Evidence map›Paper›PMID 28303589›Full record

ArticleStatistics in medicine2017

Secondary phenotype analysis in ascertained family designs: application to the Leiden longevity study.

Renaud Tissier, Roula Tsonaka, Simon P Mooijaart, Eline Slagboom, Jeanine J Houwing-Duistermaat

Abstract read
In one paragraph

Article in Statistics in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Genetic Vulnerability to Social Anxiety Disorder.Current topics in behavioral neurosciences · 2025
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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

5 authors.

Renaud TissierDepartment of Medical Statistics and Bioinformatics, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-9665-883X
Roula TsonakaDepartment of Medical Statistics and Bioinformatics, Leiden University Medical Centre, Leiden, The Netherlands.
Simon P MooijaartDepartment of Gerontology and Geriatrics, Leiden University Medical Centre, Leiden, The Netherlands.
Eline SlagboomDepartment of Molecular Epidemiology, Leiden University Medical Centre, Leiden, The Netherlands.
Jeanine J Houwing-DuistermaatDepartment of Medical Statistics and Bioinformatics, Leiden University Medical Centre, Leiden, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The case-control design is often used to test associations between the case-control status and genetic variants. In addition to this primary phenotype, a number of additional traits, known as secondary phenotypes, are routinely recorded, and typically, associations between genetic factors and these secondary traits are studied too. Analysing secondary phenotypes in case-control studies may lead to biased genetic effect estimates, especially when the marker tested is associated with the primary phenotype and when the primary and secondary phenotypes tested are correlated. Several methods have been proposed in the literature to overcome the problem, but they are limited to case-control studies and not directly applicable to more complex designs, such as the multiple-cases family studies. A proper secondary phenotype analysis, in this case, is complicated by the within families correlations on top of the biased sampling design. We propose a novel approach to accommodate the ascertainment process while explicitly modelling the familial relationships. Our approach pairs existing methods for mixed-effects models with the retrospective likelihood framework and uses a multivariate probit model to capture the association between the mixed type primary and secondary phenotypes. To examine the efficiency and bias of the estimates, we performed simulations under several scenarios for the association between the primary phenotype, secondary phenotype and genetic markers. We will illustrate the method by analysing the association between triglyceride levels and glucose (secondary phenotypes) and genetic markers from the Leiden Longevity Study, a multiple-cases family study that investigates longevity. © 2017 The Authors. Statistics in Medicine Published by JohnWiley & Sons Ltd.

Indexed as

Models, GeneticModels, StatisticalBiostatisticsBlood GlucoseComputer SimulationFamilyGenetic Association StudiesGenetic MarkersHumansLikelihood FunctionsLongevityNetherlandsPhenotypePolymorphism, Single NucleotideRetrospective StudiesTriglyceridesBlood GlucoseGenetic MarkersTriglyceridesascertainmentfamily datagenetic association and heritabilitymixed modelsmultivariate probit model

Identifiers

PMID28303589
PMCPMC5485037

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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.