoor air-quality sensors could support personalized asthma prevention, but their nonlinear measurement error, delayed exposure effects, time-varying confounding, and heterogeneous lower-tail responses limit risk estimation. We present CAUSALQUANT-ASTHMA, a measurement-error-aware causal quantile distributed-lag framework for short-horizon peak expiratory flow analysis. Sparse reference measurements train a nonlinear calibration model; stabilized sequential generalized-propensity weights address measured exposure assignment; and a susceptibility-modulated, smooth, noncrossing quantile model estimates lag-specific and sustained-exposure contrasts. Because no authorized cohort simultaneously provided dense indoor sensing, reference co-location, and outcome-compatible longitudinal data, evaluation used five semi-synthetic panels with known counterfactual truth, 150 patients and 12,600 patient-days per realization. Across eight methods, CAUSALQUANT achieved a dose-response integrated absolute error of 0.304 plus or minus 0.094, improving 24.2 percent over the strongest measurement-error and propensity-weighted baseline. It also obtained the lowest overall pinball loss, 1.065, while maintaining zero quantile crossings and 78.1 percent coverage for the nominal 80 percent interval. Sensor calibration reduced held-out exposure RMSE by 33.7 percent. Stress tests quantified degradation under sensor noise, missing personal measurements, and hidden confounding. These findings establish methodological feasibility and reproducibility, not clinical effectiveness; prospective, governance-approved external validation is required before patient-level interpretation or deployment.
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BibTeX
@misc{alkobaisi2026measurementerroraware,
title = {{Measurement-Error-Aware Causal Distributed-Lag Quantile Modeling of Indoor Air Pollution and Short-Term Lung-Function Deterioration}},
author = {Shayma Alkobaisi and Anas Ali},
howpublished = {arXiv},
year = {2026},
month = sep,
doi = {10.48550/arxiv.2609.31646},
eprint = {2609.31646},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2609.31646},
note = {CC BY 4.0},
}
RIS
TY - UNPB
TI - Measurement-Error-Aware Causal Distributed-Lag Quantile Modeling of Indoor Air Pollution and Short-Term Lung-Function Deterioration
AU - Shayma Alkobaisi
AU - Anas Ali
PY - 2026
DA - 2026/09/12
PB - arXiv
DO - 10.48550/arxiv.2609.31646
UR - https://arxiv.org/abs/2609.31646
AB - Low-cost indoor air-quality sensors could support personalized asthma prevention, but their nonlinear measurement error, delayed exposure effects, time-varying confounding, and heterogeneous lower-tail responses limit risk estimation. We present CAUSALQUANT-ASTHMA, a measurement-error-aware causal quantile distributed-lag framework for short-horizon peak expiratory flow analysis. Sparse reference measurements train a nonlinear calibration model; stabilized sequential generalized-propensity weights address measured exposure assignment; and a susceptibility-modulated, smooth, noncrossing quantile model estimates lag-specific and sustained-exposure contrasts. Because no authorized cohort simultaneously provided dense indoor sensing, reference co-location, and outcome-compatible longitudinal data, evaluation used five semi-synthetic panels with known counterfactual truth, 150 patients and 12,600 patient-days per realization. Across eight methods, CAUSALQUANT achieved a dose-response integrated absolute error of 0.304 plus or minus 0.094, improving 24.2 percent over the strongest measurement-error and propensity-weighted baseline. It also obtained the lowest overall pinball loss, 1.065, while maintaining zero quantile crossings and 78.1 percent coverage for the nominal 80 percent interval. Sensor calibration reduced held-out exposure RMSE by 33.7 percent. Stress tests quantified degradation under sensor noise, missing personal measurements, and hidden confounding. These findings establish methodological feasibility and reproducibility, not clinical effectiveness; prospective, governance-approved external validation is required before patient-level interpretation or deployment.
ER -