Literature DB >> 16648417

Fractional excretion of angiogenic factors in women with severe preeclampsia.

Catalin S Buhimschi1, Lissa Magloire, Edmund Funai, Errol R Norwitz, Edward Kuczynski, Ryan Martin, Susan Richman, Seth Guller, Charles J Lockwood, Irina A Buhimschi.   

Abstract

OBJECTIVE: We estimated the fractional excretions of soluble fms-like tyrosine kinase 1 (sFlt-1), vascular endothelial growth factor, and placental growth factor of severely preeclamptic women at the time of disease clinical manifestation.
METHODS: Levels of free sFlt-1, vascular endothelial growth factor, and placental growth factor were measured by immunoassay from time-matched serum-urine samples from 64 women in the following groups: nonpregnant reproductive aged (n = 9), healthy pregnant controls (n = 13), mildly preeclamptic women (n = 15), and women with severe preeclampsia (n = 27). Urinary concentrations of angiogenic factors were normalized to creatinine and fractional excretions calculated. Correlations were estimated between fractional excretions of angiogenic factors, albuminuria, nonspecific proteinuria and urine protein-to-creatinine ratio.
RESULTS: Severely preeclamptic women had more than double urinary vascular endothelial growth factor (P = .01) and fractional excretion of vascular endothelial growth factor compared with mildly preeclamptic women (P = .007) or pregnant controls (P < .001). Serum, urine and fractional excretion levels of sFlt-1 were much higher among severely preeclamptic women compared with all the other pregnant groups (P < .001). Conversely, severely preeclamptic women had lower serum placental growth factor levels compared with healthy pregnant women (P < .05) and mildly preeclamptic groups (P < .05). Severely preeclamptic women had increased fractional excretions of placental growth factor, albumin, proteinuria, and random urine total protein/creatinine ratio. Among severely preeclamptic women there was no correlation between proteinuria and fractional excretion of vascular endothelial growth factor (r = 0.30, P = .127) or sFlt-1 (r = 0.35, P = .07). There was a significant correlation between fractional excretion for placental growth factor, random urine total protein/creatinine ratio (r = 0.60, P = .002), and nonspecific proteinuria (r = 0.50, P = .01).
CONCLUSION: Severe preeclampsia is characterized by increased fractional excretion of angiogenic factors and especially of vascular endothelial growth factor, likely reflecting 2 separate phenomena that may have additive effects: "endogenous" renal production and glomerular "leakage."

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Year:  2006        PMID: 16648417     DOI: 10.1097/01.AOG.0000207698.74104.4f

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  9 in total

1.  Accreta complicating complete placenta previa is characterized by reduced systemic levels of vascular endothelial growth factor and by epithelial-to-mesenchymal transition of the invasive trophoblast.

Authors:  Mark J Wehrum; Irina A Buhimschi; Carolyn Salafia; Stephen Thung; Mert O Bahtiyar; Erica F Werner; Katherine H Campbell; Christine Laky; Anna K Sfakianaki; Guomao Zhao; Edmund F Funai; Catalin S Buhimschi
Journal:  Am J Obstet Gynecol       Date:  2011-02-12       Impact factor: 8.661

2.  Proteomic profiling of urine identifies specific fragments of SERPINA1 and albumin as biomarkers of preeclampsia.

Authors:  Irina A Buhimschi; Guomao Zhao; Edmund F Funai; Nathan Harris; Isaac E Sasson; Ira M Bernstein; George R Saade; Catalin S Buhimschi
Journal:  Am J Obstet Gynecol       Date:  2008-11       Impact factor: 8.661

3.  Fractional excretion of tumor necrosis factor-alpha in women with severe preeclampsia.

Authors:  Michael Cackovic; Catalin S Buhimschi; Guomao Zhao; Edmund F Funai; Errol R Norwitz; Edward Kuczynski; Charles J Lockwood; Irina A Buhimschi
Journal:  Obstet Gynecol       Date:  2008-07       Impact factor: 7.661

4.  Decreased nephrin and GLEPP-1, but increased VEGF, Flt-1, and nitrotyrosine, expressions in kidney tissue sections from women with preeclampsia.

Authors:  Shuang Zhao; Xin Gu; Lynn J Groome; Yuping Wang
Journal:  Reprod Sci       Date:  2009-06-15       Impact factor: 3.060

5.  The elevation in circulating anti-angiogenic factors is independent of markers of neutrophil activation in preeclampsia.

Authors:  Wenda Ramma; Irina A Buhimschi; Guomao Zhao; Antonette T Dulay; Unzila Ali Nayeri; Catalin S Buhimschi; Asif Ahmed
Journal:  Angiogenesis       Date:  2012-03-08       Impact factor: 9.596

Review 6.  Is inflammation the cause of pre-eclampsia?

Authors:  Wenda Ramma; Asif Ahmed
Journal:  Biochem Soc Trans       Date:  2011-12       Impact factor: 5.407

7.  Endocan, a Soluble Marker of Endothelial Cell Activation Is a Molecular Marker of Disease Severity in Women with Preeclampsia.

Authors:  Sarah N Cross; Irina A Buhimschi; Christina Duzyj Buniak; Lydia Shook; Megan McCarthy; John Hardy; Yara El-Helou; Guomao Zhao; Catalin S Buhimschi
Journal:  Reprod Sci       Date:  2022-02-03       Impact factor: 2.924

8.  Maternal circulating levels of activin A, inhibin A, sFlt-1 and endoglin at parturition in normal pregnancy and pre-eclampsia.

Authors:  Aparna Reddy; Sangeeta Suri; Ian L Sargent; Christopher W G Redman; Shanthi Muttukrishna
Journal:  PLoS One       Date:  2009-02-11       Impact factor: 3.240

Review 9.  Unravelling the theories of pre-eclampsia: are the protective pathways the new paradigm?

Authors:  Asif Ahmed; Wenda Ramma
Journal:  Br J Pharmacol       Date:  2015-03       Impact factor: 8.739

  9 in total

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