Skip Navigation



Hum. Reprod. Advance Access published online on February 27, 2004

Human Reproduction, doi:10.1093/humrep/deh179
© 2004 by European Society of Human Reproduction and Embryology
This Article
Right arrow FREE Full Text (PDF ) Freely available
Right arrow All Versions of this Article:
19/4/1025    most recent
deh179v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Sacks, G.P.
Right arrow Articles by Trew, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sacks, G.P.
Right arrow Articles by Trew, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received August 11, 2003
Revised November 13, 2003
Accepted December 12, 2003

Article

Maternal C-reactive protein levels are raised at 4 weeks gestation

G.P. Sacks 1*, L. Seyani 1, S. Lavery 1, and G. Trew 1

1 Department of Reproductive Medicine, Hammersmith Hospital, Du Cane Road, London W12 0HS, UK

* To whom correspondence should be addressed. E-mail: g.sacks{at}imperial.ac.uk.


   Abstract

BACKGROUND: The aim of this study was to determine whether there is evidence of a systemic maternal inflammatory response in very early pregnancy. METHODS: Successive women receiving treatment by IVF or ICSI had serum C-reactive protein (CRP) levels measured on the day of their pregnancy blood test at 4 weeks gestation (14 days post-egg collection). Women with positive {beta}HCG levels had ongoing pregnancies confirmed by serial transvaginal ultrasound scans up to 8 weeks gestation. RESULTS: Pregnant women (n = 40) were significantly younger (mean age 34 years) than women who failed to become pregnant (n = 95, mean age 37 years, P < 0.001), received significantly lower treatment doses of recombinant FSH (2000 versus 2400 IU, P < 0.05) and had significantly more eggs collected (11 versus 8, P < 0.01). There were no significant differences in body mass index, parity, a history of smoking, endometriosis or polycystic ovaries, pre-treatment CRP levels and white cell counts, peak serum estradiol levels and numbers of embryos transferred. Pregnant women had significantly higher CRP levels (median 3.68 mg/l) than those who were not pregnant (median 1.495 mg/l, P < 0.0001), a difference that persisted after excluding potential confounding variables. Six pregnant women with ovarian hyperstimulation syndrome had higher CRP levels than those who did not (P < 0.01). CONCLUSIONS: This well-controlled study is the first to demonstrate that maternal CRP levels are raised as early as 4 weeks gestation and thus that the maternal inflammatory response is established during the earliest phases of implantation. It is hypothesized that an abnormal response (either exaggerated or absent) could cause some cases of miscarriage.

Key words: Key words: C-reactive protein/early pregnancy/inflammatory response/IVF/miscarriage


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Reproductive SciencesHome page
J. V. Ilekis, U. M. Reddy, and J. M. Roberts
Review Article: Preeclampsia A Pressing Problem: An Executive Summary of a National Institute of Child Health and Human Development Workshop
Reproductive Sciences, September 1, 2007; 14(6): 508 - 523.
[Abstract] [PDF]


Home page
Hum ReprodHome page
F. Prefumo, D. C Gaze, A. T Papageorghiou, P. O Collinson, and B. Thilaganathan
First trimester maternal serum ischaemia-modified albumin: a marker of hypoxia-ischaemia-driven early trophoblast development
Hum. Reprod., July 1, 2007; 22(7): 2029 - 2032.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
F. M. Stewart, D. J. Freeman, J. E. Ramsay, I. A. Greer, M. Caslake, and W. R. Ferrell
Longitudinal Assessment of Maternal Endothelial Function and Markers of Inflammation and Placental Function throughout Pregnancy in Lean and Obese Mothers
J. Clin. Endocrinol. Metab., March 1, 2007; 92(3): 969 - 975.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
S. A. Bainbridge, L. Belkacemi, M. Dickinson, C. H. Graham, and G. N. Smith
Carbon Monoxide Inhibits Hypoxia/Reoxygenation-Induced Apoptosis and Secondary Necrosis in Syncytiotrophoblast
Am. J. Pathol., September 1, 2006; 169(3): 774 - 783.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
T. R. Sweeney, A. H. Moser, J. K. Shigenaga, C. Grunfeld, and K. R. Feingold
Decreased nuclear hormone receptor expression in the livers of mice in late pregnancy
Am J Physiol Endocrinol Metab, June 1, 2006; 290(6): E1313 - E1320.
[Abstract] [Full Text] [PDF]


Home page
Diabetes CareHome page
X. Chen, T. O. Scholl, and T. P. Stein
Association of Elevated Serum Ferritin Levels and the Risk of Gestational Diabetes Mellitus in Pregnant Women: The Camden Study
Diabetes Care, May 1, 2006; 29(5): 1077 - 1082.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
D.M. Wunder, R. Kretschmer, and N.A. Bersinger
Concentrations of leptin and C-reactive protein in serum and follicular fluid during assisted reproductive cycles
Hum. Reprod., May 1, 2005; 20(5): 1266 - 1271.
[Abstract] [Full Text] [PDF]


Home page
Reproductive SciencesHome page
R. Orvieto
Controlled Ovarian Hyperstimulation--An Inflammatory State
Reproductive Sciences, October 1, 2004; 11(7): 424 - 426.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.