Pelvic Inflammatory Disease linked to Increased Risk of Serous Borderline Ovarian Tumors, study

The similarity between fallopian tube cells and serous borderline ovarian tumors points to a potential origin link, with salpingitis suggested as a contributing factor in the development of BOTs. Considering this, Sarah Jonsson, Department of Clinical Sciences, Obstetrics and Gynecology, Umeå University, Umeå, Sweden, and colleagues aimed to investigate the potential relationship between pelvic inflammatory disease (PID) and the risk of developing BOT.

For this purpose, the researchers conducted a national population-based case-control study in Sweden, including women diagnosed with borderline ovarian tumors from 1999 to 2020, along with ten matched controls. They analyzed data from nationwide registers using conditional logistic regression, adjusting for factors such as age, residential district, educational level, and parity.

The following were the key findings of the study:

• Among 4782 cases and 45,167 controls, 2.0% of cases and 1.3% of controls had a history of PID.
• Previous PID was associated with an increased risk of BOT overall (aOR, 1.48).
• A significant association was observed with serous tumors (aOR, 1.76), while not with mucinous tumors (aOR, 0.95).
• A dose-response relationship was noted between the number of PID episodes and serous BOT risk.

"This study shows that pelvic inflammatory disease is linked to a heightened risk of serous borderline ovarian tumors, with evidence of a dose-response relationship. The findings emphasize the significant implications of upper reproductive tract infections and inflammation. This highlights the necessity for further exploration of the biological mechanisms involved and the potential effects of PID on the development of serous BOT," the researchers concluded.

Reference:

Jonsson, S., Jonsson, H., Lundin, E., Häggström, C., & Idahl, A. Pelvic inflammatory disease and risk of borderline ovarian tumors: A national population-based case–control study in Sweden. International Journal of Cancer. https://doi.org/10.1002/ijc.35180