ArticleBiostatistics (Oxford, England)2026
Flexible nonparametric assessment of time-lag bias in meta-analysis.
Article in Biostatistics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Time-lag bias occurs when studies with larger or statistically significant effects appear in print sooner than those with smaller or null effects, which can inflate early meta-analytic estimates and mislead decision makers. Existing diagnostics typically rely on cumulative meta-analysis or meta-regression of effects on publication time. These approaches are vulnerable to repeated-testing inflation and loss of power when temporal trends are nonlinear. We propose a family of flexible nonparametric statistics that summarize standardized pairwise differences between early and later studies, each emphasizing different magnitudes of temporal contrast, and a hybrid test that adaptively combines evidence across these differences via permutation. The procedure controls type I error under exchangeability of publication order and is sensitive to diverse temporal patterns, including linear trends, early outliers, and oscillations in effect sizes over time. Simulations across 9 scenarios, with and without heterogeneity, show that the hybrid test maintains the nominal error rate and improves statistical power relative to linear meta-regression when temporal trends are nonlinear. In 2 clinical meta-analyses, our method detects pronounced time-lag patterns that standard regression misses. We provide guidance for practice and discuss practical considerations for detecting and interpreting time-lag bias in meta-analyses.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.