Lozowchuk Alexandria, Carroll Judith E, Hobel Calvin, Coussons-Read Mary, Dunkel Schetter Christine, Ross Kharah M
Psychology Department, University of Calgary, Calgary, AB, Canada.
Cousins Center for Psychoneuroimmunology, Department of Psychiatry & Biobehavioral Sciences, Jane & Terry Semel Institute for Neuroscience and Human Behavior, University of California - Los Angeles, Los Angeles, CA, United States.
Brain Behav Immun. 2023 Nov;114:407-413. doi: 10.1016/j.bbi.2023.09.007. Epub 2023 Sep 11.
Inflammatory activity during pregnancy and the postpartum period shifts systematically due to pregnancy progression, delivery, and postpartum recovery. Factors that deregulate inflammatory activity increase the risk for adverse pregnancy outcomes and slower postpartum recovery. The IL-6:IL-10 or TNF-α:IL-10 ratio is potentially one way to capture peripheral inflammatory regulation; higher values indicate that anti-inflammatory IL-10 is less effective at regulating pro-inflammatory TNF-α or IL-6, skewing towards maladaptive pro-inflammatory profiles. Associations between partner relationship quality and IL-6:IL-10 or TNF-α:IL-10 trajectories during pregnancy and the postpartum period have not been assessed. The purpose of this study was to test whether partner relationship quality (support, conflict) is associated with attenuated IL-6, IL-10, TNF-α, TNF-α:IL-10 or IL-6:IL-10 trajectories from the third trimester to the postpartum period.
A sample of 162 women from the Healthy Babies Before Birth study reported on partner relationship quality (support and conflict) using the Social Support Effectiveness Questionnaire during the third trimester. Plasma samples were collected in the third trimester and at 1-, 6- and 12-months postpartum, and assayed for TNF-α, IL-6 and IL-10. Associations between both indicators of relationship quality (support and conflict) and TNF-α, IL-6, IL-10, IL-6:IL-10, TNF-α:IL-10 trajectories were tested using multi-level modelling, controlling for sociodemographic, pregnancy and health variables.
Partner support interacted with time to predict IL-6:IL-10 trajectories, linear: b = -0.176, SE = 0.067, p =.010, quadratic: b = 0.012, SE = 0.005, p =.009. Lower partner support was associated with steeper increases in IL-6:IL-10 from the third trimester to 6 months postpartum, followed by steeper decreases in IL-6:IL-10 from 6 months postpartum to a year after birth. Partner conflict was not associated with IL-6:IL-10 levels at study entry, b = 0.233, SE = 0.219, p =.290, or over time, p's > 0.782. Neither indicator of partner relationship quality was associated with TNF-α, IL-6, IL-10, or TNF-α:IL-10 trajectories, p's > 0.205.
Lower partner support may be associated with reduced moderation of IL-6 by IL-10 between pregnancy and a year postpartum, with possible consequences for maternal health and well-being.
孕期及产后炎症活动会因妊娠进展、分娩及产后恢复而系统性地发生变化。炎症活动失调的因素会增加不良妊娠结局及产后恢复缓慢的风险。白细胞介素-6(IL-6)与白细胞介素-10(IL-10)的比值或肿瘤坏死因子-α(TNF-α)与IL-10的比值可能是反映外周炎症调节的一种方式;比值越高表明抗炎性的IL-10在调节促炎性的TNF-α或IL-6方面效果越差,从而倾向于适应不良的促炎状态。伴侣关系质量与孕期及产后IL-6与IL-10或TNF-α与IL-10变化轨迹之间的关联尚未得到评估。本研究的目的是检验伴侣关系质量(支持、冲突)是否与妊娠晚期至产后IL-6、IL-10、TNF-α、TNF-α与IL-10或IL-6与IL-10的变化轨迹减弱有关。
来自“出生前健康宝宝”研究的162名女性样本在妊娠晚期使用社会支持有效性问卷报告了伴侣关系质量(支持和冲突)。在妊娠晚期以及产后1个月、6个月和12个月采集血浆样本,检测TNF-α、IL-6和IL-10。使用多层次模型检验关系质量的两个指标(支持和冲突)与TNF-α、IL-6、IL-10、IL-6与IL-10、TNF-α与IL-10变化轨迹之间的关联,并对社会人口统计学、妊娠和健康变量进行控制。
伴侣支持与时间相互作用以预测IL-6与IL-10的变化轨迹,线性关系:b = -0.176,标准误 = 0.067,p = 0.010,二次关系:b = 0.012,标准误 = 0.005,p = 0.009。伴侣支持较低与妊娠晚期至产后6个月IL-6与IL-10的急剧上升有关,随后是产后6个月至产后一年IL-6与IL-10的急剧下降。伴侣冲突与研究开始时IL-6与IL-10水平无关,b = 0.233,标准误 = 0.219,p = 0.290,随时间变化也无关,p值 > 0.782。伴侣关系质量的两个指标均与TNF-α、IL-6、IL-10或TNF-α与IL-10的变化轨迹无关,p值 > 0.205。
伴侣支持较低可能与妊娠至产后一年期间IL-10对IL-6的调节作用减弱有关,这可能会对母亲的健康和幸福产生影响。