Evidence map›Paper›PMID 42192518›Full record

ArticleBMC public health2026

Spatial analysis of predictors of prostate cancer incidence in the united states using multiscale geographically weighted regression (MGWR).

Yang Liu, Peihai Zhang, Ziyang Ma, Jintao Wei

Abstract read
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Article in BMC public health, 2026. 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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yang LiuHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China.
Peihai ZhangHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China. zhangpeihai@cdutcm.edu.cn.
Ziyang MaHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China.
Jintao WeiHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China.

Funding

Sichuan Provincial Administration of Traditional Chinese Medicine 25ZDIZX018
6 · The paper itself

Abstract

backgroundProstate cancer incidence varies markedly across the United States (U.S.), yet the broad contextual predictors associated with this variation and the spatial scales at which these associations operate remain insufficiently characterized within a unified spatial framework.

objectiveThis study aimed to examine annual state-level associations between prostate cancer incidence and selected contextual predictors across the U.S. from 2018 to 2022 using Multiscale Geographically Weighted Regression (MGWR).

methodsFive annual state-level datasets covering the 50 U.S. states were assembled for 2018-2022. After exploratory spatial analysis, correlation screening, collinearity diagnostics, theory-informed re-evaluation, and representative-year sensitivity analyses, six predictors were retained for the final annual models: elevation, rainfall, atmospheric pressure, obesity prevalence, the percentage of males aged 65 years and older among the male population, and the percentage of the Black or African American alone population. Ordinary Least Squares (OLS), Geographically Weighted Regression (GWR), and MGWR were fitted separately for each annual dataset. Model performance was compared using R², adjusted R², residual sum of squares, corrected Akaike information criterion (AICc), bandwidth diagnostics, and residual spatial autocorrelation.

resultsAcross all five annual analyses, MGWR showed the most favorable overall performance, with adjusted R² values ranging from 0.555 to 0.618 and AICc values ranging from 124.934 to 132.779. MGWR also identified variable-specific adaptive bandwidths ranging from 24 to 40 nearest neighbors, indicating spatial scale heterogeneity among predictors. Local coefficient surfaces showed clear spatial non-stationarity in both coefficient magnitude and, for some predictors, coefficient direction. Residual Moran's I tests were non-significant for all five annual models, suggesting that substantial residual spatial autocorrelation had been reduced after model fitting. Multivariate clustering of standardized local coefficients further revealed recurring regional groupings in coefficient-pattern similarity.

conclusionAt the state level in the U.S., prostate cancer incidence was associated with geographically differentiated contextual patterns rather than a single spatially uniform relationship structure. In this setting, the main value of MGWR lay in its ability to characterize multi-scale and regionally varying association patterns across repeated annual spatial analyses. These findings may support geographically differentiated surveillance and future hypothesis generation while underscoring the importance of considering spatial heterogeneity in ecological studies of prostate cancer incidence.

Indexed as

Prostatic NeoplasmsSpatial RegressionAgedHumansIncidenceMaleSpatial AnalysisUnited StatesEnvironmental factorsMGWRProstate cancerSpatial heterogeneityU.S

Identifiers

PMID42192518
PMCPMC13390135

What Socratic holds

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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.