Evidence map›Paper›PMID 25153242›Full record

ArticleThe international journal of biostatistics2014

Optimal design strategies for sibling studies with binary exposures.

Zhigang Li, Ian W McKeague, Lambert H Lumey

Abstract read
In one paragraph

Article in The international journal of biostatistics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Zhigang Li
Ian W McKeague
Lambert H Lumey

Funding

Post-selection inference and trajectory analysisR01GM095722 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MCKEAGUE, IAN WRAY · 2011 to 2018
$1.5M
Prenatally induced DNA methylation profiles and disease risk at age 60R01AG042190 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LUMEY, L H · 2011 to 2013
$989k
Design and Analysis of Palliative Care Trials Evaluating Early InterventionsR03NR014915 · NINR · DARTMOUTH COLLEGE · PI LI, ZHIGANG · 2014 to 2015
$160k
NIA NIH HHS R01 AG042190NIA NIH HHS R01AG042190-03NIGMS NIH HHS R01 GM095722NIGMS NIH HHS R01GM095722-01NINR NIH HHS 1R03NR014915-01NINR NIH HHS R03 NR014915
6 · The paper itself

Abstract

Sibling studies have become increasingly popular because they provide better control over confounding by unmeasured family-level risk factors than can be obtained in standard cohort studies. However, little attention has been devoted to the development of efficient design strategies for sibling studies in terms of optimizing power. We here address this issue in commonly encountered types of sibling studies, allowing for continuous and binary outcomes and varying numbers of exposed and unexposed siblings. For continuous outcomes, we show that in families with sibling pairs, optimal study power is obtained by recruiting discordant (exposed-control) pairs of siblings. More generally, balancing the exposure status within each family as evenly as possible is shown to be optimal. For binary outcomes, we elucidate how the optimal strategy depends on the variation of the binary response; as the within-family correlation increases, the optimal strategy tends toward only recruiting discordant sibling pairs (as in the case of continuous outcomes). R code for obtaining the optimal strategies is included.

Indexed as

Epidemiologic Research DesignModels, StatisticalSiblingsHumansSample Size

Identifiers

PMID25153242
PMCPMC4412035

What OpenQuestion holds

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Registered trials

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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.