Link directly to the doctoral thesis and the whole abstract
Background:
Persistent human papillomavirus (HPV) infection causes cervical intraepithelial neoplasia (CIN). Excisional treatment of CIN has been linked to increased risk of preterm delivery (PTD). The specific mechanism behind is however unclear. Also untreated CIN has been associated with an increased risk of PTD. It is unknown whether this is attributable to the HPV infection itself or other causes.
Aims: To examine whether HPV infection, untreated CIN and/or previous treatment for CIN is associated with PTD and other adverse obstetric outcomes. To study possible causal pathways for an association, including cone length of treatment, changes in cervical microbiota and infectious complications.
Results:
Paper I; HPV infection (HPVtest) compared to NCC was associated with PTD (aOR 1.2, 95% CI 1.0-1.4), and preterm prelabor rupture of membranes (pPROM) (aOR 1.5, 1.2-2.0), but treated women had higher risk compared to women with HPV infection; PTD (aOR 1.7, 1.4-2.0), pPROM (aOR 1.6, 1.2-2.0). Treatment but also HPV infection were associated with increased risk of neonatal mortality and PROM at term and treatment also with chorioamnionitis and neonatal sepsis. Paper II; Treatment was associated with an increased risk of PTD (aOR 1.6, 1.2-2.1), pPROM (aOR 2.7, 1.7-4.5), and PROM at term compared to women with CIN, and risks increased with cone length. Small treatments (≤10 mm) were also associated with increased risk for PTD and pPROM. Paper III; Women positive for high-risk-HPV genotypes at mid-pregnancy had a higher frequency of PTD compared to those negative for high-risk-HPV, but comparisons were non-significant. Paper IV; Treatment resulted in a reduction of non-Lactobacillus bacterial species. More types of bacterial species were detected in women planned for LEEP than in women with NCC. Conclusion: Women with HPV infection have increased risk of PTD, pPROM and neonatal mortality. Excisional treatment for CIN, also minor excisions, increases the risks for PTD and pPROM further compared to having untreated CIN/HPV infection. The risks increase with cone length. Previous treatment is also associated with increased risk of PROM at term and maternal and neonatal infectious complications. Treatment appears not to result in a more diverse or dysbiotic cervical microbiota while CIN is associated with increased bacterial diversity.
