Evidence map›Paper›PMID 25255808›Full record

ArticleAmerican journal of epidemiology2014

Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.

Amit D Joshi, Sara Lindström, Anika Hüsing, Myrto Barrdahl, Tyler J VanderWeele, Daniele Campa, Federico Canzian, Mia M Gaudet, Jonine D Figueroa, Laura Baglietto and 35 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in American journal of epidemiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Development of a Breast Cancer Risk Prediction Model Integrating Monogenic, Polygenic, and Epidemiologic Risk.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2024
    Article
  2. Article
  3. Obesity, Adiposity, and Risk of Symptomatic Gallstone Disease According to Genetic Susceptibility.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2022
    Article
  4. Article
  5. Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
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  19. Previous GWAS hits in relation to young-onset breast cancer.Breast cancer research and treatment · 2017
    Article
  20. MiRNA-binding site functional polymorphisms in DNA repair genes RAD51, RAD52, and XRCC2 and breast cancer risk in Chinese population.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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

45 authors at 1 institution in 1 country.

Amit D Joshi
Sara Lindström
Anika Hüsing
Myrto Barrdahl
Tyler J VanderWeele
Daniele Campa
Federico Canzian
Mia M Gaudet
Jonine D Figueroa
Laura Baglietto
Christine D Berg
Julie E Buring
Stephen J Chanock
María-Dolores Chirlaque
W Ryan Diver
Laure Dossus
Graham G Giles
Christopher A Haiman
Susan E Hankinson
Brian E Henderson
Robert N Hoover
David J Hunter
Claudine Isaacs
Rudolf Kaaks
Laurence N Kolonel
Vittorio Krogh
Loic Le Marchand
I-Min Lee
Eiliv Lund
Catherine A McCarty
Kim Overvad
Petra H Peeters
Elio Riboli
Fredrick Schumacher
Gianluca Severi
Daniel O Stram
Malin Sund
Michael J Thun
Ruth C Travis
Dimitrios Trichopoulos
Walter C Willett
Shumin Zhang
Regina G Ziegler
Peter Kraft
Breast and Prostate Cancer Cohort Consortium (BPC3)
Harvard University · US

Funding

Hormone-Related CancersZIACP010126 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI GIERACH, GRETCHEN · 2009 to 2025
$103.5M
Understanding Ethnic Differences in Cancer: The Multiethnic Cohort StudyUM1CA164973 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI HENDERSON, BRIAN E, LE MARCHAND, LOIC · 2012 to 2014
$11.3M
Characterizing Genetic Susceptibility to Breast and Prostate Cancer; the BPC3U01CA098758 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HENDERSON, BRIAN E · 2003 to 2010
$11.0M
Characterizing Genetic Susceptibility to Breast and Prostate Cancer; the BPC3U01CA098233 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI HUNTER, DAVID JOHN · 2003 to 2010
$10.8M
Epidemiologic StudiesU19CA148065 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI AHSAN, HABIBUL, BRUGGE, JOAN SIEFERT · 2010 to 2014
$10.6M
Characterizing Genetic Susceptibility to Breast and Prostate Cancer; the BPC3U01CA098216 · NCI · INTERNATIONAL AGENCY FOR RES ON CANCER · PI RIBOLI, ELIO · 2003 to 2011
$7.4M
Characterizing Genetic Susceptibility to Breast and Prostate Cancer: The BPC3.U01CA098710 · NCI · AMERICAN CANCER SOCIETY, INC. · PI GAPSTUR, SUSAN M · 2003 to 2011
$4.2M
Cancer Research UK 16491Intramural NIH HHSNCI NIH HHS CA148065NCI NIH HHS U01 CA098216NCI NIH HHS U01 CA098233NCI NIH HHS U01 CA098710NCI NIH HHS U01 CA098758NCI NIH HHS U01-CA98216NCI NIH HHS U01-CA98233NCI NIH HHS U01-CA98710NCI NIH HHS U01-CA98758NCI NIH HHS U19 CA148065NCI NIH HHS U19-CA148065NCI NIH HHS UM1 CA164973
6 · The paper itself

Abstract

Additive interactions can have public health and etiological implications but are infrequently reported. We assessed departures from additivity on the absolute risk scale between 9 established breast cancer risk factors and 23 susceptibility single-nucleotide polymorphisms (SNPs) identified from genome-wide association studies among 10,146 non-Hispanic white breast cancer cases and 12,760 controls within the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium. We estimated the relative excess risk due to interaction and its 95% confidence interval for each pairwise combination of SNPs and nongenetic risk factors using age- and cohort-adjusted logistic regression models. After correction for multiple comparisons, we identified a statistically significant relative excess risk due to interaction (uncorrected P = 4.51 × 10(-5)) between a SNP in the DNA repair protein RAD51 homolog 2 gene (RAD51L1; rs10483813) and body mass index (weight (kg)/height (m)(2)). We also compared additive and multiplicative polygenic risk prediction models using per-allele odds ratio estimates from previous studies for breast-cancer susceptibility SNPs and observed that the multiplicative model had a substantially better goodness of fit than the additive model.

Indexed as

Polymorphism, Single NucleotideAllelesAustraliaBiomarkers, TumorBody Mass IndexBreast NeoplasmsCase-Control StudiesCohort StudiesDNA-Binding ProteinsEuropeFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedBiomarkers, TumorDNA-Binding ProteinsRAD51B protein, humanRAD51 protein, humanRad51 Recombinaseadditive interactionsbreast cancergenome-wide association studiessingle-nucleotide polymorphisms

Identifiers

PMID25255808
PMCPMC4224360
OpenAlexW2170740290

What OpenQuestion holds

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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.