Evidence map›Paper›PMID 42429185›Full record

ArticleBiostatistics (Oxford, England)2026

Data-augmented multistate modeling for chronic disease processes using cross-sectional studies: application to HPV and cervical precancer.

Fangya Mao, Nicole G Campos, Li C Cheung

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2026. 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
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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

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.

Fangya MaoBiostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Rockville, MD, 20850, United States.ORCID 0000-0003-1162-4348
Nicole G CamposCenter for Health Decision Science, Harvard T.H. Chan School of Public Health, 677 Huntington Avenue, Boston, MA, 02115, United States.
Li C CheungBiostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 9609 Medical Center Drive, Rockville, MD, 20850, United States.ORCID 0000-0003-1625-4331

Funding

NIH HHS
6 · The paper itself

Abstract

Understanding the population-level natural history of human papillomavirus (HPV) infection and cervical precancer is essential for informing effective prevention strategies. Multistate models provide a principled framework for characterizing disease progression by modeling transitions among discrete health states. However, intensity-based multistate analyses typically require longitudinal data, which are often costly and logistically difficult to obtain, whereas cross-sectional data are more widely available, particularly in resource-limited settings. We develop a semi-Markov multistate model that captures HPV infection dynamics and cervical precancer progression, including recurrent transitions between HPV-infected and uninfected states. To enable estimation from cross-sectional data, we propose a two-step approach that combines local cross-sectional observations with external information on transferable transition intensities. First, biologically driven transition intensities are estimated from external data under a transferability assumption. Second, these estimates are incorporated into an approximate likelihood to infer population-specific transition intensities shaped by local epidemiological and behavioral factors. Simulation studies and applications to 2 populations demonstrate the performance of the proposed method and its practical utility.

Indexed as

Models, StatisticalPapillomavirus InfectionsPrecancerous ConditionsUterine Cervical NeoplasmsChronic DiseaseCross-Sectional StudiesDisease ProgressionFemaleHuman Papillomavirus VirusesHumansMarkov Chainscervical precancercross-sectional datahuman papillomavirusmultistate modelsrecurrent processessemi-Markov models

Identifiers

PMID42429185
PMCPMC13351745

What OpenQuestion holds

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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.