Evidence map›Paper›PMID 24373701›Full record

ArticleCancer epidemiology2014

Breast cancer susceptibility loci in association with age at menarche, age at natural menopause and the reproductive lifespan.

Shaneda Warren Andersen, Amy Trentham-Dietz, Ronald E Gangnon, John M Hampton, Halcyon G Skinner, Corinne D Engelman, Barbara E Klein, Linda J Titus, Kathleen M Egan, Polly A Newcomb

Abstract readValidation Study
In one paragraph

Article in Cancer epidemiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Genetic Variation and Hot Flashes: A Systematic Review.The Journal of clinical endocrinology and metabolism · 2020
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Genetics of pubertal timing.Current opinion in pediatrics · 2018
    Review
  6. Article
  7. Article
  8. Interaction between common breast cancer susceptibility variants, genetic ancestry, and nongenetic risk factors in Hispanic women.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2015
    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

10 authors.

Shaneda Warren AndersenUniversity of Wisconsin, Carbone Cancer Center, Madison, WI 53726, USA; Department of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA. Electronic address: snandersen@uwalumni.com.
Amy Trentham-DietzUniversity of Wisconsin, Carbone Cancer Center, Madison, WI 53726, USA; Department of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA.
Ronald E GangnonDepartment of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA.
John M HamptonUniversity of Wisconsin, Carbone Cancer Center, Madison, WI 53726, USA.
Halcyon G SkinnerDepartment of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA.
Corinne D EngelmanDepartment of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA.
Barbara E KleinDepartment of Ophthalmology and Visual Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI 53726, USA.
Linda J TitusNorris Cotton Cancer Center, Dartmouth Medical School, Lebanon, NH 03756, USA.
Kathleen M EganDivision of Cancer Prevention and Control, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Polly A NewcombUniversity of Wisconsin, Carbone Cancer Center, Madison, WI 53726, USA; Cancer Prevention Program, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
THE EPIDEMIOLOGY OF AGE-RELATED OCULAR DISEASEU10EY006594 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI KLEIN, RONALD · 1987 to 2018
$17.3M
Scientific and Technical CoreP2CHD047873 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI Katherine J. Curtis · 2014 to 2026
$5.1M
PHYSICAL ACTIVITY, LIFESTYLE AND OVARIAN CANCER RISKR01CA047147 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI NEWCOMB, POLLY A · 1988 to 2007
$2.6M
Training and Research in Colon Cancer SurvivalK05CA152715 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 2010 to 2019
$991k
HORMONES, LIFESTYLE AND BREAST CANCERR01CA047305 · NCI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI EGAN, KATHLEEN · 1988 to 1999
–
HORMONES, LIFESTYLE, AND BREAST CANCERR01CA069664 · NCI · DARTMOUTH COLLEGE · PI TITUS-ERNSTOFF, LINDA · 1996 to 1999
–
Intramural NIH HHSNCI NIH HHS CA47147NCI NIH HHS K05 CA152715NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA047147NCI NIH HHS R01 CA047305NCI NIH HHS R01 CA069664NEI NIH HHS U10 EY006594NEI NIH HHS U10EY06594NICHD NIH HHS P2C HD047873
6 · The paper itself

Abstract

backgroundGenome-wide association studies have identified single nucleotide polymorphisms (SNPs) associated with breast cancer risk. Some of these loci have unknown functional significance and may mediate the effects of hormonal exposures on breast cancer risk. We examined relationships between breast cancer susceptibility variants and menstrual/reproductive factors using data from two population-based studies.

methodsThe first analysis was based on a sample of 1328 women age 20-74 who participated as controls in a case-control study of breast cancer conducted in three U.S. states. We evaluated the associations between age at menarche, age at natural menopause and the reproductive lifespan with 13 previously identified breast cancer variants. Associations were also examined with a genetic score created as the sum of at-risk alleles across the 13 variants. For validation, significant results were evaluated in a second dataset comprised 1353 women age 43-86 recruited as part of a cohort study in Wisconsin.

resultsNeither the genetic score nor any of the 13 variants considered individually were associated with age at menarche or reproductive lifespan. Two SNPs were associated with age at natural menopause; every increase in the minor allele (A) of rs17468277 (CASP8) was associated with a 1.12 year decrease in menopause age (p=0.02). The minor allele (G) of rs10941679 (5p12) was associated with a 1.01 year increase in age at natural menopause (p=0.01). The results were not replicated in the validation cohort (B=-0.61, p=0.14 and B=-0.01, p=.0.98, respectively).

conclusionsThe evaluated variants and reproductive experiences may work through separate pathways to influence breast cancer risk.

Indexed as

Genetic Predisposition to DiseaseAdultAgedBreast NeoplasmsCase-Control StudiesCohort StudiesFemaleHumansMenarcheMenopauseMiddle AgedPolymorphism, Single NucleotideReproductive HistoryRisk FactorsUnited StatesYoung AdultBreast cancerBreast cancer susceptibility lociEpidemiologyMenstrual factors

Identifiers

PMID24373701
PMCPMC4023814

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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.