Publicação
Lipid, Oxidative and Inflammatory Profile and Alterations in the Enzymes Paraoxonase and Butyrylcholinesterase in Plasma of Patients with Homocystinuria Due CBS Deficiency: The Vitamin B12 and Folic Acid Importance
| dc.contributor.author | Vanzin, C.S. | |
| dc.contributor.author | Mescka, C.P. | |
| dc.contributor.author | Donida, B. | |
| dc.contributor.author | Hammerschimidt, T.G. | |
| dc.contributor.author | Ribas, G.S. | |
| dc.contributor.author | Kolling, J. | |
| dc.contributor.author | Scherer, E.B. | |
| dc.contributor.author | Vilarinho, Laura | |
| dc.contributor.author | Nogueira, Célia | |
| dc.contributor.author | Coitinho, A.S. | |
| dc.contributor.author | Wajner, M. | |
| dc.contributor.author | Wyse, A.T. | |
| dc.contributor.author | Vargas, C.R. | |
| dc.date.accessioned | 2016-03-30T11:47:38Z | |
| dc.date.available | 2016-09-01T00:30:09Z | |
| dc.date.issued | 2015-08 | |
| dc.description.abstract | Cystathionine-β-synthase (CBS) deficiency is the main cause of homocystinuria. Homocysteine (Hcy), methionine, and other metabolites of Hcy accumulate in the body of affected patients. Despite the fact that thromboembolism represents the major cause of morbidity in CBS-deficient patients, the mechanisms of cardiovascular alterations found in homocystinuria remain unclear. In this work, we evaluated the lipid and inflammatory profile, oxidative protein damage, and the activities of the enzymes paraoxonase (PON1) and butyrylcholinesterase (BuChE) in plasma of CBS-deficient patients at diagnosis and during the treatment (protein-restricted diet supplemented with pyridoxine, folic acid, betaine, and vitamin B12). We also investigated the effect of folic acid and vitamin B12 on these parameters. We found a significant decrease in HDL cholesterol and apolipoprotein A1 (ApoA-1) levels, as well as in PON1 activity in both untreated and treated CBS-deficient patients when compared to controls. BuChE activity and IL-6 levels were significantly increased in not treated patients. Furthermore, significant positive correlations between PON1 activity and sulphydryl groups and between IL-6 levels and carbonyl content were verified. Moreover, vitamin B12 was positively correlated with PON1 and ApoA-1 levels, while folic acid was inversely correlated with total Hcy concentration, demonstrating the importance of this treatment. Our results also demonstrated that CBS-deficient patients presented important alterations in biochemical parameters, possibly caused by the metabolites of Hcy, as well as by oxidative stress, and that the adequate adherence to the treatment is essential to revert or prevent these alterations. | pt_PT |
| dc.description.sponsorship | This work was supported in part by grants from CAPES, CNPq, and FIPE/HCPA-Brazil. | pt_PT |
| dc.identifier.citation | Cell Mol Neurobiol. 2015 Aug;35(6):899-911. doi: 10.1007/s10571-015-0185-7. Epub 2015 Mar 25. | pt_PT |
| dc.identifier.doi | 10.1007/s10571-015-0185-7 | pt_PT |
| dc.identifier.issn | 0272-4340 | |
| dc.identifier.uri | http://hdl.handle.net/10400.18/3759 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.publisher | Springer Verlag (Germany) | pt_PT |
| dc.relation.publisherversion | http://link.springer.com/article/10.1007%2Fs10571-015-0185-7 | pt_PT |
| dc.subject | Doenças Genéticas | pt_PT |
| dc.subject | Homocysteine | pt_PT |
| dc.subject | Lipid Profile | pt_PT |
| dc.subject | Inflammation | pt_PT |
| dc.subject | Paraoxonase | pt_PT |
| dc.subject | Butyrylcholinesterase | pt_PT |
| dc.subject | Vitamin B12 | pt_PT |
| dc.subject | Folic Acid | pt_PT |
| dc.title | Lipid, Oxidative and Inflammatory Profile and Alterations in the Enzymes Paraoxonase and Butyrylcholinesterase in Plasma of Patients with Homocystinuria Due CBS Deficiency: The Vitamin B12 and Folic Acid Importance | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 911 | pt_PT |
| oaire.citation.startPage | 899 | pt_PT |
| oaire.citation.title | Cellular and Molecular Neurobiology | pt_PT |
| oaire.citation.volume | 35(6) | pt_PT |
| rcaap.rights | embargoedAccess | pt_PT |
| rcaap.type | article | pt_PT |