Evidence map›Paper›PMID 36786871›Full record

ArticleCancer causes & control : CCC2023

A comparison of analytic approaches for investigating the obesity paradox in kidney cancer.

Linnea T Olsson, Carolyn E Eberle, Stacey Petruzella, Whitney R Robinson, Helena Furberg

Open access · greenAbstract read
In one paragraph

Article in Cancer causes & control : CCC, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Observational
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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

5 authors at 2 institutions in 1 country.

Linnea T OlssonDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Carolyn E EberleDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Stacey PetruzellaDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Whitney R Robinson *Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Helena Furberg *Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA. furberga@mskcc.org.ORCID http://orcid.org/0000-0003-1887-514X
University of North Carolina at Chapel Hill · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Body composition and the obesity paradox in clear cell renal cell carcinomaR01CA233885 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI FURBERG-BARNES, ANNA HELENA · 2019 to 2023
$3.3M
Resolving the obesity paradox in kidney cancer"R03CA212720 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROBINSON, WHITNEY RAGAN · 2017 to 2018
$184k
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA233885NCI NIH HHS R03 CA212720
6 · The paper itself

Abstract

purposeBody mass index (BMI) and kidney cancer mortality are inconsistently associated in the scientific literature. To understand how study design affects results, we contrasted associations between pre-diagnosis BMI and mortality under different analytic scenarios in a large, population-based prospective cohort study.

methodsUsing data from the NIH-AARP Diet and Health Study (1995-2011), we constructed two cohorts: a "full at-risk" cohort with no kidney cancer history at baseline (n = 252,845) and an "incident cancer" subset who developed kidney cancer during follow-up (n = 1,652). Cox Proportional Hazards models estimated hazard ratios (HR) and 95% confidence intervals (CI) between pre-diagnosis BMI and mortality for different outcomes (all-cause and cancer-specific mortality), in the different cohorts (full at-risk vs. incident cancer cohort), and with different covariates (minimally vs. fully adjusted). For the incident cancer cohort, we also examined time to mortality using different timescales: from enrollment or diagnosis.

resultsIn the full at-risk study population, higher pre-diagnosis BMI was associated with greater cancer-specific mortality in fully adjusted multivariable models, particularly for obese participants [HR, (95% CI): 1.76, (1.38-2.25)]. This association was less pronounced in the incident cancer cohort [1.50, (1.09-2.07)]. BMI was not strongly associated with all-cause mortality in either cohort in fully adjusted models [full cohort: 1.03, (1.01, 1.06); incident cancer cohort: 1.20, (0.97, 1.48)].

conclusionsPopulations characterized by high adult BMI will likely experience greater population burdens of mortality from kidney cancer, partially because of higher rates of kidney cancer diagnosis. Questions regarding overall mortality burden and post-diagnosis cancer survivorship are distinct and require different study designs.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAdultBody Mass IndexHumansObesityObesity ParadoxProportional Hazards ModelsProspective StudiesRisk FactorsBMI paradoxCausal inferenceEpidemiologyMethodologicalObesity paradoxRisk factors for cancer mortality

Identifiers

PMID36786871
PMCPMC10448500
OpenAlexW4320710536

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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.