Evidence map›Paper›PMID 40313270›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Quantify the Contribution of Modifiable Risk Factors for Progression of MGUS to Multiple Myeloma.

Mei Wang, Byron Sigel, Lawrence Liu, John H Huber, Mengmeng Ji, Martin W Schoen, Kristen M Sanfilippo, Theodore S Thomas, Graham A Colditz, Shi-Yi Wang and 1 more

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. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

5 · Who and what money

Authors and funding

11 authors.

Byron Sigel
Lawrence Liu
John H Huber
Martin W Schoen
Kristen M Sanfilippo
Theodore S Thomas
Shi-Yi Wang
Su-Hsin Chang

Funding

Comparative modeling of multiple myeloma across myeloma control continuuum: prevention, treatment, and disparity reductionU01CA265735 · NCI · WASHINGTON UNIVERSITY · PI CHANG, SU-HSIN, WANG, SHIYI · 2021 to 2025
$3.2M
Addressing racial disparities in monoclonal gammopathy of undetermined significance and progression to multiple myeloma from a prevention perspectiveR01CA253475 · NCI · WASHINGTON UNIVERSITY · PI CHANG, SU-HSIN · 2020 to 2022
$1.1M
NCI NIH HHS R01 CA253475NCI NIH HHS U01 CA265735
6 · The paper itself

Abstract

backgroundMultiple myeloma (MM), the most common plasma cell dyscrasia in the U.S., is preceded by an asymptomatic precursor monoclonal gammopathy of undetermined significance (MGUS). Although several risk factors for MGUS progression are known, their relative contributions remain unclear. Unlike other malignancies, such evidence is lacking for MM despite its high burden.

objectiveTo quantify contributions of modifiable risk factors to MGUS progression to MM to inform prevention.

designRetrospective cohort study conducted from 1/1/2024-12/31/2024.

settingNationwide U.S. Veterans Health Administration (VHA).

participantsPatients with MGUS (IgG, IgA, or light chain) diagnosed from 10/1/1999-12/31/2023.

interventionsModifiable risk factors including excess body mass index (BMI), chemical exposure, and comorbidities. MEASUREMENTS: Excess body mass index was defined as BMI ≥25 kg/m2, chemical exposure was measured by prior exposure to Agent Orange, comorbidities were summarized using Charlson Comorbidity Index. Multivariable-adjusted population attributable fractions (aPAF) was calculated for each modifiable risk factor. The aPAF estimates the proportion of progression in patients diagnosed with MGUS that could have been prevented, if a given risk factor were absent.

resultsThe cohort included 35,073 MGUS patients (33,670 [96.0%] male and 23,218 [66.2%] White), of whom 2,895 (8.3%) progressed to MM. Median age at MGUS diagnosis was 71.8 (IQR: 64.4-78.6) years. Among all evaluated risk factors, excess BMI was the leading factor (Black: aPAF=27.1%, 95% CI 19.5-34.0%; White: 27.2%, 95% CI 20.3-33.4%; All: aPAF=27.1%, 95% CI: 22.1-31.9%). LIMITATIONS: Potential residual confounding, limited generalizability beyond the VHA population.

conclusionOur study highlights the potential for weight management as a key strategy in reducing the risk of progression to MM in Black and White patients diagnosed with MGUS. PRIMARY FUNDING SOURCE: National Institutes of Health.

Identifiers

PMID40313270
PMCPMC12045440

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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.