Fetal microchimerism by mode of delivery: a prospective cohort study.

作者: R Shree , WE Harrington , SB Kanaan , A Forsyth , E Cousin

DOI: 10.1111/1471-0528.15432

关键词:

摘要: Objective To compare fetal microchimerism (FMc) in pregnancies with uncomplicated vaginal delivery (VD) versus caesarean (CD). Design Prospective cohort study. Setting University of Washington and Fred Hutchinson Cancer Research Center, USA. Population Women delivering singleton without pertinent antenatal complications deliveries (n = 36). Methods We collected maternal predelivery, postdelivery umbilical cord blood for each mother-baby pair. Following genotyping, FMc was measured quantitative polymerase chain reaction assays targeting fetus-specific polymorphisms. Quantification is expressed as genome equivalents (gEq) DNA/100 000 total gEq tested. detection evaluated by logistic regression while controlling number cell tested clinically relevant covariates. concentrations were compared using negative binomial the same covariates predelivery positivity. Main outcome measure Detection concentration mode delivery. Results Twenty-four pairs had a VD 12 CD. Postdelivery higher following CD than after (58.3% 16.7%, P 0.02). After covariates, likelihood almost nine-fold (odds ratio 8.8, 95% CI 1.6-47.6; 0.01). With respect to concentration, rate adjusted model 14.7 (95% 3.2-66.8; 0.001). Conclusion peripheral are significantly VD. As associated long-term health, our findings suggest that may impact this risk. Tweetable abstract Greater found

参考文章(31)
N.C. Lambert, J.L. Nelson, K.M. Adams Waldorf, H.S. Gammill, J. Lucas, T.M. Aydelotte, W.M. Leisenring, Dynamic changes in fetal microchimerism in maternal peripheral blood mononuclear cells, CD4+ and CD8+ cells in normal pregnancy. Placenta. ,vol. 31, pp. 589- 594 ,(2010) , 10.1016/J.PLACENTA.2010.04.013
Hilary S. Gammill, J. Lee Nelson, Naturally acquired microchimerism. The International Journal of Developmental Biology. ,vol. 54, pp. 531- 543 ,(2010) , 10.1387/IJDB.082767HG
Sean Maloney, Anajane Smith, Daniel E. Furst, David Myerson, Kate Rupert, Paul C. Evans, J. Lee Nelson, Microchimerism of maternal origin persists into adult life Journal of Clinical Investigation. ,vol. 104, pp. 41- 47 ,(1999) , 10.1172/JCI6611
Hilary S. Gammill, Katherine A. Guthrie, Tessa M. Aydelotte, Kristina M. Adams Waldorf, J. Lee Nelson, Effect of parity on fetal and maternal microchimerism: interaction of grafts within a host? Blood. ,vol. 116, pp. 2706- 2712 ,(2010) , 10.1182/BLOOD-2010-02-270942
Hilary S. Gammill, Tessa M. Aydelotte, Katherine A. Guthrie, Evangelyn C. Nkwopara, J. Lee Nelson, Cellular Fetal Microchimerism in Preeclampsia Hypertension. ,vol. 62, pp. 1062- 1067 ,(2013) , 10.1161/HYPERTENSIONAHA.113.01486
D. W. Bianchi, G. K. Zickwolf, G. J. Weil, S. Sylvester, M. A. DeMaria, Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum Proceedings of the National Academy of Sciences of the United States of America. ,vol. 93, pp. 705- 708 ,(1996) , 10.1073/PNAS.93.2.705
Kristina M. Adams Waldorf, J. Lee Nelson, Autoimmune disease during pregnancy and the microchimerism legacy of pregnancy. Immunological Investigations. ,vol. 37, pp. 631- 644 ,(2008) , 10.1080/08820130802205886
R. Saiki, D. Gelfand, S Stoffel, S. Scharf, R Higuchi, G. Horn, K. Mullis, H. Erlich, Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase Science. ,vol. 239, pp. 487- 491 ,(1988) , 10.1126/SCIENCE.2448875
Vijayakrishna K. Gadi, Fetal microchimerism in breast from women with and without breast cancer Breast Cancer Research and Treatment. ,vol. 121, pp. 241- 244 ,(2010) , 10.1007/S10549-009-0548-1
Nathalie C. Lambert, Y. M. Dennis Lo, Timothy D. Erickson, Tracy S. Tylee, Katherine A. Guthrie, Daniel E. Furst, J. Lee Nelson, Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer Blood. ,vol. 100, pp. 2845- 2851 ,(2002) , 10.1182/BLOOD-2002-01-0295