Introduction
Inflammatory bowel disease (IBD) commonly affects women of reproductive age. Although both pregnancy and IBD have been associated with an increased risk of major adverse cardiovascular events (MACE), the risk of MACE during pregnancy and after delivery among women with IBD is not well characterized.
Aims & Methods
We conducted a population-based cohort and case-control study including all women with a delivery resulting in live birth in Switzerland between 2012 and 2022. Women with and without IBD were followed from discharge after delivery hospitalization to assess the risk of MACE, defined as a composite of acute myocardial infarction, stroke, hospitalization for heart failure, or all-cause mortality. Follow-up was divided into a postpartum period (≤3 months) and long-term follow-up. Women were censored at the time of a subsequent pregnancy, an outcome event, or the end of the study period. Weighted hazard ratios (HR) were estimated using Cox regression. To study the MACE risk during pregnancy (divided into pregnancy period [defined as 10 months prior to delivery hospitalization excluding delivery hospitalization] and delivery hospitalization), we conducted a case-control study and estimated odds ratios (OR) using weighted logistic regression. In both analyses, stabilized inverse probability of treatment weighting (IPTW) was used to balance baseline covariates.
Results
Among 658,776 women with a delivery resulting in live birth, 1,831 had IBD (Crohn's disease, n=1,021; ulcerative colitis, n=810). During a median follow-up of 3.4 years, MACE occurred in 9 women with IBD (incidence rate [IR], 8.7 per 100,000 person-years) and 1,398 women without IBD (IR, 3.9 per 100,000 person-years), yielding a weighted HR of 2.21 (95% confidence interval [CI], 1.05-4.64). This association was primarily driven by stroke (HR, 3.06; 95% CI, 1.02-9.16), whereas no significant associations were observed for the other MACE components. Most events occurred beyond 3 months after delivery in both groups (women with IBD: 89%; women without IBD: 84%). No significant differences were observed according to IBD subtype or other predefined subgroups (age, multiple gestation, prior MACE, prior VTE). In the case-control analysis, IBD was not associated with increased MACE risk during pregnancy (odds ratio [OR], 0.73; 95% CI, 0.10-5.26) or at delivery hospitalization (OR, 1.62; 95% CI, 0.30-8.73).
Period
| Events in Women with IBD
| Events in Women without IBD
| HR / OR
| P-value
|
N (%)
| N (%)
| (95% CI)
|
Pregnancy
| 1 (0.05)
| 88 (0.01)
| 0.73 (0.10-5.26)
| 0.76
|
Delivery Hospitalization
| 2 (0.11)
| 235 (0.04)
| 1.62 (0.30-8.73)
| 0.58
|
Postpartum Period
| 1 (0.05)
| 226 (0.03)
| 0.29 (0.04-2.03)
| 0.21
|
Long-term Follow-Up
| 9 (0.49)
| 1,398 (0.21)
| 2.21 (1.05-4.64)
| 0.04
|
Table 1: MACE risk across pregnancy and postpartum periods in women with and without IBD.
IPTW-adjusted. Pregnancy and delivery hospitalization: OR (weighted logistic regression); postpartum period and long-term follow-up: HR (weighted Cox regression).
Conclusion
Among women with a delivery resulting in live birth, IBD was not associated with an increased MACE risk during pregnancy or the postpartum period. However, women with IBD had a more than twofold higher long-term risk of MACE after delivery, primarily driven by stroke. These findings support consideration of long-term cardiovascular risk assessment in women with IBD after pregnancy.