Evidence map›Paper›PMID 37398345›Full record

ArticlebioRxiv : the preprint server for biology2024

Study design features increase replicability in cross-sectional and longitudinal brain-wide association studies.

Kaidi Kang, Jakob Seidlitz, Richard A I Bethlehem, Jiangmei Xiong, Megan T Jones, Kahini Mehta, Arielle S Keller, Ran Tao, Anita Randolph, Bart Larsen and 22 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

32 authors.

Kaidi KangDepartment of Biostatistics, Vanderbilt University Medical Center.ORCID 0000-0003-0922-5727
Jakob SeidlitzDepartment of Child and Adolescent Psychiatry and Behavioral Sciences, The Children's Hospital of Philadelphia.
Richard A I BethlehemDepartment of Psychology, University of Cambridge.ORCID 0000-0002-0714-0685
Jiangmei XiongDepartment of Biostatistics, Vanderbilt University Medical Center.ORCID 0000-0002-7481-765X
Megan T JonesDepartment of Biostatistics, Vanderbilt University Medical Center.
Kahini MehtaDepartment of Psychiatry, University of Pennsylvania.ORCID 0000-0001-9466-100X
Arielle S KellerDepartment of Psychiatry, University of Pennsylvania.ORCID 0000-0003-4708-1672
Ran TaoDepartment of Biostatistics, Vanderbilt University Medical Center.
Anita RandolphDepartment of Pediatrics, University of Minnesota Medical School.
Bart LarsenDepartment of Pediatrics, University of Minnesota Medical School.
Brenden Tervo-ClemmensDepartment of Department of Psychiatry & Behavioral Sciences, University of Minnesota Medical School.
Eric FeczkoDepartment of Pediatrics, University of Minnesota Medical School.
Oscar Miranda DominguezDepartment of Pediatrics, University of Minnesota Medical School.
Steve NelsonDepartment of Pediatrics, University of Minnesota Medical School.
Lifespan Brain Chart Consortium
3R-BRAIN
AIBL
Alzheimer’s Disease Neuroimaging Initiative
Alzheimer’s Disease Repository Without Borders Investigators
CALM Team
CCNP
COBRE
cVEDA
Harvard Aging Brain Study
IMAGEN
POND
PREVENT-AD Research Group
Jonathan SchildcroutDepartment of Biostatistics, Vanderbilt University Medical Center.
Damien FairDepartment of Pediatrics, University of Minnesota Medical School.
Theodore D SatterthwaiteDepartment of Psychiatry, University of Pennsylvania.
Aaron Alexander-BlochDepartment of Child and Adolescent Psychiatry and Behavioral Sciences, The Children's Hospital of Philadelphia.
Simon VandekarDepartment of Biostatistics, Vanderbilt University Medical Center.

Funding

Vascular factors, physical activity, and inflammation as modulators of neurodegenerative and cognitive trajectories (Project 2)P01AG036694 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Hyun-Sik Yang · 2010 to 2026
$50.2M
The Genetics of Personalized Functional MRI NetworksR01MH132934 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI Aaron Felix Alexander-Bloch · 2023 to 2026
$4.2M
Precision brain charts for imaging-genomics of schizophrenia and the psychosis spectrumR01MH133843 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI Aaron Felix Alexander-Bloch · 2023 to 2026
$3.2M
Semiparametric Inference for Psychiatric NeuroimagingR01MH123563 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI VANDEKAR, SIMON NEIL · 2020 to 2024
$2.1M
Combined brain and gene network approaches to the developmental hypothesis of schizophreniaK08MH120564 · NIMH · YALE UNIVERSITY · PI ALEXANDER-BLOCH, AARON FELIX · 2019 to 2023
$923k
NIA NIH HHS P01 AG036694NIMH NIH HHS K08 MH120564NIMH NIH HHS R01 MH123563NIMH NIH HHS R01 MH132934NIMH NIH HHS R01 MH133843
6 · The paper itself

Abstract

Brain-wide association studies (BWAS) are a fundamental tool in discovering brain-behavior associations. Several recent studies showed that thousands of study participants are required for good replicability of BWAS because the standardized effect sizes (ESs) are much smaller than the reported standardized ESs in smaller studies. Here, we perform analyses and meta-analyses of a robust effect size index using 63 longitudinal and cross-sectional magnetic resonance imaging studies from the Lifespan Brain Chart Consortium (77,695 total scans) to demonstrate that optimizing study design is critical for increasing standardized ESs and replicability in BWAS. A meta-analysis of brain volume associations with age indicates that BWAS with larger variability in covariate have larger reported standardized ES. In addition, the longitudinal studies we examined reported systematically larger standardized ES than cross-sectional studies. Analyzing age effects on global and regional brain measures from the United Kingdom Biobank and the Alzheimer's Disease Neuroimaging Initiative, we show that modifying longitudinal study design through sampling schemes improves the standardized ESs and replicability. Sampling schemes that improve standardized ESs and replicability include increasing between-subject age variability in the sample and adding a single additional longitudinal measurement per subject. To ensure that our results are generalizable, we further evaluate these longitudinal sampling schemes on cognitive, psychopathology, and demographic associations with structural and functional brain outcome measures in the Adolescent Brain and Cognitive Development dataset. We demonstrate that commonly used longitudinal models can, counterintuitively, reduce standardized ESs and replicability. The benefit of conducting longitudinal studies depends on the strengths of the between- versus within-subject associations of the brain and non-brain measures. Explicitly modeling between- versus within-subject effects avoids averaging the effects and allows optimizing the standardized ESs for each separately. Together, these results provide guidance for study designs that improve the replicability of BWAS.

Identifiers

PMID37398345
PMCPMC10312450

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.