Evidence map›Paper›PMID 42871646›Full record

ArticleEClinicalMedicine2026

MGUS in Black individuals in Soweto, South Africa screened by mass spectrometry: results of the PROMISE South Africa study.

David J Lee, Wenlong C Chen, Luca Bertamini, Habib El-Khoury, Sabine Allam, Grace Fleming, Jean-Baptiste Alberge, Jacqueline Perry, Maya I Davis, Elizabeth Lightbody and 16 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 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
–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

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

26 authors.

David J LeeDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Wenlong C ChenStrengthening Oncology Services Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Luca BertaminiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Habib El-KhouryDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Sabine AllamDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Grace FlemingDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jean-Baptiste AlbergeDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jacqueline PerryDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Maya I DavisDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Elizabeth LightbodyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Lindokuhle N GoqwanaFaculty of Health Sciences, Division of Internal Medicine, School of Clinical Medicine, University of the Witwatersrand, Johannesburg, South Africa.
Vinitha PhilipClinical Haematology Unit, Faculty of Health Sciences, Department of Medicine, Chris Hani Baragwanath Academic Hospital, University of the Witwatersrand, Johannesburg, South Africa.
Audrey Pentz BRadStrengthening Oncology Services Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Thulisile Hlubi Dip TchgStrengthening Oncology Services Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Robert ReddDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Dhananjay SakrikarBinding Site, part of Thermo Fisher Scientific, Rochester, MN, USA.
David BarnidgeBinding Site, part of Thermo Fisher Scientific, Rochester, MN, USA.
Mark C PerkinsWaters Corporation, England, UK.
Stephen HardingThe Binding Site Group Ltd., Birmingham, UK.
Julia ColchieDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Elizabeth W KarlsonHarvard Medical School, Boston, MA, USA.
Timothy R RebbeckDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Gad GetzHarvard Medical School, Boston, MA, USA.
Maureen JoffeStrengthening Oncology Services Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Irene M GhobrialDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Catherine R MarinacDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Funding

Pathways to Mentorship and Research: Training the Next Generation Physician-ScientistsR25AI147393 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2019 to 2024
$1.8M
MGH Next Generation Physician-Scientist Through Stimulating Access to Research in Residency Program (MGH-Next Gen StARR)R38HL150212 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI VYAS, JATIN M · 2020 to 2023
$1.3M
Repurposing Metformin for the Prevention of Disease Progression in Precursor Multiple MyelomaK22CA251648 · NCI · DANA-FARBER CANCER INST · PI MARINAC, CATHERINE · 2020 to 2022
$577k
Prolonged Nightly Fasting as a Behavioral Intervention for Obesity Reduction and the Prevention of Progression in Precursor Multiple MyelomaR21CA256644 · NCI · DANA-FARBER CANCER INST · PI MARINAC, CATHERINE · 2022 to 2023
$453k
NCI NIH HHS K22 CA251648NCI NIH HHS R21 CA256644NHLBI NIH HHS R38 HL150212NIAID NIH HHS R25 AI147393
6 · The paper itself

Abstract

Background: Only few studies have screened for monoclonal gammopathy of undetermined significance (MGUS) among Black Africans in sub-Saharan Africa, with mixed results. Methods: In this cross-sectional study, we enrolled 2004 Black Africans aged 40-75 years from Soweto, South Africa, from January 2021 to August 2023. Participants completed an interview-guided exposure survey, underwent height and weight measurements, and provided blood samples that were screened for MGUS by matrix-assisted laser desorption ionisation-time of flight mass spectrometry. The primary outcome was the prevalence of MGUS, assessed from blood samples collected at the participants' single study visit. Prevalence was compared to those of high-risk United States (US)-based cohorts screened by the same method. Multivariable logistic regression models evaluated associations between exposures and MGUS. Findings: Prevalences of heavy-chain and light-chain MGUS among Black Africans were 12% and 3%. MGUS prevalence among Black Africans were similar to or higher than those of high-risk populations in the US. In multivariable modelling within the South Africa cohort, human immunodeficiency virus (HIV) was associated with MGUS (odds ratio [OR], 1.67; 95% confidence interval [CI], 1.27-2.21; p < 0.001). Smoking was associated with MGUS (<20 pack-years vs never smoking: OR, 1.55; 95% CI, 1.14-2.12; p = 0.01 and ≥20 pack-years vs never smoking: OR, 1.76; 95% CI, 1.21-2.56; p = 0.003). Body mass index (BMI) of ≥30 kg/m Interpretation: Results suggest Black South Africans represent a high-risk population with an increased likelihood of having MGUS. HIV, smoking, and physical activity may contribute to prevalence patterns. Prospective studies are needed to further elucidate the role of these risk factors in MGUS development and to identify strategies for early detection, risk stratification, and prevention. Funding: Stand Up To Cancer Dream Team, Multiple Myeloma Research Foundation, and National Institutes of Health.

Indexed as

Cancer preventionMGUSMultiple myelomaRisk factors

Identifiers

PMID42871646
PMCPMC13659611

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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.