| name | bio-causal-genomics-mediation-analysis |
| description | Decompose total effects into direct and indirect paths through mediators using mediation, CMAverse 4-way, HIMA/HIMA2 high-dimensional, BAMA, two-step / MVMR mediation, or double-ML medDML. Use when testing whether a molecular phenotype (expression, methylation, protein) mediates a treatment-outcome relationship, decomposing exposure-mediator interaction via VanderWeele 4-way, screening high-dimensional EWAS mediators, or running MR-based mediation when sequential ignorability is implausible. |
| origin | openai4s |
| category | bioskills/causal-genomics |
| metadata | {"tool_type":"mixed","primary_tool":"mediation","third_party":{"name":"GPTomics/bioSkills","repository":"https://github.com/GPTomics/bioSkills","commit":"d91ed3d563019e649dc854c56ccd62551359488a","license":"MIT"}} |
Version Compatibility
Reference examples tested with: R 4.3+, mediation 4.5.0+, CMAverse 0.1.0+ (GitHub BS1125/CMAverse), HIMA >= 2.3.0 (GitHub YinanZheng/HIMA; archived from CRAN 2026-07), bama 1.3+, causalweight 1.0.5+ (medDML), MVMR 0.4+, TwoSampleMR 0.6+, EValue 4.1+, gesttools 1.3+, ipw 1.0.11+.
Before using code patterns, verify installed versions match. If versions differ:
- R:
packageVersion('<pkg>') then ?function_name to verify parameters
- HIMA must be pinned at
>= 2.3.0 for the code patterns below; the formula interface hima(formula, data.pheno, data.M, mediator.type, penalty, ...) was introduced in 2.3.0. On HIMA 2.2.x the classic engine is the top-level hima(X, Y, M, COV.XM=, COV.MY=, Y.family=, penalty=) (positional order X, Y, M) with no formula interface; HIMA 2.2.x is NOT API-compatible with the examples here.
- In 2.3+ the classic engine is
hima_classic(X, M, Y, COV.XM=, COV.MY=, Y.type=) (positional order X, M, Y; outcome type via Y.type, not Y.family); use it only to reproduce the original 2016-2021 SIS+penalty pipelines.
If code throws an error, introspect the installed package (?hima, args(cmest)) and adapt the example to match the actual API rather than retrying.
Mediation Analysis
"Does expression of GENE_X mediate the SNP-to-disease effect?" -> Decompose the total effect of a treatment (genotype, exposure) on an outcome into direct and indirect paths through one or more mediators, with explicit handling of exposure-mediator interaction, sensitivity to unmeasured confounding, and high-dimensional mediator screening.
- R (single-mediator, observational, sequential-ignorability assumed):
mediation::mediate(med_model, out_model, treat='X', mediator='M', boot=TRUE, sims=5000)
- R (4-way decomposition with exposure-mediator interaction):
CMAverse::cmest(...EMint=TRUE, estimation='paramfunc', inference='bootstrap', nboot=1000)
- R (high-dimensional / EWAS mediators):
HIMA::hima(Y ~ X + covariates, data.pheno, data.M, mediator.type='gaussian', penalty='DBlasso') (modern v2.3+ formula interface)
- R (MR-based mediation): two-step
TwoSampleMR with independent instruments OR MVMR::ivw_mvmr for joint direct effect
- R (doubly-robust double-ML):
causalweight::medDML(y, d, m, x)
Sequential ignorability (no unmeasured confounder of treatment-mediator, mediator-outcome, treatment-outcome) is the single load-bearing assumption of observational mediation and is fundamentally untestable. Every report should include a sensitivity result (Imai's rho via medsens() or a mediational E-value).
Algorithmic Taxonomy
| Method | Framework | Handles E-M interaction | High-D mediators | Min n | Fails when |
|---|
| Baron-Kenny (1986) | Additive regression-based product/difference | No | No | ~100 | Any non-linearity, interaction, or binary outcome; deprecated for causal inference |
| Imai mediation R (Imai 2010 Psychol Methods) | Counterfactual ACME/ADE with bootstrap | Yes (via interaction term in outcome model) | No | ~200 | Sequential ignorability violated; exposure-induced M-Y confounder; rare binary outcome with logistic outcome model |
| VanderWeele 4-way (VanderWeele 2014 Epidemiology 25:749; 2015 OUP) | CDE + PIE + INTref + INTmed decomposition | Native | No | ~300 | Without interaction term reduces to standard mediation; binary outcome needs rare-disease assumption |
| CMAverse (Shi 2021 Epidemiology 32:e20) | 6 estimators: regression (rb), weighting (wb), IORW (iorw), natural effect models (ne), MSM (msm), g-formula (gformula) | Yes | No (single M, or M-vector) | ~300 | Estimator-specific; wb fails with rare exposure; msm needs censoring weights for survival |
| HIMA1 / hima_classic (Zhang 2016 Bioinformatics 32:3150) | SIS screen by beta (M->Y) + MCP penalty | No | Yes (up to ~10k) | ~150 + p>>n | Misses mediators with strong alpha and weak beta; screening-step false-negatives |
| HIMA2 / hima (Perera 2022 BMC Bioinformatics 23:296) | SIS screen by alpha*beta (indirect effect) + de-biased Lasso (DBlasso) | No (linear by default) | Yes | ~150 | Outcome family limited (gaussian/binomial); HIMA-Cox for survival; HIMA-Pois for count |
| HILAMA (Wang et al 2025) | High-D mediation with latent confounders | No | Yes (>= 100k) | ~500 | Newer; benchmarks evolving; requires latent-factor specification |
| BAMA (Song 2020 Biometrics) | Bayesian high-D continuous shrinkage | No | Yes (~5k) | ~200 | Slow MCMC; prior sensitivity for very weak mediators |
Methodology evolves; verify against the current CMAverse vignette and the Steen / Vansteelandt natural-effects-model literature before locking analytic choices. Difference-in-coefficients and product-of-coefficients give identical estimates in fully linear-Gaussian models but DIVERGE for any non-linear outcome model (logistic, Cox, Poisson); the counterfactual ACME from mediation::mediate() is the correct quantity for non-linear outcomes.
4-Way Decomposition Framework
VanderWeele 4-way explicitly separates effects from exposure-mediator interaction:
Total Effect = CDE + INTref + INTmed + PIE
| Component | Meaning | Active when |
|---|
| CDE | Controlled direct effect (with mediator fixed at reference level) | E directly affects Y |
| INTref | Interaction-reference -- needs interaction AND exposure | E*M interaction with mediator at reference |
| INTmed | Mediated interaction -- needs interaction AND exposure AND mediation | E shifts M which then interacts with E |
| PIE | Pure indirect effect (older "mediation" quantity) | E shifts M which shifts Y additively |
Without an exposure-mediator interaction term, INTref = INTmed = 0 and the decomposition collapses to CDE + PIE (= ADE + ACME). With interaction present, traditional ACME mixes PIE and INTmed; the 4-way separation is the only framework that disentangles them. Most epidemiology applications include the interaction term and report all four components (Valeri & VanderWeele 2013 Psychol Methods).
Decision Tree by Scenario
| Scenario | Recommended pipeline |
|---|
| Observational, single measured mediator, no plausible E-M interaction, continuous outcome | mediation::mediate() with boot=TRUE, sims=5000; always run medsens() |
| Observational, single mediator, suspected E-M interaction, any outcome family | CMAverse::cmest(..., EMint=TRUE) -> read CDE, PIE, INTref, INTmed |
| Observational, BINARY outcome, rare disease (< 10%) | cmest(yreg='logistic', EMint=TRUE, casecontrol=FALSE) -- OR-based 4-way decomposition is valid under rare-disease |
| Observational, survival outcome | cmest(yreg='coxph') OR HIMA::hima_cox for high-D; report HRs |
| High-D mediators (EWAS, transcriptome-wide), continuous outcome | HIMA::hima(formula, data.pheno, data.M, mediator.type='gaussian', penalty='DBlasso'); report sigcut (FDR threshold, default 0.05) |
| High-D mediators with latent confounding (very-high-D EWAS) | HILAMA (2025) |
| High-D mediators with Bayesian shrinkage (small n, ~5k features) | bama::bama() |
| Strong genetic IVs for exposure available, single mediator with own IVs | Two-step MR with independent instruments + Steiger filter on mediator |
| Both E and M have IVs but instruments are weak / correlated | MVMR-mediation with conditional F > 10 each |
| Observational with rich confounder set, want doubly-robust estimate | causalweight::medDML (double-debiased ML) |
| Longitudinal with time-varying confounding | g-formula via CMAverse::cmest(estimation='gformula') OR gfoRmula package |
| Exposure-induced confounder of M-Y exists | Interventional indirect effects (Vansteelandt & Daniel 2017); CMAverse::cmest(estimation='msm') |
Sequential Ignorability and Why It Always Needs Sensitivity
Observational mediation requires three no-unmeasured-confounding assumptions. The third (M-Y unmeasured confounder, after conditioning on E) is the most common violator in genomic mediation because biological confounders (cell composition, batch effects, technical mediators) frequently affect both M and Y.
Sequential ignorability untestable
Trigger: Always, by design.
Mechanism: No statistical test can detect an unmeasured confounder of M-Y. Bootstrap CIs assume the assumption holds; they do NOT propagate uncertainty about it.
Symptom: Significant ACME with no sensitivity reported -> reviewer rejects.
Fix: Report at least one of:
- Imai's rho sensitivity:
medsens(med_result, rho.by=0.05, sims=1000); the critical rho where ACME crosses 0; |rho_crit| > 0.3 is "reasonably robust" (Imai 2010), |rho_crit| < 0.1 is highly sensitive.
- Mediational E-value (Smith & VanderWeele 2019 Epidemiology 30:835): minimum risk-ratio strength of an unmeasured confounder needed to nullify the observed indirect effect; computed via
EValue::evalues.OLS() for linear outcomes or by-hand from ACME risk ratio bounds.
- Reporting BOTH rho-based and E-value sensitivity is standard for high-stakes claims.
Methods-Section Defense of Sequential Ignorability
Template sentence for the methods write-up: "We assumed sequential ignorability conditional on {age, sex, ancestry PCs, cell composition, batch, smoking}. Robustness was assessed via Imai rho_crit at the ACME contrast (medsens, sims = 1000) and the mediational E-value on the risk-ratio scale (Smith & VanderWeele 2019 Epidemiology 30:835)."
Quantitative interpretation thresholds:
- rho_crit: |rho_crit| > 0.3 robust; 0.1-0.3 moderately sensitive; < 0.1 highly sensitive (Imai 2010).
- E-value: E > 2 robust to plausible biological confounding; 1.5-2 moderate; < 1.5 fragile (Smith & VanderWeele 2019).
For high-stakes claims (clinical, drug-target, regulatory submissions) report BOTH rho_crit and the mediational E-value; for exploratory work either alone suffices.
Exposure-induced M-Y confounder
Trigger: A covariate L sits between E and Y, AND is affected by E, AND confounds M-Y.
Mechanism: Standard regression-based mediation cannot adjust for L without blocking part of the indirect effect (collider stratification bias). Adjusting biases CDE; not adjusting biases ACME.
Symptom: Sensitivity to confounder set; ACME flips sign when L is added vs removed.
Operational identification: From the DAG, L is a covariate of M and Y that is also affected by E. VanderWeele TJ, Vansteelandt S & Robins JM 2014 (Epidemiology 25:300) give the criterion: if L is adjusted, part of the indirect E -> L -> M -> Y pathway is blocked; if L is not adjusted, L confounds the M-Y leg. Both are wrong under natural-effects; the natural indirect effect is simply not identified.
Fix: Switch to interventional indirect effects (Vansteelandt & Daniel 2017 Epidemiology 28:258), NOT natural indirect effects. Use CMAverse::cmest(estimation='msm') with stabilized inverse-probability weights (yields the randomized-interventional analogue), gfoRmula (parametric g-formula), or randomized/interventional indirect effects (Lin SH & VanderWeele TJ 2017 J Causal Inference 5:20150027). The interventional indirect is identified under weaker assumptions than the natural indirect.
HIMA covariate or data.pheno error
Trigger: data.pheno contains factor columns with NA, or formula references columns missing from data.pheno.
Mechanism: HIMA v2.3+ uses a formula interface and constructs the design matrix internally from data.pheno; missing values or unparseable formulas surface as cryptic glmnet errors.
Symptom: Pipeline fails inside hima() with a non-obvious storage.mode or model.matrix error.
Fix: Pre-clean data.pheno (drop NA rows for the variables in the formula; convert factors with factor(); ensure all RHS variables exist as columns). Example:
dat <- na.omit(dat[, c('outcome', 'exposure', 'age', 'sex', 'batch', 'pc1', 'pc2')])
dat$batch <- factor(dat$batch)
result <- hima(outcome ~ exposure + age + sex + batch + pc1 + pc2,
data.pheno=dat, data.M=M_matrix, mediator.type='gaussian')
HIMA mediator-type vs outcome-type mismatch
Trigger: Survival outcome (Surv() on LHS) with mediator.type='compositional' chosen against text mediator panel; or count mediators passed as 'gaussian'.
Mechanism: HIMA v2.3+ auto-detects outcome family from the LHS of formula (continuous, binary, survival, count); mediator.type is set for the mediator data only ('gaussian', 'negbin', 'compositional'). Mismatching mediator-type to the actual mediator distribution biases the screening step.
Symptom: Hazard / rate ratios for indirect effects look implausible; many "significant" mediators fail replication.
Fix: Set mediator.type='gaussian' for continuous (e.g., methylation beta, log-CPM expression), 'negbin' for raw count (RNA-seq), 'compositional' for relative-abundance microbiome. Verify by ?hima in the installed version since the catalogue of mediator types has expanded across releases.
Bootstrap iterations too low
Trigger: sims=100 or sims=500 in early exploration left in for the final report.
Mechanism: ACME CIs from bootstrap have Monte-Carlo error that scales as 1/sqrt(sims); at sims=500 the 95% CI bounds have ~5% MC noise, enough to flip the conclusion at the boundary.
Symptom: Re-running mediate() with a different set.seed() gives substantially different CI bounds.
Fix: sims=1000 minimum for any reported result; sims=5000 for publication; sims=10000 if proximity to zero matters. BCa CIs (boot.ci.type='bca' in mediate()) are slightly more accurate than percentile CIs near zero but require more sims for stability.
Two-step MR instrument independence
Trigger: Same set of SNPs used as instruments for E in step 1 and for M in step 2.
Mechanism: If a SNP affects both E and M, the M-instrument violates exclusion restriction (the SNP-Y association is not exclusively through M). Estimates are biased toward the direct effect.
Symptom: Two-step MR shows large indirect effect; replacing M-instruments with non-overlapping SNPs makes it vanish.
Fix: Apply Steiger filter on the mediator: keep only SNPs where the SNP-M F-statistic exceeds SNP-E F-statistic (or where SNP explains more variance in M than E). For MVMR-mediation, require conditional F > 10 for each exposure independently (Sanderson 2019 IJE 48:713).
Difference vs product of coefficients diverge for non-linear outcomes
Trigger: Binary or survival outcome modeled with logistic / Cox.
Mechanism: Difference = total - direct; product = alpha * beta. Equivalent under linear-Gaussian; diverge under any link function. Counterfactual ACME from mediation::mediate() is the correct quantity; hand-computed product-of-coefficients on logistic output is biased except under rare-disease.
Fix: Report only counterfactual ACME (Imai or CMAverse). For OR-based 4-way decomposition on rare outcomes (<= 10%), Valeri & VanderWeele 2013 formulas apply; for common outcomes use risk-ratio scale or marginal effects rather than ORs.
Required Reporting for Publication
| Component | Required |
|---|
| ACME estimate + 95% CI (BCa preferred) | Yes |
| ADE + 95% CI | Yes |
| Total effect | Yes |
| Proportion mediated | Yes when total > effect-size threshold |
| Bootstrap method + sims | percentile / BCa; min 1000, recommend 5000 |
| Sequential ignorability sensitivity | rho_crit (medsens) OR mediational E-value |
| Exposure-mediator interaction test | Coefficient + p; 4-way decomposition if significant |
| Confounder set justification | DAG description |
| Mediator measurement reliability | Cite |
| Sample size + missing-data handling | Yes |
| Mediator / exposure scale | Standardized? log? raw? |
Reference: AGReMA guideline (Lee H et al 2021 JAMA 326:1045) and MacKinnon 2008 Introduction to Statistical Mediation Analysis.
Reconciliation: Observational vs MR Mediation
| Pattern | Likely cause | Action |
|---|
| Observational ACME significant; MR-mediation null | Unmeasured M-Y confounding inflated observational estimate; OR weak IVs in MR | Re-run observational with medsens(); if rho_crit < 0.1, trust MR null |
| Observational ACME null; MR-mediation significant | Measurement error in M attenuated observational estimate | Trust MR (regression-dilution-free) IF instruments pass Steiger and pleiotropy tests (MR-Egger intercept, MR-PRESSO) |
| Both significant with same sign | Convergent evidence | High-confidence mediation; report effect size from the more-conservative estimate |
| Both significant with opposite signs | At least one is biased; revisit confounder structure and IV assumptions | Do not pool; investigate via cross-method sensitivity |
Operational rule for high-stakes claims (clinical / drug-target mediation): Require (1) significant observational ACME, (2) Imai rho_crit > 0.2 OR mediational E-value > 1.5, (3) directionally consistent MR-mediation result OR documented absence of valid instruments. Single-method mediation claims should be reported as exploratory.
Anticipated Reviewer Pushback
| Pushback | Standard response |
|---|
| "Sequential ignorability?" | Imai rho_crit reported via medsens; mediational E-value reported on the risk-ratio scale |
| "Exposure-induced confounder of M-Y?" | DAG drawn; if L present, switch to CMAverse::cmest(estimation='msm') for interventional indirect effect (Vansteelandt & Daniel 2017) |
| "Why this bootstrap method?" | BCa with sims=5000 for publication; percentile fallback when BCa fails to converge (acceleration estimate unstable at boundary) |
| "Why was MR-mediation not done?" | If valid IVs for E and M exist: two-step MR or MVMR-mediation done (see code below); if not, documented absence of trans-instruments |
| "Mediator measured with error?" | Regression calibration (Carroll 2006 Measurement Error in Nonlinear Models) OR sensitivity analysis assuming reliability r = 0.7 (Valeri & VanderWeele 2014) |
| "Why HIMA2 not BAMA?" | HIMA2 = frequentist + FDR control + faster; BAMA = Bayesian when prior information is available; sample-size justification given against simulation rule-of-thumb |
| "Proportion mediated unstable?" | When |
Quantitative Thresholds
| Quantity | Threshold | Source / Rationale |
|---|
sims (bootstrap iterations) | >= 1000 exploratory, >= 5000 publication | Imai 2010; MC error scales 1/sqrt(sims) |
| Proportion mediated -- meaningful | > 0.2 | Convention; weak guideline only -- effect size in absolute terms matters more (MacKinnon 2008) |
| Proportion mediated -- "most of the effect" | > 0.5-0.8 | Convention |
| Imai rho_crit -- robust | > 0.3 | Imai 2010 Psychol Methods 15:309 |
| Imai rho_crit -- sensitive | < 0.1 | Same |
| Mediational E-value -- robust | > 2.0 (working convention; the original Smith & VanderWeele 2019 E-value framework does not prescribe a specific cutoff -- magnitude is context-dependent) | Smith & VanderWeele 2019 Epidemiology 30:835 |
| HIMA FDR cutoff | BH FDR < 0.05 | Default; report q-values not raw p |
| MVMR conditional F per exposure | > 10 each | Sanderson 2019 IJE 48:713 |
| Two-step MR -- F for both stages | > 10 each | Burgess weak-instrument convention |
| Sample size -- single-mediator (Imai) | >= 200 for stable bootstrap | Simulation rule-of-thumb |
| Sample size -- HIMA EWAS | >= 150 with p_mediators up to ~10k | Zhang 2016 simulations |
| Rare-outcome cutoff for OR-based 4-way | outcome prevalence <= 10% | Valeri & VanderWeele 2013 |
Working Code Patterns
Single-Mediator Observational with Sensitivity
Goal: Decompose a genotype-disease effect via measured molecular mediator with explicit sensitivity to unmeasured M-Y confounding.
Approach: Fit mediator and outcome models, bootstrap ACME/ADE, run medsens() for Imai rho-based sensitivity.
library(mediation)
med_model <- lm(expression ~ genotype + age + sex + pc1 + pc2 + pc3, data=dat)
out_model <- glm(disease ~ genotype + expression + age + sex + pc1 + pc2 + pc3,
data=dat, family=binomial)
med_result <- mediate(med_model, out_model,
treat='genotype', mediator='expression',
boot=TRUE, sims=5000, boot.ci.type='bca')
summary(med_result)
sens <- medsens(med_result, rho.by=0.05, effect.type='indirect', sims=1000)
summary(sens)
d0, z0, n0, tau.coef slots return ACME, ADE, proportion mediated, total effect.
4-Way Decomposition with Exposure-Mediator Interaction
Goal: Separate CDE, PIE, INTref, INTmed when exposure-mediator interaction is biologically plausible (e.g., gene-environment interaction modifying mediator effect).
Approach: Use CMAverse regression-based estimator with EMint=TRUE; bootstrap CIs.
library(CMAverse)
result_4way <- cmest(
data=dat, model='rb',
outcome='disease', exposure='genotype', mediator='expression',
basec=c('age','sex','pc1','pc2'),
EMint=TRUE,
mreg=list('linear'), yreg='logistic',
astar=0, a=1, mval=list(0),
estimation='paramfunc', inference='bootstrap', nboot=1000
)
summary(result_4way)
CMAverse reports the 4-way decomposition (Vanderweele 2014): for continuous outcomes the components are cde, intref, intmed, pnie (or pie), te, pm; for non-continuous outcomes (logistic / Cox / Poisson) the ratio versions Rcde, Rpnde, Rtnde, Rpnie, Rtnie are reported. When EMint=TRUE, additional proportion-attributable-to-interaction terms (int, pe) are included. Verify column names with summary(result)$results in the installed CMAverse version, since naming has evolved.
High-Dimensional EWAS Mediation (HIMA2)
Goal: Among thousands of candidate CpG mediators, identify those mediating an exposure-outcome effect with FDR control.
Approach: HIMA v2.3+ uses a formula interface and auto-detects outcome family (Gaussian / binomial / Cox / Poisson). Screening + MCP/DBlasso penalisation + joint significance with BH; the sigcut argument controls the FDR threshold (default 0.05).
library(HIMA)
dat <- na.omit(dat[, c('outcome', 'exposure', 'age', 'sex', 'cell_pc1', 'cell_pc2')])
M_matrix <- as.matrix(beta_values)
result <- hima(
outcome ~ exposure + age + sex + cell_pc1 + cell_pc2,
data.pheno=dat,
data.M=M_matrix,
mediator.type='gaussian', # 'negbin' for count, 'compositional' for microbiome
penalty='DBlasso', # default; alternatives 'MCP', 'SCAD', 'lasso'
scale=TRUE,
sigcut=0.05,
parallel=TRUE, ncore=8, verbose=TRUE
)
# result is a data.frame of significant mediators below sigcut
For survival outcomes wrap the LHS as Surv(time, status); HIMA auto-routes to Cox. The old hima_classic() (Zhang 2016 original) is still exported but screens by beta only and misses mediators with strong alpha + weak beta -- prefer the wrapper hima() unless reproducing a 2016-2021 paper.
For highly-correlated mediators (CpG-island clusters, gene-module co-expression): HIMA uses joint significance with BH-FDR on max(p_alpha, p_beta) and handles correlation only weakly. Within hima(), set penalty='MCP' for stronger correlation handling; alternatively pre-reduce the mediator panel by principal components or by clustering correlated mediators and screening the cluster centroid (VanderWeele & Vansteelandt 2014 Epidemiol Methods 2:95).
Time-Varying Mediation Methods
When the mediator is measured at multiple timepoints (or exposure varies over time), natural-effects estimands are not identified; switch to one of:
- g-formula (parametric or Monte Carlo):
gfoRmula::gformula_continuous_eof(); CMAverse::cmest(estimation='gformula')
- g-estimation of a structural nested mean model:
gesttools::gestSingle() / gestMultiple()
- Marginal structural model with stabilized IPTW:
ipw::ipwtm() followed by glm(..., weights=sw)
- Sequential mediation for K timepoints: VanderWeele & Tchetgen Tchetgen 2017 JRSSB 79:917
Choose based on the experimental structure:
-
= 3 timepoints required for g-methods to identify time-varying indirect effects
- Longitudinal mediator measurement at EACH timepoint is required (not just baseline)
- MSM is preferred when treatment is binary and time-varying; g-formula when continuous
- Sequential mediation when the causal ordering of multiple mediators is known and stable across time
MR-Mediation: Two-Step vs MVMR-Mediation
Decision tree:
- Independent instrument sets available for E and M -> two-step MR (Burgess 2015 IJE 44:484)
- E and M share instruments (common in cis-eQTL / cis-pQTL mediator cases) -> MVMR-mediation (Carter & Sanderson 2021 Eur J Epidemiol 36:465)
- Both feasible -> report both (triangulation)
Two-step code sketch:
library(TwoSampleMR)
exp_E <- extract_instruments('ieu-a-2', clump=TRUE)
m_E <- extract_outcome_data(exp_E$SNP, 'ieu-b-30')
dat_EM <- harmonise_data(exp_E, m_E)
mr_EM <- mr(dat_EM)
exp_M <- extract_instruments('ieu-b-30', clump=TRUE)
exp_M_indep <- exp_M[!exp_M$SNP %in% exp_E$SNP, ]
exp_M_indep <- steiger_filtering(exp_M_indep)
out_M <- extract_outcome_data(exp_M_indep$SNP, 'ieu-a-7')
dat_MY <- harmonise_data(exp_M_indep, out_M)
mr_MY <- mr(dat_MY)
Indirect effect = beta_EM * beta_MY (product of coefficients). CI via delta method or parametric bootstrap of the joint (beta_EM, beta_MY) distribution. Steiger filter on M-instruments is mandatory to ensure the M -> Y direction (not Y -> M).
MR-Mediation: Total Minus Direct via MVMR
Goal: Estimate the proportion of a genetic-instrument-identified causal effect that flows through a mediator, using independent IVs for E and (E + M).
Approach: Univariable MR for total E->Y; MVMR for direct E->Y conditional on M; indirect = total - direct via delta-method CI.
library(TwoSampleMR); library(MVMR)
total <- mr_ivw(beta_E, beta_Y, se_E, se_Y)
mvmr_dat <- format_mvmr(BXGs=cbind(beta_E, beta_M),
BYG=beta_Y, seBXGs=cbind(se_E, se_M), seBYG=se_Y, RSID=snps)
fstat <- strength_mvmr(mvmr_dat, gencov=0)
mvmr_fit <- ivw_mvmr(mvmr_dat)
direct <- mvmr_fit[1, 'Estimate']
direct_se <- mvmr_fit[1, 'Std. Error']
indirect <- total$b - direct
indirect_se <- sqrt(total$se^2 + direct_se^2)
indirect_ci <- indirect + c(-1.96, 1.96) * indirect_se
Require fstat conditional F > 10 for both E and M independently. If fstat < 10, use Q-statistic-adjusted IVW (qhet_mvmr) or report the result as weak-instrument-limited.
Double-ML Doubly-Robust Mediation
Goal: Avoid model misspecification of both mediator and outcome models via cross-fitted ML nuisance estimators.
Approach: causalweight::medDML uses random forests (or other learners) with sample splitting to estimate nuisance parameters; final estimator is doubly robust.
library(causalweight)
result_dml <- medDML(
y=dat$outcome, d=dat$treatment, m=dat$mediator,
x=as.matrix(dat[, covariates]),
trim=0.05, order=1
)
Reports direct, indirect (via mediator), and total effects with influence-function-based standard errors. Robust to non-linearity and interactions; assumes sequential ignorability still.
Mediational E-Value for Sensitivity
Goal: Report the minimum strength of an unmeasured M-Y confounder required to nullify the observed indirect effect.
Approach: Convert ACME and its CI to a risk-ratio scale, then apply VanderWeele E-value formula.
library(EValue)
acme_rr <- exp(med_result$d0)
acme_lower_rr <- exp(med_result$d0.ci[1])
evalues.RR(acme_rr, lo=acme_lower_rr, hi=NULL)
For binary outcomes, convert ACME on probability scale to RR; for continuous, use evalues.OLS() with the standardized indirect effect. E-value > 2 indicates a confounder would need >2-fold associations with both M and Y to nullify the indirect effect (Smith & VanderWeele 2019).
Tool Install Notes
| Package | Source | Notes |
|---|
| mediation | CRAN | install.packages('mediation'); actively maintained (Imai group) |
| CMAverse | GitHub | remotes::install_github('BS1125/CMAverse'); NOT on CRAN; 6 estimators in one interface |
| HIMA | GitHub | remotes::install_github('YinanZheng/HIMA'); archived from CRAN 2026-07 (needs archived scalreg); v2.x renamed hima() to HIMA2 -- verify with ?hima |
| bama | CRAN | install.packages('bama'); Bayesian; slow MCMC |
| causalweight | CRAN | install.packages('causalweight'); medDML for double-ML mediation |
| EValue | CRAN | install.packages('EValue'); for mediational E-values |
| TwoSampleMR | r-universe | See causal-genomics/mendelian-randomization for setup |
| MVMR | r-universe | remotes::install_github('WSpiller/MVMR'); for MVMR-mediation |
| gfoRmula | CRAN | For longitudinal / time-varying confounders |
Common Errors
| Error / symptom | Cause | Solution |
|---|
Error in storage.mode(x) <- "double" inside hima() | NA in data.pheno columns referenced by formula, or unconverted factors | na.omit(data.pheno) first; ensure all RHS vars in formula are numeric or factor |
| ACME significant, ADE significant, total NOT significant | Suppression / inconsistent mediation | Report transparently; effect partitioning can exceed total in suppression |
medsens() errors on glm outcome | medsens requires linear OR probit (not logit) outcome | Refit outcome as glm(..., family=binomial(link='probit')) |
mediate() runs forever with binary outcome | sims=5000 with bootstrap and small n | Use sims=1000 exploratory; verify model converges first; consider parallel via parallel='multicore' |
CMAverse cmest() reports NaN for pm | Total effect crosses zero -> proportion ill-defined | Report ACME and TE separately; pm is unstable when |
Different ACME between mediation and CMAverse rb | Default astar/a levels differ; binary mediator handled differently | Set astar=0, a=1 explicitly; for binary mediator pass mval=list(0) |
| HIMA returns zero significant mediators | Screening too aggressive; or no true mediators | Try topN=2*sqrt(n) instead of default; verify with permutation null |
| Two-step MR shows indirect > total | Steiger reversal: M actually causes E; or pleiotropic SNPs | Run MR-Steiger filter; use MR-PRESSO for pleiotropy |
medDML trim removes most data | Severe positivity violation -- few units with overlapping treatment/mediator distributions | Tighten covariate set; check propensity score distributions |
References
- Baron RM, Kenny DA 1986 J Pers Soc Psychol 51:1173 (original product-of-coefficients)
- Imai K, Keele L, Tingley D 2010 Psychol Methods 15:309 (counterfactual mediation, sequential ignorability)
- VanderWeele TJ 2014 Epidemiology 25:749 (4-way decomposition)
- VanderWeele TJ 2015 Explanation in Causal Inference (OUP) -- canonical textbook
- Valeri L, VanderWeele TJ 2013 Psychol Methods 18:137 (binary outcomes; rare-disease 4-way)
- Vansteelandt S, Daniel RM 2017 Epidemiology 28:258 (interventional / randomized indirect effects)
- Shi B et al 2021 Epidemiology 32:e20 (CMAverse package; 6 estimators)
- Zhang H et al 2016 Bioinformatics 32:3150 (HIMA original)
- Perera C et al 2022 BMC Bioinformatics 23:296 (HIMA2 alpha-beta screening)
- Song Y et al 2020 Biometrics 76:700 (BAMA Bayesian high-D mediation)
- Burgess S et al 2015 IJE 44:484 (network / two-step MR)
- Sanderson E et al 2019 IJE 48:713 (MVMR conditional F-statistic)
- Carter AR & Sanderson E 2021 Eur J Epidemiol 36:465 (MVMR-mediation)
- Farbmacher H et al 2022 Econometrics J 25:277 (medDML / double-ML mediation)
- Smith LH, VanderWeele TJ 2019 Epidemiology 30:835 (mediational E-value)
Related Skills
- causal-genomics/mendelian-randomization - IV-based causal inference; foundation for MR-mediation
- causal-genomics/pleiotropy-detection - MR-mediation instrument validity hinges on pleiotropy diagnostics (MR-Egger intercept, MR-PRESSO)
- causal-genomics/colocalization-analysis - Confirm shared causal variant before causal mediation
- causal-genomics/fine-mapping - Identify the causal variant driving the exposure
- methylation-analysis/differential-cpg-testing - Per-CpG inputs for HIMA EWAS mediation
- differential-expression/deseq2-basics - Expression inputs for eQTL mediation
- multi-omics-integration/mofa-integration - Multi-layer mediator construction
- population-genetics/association-testing - GWAS summary statistics for MR-mediation
- clinical-biostatistics/effect-measures - Risk-ratio / odds-ratio scales for binary outcomes
- machine-learning/model-validation - Cross-fitting and sample splitting for medDML
