4.4 Article

Association of depressive symptoms with inflammatory biomarkers among pregnant African-American women

期刊

JOURNAL OF REPRODUCTIVE IMMUNOLOGY
卷 94, 期 2, 页码 202-209

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jri.2012.01.007

关键词

Race disparity; Pregnancy; Inflammation; Cytokine; Depressive symptoms

资金

  1. Institute for Population Sciences, Health Assessment, Administration, Services, and Economics (INPHAASE)

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Depression and inflammation are associated with poorer birth outcomes. African-American women have higher levels of inflammatory biomarkers, more depressive symptoms, and a disparate burden of poorer birth outcomes, but the association between depressive symptoms and inflammation within this higher-risk group is unknown. We examined this association among African-American women in the second trimester of pregnancy and additionally tested whether body mass index (BMI) mediates or moderates this relationship. We recruited 187 women from the obstetrics clinics of a large urban health system. Depression symptoms were measured with the Center for Epidemiological Studies Depression (CES-D) scale and inflammatory biomarkers (high-sensitivity C-reactive protein [hs-CRP], interleukin [IL]-6, IL-10, IL-1 beta, and tumor necrosis factor-alpha [TNF-alpha]) with enzyme immunoassays. Multivariate regression models were fitted to determine the association between CES-D score and each inflammatory biomarker. CES-D was not associated with hs-CRP or TNF-alpha CES-D was directly associated with IL-1 beta (P = 0.03). BMI moderated the relationship between CES-D and IL-6 (P < 0.01) and IL-10 (P = 0.04): in leaner women, depressive symptoms were associated with higher IL-6 and IL-10 levels, whereas in heavier women, depressive symptoms were associated with lower IL-10 levels. BMI did not mediate the relationship between CES-D and inflammation. We conclude that depressive symptoms are associated with increased inflammation among pregnant African-American women. Future studies are needed to examine if depression, mediated through inflammation, increases the risk of adverse pregnancy outcomes in African-American women. (c) 2012 Elsevier Ireland Ltd. All rights reserved.

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