Evidence map›Paper›PMID 38818035›Full record

ArticleFrontiers in genetics2024

Longitudinal method comparison: modeling polygenic risk for post-traumatic stress disorder over time in individuals of African and European ancestry.

Kristin Passero, Jennie G Noll, Shefali Setia Verma, Claire Selin, Molly A Hall

Abstract read
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Article in Frontiers in genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kristin PasseroVirginia Institute of Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, United States.
Jennie G NollDepartment of Psychology, Mount Hope Family Center, University of Rochester, Rochester, NY, United States.
Shefali Setia VermaDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Claire SelinCenter for Childhood Deafness, Language, and Learning, Boys Town National Research Hospital, Omaha, NE, United States.
Molly A HallDepartment of Genetics and Institute for Biomedical Informatics, University of Pennsylvania, Philadelphia, PA, United States.

Funding

Translational Research that Adapts New Science FORMaltreatment prevention (TRANSFORM)P50HD096698 · NICHD · UNIVERSITY OF ROCHESTER · PI JENNIE G NOLL, Sheree Lynn Toth · 2018 to 2026
$16.5M
Methods for Enhancing Polygenic Risk Prediction Models for Complex DiseaseR01HL169458 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Dokyoon Kim, MARYLYN D RITCHIE · 2023 to 2026
$3.1M
Abused and non-abused females' high-risk online behaviors: Impact on developmentR01HD073130 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI NOLL, JENNIE G · 2012 to 2016
$2.9M
Creating the Next Generation of Scholars in CM Science (CMT32)T32HD101390 · NICHD · PENNSYLVANIA STATE UNIVERSITY, THE · PI Erika Lunkenheimer, Hannah Milena Caroline Schreier · 2020 to 2026
$1.9M
NHLBI NIH HHS R01 HL169458NICHD NIH HHS P50 HD096698NICHD NIH HHS R01 HD073130NICHD NIH HHS T32 HD101390
6 · The paper itself

Abstract

Cross-sectional data allow the investigation of how genetics influence health at a single time point, but to understand how the genome impacts phenotype development, one must use repeated measures data. Ignoring the dependency inherent in repeated measures can exacerbate false positives and requires the utilization of methods other than general or generalized linear models. Many methods can accommodate longitudinal data, including the commonly used linear mixed model and generalized estimating equation, as well as the less popular fixed-effects model, cluster-robust standard error adjustment, and aggregate regression. We simulated longitudinal data and applied these five methods alongside naïve linear regression, which ignored the dependency and served as a baseline, to compare their power, false positive rate, estimation accuracy, and precision. The results showed that the naïve linear regression and fixed-effects models incurred high false positive rates when analyzing a predictor that is fixed over time, making them unviable for studying time-invariant genetic effects. The linear mixed models maintained low false positive rates and unbiased estimation. The generalized estimating equation was similar to the former in terms of power and estimation, but it had increased false positives when the sample size was low, as did cluster-robust standard error adjustment. Aggregate regression produced biased estimates when predictor effects varied over time. To show how the method choice affects downstream results, we performed longitudinal analyses in an adolescent cohort of African and European ancestry. We examined how developing post-traumatic stress symptoms were predicted by polygenic risk, traumatic events, exposure to sexual abuse, and income using four approaches-linear mixed models, generalized estimating equations, cluster-robust standard error adjustment, and aggregate regression. While the directions of effect were generally consistent, coefficient magnitudes and statistical significance differed across methods. Our in-depth comparison of longitudinal methods showed that linear mixed models and generalized estimating equations were applicable in most scenarios requiring longitudinal modeling, but no approach produced identical results even if fit to the same data. Since result discrepancies can result from methodological choices, it is crucial that researchers determine their model

Indexed as

longitudinal analysis methodslongitudinal method comparisonpolygenic risk scorespost-traumatic stress disorderrepeated measuressimulation study

Identifiers

PMID38818035
PMCPMC11137250

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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.