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Pathway Lasso: Estimate and Select Sparse Mediation Pathways with High Dimensional Mediators

Machine Learning · Submitted 24 Mar 2016

abstract compiled · 2026-09-23 · no language-model review

The authors' main claim On both simulated data and a real fMRI dataset, the proposed approach yields higher pathway selection accuracy and lower estimation bias than other competing methods.

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arXiv ID1603.07749 (version 1)
Pith IDJU6D3WUQ, Pith's permanent record of this paper and its review
CitationXi Luo, Yi Zhao. "Pathway Lasso: Estimate and Select Sparse Mediation Pathways with High Dimensional Mediators." arXiv:1603.07749 (2016). https://pith.science/paper/JU6D3WUQ
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What the abstract itself states, as probabilities: claims first 0.07 · states limitation 0.10 · human participants 0.58 · controlled comparison 0.06 · randomized assignment 0.03 · states quantitative result 0.06 · compares with prior results 0.94 · mentions code or data availability 0.02.

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arXiv listing abstract v1. Results and the main claim are underlined; .

In many scientific studies, it becomes increasingly important to delineate the causal pathways through a large number of mediators, such as genetic and brain mediators. Structural equation modeling (SEM) is a popular technique to estimate the pathway effects, commonly expressed as products of coefficients. However, it becomes unstable to fit such models with high dimensional mediators, especially for a general setting where all the mediators are causally dependent but the exact causal relationships between them are unknown. This paper proposes a sparse mediation model using a regularized SEM approach, where sparsity here means that a small number of mediators have nonzero mediation effects between a treatment and an outcome. To address the model selection challenge, we innovate by introducing a new penalty called Pathway Lasso. This penalty function is a convex relaxation of the non-convex product function, and it enables a computationally tractable optimization criterion to estimate and select many pathway effects simultaneously. We develop a fast ADMM-type algorithm to compute the model parameters, and we show that the iterative updates can be expressed in closed form. On both simulated data and a real fMRI dataset, the proposed approach yields higher pathway selection accuracy and lower estimation bias than other competing methods.

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What the classifier reports for each sentence. The number is the probability it gave the label.
#sentencerolethe authors' own workstates the main conclusionstrength
s0 In many scientific studies, it becomes increasingly important to delineate the causal pathways through a large number of mediators, such as genetic and brain mediators. background 1.00 0.04 0.02 asserted 0.92
s1 Structural equation modeling (SEM) is a popular technique to estimate the pathway effects, commonly expressed as products of coefficients. background 1.00 0.04 0.02 asserted 1.00
s2 However, it becomes unstable to fit such models with high dimensional mediators, especially for a general setting where all the mediators are causally dependent but the exact causal relationships between them are unknown. gap 0.61 0.09 0.02 asserted 0.99
s3 This paper proposes a sparse mediation model using a regularized SEM approach, where sparsity here means that a small number of mediators have nonzero mediation effects between a treatment and an outcome. contribution 0.68 0.75 0.10 asserted 0.99
s4 To address the model selection challenge, we innovate by introducing a new penalty called Pathway Lasso. contribution 0.98 0.94 0.05 asserted 1.00
s5 This penalty function is a convex relaxation of the non-convex product function, and it enables a computationally tractable optimization criterion to estimate and select many pathway effects simultaneously. method 0.72 0.89 0.10 asserted 1.00
s6 We develop a fast ADMM-type algorithm to compute the model parameters, and we show that the iterative updates can be expressed in closed form. method 0.97 0.97 0.04 asserted 1.00
s7 On both simulated data and a real fMRI dataset, the proposed approach yields higher pathway selection accuracy and lower estimation bias than other competing methods. result 1.00 0.96 0.85 asserted 1.00

What kind of paper the classifier reports this is: method or tool 1.00 · evidence from simulation or computation 0.93.

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Original abstract

In many scientific studies, it becomes increasingly important to delineate the causal pathways through a large number of mediators, such as genetic and brain mediators. Structural equation modeling (SEM) is a popular technique to estimate the pathway effects, commonly expressed as products of coefficients. However, it becomes unstable to fit such models with high dimensional mediators, especially for a general setting where all the mediators are causally dependent but the exact causal relationships between them are unknown. This paper proposes a sparse mediation model using a regularized SEM approach, where sparsity here means that a small number of mediators have nonzero mediation effects between a treatment and an outcome. To address the model selection challenge, we innovate by introducing a new penalty called Pathway Lasso. This penalty function is a convex relaxation of the non-convex product function, and it enables a computationally tractable optimization criterion to estimate and select many pathway effects simultaneously. We develop a fast ADMM-type algorithm to compute the model parameters, and we show that the iterative updates can be expressed in closed form. On both simulated data and a real fMRI dataset, the proposed approach yields higher pathway selection accuracy and lower estimation bias than other competing methods.

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