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A Matched Case-Control Study Examining the Association Between Exposure to Depot Medroxyprogesterone Acetate and
Russell Griffin1, Rebecca Arend2
1Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Abstract:
The recent literature has reported an increased association between the use of depot medroxyprogesterone acetate (dMPA) and cerebral meningioma (CM). Prior studies have been limited in generalizability and did not use an active comparator as a control. The current matched case-control study utilized a bootstrapped sampling design, matching 241 CM cases with controls (i.e., women diagnosed with non-meningioma brain, breast, or skin tumor, one control per type for three total) on age ± 5 years and diagnosis date ± 3 months. Conditional logistic regression was used to estimate odds ratios (ORs) compared with an active (norethindrone or levonorgestrel) and non-active control group. Exposure to dMPA at any time point was not associated with the diagnosis of cerebral meningioma (OR 1.75, 95% CI 0.81-4.95). Exposure to dMPA within a year of diagnosis was associated with the diagnosis of CM compared to both an active control (OR 3.38, 95% CI 1.13-9.70) and a non-active control (OR 6.90, 95% CI 2.31-17.58). This association was also present for those who were exposed within two years prior when compared to a non-active control (OR 3.54, 95% CI 1.50-11.88) but not an active control. Combined with the prior literature, the current results suggest that future research is warranted to understand this association.
Insights
Depot medroxyprogesterone acetate (dMPA) use showed no overall link to cerebral meningioma (CM). However, recent dMPA exposure was associated with increased CM risk, particularly when compared to non-active controls.
Area of Science:
- Neuro-oncology
- Endocrinology
- Epidemiology
Background:
- Recent literature suggests a potential link between depot medroxyprogesterone acetate (dMPA) and cerebral meningioma (CM).
- Previous studies lacked generalizability and active comparators, necessitating further investigation.
- Understanding this association is crucial for patient safety and informed clinical practice.
Purpose of the Study:
- To investigate the association between dMPA use and the risk of developing cerebral meningioma (CM).
- To address limitations of prior studies by employing an active comparator group.
- To provide robust epidemiological data on dMPA and CM risk.
Main Methods:
- A matched case-control study design was utilized.
- 241 CM cases were matched with controls (diagnosed with non-meningioma brain, breast, or skin tumors) on age and diagnosis date.
- Conditional logistic regression was used to estimate odds ratios (ORs) comparing dMPA exposure against active and non-active controls.
Main Results:
- Overall dMPA exposure was not significantly associated with cerebral meningioma (OR 1.75).
- Exposure to dMPA within one year of diagnosis showed a significant association with CM risk (OR 3.38 vs. active control; OR 6.90 vs. non-active control).
- Exposure within two years prior to diagnosis was associated with CM risk compared to non-active controls (OR 3.54).
Conclusions:
- While overall dMPA use was not linked to CM, recent exposure (within 1-2 years) demonstrated a significant association.
- These findings, in conjunction with existing literature, highlight the need for further research into the dMPA-CM relationship.
- The results underscore the importance of considering recent hormonal contraceptive use in the differential diagnosis of cerebral meningioma.
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