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Am J Obstet Gynecol. 2010 Feb;202(2):161.e1-161.e11. doi: 10.1016/j.ajog.2009.09.016. Epub 2009 Oct 21.

An automated method for the determination of the sFlt-1/PIGF ratio in the assessment of preeclampsia.

Author information

1
Department of Obstetrics, Campus Virchow-Clinic, Charité University Medicine, Berlin, Germany.

Abstract

OBJECTIVE:

The angiogenic and antiangiogenic factors soluble fms-like tyrosine kinase (sFlt)-1 and placental growth factor (PIGF) have been implicated in the mechanisms of disease responsible for preeclampsia (PE). Moreover, it has been proposed that the concentrations of these markers in maternal serum/plasma may have predictive value. This study evaluates a newly developed Elecsys (Roche, Penzberg, Germany) assay for sFlt-1 and PIGF and tests the value of the sFlt-1/PIGF ratio in the assessment of PE.

STUDY DESIGN:

This multicenter case-control study included 351 patients: 71 patients with PE and 280 gestational age-matched control subjects from 5 European study centers. A total of 595 serum samples were measured for sFlt-1 and PIGF using an automated platform.

RESULTS:

Maternal serum concentrations of sFlt-1 and PIGF significantly separated healthy women and women with PE. The sFlt-1/PIGF ratio had an area under the receiver operating characteristic curve of 0.95. The best performance was obtained in the identification of early-onset PE (area under the receiver operating characteristic curve of 0.97).

CONCLUSION:

Measurement of sFlt-1 and PIGF and calculation of sFlt-1/PIGF ratio can be performed quickly and in a platform available in clinical laboratories. This is a substantial step forward in bringing the determination of these analytes to clinical practice in obstetrics. We propose that sFlt-1, PIGF, and sFlt-1/PIGF ratio may be of value in the prediction of PE and in the differential diagnosis of patients with atypical presentations of PE, and perhaps in the differential diagnosis of women with chronic hypertension suspected to develop superimposed PE.

PMID:
19850276
DOI:
10.1016/j.ajog.2009.09.016
[Indexed for MEDLINE]

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