Evidence map›Paper›PMID 26220747›Full record

ArticleNeuroImage2015

A cautionary note on using secondary phenotypes in neuroimaging genetic studies.

Junghi Kim, Wei Pan, Alzheimer's Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in NeuroImage, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Brain Imaging Genomics: Integrated Analysis and Machine Learning.Proceedings of the IEEE. Institute of Electrical and Electronics Engineers · 2020
    Article
  4. Review
  5. Article
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.

Junghi KimDivision of Biostatistics, University of Minnesota, USA.
Wei PanDivision of Biostatistics, University of Minnesota, USA. Electronic address: weip@biostat.umn.edu.
Alzheimer's Disease Neuroimaging Initiative

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Association analysis of rare variants with sequencing dataR01HL116720 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, WEI, PENG · 2013 to 2020
$3.3M
Powerful Inference and Prediction for Genetic AssociationR01HL105397 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2011 to 2018
$2.9M
New Machine Learning Tools for Biomedical DataR01GM081535 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2007 to 2014
$2.2M
Statistical Methods for Genomic DataR01GM113250 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2014 to 2017
$702k
NHLBI NIH HHS R01 HL105397NHLBI NIH HHS R01HL105397NHLBI NIH HHS R01 HL116720NHLBI NIH HHS R01HL116720NIA NIH HHS U01 AG024904NIGMS NIH HHS R01 GM081535NIGMS NIH HHS R01GM081535NIGMS NIH HHS R01 GM113250NIGMS NIH HHS R01GM113250
6 · The paper itself

Abstract

Almost all genome-wide association studies (GWASs), including Alzheimer's Disease Neuroimaging Initiative (ADNI), are based on the case-control study design, implying that the resulting case-control data are likely a biased, not random, sample of the target population. Although association analysis of the disease (e.g. Alzheimer's disease in the ADNI) can be conducted using a standard logistic regression by ignoring the biased case-control sampling, a standard linear regression analysis on a secondary phenotype (e.g. any neuroimaging phenotype in the ADNI) may in general lead to biased inference, including biased parameter estimates, inflated Type I errors and reduced power for association testing. Despite of this well known result in genetic epidemiology, to our surprise, all the published studies on secondary phenotypes with the ADNI data have ignored this potential problem. Here we aim to answer whether such a standard analysis of a secondary phenotype is valid or problematic with the ADNI data. Through both real data analyses and simulation studies, we found that, strikingly, such an analysis was generally valid (with only small biases or slightly inflated Type I errors) for the ADNI data, though cautions must be taken when analyzing other data. We also illustrate applications and possible problems of two methods specifically developed for valid analysis of secondary phenotypes.

Indexed as

Alzheimer DiseaseData Interpretation, StatisticalGenotypePhenotypeSelection BiasAgedAged, 80 and overBrainComputer SimulationGenome-Wide Association StudyHumansMiddle AgedNeuroimagingResearch DesignADNIBiased samplingCase–control designGWASInverse probability weightingLinear regressionLogistic regressionSPREG

Identifiers

PMID26220747
PMCPMC4604049

What OpenQuestion holds

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Registered trials

None linked

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.