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Elevated systemic galectin-1 levels characterize HELLP syndrome.

Schnabel, Annegret et al · Elsevier Ireland · 2016

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Galectin-1 (gal-1), a member of a family of conserved β-galactoside-binding proteins, has been shown to exert a key role during gestation. Though gal-1 is expressed at higher levels in the placenta from HELLP patients, it is still poorly understood whether systemic gal-1 levels also differ in HELLP patients. In the present study, we evaluated the systemic expression of gal-1, together with the angiogenic factors, placental growth factor (PlGF) and soluble fms-like tyrosine kinase 1 (sFlt-1) in conjunction with HELLP syndrome severity. Systemic levels of gal-1 and sFlt-1 were elevated in patients with both early- and late-onset HELLP syndrome as compared to healthy controls. In contrast, peripheral PlGF levels were decreased in early- and late-onset HELLP. A positive correlation between systemic gal-1 levels and sFlt-1/PlGF ratios was found in early onset HELLP patients. Our results show that HELLP syndrome is associated with increased circulating levels of gal-1; integrating systemic gal-1 measurements into the diagnostic analyses of pregnant women may provide more effective prediction of HELLP syndrome development Fil: Schnabel, Annegret. Universitat Regensburg; Alemania Fil: Blois, Sandra M.. Charité-Universitätsmedizin Berlin; Alemania

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APA 7

Schnabel, A. E. A. (2016). Elevated systemic galectin-1 levels characterize HELLP syndrome. http://hdl.handle.net/11336/43966

MLA

Schnabel, Annegret et al. "Elevated systemic galectin-1 levels characterize HELLP syndrome." 2016. http://hdl.handle.net/11336/43966.

Chicago

Schnabel, Annegret et al. 2016. "Elevated systemic galectin-1 levels characterize HELLP syndrome.". http://hdl.handle.net/11336/43966.

Harvard

Schnabel, A. E. A. 2016, Elevated systemic galectin-1 levels characterize HELLP syndrome, Elsevier Ireland, available at: http://hdl.handle.net/11336/43966 [Accessed 8 Aug. 2026].

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Title
Elevated systemic galectin-1 levels characterize HELLP syndrome.
Author / contributors
Schnabel, Annegret et al
Publisher
Elsevier Ireland
Publication year
2016
ISSN
0165-0378
ISSN
0165-0378
Language
English

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