Literature DB >> 16681647

Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.

Vikki G Nolan1, Adeboye Adewoye, Clinton Baldwin, Ling Wang, Qianli Ma, Diego F Wyszynski, John J Farrell, Paola Sebastiani, Lindsay A Farrer, Martin H Steinberg.   

Abstract

Cutaneous leg ulcers are common in sickle cell anaemia and their risk might be genetically determined. Sickle cell anaemia patients were studied to examine the relationship of leg ulcers with haemolysis and with single nucleotide polymorphisms (SNPs) in candidate genes that could affect sickle vasoocclusion. Leg ulcer patients had lower haemoglobin levels and higher levels of lactate dehydrogenase, bilirubin, aspartate transaminase and reticulocytes than did control patients with sickle cell anaemia but without leg ulcers. Age-adjusted comparisons showed that sickle cell anaemia-alpha thalassaemia was more frequent among controls than cases. These results strongly suggested that the likelihood of having leg ulcers was related to the intensity of haemolysis. 215 SNPs in more than 100 candidate genes were studied. Associations were found with SNPs in Klotho, TEK and several genes in the TGF-beta/BMP signalling pathway by genotypic association analyses. KL directly or indirectly promotes endothelial nitric oxide (NO) production and the TEK receptor tyrosine kinase is involved in angiogenesis. The TGF-beta/BMP signalling pathway modulates wound healing and angiogenesis, among its other functions. Haemolysis-driven phenotypes, such as leg ulcers, could be improved by agents that reduce sickle erythrocyte density or increase NO bioavailability.

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Year:  2006        PMID: 16681647      PMCID: PMC1679888          DOI: 10.1111/j.1365-2141.2006.06074.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  64 in total

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  57 in total

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Review 2.  Genetic modifiers of sickle cell disease.

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Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

5.  Erythrocytapheresis: Do Not Forget a Useful Therapy!

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Review 7.  Cardiovascular abnormalities in sickle cell disease.

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Review 8.  Role of the hemostatic system on sickle cell disease pathophysiology and potential therapeutics.

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10.  Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

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