Evidence map›Paper›PMID 24502445›Full record

ArticleLymphatic research and biology2014

Cytokine candidate genes predict the development of secondary lymphedema following breast cancer surgery.

Geraldine Leung, Christina Baggott, Claudia West, Charles Elboim, Steven M Paul, Bruce A Cooper, Gary Abrams, Anand Dhruva, Brian L Schmidt, Kord Kober and 7 more

Open access · greenAbstract read
In one paragraph

Article in Lymphatic research and biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Etiology and treatment of cancer-related secondary lymphedema.Clinical & experimental metastasis · 2024
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Secondary lymphedema from cancer therapy.Clinical & experimental metastasis · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
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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 2 institutions in 1 country.

Geraldine Leung1 School of Nursing, University of California , San Francisco, California.
Christina Baggott
Claudia West
Charles Elboim
Steven M Paul
Bruce A Cooper
Gary Abrams
Anand Dhruva
Brian L Schmidt
Kord Kober
John D Merriman
Heather Leutwyler
John Neuhaus
Dale Langford
Betty J Smoot
Bradley E Aouizerat
Christine Miaskowski
University of California, San Francisco · USNew York University · US

Funding

UCSF CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024131 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSTON, S. CLAIBORNE · 2006 to 2011
$111.2M
Symptom Management After Breast Cancer SurgeryR01CA107091 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIASKOWSKI, CHRISTINE A. · 2003 to 2008
$4.5M
Long-term Arm Morbidity Following Breast Cancer TreatmentR01CA118658 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIASKOWSKI, CHRISTINE A. · 2006 to 2010
$3.5M
A Whole Systems Approach to the Study of Ayurveda for Cancer SurvivorshipK23AT005340 · NCCIH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DHRUVA, ANAND · 2009 to 2013
$635k
Identification of Genetic Markers Associated With Attentional FatigueF31NR012604 · NINR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MERRIMAN, JOHN D. · 2010 to 2013
$95k
NCCIH NIH HHS K23 AT005340NCI NIH HHS CA107091NCI NIH HHS CA118658NCI NIH HHS R01 CA107091NCI NIH HHS R01 CA118658NCRR NIH HHS RR624130NCRR NIH HHS UL1 RR024131
6 · The paper itself

Abstract

backgroundLymphedema (LE) is a frequent complication following breast cancer treatment. While progress is being made in the identification of phenotypic risk factors for the development of LE, little information is available on the molecular characterization of LE. The purpose of this study was to determine if variations in pro- and anti-inflammatory cytokine genes were associated with LE following breast cancer treatment. METHODS AND

resultsBreast cancer patients completed a number of self-report questionnaires. LE was evaluated using bioimpedance spectroscopy. Genotyping was done using a custom genotyping array. No differences were found between patients with (n=155) and without LE (n=387) for the majority of the demographic and clinical characteristics. Patients with LE had a significantly higher body mass index, more advanced disease, and a higher number of lymph nodes removed. Genetic associations were identified for three genes (i.e., interleukin (IL4) 4 (rs2227284), IL 10 (rs1518111), and nuclear kappa factor beta 2 (NFKB2 (rs1056890)) associated with inflammatory responses.

conclusionsThese genetic associations suggest a role for a number of pro- and anti-inflammatory genes in the development of LE following breast cancer treatment.

Indexed as

AdultAgedBreast NeoplasmsCytokinesElectric ImpedanceFemaleGenetic Predisposition to DiseaseGenotypeHumansLymphedemaMastectomyMiddle AgedOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideSurveys and QuestionnairesCytokines

Identifiers

PMID24502445
PMCPMC3961780
OpenAlexW2130541856

What OpenQuestion holds

Textmetadata
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.