4.5 Article

Meta-analysis of non-linear exposure-outcome relationships using individual participant data: A comparison of two methods

Journal

STATISTICS IN MEDICINE
Volume 38, Issue 3, Pages 326-338

Publisher

WILEY
DOI: 10.1002/sim.7974

Keywords

fractional polynomials; meta-analysis; multivariate meta-analysis; prognostic research; random effects models

Funding

  1. Medical Research Council [MC_UU_12023/21]
  2. UK Medical Research Council [G0800270]
  3. British Heart Foundation [SP/09/002]
  4. British Heart Foundation Cambridge Cardiovascular Centre of Excellence
  5. National Institute for Health Research Cambridge Biomedical Research Centre
  6. MRC [MR/L003120/1, G0800270, MC_UU_12023/21] Funding Source: UKRI

Ask authors/readers for more resources

Non-linear exposure-outcome relationships such as between body mass index (BMI) and mortality are common. They are best explored as continuous functions using individual participant data from multiple studies. We explore two two-stage methods for meta-analysis of such relationships, where the confounder-adjusted relationship is first estimated in a non-linear regression model in each study, then combined across studies. The metacurve approach combines the estimated curves using multiple meta-analyses of the relative effect between a given exposure level and a reference level. The mvmeta approach combines the estimated model parameters in a single multivariate meta-analysis. Both methods allow the exposure-outcome relationship to differ across studies. Using theoretical arguments, we show that the methods differ most when covariate distributions differ across studies; using simulated data, we show that mvmeta gains precision but metacurve is more robust to model mis-specification. We then compare the two methods using data from the Emerging Risk Factors Collaboration on BMI, coronary heart disease events, and all-cause mortality (>80 cohorts, >18 000 events). For each outcome, we model BMI using fractional polynomials of degree 2 in each study, with adjustment for confounders. For metacurve, the powers defining the fractional polynomials may be study-specific or common across studies. For coronary heart disease, metacurve with common powers and mvmeta correctly identify a small increase in risk in the lowest levels of BMI, but metacurve with study-specific powers does not. For all-cause mortality, all methods identify a steep U-shape. The metacurve and mvmeta methods perform well in combining complex exposure-disease relationships across studies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available