2011
DOI: 10.1111/j.1538-7836.2011.04494.x
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A functional variant in the thrombospondin‐1 gene and the risk of small for gestational age infants

Abstract: Summary.  Introduction: Thrombospondin‐1 (TSP‐1) is a prothrombotic and anti‐angiogenic glycoprotein expressed in the placenta. A functional single nucleotide polymorphism in the TSP‐1 gene (TSP‐1 A2210G) is a risk factor for familial premature myocardial infarction. Small for gestational age (SGA) infants are at increased risk of coronary artery disease in adult life and common genetic factors may underlie both conditions. We investigated the association of TSP‐1 A2210G in SGA infants and their parents. Metho… Show more

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Cited by 22 publications
(13 citation statements)
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“…Replacement of an asparagine residue with a serine at residue 700 of TSP1 led to a protein variant that, in cell culture experiments, promoted pro-thrombotic phenomena, including augmented fibrinogen binding and enhanced platelet aggregation (Narizhneva et al 2004). The presence of the TSP-1 A2210G variant has been associated with the small for gestational age phenotype (itself a risk factor for coronary artery disease) in newborns from affected parents (Andraweera et al 2011). Additionally, umbilical cord blood endothelial cells from low birth weight infants (also known to be at risk for cardiovascular disease) were found to overexpress TSP1 and this was associated with decreased angiogenic activity in these cells (Ligi et al 2011).…”
Section: The Cd47-tsp1 Signaling Axis In Human Cvdmentioning
confidence: 99%
“…Replacement of an asparagine residue with a serine at residue 700 of TSP1 led to a protein variant that, in cell culture experiments, promoted pro-thrombotic phenomena, including augmented fibrinogen binding and enhanced platelet aggregation (Narizhneva et al 2004). The presence of the TSP-1 A2210G variant has been associated with the small for gestational age phenotype (itself a risk factor for coronary artery disease) in newborns from affected parents (Andraweera et al 2011). Additionally, umbilical cord blood endothelial cells from low birth weight infants (also known to be at risk for cardiovascular disease) were found to overexpress TSP1 and this was associated with decreased angiogenic activity in these cells (Ligi et al 2011).…”
Section: The Cd47-tsp1 Signaling Axis In Human Cvdmentioning
confidence: 99%
“…A single nucleotide polymorphism in the TSP-1 gene (TSP-1 2210A/G) was reported to be a significant risk factor for familial premature myocardial infarction, hypertension, and renal disease, which was associated with SGA, suggesting that TSP-1 polymorphism may be associated with the risk of vascular disorders across the course of life. 17 In a rat study, TSP-1 expression was more prominent, especially in peritubular interstitial space. The percentage of glomeruli with positive intraglomerular TSP-1 staining was 19.3 (SD4.5) %; (P<0.0001).…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, previous publications showed that birth weight was a risk factor for increased TSP-1 levels. 16,17 Isenberg et al reported that the expression of TSP-1 in wild type mice born SGA and aged between 14 to 18 months demonstrated greater degrees of ischemia in the glomeruli and tubulointerstitium of the kidney and formed atherosclerosis in the vessel walls. TSP-1 level was related to birth weight.…”
Section: Discussionmentioning
confidence: 99%