Bias assessment and correction for Levin's population attributable fraction in the presence of confounding.

John Ferguson, Alberto Alvarez, Martin Mulligan, Conor Judge, Martin O'Donnell
Author Information
  1. John Ferguson: HRB Clinical Research Facility Galway, University of Galway, Galway, Ireland. john.ferguson@universityofgalway.ie. ORCID
  2. Alberto Alvarez: HRB Clinical Research Facility Galway, University of Galway, Galway, Ireland.
  3. Martin Mulligan: HRB Clinical Research Facility Galway, University of Galway, Galway, Ireland.
  4. Conor Judge: HRB Clinical Research Facility Galway, University of Galway, Galway, Ireland.
  5. Martin O'Donnell: HRB Clinical Research Facility Galway, University of Galway, Galway, Ireland.

Abstract

In 1953, Morton Levin introduced a simple approach to estimating population attributable fractions (PAF) depending only on risk factor prevalence and relative risk. This formula and its extensions are still in widespread use today, particularly to estimate PAF in populations where individual data is unavailable. Unfortunately, Levin's approach is known to be asymptotically biased for the PAF when the risk factor-disease relationship is confounded even if relative risks that are correctly adjusted for confounding are used in the estimator. Here we describe a simple re-expression of Miettinen's estimand that depends on the causal relative risk, the unadjusted relative risk and the population risk factor prevalence. While this re-expression is not new, it has been underappreciated in the literature, and the associated estimator may be useful in estimating PAF in populations when individual data is unavailable provided estimated adjusted and unadjusted relative risks can be transported to the population of interest. Using the re-expressed estimand, we develop novel analytic formulae for the relative and absolute asymptotic bias in Levin's formula, solidifying earlier work by Darrow and Steenland that used simulations to investigate this bias. We extend all results to settings with non-binary valued risk factors and continuous exposures and discuss the utility of these results in estimating PAF in practice.

Keywords

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Grants

  1. EIA 2017-017/Health Research Board

MeSH Term

Humans
Risk Factors
Bias

Word Cloud

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