Evidence map›Paper›PMID 40703807›Full record

ArticleNeuro-oncology advances

Long-term psychological and neurological outcomes among people with a history of non-malignant meningioma in the UK Biobank cohort.

Diana R Withrow, Fahad S Al-Huda, Helen Bulbeck, Krishnan Bhaskaran, Robin Grant, Usama Ali, Pieter Pretorius, Jason L Oke, Brian D Nicholson

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

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Diana R WithrowNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford.ORCID https://orcid.org/0000-0002-9757-040X
Fahad S Al-HudaNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford.
Helen Bulbeckbrainstrust, Cowes, Isle of Wight.ORCID https://orcid.org/0000-0002-6775-5251
Krishnan BhaskaranDepartment of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London.ORCID https://orcid.org/0000-0001-5364-8757
Robin GrantDepartment of Clinical Neurosciences, Royal Infirmary of Edinburgh, Edinburgh.ORCID https://orcid.org/0000-0003-2597-9510
Usama AliNuffield Department of Population Health, University of Oxford, Oxford.ORCID https://orcid.org/0000-0003-0313-4429
Pieter PretoriusDepartment of Neuroradiology, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust.
Jason L OkeAbbott Diabetes Care, Witney, Oxfordshire.
Brian D NicholsonNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Meningiomas are among the most common brain tumours in the United Kingdom and incidence is increasing. Up to 90% of meningiomas are Grade 1 (non-malignant) and have high survival. Brain tumour survivors are at risk of psychological and neurological late effects but risks in persons with non-malignant meningioma are not well characterized. Methods: We used UK Biobank, a cohort of approximately 500 000 adults recruited ages 40-69 during 2006-2010. Non-malignant meningioma patients were identified through linked cancer registry data. Follow-up for 10 outcomes was based on linkage to Hospital Episode Statistics. Standardized incidence ratios (SIRs) compared risks in meningioma patients to rates from UK Biobank overall, adjusted for age, sex, and calendar time. Results: Four hundred and sixty-seven individuals were diagnosed with non-malignant meningioma after joining UK Biobank (77% female). Median age at diagnosis was 65 and median follow-up was 5 years. Persons with meningioma had significantly increased risks of 9 of 10 sequelae studied. The lowest SIR was for stroke (1.3, 95% confidence interval [CI] 0.6-2.9) and the highest SIRs were for epilepsy (18.9, 95%CI: 13.3-26.9) and visual disturbances (6.6, 95%CI: 3.3-13.1). SIRs for depression, anxiety, headache, fatigue, hearing loss, limb weakness, and cognitive issues (in ascending order) ranged from 2.3 (95%CI: 1.6-3.4) to 4.4 (95%CI: 2.8-6.9). Conclusions: By providing preliminary evidence of excess risk of a range of long-term sequelae, this research can provide insight into future risks and validate survivor experience for people diagnosed with non-malignant meningioma and build momentum for future research using larger population-based databases and primary care records.

Indexed as

brain tumourslate effectsmeningiomasurvivorship

Identifiers

PMID40703807
PMCPMC12284636

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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.