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Title: Getting too sweet: galectin-1 dysregulation in gestational diabetes mellitus
Authors: Blois, Sandra M.
Gueuvoghlanian-Silva, Barbara Y. [UNIFESP]
Tirado-Gonzalez, Irene
Torloni, Maria Regina [UNIFESP]
Freitag, Nancy
Mattar, Rosiane [UNIFESP]
Conrad, Melanie L.
Unverdorben, Laura
Barrientos, Gabriela
Knabl, Julia
Toldi, Gergely
Molvarec, Attila
Rose, Matthias
Markert, Udo R.
Jeschke, Udo
Daher, Silvia [UNIFESP]
Med Univ Berlin
Universidade Federal de São Paulo (UNIFESP)
Univ Hosp Jena
Univ Munich
Semmelweis Univ
Keywords: galectin-1
gestational diabetes
Issue Date: 1-Jul-2014
Publisher: Oxford Univ Press
Citation: Molecular Human Reproduction. Oxford: Oxford Univ Press, v. 20, n. 7, p. 644-649, 2014.
Abstract: Galectin-1 (gal-1) is a prototype carbohydrate-binding protein, whose dysregulation is associated with adverse pregnancy outcomes such as spontaneous abortion and pre-eclampsia. Furthermore, it is known that faulty gal-1 protein production or gene regulation can be caused by single-nucleotide polymorphisms in the LGALS1 gene. Gestational diabetes mellitus (GDM) is also an adverse pregnancy outcome and the most common metabolic disorder during gestation. However, gal-1 expression patterns during GDM remain largely unknown. Our aims were to define local and peripheral gal-1 expression patterns during pregnancy, and to investigate LGALS1 gene polymorphisms in GDM patients. Circulating gal-1 levels were determined by ELISA in GDM patients and normal pregnant controls, and LGALS1 gene polymorphisms were assessed for association with GDM. Placental tissues were collected from control and GDM term pregnancies to evaluate local gal-1 expression by immunofluorescence. Our results show that GDM is associated with a failure to increase circulating gal-1 levels during the second and third trimester, as well as overexpression of gal-1 in placental tissue. Additionally, the LGALS1 polymorphism rs4820294 was associated with the development of GDM. in pregnancies complicated by GDM, we observed gal-1 dysregulation both locally in the placenta and peripherally in the circulation. Furthermore, the association between the LGALS1 polymorphism and GDM may indicate a genetic contribution to this adverse pregnancy outcome.
ISSN: 1360-9947
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