Evidence map›Paper›PMID 32124188›Full record

ArticleCancer causes & control : CCC2020

Infectious mononucleosis, immune genotypes, and non-Hodgkin lymphoma (NHL): an InterLymph Consortium study.

Niquelle Brown Wadé, Cindy M Chang, David Conti, Joshua Millstein, Christine Skibola, Alexandra Nieters, Sophia S Wang, Silvia De Sanjose, Eleanor Kane, John J Spinelli and 10 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Cancer causes & control : CCC, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 14 institutions in 7 countries.

Niquelle Brown WadéDepartment of Preventive Medicine, Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Cindy M ChangDivision of Population Health Sciences, Center for Tobacco Products, Food and Drug Administration, Bethesda, MD, USA.
David ContiDepartment of Preventive Medicine, Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Joshua MillsteinDepartment of Preventive Medicine, Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Christine SkibolaDepartment of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Alexandra NietersCenter for Chronic Immunodeficiency (CCI), University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.
Sophia S WangDepartment of Computational and Quantitative Medicine, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Silvia De SanjoseSexual and Reproductive Health, PATH, Seattle, WA, USA.
Eleanor KaneDepartment of Health Sciences, University of York, York, YO10 5DD, UK.
John J SpinelliPopulation Oncology, BC Cancer Agency, Vancouver, Canada.
Paige BracciDepartment of Epidemiology and Biostatistics, University of California at San Francisco, San Francisco, CA, USA.
Yawei ZhangDepartment of Surgery, Yale School of Medicine and Yale School of Public Health, New Haven, CT, USA.
Susan SlagerDepartment of Epidemiology, Mayo Clinic, Rochester, MN, USA.
Jun WangDepartment of Preventive Medicine, Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Henrik HjalgrimDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Karin Ekstrom SmedbyKarolinska Institutet, Sweden University Hospital, Karolinska University, Stockholm, Sweden.
Elizabeth E BrownDepartment of Pathology, O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Ruth F JarrettMRC-University of Glasgow Centre for Virus Research, Glasgow, Scotland.
Wendy CozenDepartment of Preventive Medicine, Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. wcozen@med.usc.edu.ORCID 0000-0003-3415-8247
InterLymph Consortium Immunology and Infection Working Group
University of Southern California · USBC Cancer Agency · CACity of Hope · USEmory University · USKarolinska University Hospital · SEMayo Clinic · USMRC University of Glasgow Centre for Virus Research · GBProgram for Appropriate Technology in Health · USStatens Serum Institut · DKUniversity of Alabama at Birmingham · USUniversity of California, San Francisco · USUniversity of Freiburg · DEUniversity of York · GBYale University · US

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MYLES G COCKBURN · 1985 to 2026
$181.4M
XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
CALIFORNIA COORDINATED CANCER PREVENTION & CONTROL PROGRAMU58DP003862 · DP · CALIFORNIA STATE DEPT OF PUBLIC HEALTH · PI SNIPES, KURT P · 2012 to 2014
$31.5M
TRAINING AND CAREER DEVELOPMENTU54CA118948 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI UPENDER MANNE · 2005 to 2026
$26.6M
Molecular Epidemiology of non Hodgkin's LymphomaR01CA087014 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI HOLLY, ELIZABETH A. · 2001 to 2005
$6.7M
Molecular characterization of myeloma and related asymptomatic precursor statesR01CA186646 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BROWN, ELIZABETH E, VACHON, CELINE M · 2014 to 2018
$3.0M
Genetic Susceptibility to Non-Hodgkins LymphomaR01CA104682 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI SKIBOLA, CHRISTINE F. · 2003 to 2012
$2.6M
Resequencing and Functional Studies to Identify Causal Gene Variants of LymphomaR01CA154643 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI ZHANG, JIANQING · 2011 to 2014
$2.4M
ACTIVITY OF LYMPHOTACTIN IN CHILDHOOD MALIGNANCYR01CA075014 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI BRENNER, MALCOLM K · 1997 to 2001
$507k
A genome-wide methylation study of epigenetic contributions to multiple myelomaR21CA155951 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BROWN, ELIZABETH E · 2011 to 2012
$347k
EPIDEMIOLOGY OF NON-HODGKIN'S LYMPHOMA &RETROVIRAL TESTR01CA045614 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI HOLLY, ELIZABETH A. · 1988 to 1992
–
Medical Research Council MC_UU_12014/3NCATS NIH HHS UL1 TR001863NCCDPHP CDC HHS U58 DP003862NCI NIH HHS HHSN261201000034CNCI NIH HHS HHSN261201000035CNCI NIH HHS HHSN261201000035INCI NIH HHS HHSN261201000140CNCI NIH HHS N01-CN-75014-20NCI NIH HHS P30 CA013148NCI NIH HHS P30 CA014089NCI NIH HHS P30-CA-014089NCI NIH HHS P30-CA-13148NCI NIH HHS R01 CA045614NCI NIH HHS R01-CA-045614NCI NIH HHS R01 CA087014NCI NIH HHS R01 CA104682NCI NIH HHS R01-CA-104682NCI NIH HHS R01 CA154643NCI NIH HHS R01-CA-154643NCI NIH HHS R01 CA186646NCI NIH HHS R01-CA-186646NCI NIH HHS R21 CA155951NCI NIH HHS R21-CA-155951NCI NIH HHS U54 CA118948NCI NIH HHS U54-CA-118948
6 · The paper itself

Abstract

purposeWe explored the interaction between non-Hodgkin lymphoma (NHL), infectious mononucleosis (IM) history, and immune-related genotypes in a pooled case-control analysis.

methodsA total of 7,926 NHL patients and 10,018 controls from 12 case-control studies were included. Studies were conducted during various time periods between 1988 and 2008, and participants were 17-96 years of age at the time of ascertainment/recruitment. Self-reported IM history and immune response genotypes were provided by the InterLymph Data Coordinating Center at Mayo Clinic. Odds ratios (OR) were estimated using multivariate logistic regression, and interactions were estimated using the empirical Bayes method. P

resultsThere was evidence of an interaction effect between IM history and two variants on T-cell lymphoma (TCL) risk: rs1143627 in interleukin-1B (IL1B) (p

conclusionsGenetic risk variants in IL1B and IL6 may affect the association between IM and TCL, possibly by influencing T-cell activation, growth, and differentiation in the presence of IM, thereby decreasing risk of immune cell proliferation.

Indexed as

AdolescentAdultAgedAged, 80 and overBayes TheoremCase-Control StudiesFemaleGenotypeHumansInfectious MononucleosisLymphoma, Non-HodgkinMaleMiddle AgedRisk FactorsSelf ReportYoung AdultGene–environment interactionInfectious mononucleosisInterleukin-1beta (IL1B)Interleukin-6 (IL6)Non-Hodgkin lymphomaT-cell lymphoma

Identifiers

PMID32124188
PMCPMC7534692
OpenAlexW3000385254

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Registered trials

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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.