Evidence map›Paper›PMID 38212245›Full record

Trial reportBlood advances2024

Mass spectrometry-detected MGUS is associated with obesity and other novel modifiable risk factors in a high-risk population.

David J Lee, Habib El-Khoury, Angela C Tramontano, Jean-Baptiste Alberge, Jacqueline Perry, Maya I Davis, Erica Horowitz, Robert Redd, Dhananjay Sakrikar, David Barnidge and 6 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03689595 (Predicting Progression of Developing Myeloma in a High-Risk Screened Population), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
9.5field-weighted citation impact, top 2% of its field
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.

NCT03689595 enrolling by invitationnot on this map

Predicting Progression of Developing Myeloma in a High-Risk Screened Population (PROMISE)

TypeobservationalSponsorDana-Farber Cancer InstituteRan2018 to 2033Enrolled30,000ConditionsMultiple MyelomaArmsSamples of blood (2-4 tablespoons) from 4 tubes will be collected -Analysis will be performed on the blood to test for multiple myeloma precursor conditions.
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. A Comprehensive Review of Monoclonal Gammopathy of Undetermined Significance.Journal of the advanced practitioner in oncology · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Multiple myeloma.Nature reviews. Disease primers · 2024
    Review
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

16 authors at 2 institutions in 1 country.

David J LeeDepartment of Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-0330-1824
Habib El-KhouryHarvard Medical School, Boston, MA.ORCID 0000-0002-4023-6566
Angela C TramontanoDivision of Population Sciences, Dana-Farber Cancer Institute, Boston, MA.
Jean-Baptiste AlbergeHarvard Medical School, Boston, MA.ORCID 0000-0002-4218-7294
Jacqueline PerryDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Maya I DavisDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Erica HorowitzDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-1458-330X
Robert ReddBiostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-1329-5288
Dhananjay SakrikarThe Binding Site Inc, Rochester, MN.ORCID 0000-0001-8430-0120
David BarnidgeThe Binding Site Inc, Rochester, MN.
Mark C PerkinsThe Binding Site Group Ltd, Birmingham, United Kingdom.
Stephen HardingThe Binding Site Group Ltd, Birmingham, United Kingdom.
Lorelei MucciHarvard T.H. Chan School of Public Health, Boston, MA.
Timothy R RebbeckDivision of Population Sciences, Dana-Farber Cancer Institute, Boston, MA.
Irene M GhobrialHarvard Medical School, Boston, MA.ORCID 0000-0001-7361-3092
Catherine R MarinacHarvard Medical School, Boston, MA.ORCID 0000-0002-9128-3012
Dana-Farber Cancer Institute · USHarvard University · US

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
Obesity, Molecular Biomarkers, and Multiple Myeloma PrognosisF32CA220859 · NCI · DANA-FARBER CANCER INST · PI MARINAC, CATHERINE · 2018 to 2019
$94k
NCI NIH HHS F32 CA220859NCI NIH HHS K22 CA251648NHLBI NIH HHS R38 HL150212NIAID NIH HHS R25 AI147393
6 · The paper itself

Abstract

abstractMonoclonal gammopathy of undetermined significance (MGUS) is a premalignant condition of multiple myeloma with few known risk factors. The emergence of mass spectrometry (MS) for the detection of MGUS has provided new opportunities to evaluate its risk factors. In total, 2628 individuals at elevated risk for multiple myeloma were enrolled in a screening study and completed an exposure survey (PROMISE trial). Participant samples were screened by MS, and monoclonal proteins (M-proteins) with concentrations of ≥0.2 g/L were categorized as MS-MGUS. Multivariable logistic models evaluated associations between exposures and MS outcomes. Compared with normal weight (body mass index [BMI] of 18.5 to <25 kg/m2), obesity (BMI of ≥30 kg/m2) was associated with MS-MGUS, adjusting for age, sex, Black race, education, and income (odds ratio [OR], 1.73; 95% confidence interval [CI], 1.21-2.47; P = .003). High physical activity (≥73.5 metabolic equivalent of task (MET)-hours per week vs <10.5 MET-hours per week) had a decreased likelihood of MS-MGUS (OR, 0.45, 95% CI, 0.24-0.80; P = .009), whereas heavy smoking and short sleep had increased likelihood of MS-MGUS (>30 pack-years vs never smoker: OR, 2.19; 95% CI, 1.24-3.74; P = .005, and sleep <6 vs ≥6 hours per day: OR, 2.11; 95% CI, 1.26-3.42; P = .003). In the analysis of all MS-detected monoclonal gammopathies, which are inclusive of M-proteins with concentrations of <0.2 g/L, elevated BMI and smoking were associated with all MS-positive cases. Findings suggest MS-detected monoclonal gammopathies are associated with a broader range of modifiable risk factors than what has been previously identified. This trial was registered at www.clinicaltrials.gov as #NCT03689595.

Indexed as

Monoclonal Gammopathy of Undetermined SignificanceMultiple MyelomaHumansObesityRisk Factors

Identifiers

PMID38212245
PMCPMC10997907
OpenAlexW4390765747

What OpenQuestion holds

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Registered trials

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.