Evidence map›Paper›PMID 30565280›Full record

ArticleStatistics in medicine2019

Assessing the robustness of sisVIVE in a Mendelian randomization study to estimate the causal effect of body mass index on income using multiple SNPs from understanding society.

Yanchun Bao, Paul S Clarke, Melissa Smart, Meena Kumari

Abstract readComparative Study
In one paragraph

Article in Statistics in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Identification and Inference with Invalid Instruments.Annual review of statistics and its application · 2025
    Article
  2. Wage Penalties or Wage Premiums? A Socioeconomic Analysis of Gender Disparity in Obesity in Urban China.International journal of environmental research and public health · 2020
    Article
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yanchun BaoInstitute for Social and Economic Research, University of Essex, Colchester, UK.ORCID 0000-0002-6102-5098
Paul S ClarkeInstitute for Social and Economic Research, University of Essex, Colchester, UK.
Melissa SmartInstitute for Social and Economic Research, University of Essex, Colchester, UK.
Meena KumariInstitute for Social and Economic Research, University of Essex, Colchester, UK.

Funding

Medical Research Council G1001799Medical Research Council MR/N01104X/1Medical Research Council MR/N01104X/2
6 · The paper itself

Abstract

The "some invalid, some valid instrumental variable estimator" (sisVIVE) is a lasso-based method for instrumental variables (IVs) regression of outcome on an exposure. In principle, sisVIVE is robust to some of the IVs in the analysis being invalid, in the sense of being related to the outcome variable through pathways not mediated by the exposure. In this paper, we consider the application of sisVIVE to a Mendelian randomization study in which multiple genetic variants are used as IVs to estimate the causal effect of body mass index on personal income in the presence of unobserved confounding. In addition to analyzing data from the large-scale longitudinal household survey Understanding Society, we conduct a simulation study to (a) assess the performance of sisVIVE in relation to that of competing robust methods like "MR-Egger" and "MR-Median" and (b) identify scenarios under which its absolute performance is poor. We find that sisVIVE outperforms alternative robust methods, in terms of mean-square error, across a wide range of scenarios, but that its performance is poor in absolute terms when the presence of indirect pleiotropy leads to failure of the "InSIDE" condition, which is not explicitly required for identification. We argue that this is because the consistency criterion for sisVIVE does not identify the true causal effect when InSIDE fails.

Indexed as

CausalityRegression AnalysisBody Mass IndexComputer SimulationGenetic Predisposition to DiseaseHumansIncomeMendelian Randomization AnalysisModels, GeneticPolymorphism, Single Nucleotideinstrumental variablesMendelian randomizationMR-EggerMR-Medianpleiotropic biassisVIVE

Identifiers

PMID30565280
PMCPMC6492086

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.