Evidence map›Paper›PMID 40585078›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Chronic Disease and Risk Factor Prevalence in Multiracial Subgroups: California, 2014-2023.

Tracy Lam-Hine, Michelle C Odden, Aliya Saperstein, Tainayah W Thomas, David H Rehkopf

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

5 · Who and what money

Authors and funding

5 authors.

Tracy Lam-HineStanford University School of Medicine, Department of Epidemiology and Population Health.ORCID 0000-0001-9040-2991
Michelle C OddenStanford University School of Medicine, Department of Epidemiology and Population Health.ORCID 0000-0002-5974-3648
Aliya SapersteinStanford University Department of Sociology.ORCID 0000-0002-6429-1172
Tainayah W ThomasStanford University School of Medicine, Department of Epidemiology and Population Health.ORCID 0000-0001-9094-8556
David H RehkopfStanford University School of Medicine, Department of Epidemiology and Population Health.ORCID 0000-0002-7597-6513

Funding

Diabetes, Endocrinology and Metabolism Training GrantT32DK007217 · NIDDK · STANFORD UNIVERSITY · PI Justin Pierce Annes, David Matthew Maahs · 1987 to 2026
$7.2M
NIDDK NIH HHS T32 DK007217
6 · The paper itself

Abstract

Background: Multiracial adults represent a growing U.S. population but are often grouped together or reassigned to single-race categories in public health data. Aggregation can obscure important variation across subgroups, limiting opportunities for targeted prevention. Methods: We analyzed 2014-2023 California Behavioral Risk Factor Surveillance System data (n=100,177) to estimate prevalence of 28 health indicators across racial and ethnic groups, including disaggregated Multiracial subgroups. We categorized participants based on all self-identified races and aggregated subgroups with N<50. We standardized prevalence by age and sex using 2020 California census data, calculated relative standard errors, and used survey-weighted methods to compare prevalence and subgroup differences. Results: Among 100,177 participants, Multiracial subgroups had the highest prevalence for 24 of 28 outcomes. American Indian or Alaska Native-Black and Hispanic-Black-White adults had the highest prevalence of chronic conditions, poor general health, and disability. In contrast, Asian Multiracial subgroups (e.g., Asian-Black, Asian-Pacific Islander) more often had the lowest prevalence, though Asian-White adults were not consistently the healthiest subgroup. Differences across Multiracial subgroups exceeded 20 percentage points for nearly half of all outcomes. Discussion: Wide health variation among Multiracial adults is masked by common aggregation practices. Subgroups with the highest burden may be overlooked if data are not routinely disaggregated. Public health surveillance systems should expand capacity to collect and report disaggregated race and ethnicity data to better inform prevention strategies.

Indexed as

chronic diseasedisaggregationethnicityMultiracialrace

Identifiers

PMID40585078
PMCPMC12204261

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.