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本文引用的文献

1
Perinatal mood and anxiety disorders: biomarker discovery using plasma proteomics.围产期情绪和焦虑障碍:使用血浆蛋白质组学进行生物标志物发现。
Am J Obstet Gynecol. 2023 Aug;229(2):166.e1-166.e16. doi: 10.1016/j.ajog.2023.01.012. Epub 2023 Jan 14.
2
Association between diagnosed perinatal mood and anxiety disorders and adverse perinatal outcomes.围产期情绪和焦虑障碍与不良围产期结局的关联。
J Matern Fetal Neonatal Med. 2022 Dec;35(25):9066-9070. doi: 10.1080/14767058.2021.2014450. Epub 2021 Dec 8.
3
Inflammatory and immune marker trajectories from pregnancy to one-year post-birth.从怀孕到产后一年的炎症和免疫标志物轨迹。
Cytokine. 2022 Jan;149:155758. doi: 10.1016/j.cyto.2021.155758. Epub 2021 Nov 11.
4
Maternal Mid-Gestation Cytokine Dysregulation in Mothers of Children with Autism Spectrum Disorder.自闭症谱系障碍患儿母亲妊娠中期细胞因子失调。
J Autism Dev Disord. 2022 Sep;52(9):3919-3932. doi: 10.1007/s10803-021-05271-7. Epub 2021 Sep 9.
5
Cytokine levels throughout the perinatal period.围生期的细胞因子水平。
J Matern Fetal Neonatal Med. 2022 Dec;35(25):5513-5519. doi: 10.1080/14767058.2021.1887121. Epub 2021 Feb 28.
6
Longitudinal plasma inflammatory proteome profiling during pregnancy in the Born into Life study.《生于生命研究》中妊娠期间纵向血浆炎症蛋白质组分析。
Sci Rep. 2020 Oct 20;10(1):17819. doi: 10.1038/s41598-020-74722-5.
7
Financial Toll of Untreated Perinatal Mood and Anxiety Disorders Among 2017 Births in the United States.美国 2017 年分娩人群中未经治疗的围产期情绪和焦虑障碍的经济代价。
Am J Public Health. 2020 Jun;110(6):888-896. doi: 10.2105/AJPH.2020.305619. Epub 2020 Apr 16.
8
Postpartum Care: An Approach to the Fourth Trimester.产后护理:迈向第四个三月期。
Am Fam Physician. 2019 Oct 15;100(8):485-491.
9
Socioeconomic Status, Preeclampsia Risk and Gestational Length in Black and White Women.社会经济地位、子痫前期风险与黑人和白人妇女的妊娠时长。
J Racial Ethn Health Disparities. 2019 Dec;6(6):1182-1191. doi: 10.1007/s40615-019-00619-3. Epub 2019 Jul 31.
10
The cytokine profile of women with severe anxiety and depression during pregnancy.孕妇严重焦虑和抑郁的细胞因子特征。
BMC Psychiatry. 2019 Apr 3;19(1):104. doi: 10.1186/s12888-019-2087-6.

产前情绪和焦虑障碍及相关细胞因子变化。

Prenatal mood and anxiety disorders and associated cytokine changes.

机构信息

Department of Psychology and Neuroscience, Regis University, Denver, CO, USA.

Centre for Social Sciences, Athabasca University, Athabasca, AB, Canada.

出版信息

J Affect Disord. 2024 Feb 15;347:635-644. doi: 10.1016/j.jad.2023.12.014. Epub 2023 Dec 7.

DOI:10.1016/j.jad.2023.12.014
PMID:38070749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11375962/
Abstract

BACKGROUND

We examined whether women with prenatal mood and anxiety disorders would exhibit differential pro- and anti-inflammatory marker trajectories during the prenatal and postpartum periods compared to women without these disorders.

METHODS

Approximately 179 pregnant women participated in a longitudinal study conducted in two urban areas. Blood samples for inflammatory markers were collected at six study visits. The Structured Clinical Interview for the DSM-IV (SCID) was administered to participants scoring above cutoffs on anxiety and depression. Pregnant women with SCID Axis I diagnoses of mood and/or anxiety disorders were compared to other participants on inflammatory markers. Multilevel modeling tested associations between SCID diagnoses and within-person interleukin (IL)6 and IL10 trajectories.

RESULTS

Prenatal SCID diagnoses were associated with linear, quadratic and cubic change in IL6 from prenatal to postpartum timepoints. Women with a prenatal SCID diagnosis had steeper decreases and increases in IL6 during prenatal and postpartum periods. SCID diagnoses were associated with lower IL10 in mid-pregnancy to postpartum (b = -0.078, SE = 0.019; p = .015).

LIMITATIONS

Future studies would benefit from a larger sample size and a larger number of participants with SCID diagnoses. Future research should also examine whether different prenatal Axis 1 diagnoses are associated with different patterns of immune response in pregnancy.

CONCLUSIONS

Pregnant women with prenatal mood and anxiety disorders had greater fluctuations in IL6 across prenatal and postpartum periods and lower IL10 through pregnancy and postpartum. They may have different proinflammatory states that remain after birth without a reciprocal anti-inflammatory response.

摘要

背景

我们研究了与没有这些障碍的女性相比,患有产前情绪和焦虑障碍的女性在产前和产后期间是否会表现出不同的促炎和抗炎标志物轨迹。

方法

大约 179 名孕妇参加了在两个城市进行的一项纵向研究。在六个研究访视时采集了用于炎症标志物的血液样本。使用 DSM-IV 轴 I 障碍定式临床访谈 (SCID) 对焦虑和抑郁得分高于切点的参与者进行评估。将具有 SCID 轴 I 心境和/或焦虑障碍诊断的孕妇与其他参与者的炎症标志物进行比较。多层次模型测试了 SCID 诊断与个体内白细胞介素 (IL)6 和 IL10 轨迹之间的关联。

结果

产前 SCID 诊断与从产前到产后时间点的 IL6 的线性、二次和三次变化相关。产前 SCID 诊断的女性在产前和产后期间的 IL6 下降和增加更为陡峭。SCID 诊断与妊娠中期至产后 IL10 降低相关(b=-0.078,SE=0.019;p=0.015)。

局限性

未来的研究将受益于更大的样本量和更多的 SCID 诊断参与者。未来的研究还应检查不同的产前轴 1 诊断是否与妊娠期间不同的免疫反应模式相关。

结论

患有产前情绪和焦虑障碍的孕妇在产前和产后期间的 IL6 波动更大,在妊娠和产后期间的 IL10 更低。她们在出生后可能仍然存在不同的促炎状态,而没有相应的抗炎反应。