Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Mol Psychiatry. 2024 Mar;29(3):602-610. doi: 10.1038/s41380-023-02351-1. Epub 2024 Jan 9.
Although major depression, characterized by a pro-inflammatory profile, genetically overlap with autoimmune disease (AD) and the perinatal period involve immune system adaptations and AD symptom alterations, the bidirectional link between perinatal depression (PND) and AD is largely unexplored. Hence, the objective of this study was to investigate the bidirectional association between PND and AD. Using nationwide Swedish population and health registers, we conducted a nested case-control study and a matched cohort study. From 1,347,901 pregnancies during 2001-2013, we included 55,299 incident PND, their unaffected full sisters, and 10 unaffected matched women per PND case. We identified 41 subtypes of AD diagnoses recorded in the registers and compared PND with unaffected population-matched women and full sisters, using multivariable regressions. Women with an AD had a 30% higher risk of subsequent PND (95% CI 1.2-1.5) and women exposed to PND had a 30% higher risk of a subsequent AD (95% CI 1.3-1.4). Comparable associations were found when comparing exposed women with their unaffected sisters (nested case-control OR: 1.3, 95% CI 1.2-1.5, matched cohort HR: 1.3, 95% CI 1.1-1.6), and when studying antepartum and postpartum depression. The bidirectional association was more pronounced among women without psychiatric comorbidities (nested case-control OR: 1.5, 95% CI 1.4-1.6, matched cohort HR: 1.4, 95% CI 1.4-1.5) and strongest for multiple sclerosis (nested case-control OR: 2.0, 95% CI 1.6-2.3, matched cohort HR: 1.8, 95% CI 1.0-3.1). These findings demonstrate a bidirectional association between AD and PND independent of psychiatric comorbidities, suggesting possibly shared biological mechanisms. If future translational science confirms the underlying mechanisms, healthcare providers need to be aware of the increased risk of PND among women with ADs and vice versa.
虽然重度抑郁症表现出促炎特征,与自身免疫性疾病(AD)在遗传上存在重叠,且围产期涉及免疫系统适应和 AD 症状改变,但围产期抑郁症(PND)和 AD 之间的双向联系在很大程度上仍未得到探索。因此,本研究的目的是调查 PND 和 AD 之间的双向关联。我们使用全国性的瑞典人群和健康登记处进行了嵌套病例对照研究和匹配队列研究。在 2001-2013 年期间的 1347901 例妊娠中,我们纳入了 55299 例新发 PND、未受影响的全同胞姐妹以及每例 PND 病例 10 名未受影响的匹配女性。我们从登记处记录的 41 种 AD 亚型中进行了比较,并使用多变量回归比较了 PND 与未受影响的人群匹配女性和全同胞姐妹。患有 AD 的女性发生后续 PND 的风险增加了 30%(95%CI 1.2-1.5),而暴露于 PND 的女性发生后续 AD 的风险增加了 30%(95%CI 1.3-1.4)。当将暴露于 PND 的女性与未受影响的姐妹进行比较时(嵌套病例对照 OR:1.3,95%CI 1.2-1.5,匹配队列 HR:1.3,95%CI 1.1-1.6),以及当研究产前和产后抑郁症时,也发现了类似的关联。在没有精神共病的女性中,这种双向关联更为明显(嵌套病例对照 OR:1.5,95%CI 1.4-1.6,匹配队列 HR:1.4,95%CI 1.4-1.5),对于多发性硬化症最强(嵌套病例对照 OR:2.0,95%CI 1.6-2.3,匹配队列 HR:1.8,95%CI 1.0-3.1)。这些发现表明,AD 和 PND 之间存在双向关联,与精神共病无关,提示可能存在共同的生物学机制。如果未来的转化科学证实了潜在的机制,医疗保健提供者需要意识到 AD 女性中 PND 的风险增加,反之亦然。