Prediction of placental abruption by testing for C‐reactive protein and chlamydial antibody levels in early pregnancy

Objective  Placental abruption may be a manifestation of acute and chronic inflammatory process. We wanted to assess the association of first‐trimester serum C‐reactive protein (CRP), Chlamydia pneumoniae antibodies, Chlamydia trachomatis antibodies or chlamydial heat‐shock protein 60 (CHSP60) antib...

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Veröffentlicht in:BJOG : an international journal of obstetrics and gynaecology 2008-03, Vol.115 (4), p.486-491
Hauptverfasser: Tikkanen, M, Surcel, H‐M, Bloigu, A, Nuutila, M, Hiilesmaa, V, Ylikorkala, O, Paavonen, J
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Sprache:eng
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Zusammenfassung:Objective  Placental abruption may be a manifestation of acute and chronic inflammatory process. We wanted to assess the association of first‐trimester serum C‐reactive protein (CRP), Chlamydia pneumoniae antibodies, Chlamydia trachomatis antibodies or chlamydial heat‐shock protein 60 (CHSP60) antibodies to placental abruption. Design  Retrospective case–control study. Setting  University Hospital. Population  A total of 181 women with subsequent placental abruption and 261 control women with normal pregnancy. Methods  Serum samples collected at first trimester (mean 10.4 gestational weeks) were analysed for CRP levels, C. pneumoniae‐specific immunoglobulin G (IgG) and immunoglobulin A (IgA) antibodies and C. trachomatis‐specific IgG, IgA and CHSP60 antibodies. Main outcome measure  Placental abruption. Results  The levels of CRP showed no difference between the cases and the controls (median 2.35 mg/l [interquartile range {IQR} 1.09–5.93] versus 2.28 mg/l [IQR 0.92–5.01], not significant). C. pneumoniae‐specific IgG and IgA as well as C. trachomatis‐specific IgG, IgA and CHSP60 antibody frequencies were similar between the groups. There was no association between CRP levels and chlamydial antibodies. Conclusion  These markers of inflammation in early pregnancy failed to predict subsequent placental abruption.
ISSN:1470-0328
1471-0528
DOI:10.1111/j.1471-0528.2007.01663.x