A sufficient cause based approach to the assessment of mediation

Methods

Abstract

The minimal sufficient cause (MSC) model, also known as the sufficient component cause model, has been used to facilitate understanding of several key concepts in epidemiology. To improve the understanding of mediation, we introduce a causal model for mediation that is grounded in the MSC approach. First, we describe an unbiased model for mediation, to clarify the causal meaning of previously described indirect effects. Through the use of potential outcomes and response types, we express each indirect (and direct) effect in terms of component causes within the MSC model. Second, we use an MSC-based model to illustrate a common cause of the mediator and outcome, i.e. a confounder of the mediator–outcome relationship. By describing this potential source of bias within the MSC-based model, important complexities are noted that impact the magnitude of plausible confounding. In conclusion, an MSC-based approach leads to several important insights concerning the interpretation of indirect and direct effects, as well as the potential sources of bias in mediation analysis.

Keywords

Mediation Direct and indirect effects Minimal sufficient cause model Sufficient component cause model Potential outcomes Response types 

Notes

Acknowledgements

The author would like to acknowledge Sharon Schwartz for her insightful input, guidance, and mentorship. She would also like to thank Tyler VanderWeele, Maria Glymour, and Ezra Susser for their helpful comments on this manuscript.

References

  1. 1.
    Skrabanek P. The emptiness of the black box. Epidemiology. 1994;5(5):553–5.PubMedGoogle Scholar
  2. 2.
    Susser M, Susser E. Choosing a future for epidemiology: II. From black box to Chinese boxes and eco-epidemiology. Am J Public Health. 1996;86(5):674–7.PubMedCrossRefGoogle Scholar
  3. 3.
    Weed DL. Beyond black box epidemiology. Am J Public Health. 1998;88(1):12–4.PubMedCrossRefGoogle Scholar
  4. 4.
    Hafeman D. Opening the black box: a reassessment of mediation from a counterfactual perspective. Dissertation. Columbia University, New York; 2008.Google Scholar
  5. 5.
    Susser E, et al. Psychiatric epidemiology: searching for causes of mental disorders. London: Oxford University Press; 2006. p. 422–8.Google Scholar
  6. 6.
    Marmot M, Wilkinson RG. Psychosocial and material pathways in the relation between income and health: a response to Lynch et al. BMJ. 2001;322(7296):1233–6. doi: 10.1136/bmj.322.7296.1233.PubMedCrossRefGoogle Scholar
  7. 7.
    Marmot MG, et al. Contribution of job control and other risk factors to social variations in coronary heart disease incidence. Lancet. 1997;350(9073):235–9. doi: 10.1016/S0140-6736(97)04244-X.PubMedCrossRefGoogle Scholar
  8. 8.
    Lynch JW, et al. Income inequality and mortality: importance to health of individual income, psychosocial environment, or material conditions. BMJ. 2000;320:1200–4.Google Scholar
  9. 9.
    MacKinnon DP. Analysis of mediating variables in prevention and intervention research. NIDA Res Monogr. 1994;139:127–53.PubMedGoogle Scholar
  10. 10.
    Rothman KJ, Greenland S. Modern epidemiology. 2nd ed. Philadelphia, PA: Lippincott Williams and Wilkins; 1998. 738 pp.Google Scholar
  11. 11.
    Szklo M, Nieto FJ. Epidemiology: beyond the basics. Gaithersburg, MD: Aspen Publishers; 2000.Google Scholar
  12. 12.
    Rothman KJ, Greenland S, Lash TL. Modern epidemiology. 3rd ed. Philadelphia, PA: Lippincott Williams and Wilkins; 2008. p. 200–2.Google Scholar
  13. 13.
    Pearl J. Direct and indirect effects. In: Proceedings of the American Statistical Association Joint Statistical Meetings. Minneapolis, MN: MIRA Digital Publishing; 2001.Google Scholar
  14. 14.
    Petersen ML, Sinisi SE, van der Laan MJ. Estimation of direct causal effects. Epidemiology. 2006;17(3):276–84. doi: 10.1097/01.ede.0000208475.99429.2d.PubMedCrossRefGoogle Scholar
  15. 15.
    Robins JM, Greenland S. Identifiability and exchangeability for direct and indirect effects. Epidemiology. 1992;3(2):143–55. doi: 10.1097/00001648-199203000-00013.PubMedCrossRefGoogle Scholar
  16. 16.
    Darroch J. Biologic synergism and parallelism. Am J Epidemiol. 1997;145(7):661–8.PubMedGoogle Scholar
  17. 17.
    Greenland S, Robins JM. Identifiability, exchangeability, and epidemiological confounding. Int J Epidemiol. 1986;15(3):413–9. doi: 10.1093/ije/15.3.413.PubMedCrossRefGoogle Scholar
  18. 18.
    Miettinen OS. Causal and preventive interdependence. Elementary principles. Scand J Work Environ Health. 1982;8(3):159–68.PubMedGoogle Scholar
  19. 19.
    Rothman KJ. Causes. Am J Epidemiol. 1976;104(6):587–92.PubMedGoogle Scholar
  20. 20.
    Mackie JL. The cement of the Universe: a study of causation. New York: Oxford University Press; 1974.Google Scholar
  21. 21.
    VanderWeele TJ, Robins JM. The identification of synergism in the sufficient-component-cause framework. Epidemiology. 2007;18(3):329–39. doi: 10.1097/01.ede.0000260218.66432.88.PubMedCrossRefGoogle Scholar
  22. 22.
    Ahsan H, et al. Health Effects of Arsenic Longitudinal Study (HEALS): description of a multidisciplinary epidemiologic investigation. J Expo Sci Environ Epidemiol. 2006;16(2):191–205. doi: 10.1038/sj.jea.7500449.PubMedCrossRefGoogle Scholar
  23. 23.
    Greenland S, Poole C. Invariants and noninvariants in the concept of interdependent effects. Scand J Work Environ Health. 1988;14(2):125–9.PubMedGoogle Scholar
  24. 24.
    Kaufman JS, Maclehose RF, Kaufman SA. A further critique of the analytic strategy of adjusting for covariates to identify biologic mediation. Epidemiol Perspect Innov. 2004;1(1):4. doi: 10.1186/1742-5573-1-4.PubMedCrossRefGoogle Scholar
  25. 25.
    Greenland S, Pearl J, Robins JM. Causal diagrams for epidemiologic research. Epidemiology. 1999;10(1):37–48. doi: 10.1097/00001648-199901000-00008.PubMedCrossRefGoogle Scholar
  26. 26.
    VanderWeele TJ, Robins JM. Directed acyclic graphs, sufficient causes, and the properties of conditioning on a common effect. Am J Epidemiol. 2007;166(9):1096–104. doi: 10.1093/aje/kwm179.PubMedCrossRefGoogle Scholar
  27. 27.
    Greenland S, Brumback B. An overview of relations among causal modelling methods. Int J Epidemiol. 2002;31(5):1030–7. doi: 10.1093/ije/31.5.1030.PubMedCrossRefGoogle Scholar
  28. 28.
    Flanders WD. On the relationship of sufficient component cause models with potential outcome (counterfactual) models. Eur J Epidemiol. 2006;21:847–53.Google Scholar
  29. 29.
    MacKinnon DP, Fairchild AJ, Fritz MS. Mediation analysis. Annu Rev Psychol. 2007;58:593–614. doi: 10.1146/annurev.psych.58.110405.085542.PubMedCrossRefGoogle Scholar
  30. 30.
    Judd CM, Kenny DA. Process analysis: estimating mediation in treatment evaluations. Eval Rev. 1981;5(5):602–19. doi: 10.1177/0193841X8100500502.CrossRefGoogle Scholar
  31. 31.
    Cole SR, Hernan MA. Fallibility in estimating direct effects. Int J Epidemiol. 2002;31(1):163–5. doi: 10.1093/ije/31.1.163.PubMedCrossRefGoogle Scholar
  32. 32.
    Pearl J. Causality: models, reasoning and inference. Cambridge: Cambridge University Press; 2000. p. 78–85.Google Scholar

Copyright information

© Springer Science+Business Media B.V. 2008

Authors and Affiliations

  1. 1.Department of Epidemiology, Mailman School of Public HealthColumbia UniversityNew YorkUSA

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