Evidence map›Paper›PMID 31152675›Full record

ArticleThe Journal of nutrition2019

Prediagnostic Proinflammatory Dietary Potential Is Associated with All-Cause Mortality among African-American Women with High-Grade Serous Ovarian Carcinoma.

Lauren C Peres, James R Hebert, Bo Qin, Kristin A Guertin, Elisa V Bandera, Nitin Shivappa, Tareq F Camacho, Deanna Chyn, Anthony J Alberg, Jill S Barnholtz-Sloan and 8 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in The Journal of nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

18 authors at 11 institutions in 1 country.

Lauren C PeresDepartment of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
James R HebertCancer Prevention and Control Program.
Bo QinCancer Prevention and Control Program, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Kristin A GuertinDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA.
Elisa V BanderaCancer Prevention and Control Program, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Nitin ShivappaCancer Prevention and Control Program.
Tareq F CamachoDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA.
Deanna ChynDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA.
Anthony J AlbergCancer Prevention and Control Program.
Jill S Barnholtz-SloanCase Comprehensive Cancer Center, Case Western Reserve University School of Medicine, Cleveland, OH.
Melissa L BondyDepartment of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, TX.
Michele L CoteKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI.
Ellen FunkhouserDivision of Preventive Medicine, University of Alabama at Birmingham, Birmingham, AL.
Patricia G MoormanDepartment of Community and Family Medicine, Duke University Medical Center, Durham, NC.
Edward S PetersDepartment of Epidemiology, Louisiana State University Health Sciences Center School of Public Health, New Orleans, LA.
Ann G SchwartzKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI.
Paul D TerryDepartment of Medicine, University of Tennessee Graduate School of Medicine, Knoxville, TN.
Joellen M SchildkrautDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA.
University of Virginia · USUniversity of South Carolina · USRutgers, The State University of New Jersey · USWayne State University · USBaylor College of Medicine · USCase Western Reserve University · USDuke Medical Center · USLouisiana State University Health Sciences Center New Orleans · USMoffitt Cancer Center · USUniversity of Alabama at Birmingham · USUniversity of Tennessee at Knoxville · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
Epidemiology of Ovarian Cancer in African-American WomenR01CA142081 · NCI · UNIVERSITY OF VIRGINIA · PI SCHILDKRAUT, JOELLEN M. · 2010 to 2015
$10.6M
The Role of Inflammation in the Racial Disparities in Ovarian Cancer SurvivalR00CA218681 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI PERES, LAUREN COLE · 2018 to 2020
$722k
NovaSeq Shared Instrumentation Grant for Wayne State UniversityS10OD025170 · OD · WAYNE STATE UNIVERSITY · PI RUDEN, DOUGLAS M · 2018 to 2018
$600k
The Role of Inflammation in the Racial Disparities in Ovarian Cancer SurvivalK99CA218681 · NCI · UNIVERSITY OF VIRGINIA · PI PERES, LAUREN COLE · 2017 to 2017
$95k
NCCDPHP CDC HHS U58 DP003931NCI NIH HHS HHSN261201000028CNCI NIH HHS HHSN261201200021INCI NIH HHS HHSN261201300021CNCI NIH HHS K99 CA218681NCI NIH HHS P30 CA022453NCI NIH HHS R00 CA218681NCI NIH HHS R01 CA142081NIH HHS S10 OD025170
6 · The paper itself

Abstract

backgroundChronic inflammation is associated with ovarian carcinogenesis; yet, the impact of inflammatory-related exposures on outcomes has been understudied.

objectiveGiven the poor survival of women diagnosed with ovarian cancer, especially African-Americans, we examined whether diet-associated inflammation, a modifiable source of chronic systemic inflammation measured by the dietary inflammatory index (DII), was associated with all-cause mortality among African-American women with ovarian carcinoma.

methodsData were available from 490 ovarian carcinoma patients enrolled in a population-based case-control study of African-American women with ovarian cancer, the African-American Cancer Epidemiology Study. Energy-adjusted DII (E-DII) scores were calculated based on prediagnostic dietary intake of foods alone or foods and supplements, which was self-reported using the 2005 Block Food Frequency Questionnaire. Cox proportional hazards regression was used to estimate risk of mortality overall and for the most common histotype, high-grade serous carcinoma. Additionally, we assessed interaction by age at diagnosis and smoking status.

resultsWomen included in this study had a median age of 57 y, and the majority of women were obese (58%), had late-stage disease (Stage III or IV, 66%), and had high-grade serous carcinoma (64%). Greater E-DII scores including supplements (indicating greater inflammatory potential) were associated with an increased risk of mortality among women with high-grade serous carcinoma (HR1-unit change: 1.08; 95% CI: 1.01, 1.17). Similar associations were observed for the E-DII excluding supplements, although not statistically significant (HR1-unit change: 1.07; 95% CI: 0.97, 1.17). There was an interaction by smoking status, where the positive association with mortality was present only among ever smokers (HRQuartile 4/Quartile 1: 2.36; 95% CI: 1.21, 4.60) but not among never smokers.

conclusionsGreater inflammatory potential of prediagnostic diet may adversely impact prognosis among African-American women with high-grade serous carcinoma, and specifically among ever smokers.

Indexed as

AdultAgedBlack or African AmericanCase-Control StudiesCystadenocarcinoma, SerousDietFemaleHumansInflammationMiddle AgedOvarian NeoplasmsProportional Hazards ModelsSmokingAfrican-American womencancer epidemiologydietdietary inflammatory indexgynecologic malignanciesinflammationovarian cancerrace/ethnicity

Identifiers

PMID31152675
PMCPMC6735701
OpenAlexW2946988141

What OpenQuestion holds

Textmetadata
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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.