Skip to content
Open access

Revisiting Assumptions for Membership Inference on Summary Statistics

Oct 2026 · Proceedings on Privacy Enhancing Technologies · Vol 2026, pp. 542-560 · 0 citations · 65 references
Computer Science

TL;DR

A theoretical lower bound on inference error is derived that cleanly separates a statistical term governed by pool size and feature dimensionality from a signal term capturing disease-driven shifts and shows that attack accuracy on disease-specific cohorts exceeds that on size-matched random pools by approximately 10%, a separation that grows almost threefold when measured by true-positive rate at 1% false-positive rate.

Abstract

Research studies routinely publish summary statistics such as means and standard deviations to promote transparency while protecting participant privacy. Membership inference attacks (MIAs) can exploit these statistics to determine whether a specific individual contributed to a study, posing a risk especially in biomedical and health-related settings. However, existing attacks assume the adversary holds the exact data used in the study, an assumption that rarely holds when data evolves over time. Moreover, prior work has not quantified how much of the reported accuracy stems from true individual identification rather than from group-level traits shared within disease cohorts. We investigate the robustness and interpretability of two standard attacks—the L1-distance test and the log-likelihood ratio (LLR) test—under realistic conditions where the adversary has only noisy, partial, or temporally mismatched data. We derive a theoretical lower bound on inference error that cleanly separates a statistical term governed by pool size and feature dimensionality from a signal term capturing disease-driven shifts. Empirical evaluation on cross-sectional and longitudinal miRNA datasets, validated on Fitbit activity data, confirms that both attacks tolerate substantial noise and missing features, but that real-world temporal drift degrades accuracy far more steeply than synthetic perturbations predict, and that this degradation is individual-specific. We further show that attack accuracy on disease-specific cohorts exceeds that on size-matched random pools by approximately 10%, a separation that grows almost threefold when measured by true-positive rate at 1% false-positive rate. Moreover, individuals sharing disease traits but absent from the study are frequently misclassified as members, indicating that a substantial component of reported accuracy reflects shared condition rather than individual membership.

Read PDF

Similar papers

Open access Aug 2026

Validating methods for inferring co-occurring diseases: a flexible framework for simulating synthetic data

A four-step framework to generate synthetic data for the simulation-based validation of statistical methods is proposed, broadly applicable beyond the specific medical use case, and relies on careful, domain-informed parameter curation to generate meaningful synthetic datasets.

H. Marchi, S. Schmiegel, T. Schamberger et al. · 1 citation
#machine learning Preprint Sep 2026

Membership Inference via Pairwise Likelihood Ratios

Pairwise Likelihood MIA (PL-MIA), a unified method that combines a Gaussian likelihood-ratio (GLR) statistic with population calibration and the Cauchy combination test, is proposed, demonstrating how statistical principles can turn noisy model outputs into more powerful, calibrated, and reproducible evidence for membe...

Sheng-Jie Niu, Ze-Bin Yun, Ye-Heng Ge et al. · 0 citations
Preprint Aug 2026

A normal-inverse-Wishart (NIW) Bayesian synthesizer for multivariate normal data with application to polygenic risk scores

It is shown that disclosure risk decreases with the size of the original dataset, but increases with the dimensionality of the feature space and the amount of synthetic information released, whether through the release of larger synthetic datasets or multiple generator realizations.

Rasmus Rask Kragh Jørgensen, A. Nøhr, Jan Reiter Sørensen et al. · 0 citations
Book Open access Jun 2024

A Data-Centric Decomposition of Estimator Performance in Continuous Treatment Effect Estimation

This work analyzes current benchmarking practices and introduces a novel decomposition framework that disentangles the contribution of distinct data-generating components, such as confounding, dose distribution non-uniformity, and response surface complexity, to estimator performance.

Christopher Bockel-Rickermann, Daan Caljon, Toon Vanderschueren et al. · 2 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.