Evidence map›Paper›PMID 24441287›Full record

ArticleLeukemia2014

Racial disparities in the prevalence of monoclonal gammopathies: a population-based study of 12,482 persons from the National Health and Nutritional Examination Survey.

O Landgren, B I Graubard, J A Katzmann, R A Kyle, I Ahmadizadeh, R Clark, S K Kumar, A Dispenzieri, A J Greenberg, T M Therneau and 7 more

Abstract read
In one paragraph

Article in Leukemia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed
8.5field-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.

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

109 citing papers in PubMed, 196 citations in OpenAlex.

  1. Trial
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  3. Race-Dependent Differences in Risk, Genomics, and Epstein-Barr Virus Exposure in Monoclonal Gammopathies: Results of SWOG S0120.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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  19. Opportunities to Avoid Invasive Cancer by Diagnosis and Interception of Preneoplastic Lesions and Cancer Risk Conditions.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
    Article
  20. Article

49 more citing papers are in PubMed but not listed here.

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

17 authors at 4 institutions in 1 country.

O LandgrenMultiple Myeloma Section, Center for Cancer Research, Metabolism Branch, National Cancer Institute, Rockville, MD, USA.
B I GraubardDivsion of Cancer Epidemiology and Genetics, Biostatistics Branch, National Cancer Institute, Rockville, MD, USA.
J A KatzmannDepartment of Laboratory Medicine and Pathology, College of Medicine, Mayo Clinic, Rochester, MN, USA.
R A KyleDivision of Hematology, Department of Medicine, College of Medicine, Mayo Clinic, Rochester, MN, USA.
I AhmadizadehMultiple Myeloma Section, Center for Cancer Research, Metabolism Branch, National Cancer Institute, Rockville, MD, USA.
R ClarkDepartment of Laboratory Medicine and Pathology, College of Medicine, Mayo Clinic, Rochester, MN, USA.
S K KumarDivision of Hematology, Department of Medicine, College of Medicine, Mayo Clinic, Rochester, MN, USA.
A DispenzieriDivision of Hematology, Department of Medicine, College of Medicine, Mayo Clinic, Rochester, MN, USA.
A J GreenbergDivision of Epidemiology, Department of Health Sciences Research, College of Medicine, Mayo Clinic, Rochester, MN, USA.
T M TherneauDivision of Hematology, Department of Medicine, College of Medicine, Mayo Clinic, Rochester, MN, USA.
L J MeltonDivision of Epidemiology, Department of Health Sciences Research, College of Medicine, Mayo Clinic, Rochester, MN, USA.
N CaporasoDivsion of Cancer Epidemiology and Genetics, Biostatistics Branch, National Cancer Institute, Rockville, MD, USA.
N KordeMultiple Myeloma Section, Center for Cancer Research, Metabolism Branch, National Cancer Institute, Rockville, MD, USA.
M RoschewskiMultiple Myeloma Section, Center for Cancer Research, Metabolism Branch, National Cancer Institute, Rockville, MD, USA.
R CostelloMultiple Myeloma Section, Center for Cancer Research, Metabolism Branch, National Cancer Institute, Rockville, MD, USA.
G M McQuillanCenters for Disease Control and Prevention, National Center for Health Statistics, Division of Health and Nutrition Examination Surveys, Hyattsville, MD, USA.
S V RajkumarDivision of Hematology, Department of Medicine, College of Medicine, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic · USNational Cancer Institute · USCenter for Cancer Research · USCenters for Disease Control and Prevention · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
TISSUE BANK AND CLINICAL/LABORATORY DATABASEP01CA062242 · NCI · MAYO CLINIC ROCHESTER · PI THERNEAU, TERRY M · 1994 to 2009
$12.9M
Prevalence and Progression of Monoclonal GammopathiesR01CA107476 · NCI · MAYO CLINIC ROCHESTER · PI KUMAR, SHAJI KUNNATHU, RAJKUMAR, S VINCENT · 2004 to 2018
$4.6M
CHROMOSOMAL ABNORMALITIES IN MYELOMA AS DETECTED BY FISHR01CA083724 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI FONSECA, RAFAEL · 2000 to 2013
$4.0M
Onset and biomarkers for progression of monoclonal gammopathiesR01CA168762 · NCI · MAYO CLINIC ROCHESTER · PI KUMAR, SHAJI KUNNATHU, RAJKUMAR, S VINCENT · 2012 to 2024
$3.2M
Intramural NIH HHSNCI NIH HHS CA 100707NCI NIH HHS CA107476NCI NIH HHS CA 168762NCI NIH HHS CA 62242NCI NIH HHS CA 83724NCI NIH HHS P01 CA062242NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA100707NCI NIH HHS R01 CA083724NCI NIH HHS R01 CA107476NCI NIH HHS R01 CA168762
6 · The paper itself

Abstract

Multiple myeloma (MM) incidence is markedly higher in blacks compared with whites, which may be related to a higher prevalence of monoclonal gammopathy of undetermined significance (MGUS). Our objective was to define the prevalence and risk factors of MGUS in a large cohort representative of the US population. Stored serum samples from the National Health and Nutritional Examination Survey (NHANES) III or NHANES 1999-2004 were available for 12,482 individuals of age ⩾50 years (2331 'blacks', 2475 Hispanics, 7051 'whites' and 625 'others') on which agarose-gel electrophoresis, serum protein immunofixation, serum-free light-chain assay and M-protein typing were performed. MGUS was identified in 365 participants (2.4%). Adjusted prevalence of MGUS was significantly higher (P<0.001) in blacks (3.7%) compared with whites (2.3%) (P=0.001) or Hispanics (1.8%), as were characteristics that posed a greater risk of progression to MM. The adjusted prevalence of MGUS was 3.1% and 2.1% for the North/Midwest versus South/West regions of the United States, respectively (P=0.052). MGUS is significantly more common in blacks, and more often has features associated with higher risk of progression to MM. A strong geographic disparity in the prevalence of MGUS between the North/Midwest versus the South/West regions of the United States was found, which has etiologic implications.

Indexed as

Healthcare DisparitiesAgedAged, 80 and overFemaleHealth SurveysHumansMaleMiddle AgedMonoclonal Gammopathy of Undetermined SignificanceParaproteinemiasPopulation SurveillancePrevalenceRisk FactorsUnited States

Identifiers

PMID24441287
PMCPMC4090286
OpenAlexW2027698431

What OpenQuestion holds

Textmetadata
LicenceTDM
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.