Evidence map›Paper›PMID 41388844›Full record

ArticleBiostatistics (Oxford, England)2025

Decomposition of longitudinal disparities: an application to the fetal growth-singletons study.

Sang Kyu Lee, Seonjin Kim, Mi-Ok Kim, Katherine L Grantz, Hyokyoung G Hong

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Sang Kyu LeeBiostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Rockville, MD 20892, United States.ORCID 0009-0002-7207-2102
Seonjin KimDepartment of Statistics, Miami University, 326 Data Science Building, Oxford, OH 45056, United States.ORCID 0000-0001-6058-0420
Mi-Ok KimDepartment of Epidemiology and Biostatistics, University of California San Francisco, 550 16th Street, San Francisco, CA 94158, United States.ORCID 0000-0002-7712-3653
Katherine L GrantzEpidemiology Branch, Division of Population Health Research, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 6710 Rockledge Drive, Bethesda, MD 20817, United States.ORCID 0000-0003-0276-8534
Hyokyoung G HongBiostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Rockville, MD 20892, United States.ORCID 0000-0002-4280-6243

Funding

Division of Population Health, Division of Intramural ResearchEunice Kennedy Shriver National Institute of Child Health and Human Development HHSN27500006Eunice Kennedy Shriver National Institute of Child Health and Human Development HHSN275200800003ICEunice Kennedy Shriver National Institute of Child Health and Human Development HHSN27520080 0028CNICHD NIH HHS HHSN275200800002CNICHD NIH HHS HHSN275200800002INICHD NIH HHS HHSN275200800003CNICHD NIH HHS HHSN275200800003INICHD NIH HHS HHSN275200800012CNICHD NIH HHS HHSN275200800013CNICHD NIH HHS HHSN275200800014CNICHD NIH HHS HHSN275200800028CNICHD NIH HHS HHSN275201000009C
6 · The paper itself

Abstract

Addressing health disparities across demographic groups remains a critical challenge in public health, with significant gaps in understanding how these disparities evolve over time. This paper extends the traditional Peters-Belson decomposition to a longitudinal setting, focusing on the role of a single explanatory variable, referred to as a modifier, that captures complex interactions with other covariates. The proposed method partitions disparities into 3 components: (i) the portion associated with differences in the conditional distribution of covariates, evaluated under a common distribution of the modifier across groups; (ii) the portion arising from differences in the distribution of the modifier and its interactions with other covariates; and (iii) the unexplained disparity not accounted for by observed covariates. Rather than aggregating the first 2 components into one "explained disparity," the proposed method allows for a separate characterization of temporal patterns in disparities, distinguishing those that are unassociated with the modifier from those that are associated with it. We illustrate the method using a fetal growth study, examining disparities in fetal development trajectories across racial and ethnic groups during pregnancy.

Indexed as

Fetal DevelopmentHealth Status DisparitiesModels, StatisticalEthnicityFemaleHumansLongitudinal StudiesPregnancydisparity decomposition analysislongitudinal analysisPeters-Belson approachthe Fetal Growth—Singletons Study

Identifiers

PMID41388844
PMCPMC12701353

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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.