Evidence map›Paper›PMID 36752520›Full record

ArticleJNCI cancer spectrum2023

Allostatic load and cardiovascular outcomes in males with prostate cancer.

Nickolas Stabellini, Jennifer Cullen, Marcio S Bittencourt, Justin X Moore, Lifen Cao, Neal L Weintraub, Ryan A Harris, Xiaoling Wang, Biplab Datta, Steven S Coughlin and 9 more

Open access · goldFull text read
In one paragraph

Article in JNCI cancer spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Allostatic Load and Cardiovascular Disease: A Systematic Review.American journal of preventive medicine · 2025
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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

19 authors at 9 institutions in 3 countries.

Nickolas StabelliniGraduate Education Office, Case Western Reserve University School of Medicine, Cleveland, OH, USA.ORCID 0000-0002-3135-7980
Jennifer CullenDepartment of Population and Quantitative Health Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Marcio S BittencourtDivision of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Justin X MooreCancer Prevention, Control, & Population Health Program, Department of Medicine, Medical College of Georgia at Augusta University, GA, USA.
Lifen CaoDepartment of Hematology-Oncology, University Hospitals Seidman Cancer Center, Cleveland, OH, USA.
Neal L WeintraubDepartment of Medicine, Cardiology Division, Medical College of Georgia at Augusta University, Augusta, GA, USA.
Ryan A HarrisDepartment of Medicine, Georgia Prevention Institute, Augusta University, Augusta, GA, USA.
Xiaoling WangDepartment of Medicine, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Biplab DattaDepartment of Population Health Sciences, Medical College of Georgia, Augusta University, Augusta, GA, USA.ORCID 0000-0002-2559-850X
Steven S CoughlinDepartment of Population Health Sciences, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Jorge GarciaDepartment of Hematology-Oncology, University Hospitals Seidman Cancer Center, Cleveland, OH, USA.
John ShanahanCancer Informatics, Seidman Cancer Center at University Hospitals of Cleveland, Cleveland, OH, USA.
Nelson HamerschlakOncohematology Department, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
Kristin WaiteTrans-Divisional Research Program (TDRP), Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Nathanael R FillmoreCooperative Studies Program (CSP) Informatics Center, Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC), VA Boston Healthcare System, Boston, MA, USA.
Martha TerrisUrology Section, Department of Surgery, Veterans Affairs Medical Centers, Augusta, GA, USA.
Alberto J MonteroDepartment of Hematology-Oncology, University Hospitals Seidman Cancer Center, Cleveland, OH, USA.
Jill S Barnholtz-SloanTrans-Divisional Research Program (TDRP), Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Avirup GuhaDepartment of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH, USA.ORCID 0000-0003-0253-1174
Augusta University · USUniversity Hospitals Seidman Cancer Center · USHospital Israelita Albert Einstein · BRNational Institutes of Health · USCase Comprehensive Cancer CenterHarvard University · USUniversity Hospitals of Cleveland · USUniversity of Pittsburgh · USUniversity of Ulster · GB

Funding

Neuronal HDAC9, Synaptic Plasticity and Alzheimer's DiseaseR01AG076235 · NIA · AUGUSTA UNIVERSITY · PI Xin-Yun Lu, Neal L Weintraub · 2022 to 2026
$2.8M
Innovative Approaches to Treat Duchenne Muscular Dystrophy Using iPSC-Derived Muscle ProgenitorsR01AR070029 · NIAMS · AUGUSTA UNIVERSITY · PI ASHRAF, MUHAMMAD, TANG, YAO LIANG · 2016 to 2021
$2.6M
Mechanisms of myeloperoxidase and Nox4 interactions in abdominal aortic aneurysmR01HL142097 · NHLBI · AUGUSTA UNIVERSITY · PI WEINTRAUB, NEAL L · 2018 to 2021
$2.1M
NHLBI NIH HHS R01 HL142097NIAMS NIH HHS R01 AR070029NIA NIH HHS R01 AG076235
6 · The paper itself

Abstract

backgroundCardiovascular disease (CVD) is the leading cause of death in men with prostate cancer (PC). Accumulated stress plays an important role in CVD development. The cumulative burden of chronic stress and life events can be measured using allostatic load (AL).

methodsThe initial cohort included males aged 18 years and older diagnosed with PC (2005-2019). AL was modeled as an ordinal variable (0-11). Fine-Gray competing risk regressions measured the impact of precancer diagnosis AL and postdiagnosis AL in 2-year major cardiac events (MACE). The effect of AL changes over time on MACE development was calculated via piecewise Cox regression (before, and 2 months, 6 months, and 1 year after PC diagnosis).

resultsWe included 5261 PC patients of which 6.6% had a 2-year MACE. For every 1-point increase in AL before and within 60 days after PC diagnosis, the risk of MACE increased 25% (adjusted hazard ratio [aHR] =1.25, 95% confidence interval [CI] = 1.18 to 1.33) and 27% (aHR = 1.27, 95% CI = 1.20 to 1.35), respectively. Using AL as a time-varying exposure, the risk of MACE increased 19% (aHR = 1.19, 95% CI = 1.11 to 1.27), 22% (aHR = 1.22, 95% CI = 1.14 to 1.33), 28% (aHR = 1.28, 95% CI = 1.23 to 1.33), and 31% (aHR = 1.31, 95% CI = 1.27 to 1.35) for every 1-point increase in AL before, 2 months after, 6 months after, and 1 year after PC diagnosis, respectively.

conclusionAL and its changes over time are associated with MACE in PC patients, suggesting a role of a biological measure of stress as a marker of CVD risk among men with PC.

Indexed as

AllostasisCardiovascular DiseasesProstatic NeoplasmsHumansMale

Identifiers

PMID36752520
PMCPMC10005613
OpenAlexW4319461603

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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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.