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Does exogenous hormonal therapy affect the risk of glioma among females: A systematic review and meta-analysis.
Alfuridy, Ghady; Alghamdi, Rana; Alkhoshi, Abdulaziz; Mahjari, Ahood; Alhussein, Abdullah; Alshehri, Ebtihaj; Lary, Ahmed; Sabbagh, Abdulrahman; Alomar, Soha.
Afiliación
  • Alfuridy G; College of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Alghamdi R; College of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Alkhoshi A; College of Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Mahjari A; College of Medicine, Faculty of Medicine, Najran University, Najran, Saudi Arabia.
  • Alhussein A; College of Medicine, Faculty of Medicine, King Abdulaziz University, Rabigh, Saudi Arabia.
  • Alshehri E; College of Medicine, Faculty of Medicine, King Khalid University, Abha, Saudi Arabia.
  • Lary A; Division of Neurosurgery, Department of Surgery, Faculty of Medicine, King Abdulaziz Medical City, Jeddah, Saudi Arabia.
  • Sabbagh A; Division of Neurosurgery, Department of Surgery, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Alomar S; Division of Neurosurgery, Department of Surgery, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Neurooncol Adv ; 6(1): vdad167, 2024.
Article en En | MEDLINE | ID: mdl-38405204
ABSTRACT

Background:

The effect of exogenous hormone replacement therapy (HRT) and oral contraceptive pills (OCPs) on glioma risk in females is unclear despite numerous studies; hence, we conducted a meta-analysis to evaluate this relationship.

Methods:

Studies investigating the impact of exogenous female hormones on glioma risk were retrieved by searching 4 databases from inception until September 2022. Articles of any design, such as case-control and cohort studies, proving the relative risk (RR), odds ratio (OR), or hazard ratio were included. Summary OR values were calculated using a random effects model.

Results:

Both HRT and OCP use of any duration decreased the risk of developing glioma [HRT OR = 0.78, 95% CI 0.66-0.91, P = .00; OCP OR = 0.80, 95% CI 0.67-0.96, P = .02]. When stratified by duration of use, HRT use >1 year significantly reduced glioma risk (<1 year OR = 0.82, 95% CI 0.63-1.07, P = 0.15; 1-5 years OR = 0.79, 95% CI 0.67-0.92, P = .00; 5-10 years OR = 0.80, 95% CI 0.66-0.97, P = .02; >10 years OR = 0.69, 95% CI 0.54-0.88, P = .00). In contrast, only OCP use for >10 years significantly reduced glioma risk (<1 year OR = 0.72, 95% CI 0.49-1.05, P = .09; 1-5 years OR = 0.88, 95% CI 0.72-1.02, P = .09; 5-10 years OR = 0.85, 95% CI 0.65-1.1, P = 0.21; >10 years OR = 0.58, 95% CI 0.45-0.74, P = .00).

Conclusions:

Our pooled results strongly suggest that sustained HRT and OCP use is associated with reduced risk of glioma development.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurooncol Adv Año: 2024 Tipo del documento: Article País de afiliación: Arabia Saudita

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurooncol Adv Año: 2024 Tipo del documento: Article País de afiliación: Arabia Saudita
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