Evidence map›Paper›PMID 41709045›Full record

ArticleJournal of neuro-oncology2026

The effect of sex on vestibular schwannoma incidence varies across the lifespan and modifies associations with race/ethnicity.

Kajal V Parmar, Mackenzie Price, Syed M Adil, Julia R Benedetti, Carol Kruchko, Kyle M Walsh, Quinn T Ostrom

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Kajal V Parmar *Department of Neurosurgery, Duke University School of Medicine, DUMC Box 3050, Durham, NC, USA.
Mackenzie Price *Central Brain Tumor Registry of the United States, Hinsdale, IL, USA.
Syed M AdilDepartment of Neurosurgery, Duke University School of Medicine, DUMC Box 3050, Durham, NC, USA.
Julia R BenedettiDepartment of Neurosurgery, Duke University School of Medicine, DUMC Box 3050, Durham, NC, USA.
Carol KruchkoCentral Brain Tumor Registry of the United States, Hinsdale, IL, USA.
Kyle M WalshDepartment of Neurosurgery, Duke University School of Medicine, DUMC Box 3050, Durham, NC, USA.
Quinn T OstromDepartment of Neurosurgery, Duke University School of Medicine, DUMC Box 3050, Durham, NC, USA. Quinn.Ostrom@duke.edu.

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI Laura Fish · 1985 to 2026
$174.8M
Targeted Alpha-Particle Radiotheraphy of Brain Tumors with 211At-81C6 AntibodyP50CA190991 · NCI · DUKE UNIVERSITY · PI ALI-OSMAN, FRANCIS, ASHLEY, DAVID M. · 2014 to 2023
$20.8M
NCI NIH HHS P30 CA014236NCI NIH HHS P50 CA190991U.S. Centers for Disease Control and Prevention 75D30123P17556U.S. National Cancer Institute P30CA014236
6 · The paper itself

Abstract

purposeVestibular schwannoma (VS) is a benign tumor of the eighth cranial nerve with incidence that differs by age, sex, and race/ethnicity. Prior research has not characterized how the contributions of sex and race/ethnicity to VS risk may interact or vary by age. We sought to examine the joint contributions of age, sex, and race/ethnicity to VS risk using nationally-representative data.

methodsDiagnoses of non-malignant, intracranial VS were extracted from the Central Brain Tumor Registry of the United States (CBTRUS, 2004–2020) and used to calculate average age-adjusted annual incidence rates (AAAIRs) and incidence rate ratios (IRRs). Poisson regression was used to evaluate associations of VS risk with sex, race/ethnicity, and their interaction (sex*race/ethnicity), both overall and in ten-year intervals of age.

resultsOver an eighteen-year period, 78,002 unique individuals received a new diagnosis of VS (52.9% female). Females were at elevated risk compared to males from ages 10–59, after which this trend inverted with males at increased risk. Compared to non-Hispanic White individuals, Hispanic and non-Hispanic Black individuals were at significantly reduced risk of VS throughout the lifespan. The protective effect of non-Hispanic Black race/ethnicity was apparent among both females (IRR = 0.40; 95% CI: 0.38–0.42) and males (IRR = 0.36; 95% CI: 0.34–0.38), but was significantly stronger among males (Pinteraction<0.001).

conclusionsAge significantly modifies the relationship between sex and risk of VS, while sex significantly modifies the relationship between race/ethnicity and risk of VS. Findings underscore the importance of incorporating demographic data into studies of VS biology, diagnosis, and clinical management.

Indexed as

EthnicityNeuroma, AcousticAdolescentAdultAgedAged, 80 and overBlack or African AmericanChildFemaleHispanic or LatinoHumansIncidenceMaleMiddle AgedRegistriesRisk FactorsAcoustic neuromaAfrican AmericansIncidenceRisk factorsVestibular schwannoma

Identifiers

PMID41709045
PMCPMC13215001

What Socratic holds

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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 Socratic graph.