Human brain mapping · 2025
Big Data, Small Bias: Harmonizing Diffusion MRI-Based Structural Connectomes to Mitigate Site-Related Bias in Data Integration.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Shen Rui Sherry, Parker Drew, Chen Andrew An, Yerys Benjamin E, Tunç Birkan, Roberts Timothy P L, Shinohara Russell T, Verma Ragini
Аннотация
Diffusion MRI-based structural connectomes are increasingly used to investigate brain connectivity changes associated with various disorders. However, small sample sizes in individual studies, along with highly heterogeneous disorder-related manifestations, underscore the need to pool datasets across multiple studies to be able to identify coherent and generalizable connectivity patterns linked to these disorders. Yet, combining datasets introduces site-related differences due to variations in scanner hardware or acquisition protocols. These differences highlight the necessity for statistical data harmonization to mitigate site-related effects on structural connectomes while preserving the biological information associated with participant demographics and the disorders. While several paradigms exist for harmonizing normally distributed neuroimaging measures, this paper represents the first effort to establish a harmonization framework specifically tailored for the structural connectome. We conduct a thorough investigation of various statistical harmonization methods, adapting them to accommodate the unique distributional characteristics and graph-based properties of structural connectomes. Through rigorous evaluation, we show that our MATCH algorithm, based on the gamma-distributed model, consistently outperforms existing approaches in modeling structural connectomes, enabling the effective removal of site-related biases in both edge-based and downstream graph analyses while preserving biological variability. Two real-world applications further highlight the utility of our harmonization framework in addressing challenges in multi-site structural connectome analysis. Specifically, harmonization with MATCH enhances the generalizability of connectome-based machine learning predictors to new datasets and increases statistical power for detecting group-level differences. Our work provides essential guidelines for harmonizing multi-site structural connectomes, paving the way for more robust discoveries through collaborative research in the era of team science and big data.