Evidence map›Paper›PMID 40463571›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Moving beyond risk ratios in sibling analysis: estimating clinically useful measures from family-based analysis.

Viktor H Ahlqvist, Hugo Sjöqvist, Arvid Sjölander, Daniel Berglind, Paul C Lambert, Brian K Lee, Paul Madley-Dowd

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Viktor H AhlqvistDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-1383-3194
Hugo SjöqvistDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
Arvid SjölanderDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Daniel BerglindDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
Paul C LambertDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Brian K LeeDepartment of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
Paul Madley-DowdCentre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Funding

Maternal epilepsy, antiepileptic drug use during pregnancy, and risk of autismR01NS107607 · NINDS · DREXEL UNIVERSITY · PI LEE, BRIAN KANE, MAGNUSSON, CECILIA · 2019 to 2022
$1.7M
NINDS NIH HHS R01 NS107607
6 · The paper itself

Abstract

Objective: Findings from family-based analyses, such as sibling comparisons, are often reported using only odds ratios or hazard ratios. We demonstrate how this can be improved upon by applying the marginalized between-within framework. Study Design and Setting: We provide an overview of sibling comparison methods and the marginalized between-within framework, which enables estimation of absolute risks and clinically relevant metrics while accounting for shared familial confounding. We illustrate the approach using Swedish registry data to examine the association between maternal smoking and infant mortality, estimating absolute risk differences, average treatment effects, attributable fractions, and numbers needed to harm (or treat). Results: The marginalized between-within model decomposes effects into within- and between-family components while applying a global baseline across all families. Although it typically yields similar relative estimates to conditional logistic or stratified Cox regression, the model's specification of a baseline enables the estimation of absolute measures. In the applied example, absolute measures provided more interpretable and policy-relevant insights than relative estimates alone. Code for implementation in Stata and R is provided. Conclusion: The marginalized between-within framework may strengthen the interpretability of family-based analysis by enabling absolute and policy-relevant estimates for both binary and time-to-event outcomes, moving beyond the limitations of solely relying on relative effect measures.

Indexed as

Absolute measuresFamily-based analysisMarginalized between-within modelsMaternal SmokingSibling analysisWithin-family analysis

Identifiers

PMID40463571
PMCPMC12132141

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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.