» Articles » PMID: 21990406

Frequency, Clinical Associations, and Longitudinal Course of Major Depressive Disorder in Adults with Cerebral Glioma

Overview
Journal J Clin Oncol
Specialty Oncology
Date 2011 Oct 13
PMID 21990406
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: There is a need for high-quality evidence regarding the frequency, independent clinical associations, and longitudinal course of depression in patients with cerebral glioma.

Patients And Methods: This was a twin-center, prospective, observational cohort study with 6-month follow-up. Consenting adults with a new diagnosis of cerebral glioma received the Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition to diagnose major depressive disorder (MDD). Interviews occurred shortly after the start of radiotherapy (T1), with follow-up interviews 3 months later (T2) and 6 months later (T3). Independent associations between MDD and clinical variables were analyzed using logistic regression.

Results: One hundred fifty-five patients participated. The frequency of MDD was 13.5% ± 5.4% at T1 (n = 155); 14.8% ± 6.7% at T2 (n = 108); and 6.8% ± 5.3% at T3 (n = 88). Overall, 32 individuals were diagnosed with MDD during the study period (20.6% ± 6.4%). Inter-rater diagnostic agreement for MDD was good (κ = 0.81; 95% CI, 0.60 to 1.00). Independent predictors of MDD were functional impairment (odds ratio, 3.9; 95% CI, 1.5 to 10.8) and a previous history of depression (odds ratio, 2.7; 95% CI, 0.99 to 7.3). MDD persisted for at least 3 months in half of the patients with adequate follow-up, but many depressed patients also dropped out of the study as a result of clinical deterioration.

Conclusion: In this longitudinal study, one in five patients with glioma developed clinical depression in the 6 months after starting radiotherapy. Patients with functional impairment or previous depression were at higher risk. MDD often persisted for at least 3 months. Clinicians should seek and treat depression in adults with glioma.

Citing Articles

Symptom management in isocitrate dehydrogenase mutant glioma.

Walbert T, Avila E, Boele F, Hertler C, Lu-Emerson C, van der Meer P Neurooncol Pract. 2025; 12(Suppl 1):i38-i48.

PMID: 39776527 PMC: 11703367. DOI: 10.1093/nop/npae088.


Frequency and clinical associations of common mental disorders in adults with high-grade glioma-A multicenter study.

Singer S, Schranz M, Hippler M, Kuchen R, Weiss Lucas C, Meixensberger J Cancer. 2024; 131(1):e35653.

PMID: 39550627 PMC: 11694336. DOI: 10.1002/cncr.35653.


Antidepressants and survival in glioma: Unraveling a complex puzzle.

Rooney A Neurooncol Pract. 2024; 11(2):111-112.

PMID: 38496915 PMC: 10940819. DOI: 10.1093/nop/npae010.


Association between psychiatric disorders and glioma risk: evidence from Mendelian randomization analysis.

Yang W, Han Y, He C, Zhong S, Ren F, Chen Z BMC Cancer. 2024; 24(1):118.

PMID: 38262954 PMC: 10807081. DOI: 10.1186/s12885-024-11865-y.


Chronic stress as an emerging risk factor for the development and progression of glioma.

Yi L, Lin X, She X, Gao W, Wu M Chin Med J (Engl). 2024; 137(4):394-407.

PMID: 38238191 PMC: 10876262. DOI: 10.1097/CM9.0000000000002976.