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Case-control study, 2024

Are premenstrual disorders and postpartum depression connected?

Yes, they are connected both ways. Women with premenstrual disorders are 4.76 times more likely to develop postpartum depression. Women with postpartum depression are 1.81 times more likely to develop premenstrual disorders later.

Strong study design 1,041,419 Swedish women with singleton pregnancies, 2001-2018

What they did

Analyzed Swedish medical records from 2001-2018 of 1,041,419 women with 1,803,309 pregnancies. Compared women who had postpartum depression with matched controls to see if they had premenstrual disorders before pregnancy. Then followed women after giving birth to see who developed premenstrual disorders.

What they found

Of women with postpartum depression, 2.9% had premenstrual disorders before pregnancy compared to 0.6% of controls. Women with postpartum depression had 1.81 times higher risk of developing premenstrual disorders later (7.6 per 1,000 person-years versus 3.8 per 1,000). The connection worked both directions.

What it means for you

Premenstrual disorders and postpartum depression share a root cause and may influence each other. Women with either condition should be screened for the other. The study used real medical records from a large population, making results reliable, but it cannot prove one condition causes the other.

1,041,419

Women studied

4.76

Increased risk of postpartum depression with prior PMS

1.81

Increased risk of PMS after postpartum depression

About the study

Original title
The bidirectional association between premenstrual disorders and perinatal depression: A nationwide register-based study from Sweden
Authors
Yang Q, Bränn E, Bertone-Johnson ER et al.
Journal
PLoS medicine
Year
2024
Study design
Case-control study
Participants
1,041,419
What was tested
None (observational study)
Open access
Yes
Original abstract

Background: Premenstrual disorders (PMDs) and perinatal depression (PND) share symptomology and the timing of symptoms of both conditions coincide with natural hormonal fluctuations, which may indicate a shared etiology. Yet, there is a notable absence of prospective data on the potential bidirectional association between these conditions, which is crucial for guiding clinical management. Using the Swedish nationwide registers with prospectively collected data, we aimed to investigate the bidirectional association between PMDs and PND. Methods and findings: With 1,803,309 singleton pregnancies of 1,041,419 women recorded in the Swedish Medical Birth Register during 2001 to 2018, we conducted a nested case-control study to examine the risk of PND following PMDs, which is equivalent to a cohort study, and transitioned that design into a matched cohort study with onward follow-up to simulate a prospective study design and examine the risk of PMDs after PND (within the same study population). Incident PND and PMDs were identified through clinical diagnoses or prescribed medications. We randomly selected 10 pregnant women without PND, individually matched to each PND case on maternal age and calendar year using incidence density sampling (N: 84,949: 849,482). We (1) calculated odds ratio (OR) and 95% confidence intervals (CIs) of PMDs using conditional logistic regression in the nested case-control study. Demographic factors (country of birth, educational level, region of residency, and cohabitation status) were adjusted for. We (2) calculated the hazard ratio (HR) and 95% CIs of PMDs subsequent to PND using stratified Cox regression in the matched cohort study. Smoking, BMI, parity, and history of psychiatric disorders were further controlled for, in addition to demographic factors. Pregnancies from full sisters of PND cases were identified for sibling comparison, which contrasts the risk within each set of full sisters discordant on PND. In the nested case-control study, we identified 2,488 PMDs (2.9%) before pregnancy among women with PND and 5,199 (0.6%) among controls. PMDs were associated with a higher risk of subsequent PND (OR 4.76, 95% CI [4.52,5.01]; p < 0.001). In the matched cohort with a mean follow-up of 7.40 years, we identified 4,227 newly diagnosed PMDs among women with PND (incidence rate (IR) 7.6/1,000 person-years) and 21,326 among controls (IR 3.8). Compared to their matched controls, women with PND were at higher risk of subsequent PMDs (HR 1.81, 95% CI [1.74,1.88]; p < 0.001). The bidirectional association was noted for both prenatal and postnatal depression and was stronger among women without history of psychiatric disorders (p for interaction < 0.001). Sibling comparison showed somewhat attenuated, yet statistically significant, bidirectional associations. The main limitation of this study was that our findings, based on clinical diagnoses recorded in registers, may not generalize well to women with mild PMDs or PND. Conclusions: In this study, we observed a bidirectional association between PMDs and PND. These findings suggest that a history of PMDs can inform PND susceptibility and vice versa and lend support to the shared etiology between both disorders.

Reproduced under CC-BY.

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