Cover image of the article: Homocysteine Clearance in Hemodialysis

Image Credit:Nephro-Urol Mon

Homocysteine Clearance in Hemodialysis

Authors

Rafael Fernandez Castillo1,*, Rafael J. Esteban de la Rosa2, Susana Ruiz Duran2, Yolanda Baca2, Ruth Fernndez Gallegos2, Margarita Martnez2, Fernando Pern2, Susana Pedrinaci2, Juan A. Bravo2
1Departments of Nephrology, Academic Medical Centre Virgen de las Nieves, rafaelfernandez@ugr.es, Spain
2Departments of Nephrology, Academic Medical Centre Virgen de las Nieves, Spain
*Corresponding Author: Departments of Nephrology, Academic Medical Centre Virgen de las Nieves, rafaelfernandez@ugr.es, Spain. Email: rafaelfernandez@ugr.es

Nephro-Urology Monthly:Vol. 2, issue 4; 561-566
Published online:Oct 31, 2010
Article type:Research Article
Received:Nov 24, 2009
Accepted:Jan 02, 2010
How to Cite:Castillo R, de la Rosa R, Duran S, Baca Y, Gallegos R, et al. Homocysteine Clearance in Hemodialysis. Nephro-Urol Mon. 2010;2(4):. doi:

Abstract

Background and Aims: Homocysteine is a sulphur amino acid derived from methionine. Epidemiological studies show an association between hyperhomocysteinemia and an increased cardiovascular risk, a fact that has also been confirmed in patients with chronic renal failure. This study, conducted in stage 5 chronic kidney disease patients, seeks to define the prevalence of hyperhomocysteinemia, evaluate the clearance of homocysteine with dialysis, and describe the frequency of the mutation in the mutilen-tetrahydrofolate reductase enzyme and its relationship with plasma levels of homocysteine.

Methods: The reduced percentage of homocysteine and clearance of urea were analysed every six months for seven years in patients on dialysis. Urea and total homocysteine in plasma were measured in each of these studies and the type of dialyser - low or high permeability - used and the dialysis duration was determined. A molecular study of the gene coding for mutilen-tetrahydrofolate reductase enzyme was carried out in a group of patients and any C-T point mutation at position 677 of this gene was investigated. Mutation was described as not present, heterozygous for this mutation or homozygous for lactation.

Results: Neither the average levels of homocysteine before and after dialysis or the reduction percentage of homocysteine varied with gender, although purification of urea was higher in women. Comparisons of homocysteine levels and percentage reduction in this ratio according to the ultra filtration of the dialyser used showed significant results. The molecular study of the gene in mutilen-tetrahydrofolate reductase enzyme showed that mutation was present in 54.8%: 45.2% with heterozygous polymorphism and 9.7% with homozygous.

Conclusions: Patients undergoing hemodialysis were found to have higher levels of urea and its clearance was greater with the higher the ratio of ultra filtration dialyser. Mutation of the gene in mutilen-tetrahydrofolate reductase enzyme was similar in our patients compared to the general population and had no impact on plasma levels of homocysteine.

Highlights

Full Text

Full text is available in PDF

Copyright

© 2010, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Similar Articles

30
Apr
2006
Association of Mean Arterial Blood Pressure with Plasma Total Homocysteine level, but Not with the Common C677T MTHFR Gene Mutation in Postmenopausal Iranian Women

Association of Mean Arterial Blood Pressure with Plasma Total Homocysteine level, but Not with the Common C677T MTHFR Gene Mutation in Postmenopausal Iranian Women

MA Aminzadeh,
ZA Azizi,
A Hamidi,
M Monjazeb,
GR Omrani

Aminzadeh M, Azizi Z, Hamidi A, Monjazeb M, Omrani G. Association of Mean Arterial Blood Pressure with Plasma Total Homocysteine level, but Not with the Common C677T MTHFR Gene Mutation in Postmenopausal Iranian Women. Int J Endocrinol Metab. 2006;4(2):. doi:

18
Aug
2021
The Association Between Uric Acid and Symmetric Dimethylarginine Levels in the Patients Undergoing Twice-weekly Hemodialysis

The Association Between Uric Acid and Symmetric Dimethylarginine Levels in the Patients Undergoing Twice-weekly Hemodialysis

Aida Lydia,
Yassir Yassir,
Rudy Hidayat,
Suhendro Suwarto

Lydia A, Yassir Y, Hidayat R, Suwarto S. The Association Between Uric Acid and Symmetric Dimethylarginine Levels in the Patients Undergoing Twice-weekly Hemodialysis. Nephro-Urol Mon. 2021;13(4):e117476. doi: https://doi.org/10.5812/numonthly.117476

30
Jun
2009
Does N-Acetyl Cysteine Have a Dose-Dependent Effect on Plasma Homocysteine Concentration in Patients Undergoing Hemodialysis?

Does N-Acetyl Cysteine Have a Dose-Dependent Effect on Plasma Homocysteine Concentration in Patients Undergoing Hemodialysis?

Mehdi Khosravi,
Majid Shohrati,
Kiyanush Falaknazi

Khosravi M, Shohrati M, Falaknazi K. Does N-Acetyl Cysteine Have a Dose-Dependent Effect on Plasma Homocysteine Concentration in Patients Undergoing Hemodialysis?. Nephro-Urol Mon. 2009;1(1):. doi:

30
Sep
2008
Association between Genetic Polymorphism of Methylenetetrahydrofolate Reductase with Non Familial Colorectal Cancer in Iranian Population

Association between Genetic Polymorphism of Methylenetetrahydrofolate Reductase with Non Familial Colorectal Cancer in Iranian Population

Mahdi Montazer Haghighi,
R Radpour,
M Vahedi,
SR Mohebbi,
F Khatami,
F Derakhshan
,et al.

Montazer Haghighi M, Radpour R, Vahedi M, Mohebbi S, Khatami F, et al. Association between Genetic Polymorphism of Methylenetetrahydrofolate Reductase with Non Familial Colorectal Cancer in Iranian Population. Int J Cancer Manag. 2008;1(3):e80489. doi:

31
Mar
2017
Association of Two Single-Nucleotide Polymorphisms (rs1805087 and rs1801131) with Coronary Artery Disease in Golestan Population

Association of Two Single-Nucleotide Polymorphisms (rs1805087 and rs1801131) with Coronary Artery Disease in Golestan Population

Fahimeh Baghbani-Arani,
Mohsen Kavian Telori,
Jahanbakhsh Asadi,
Esmail Samadian,
Atefeh Shirkavand

Baghbani-Arani F, Kavian Telori M, Asadi J, Samadian E, Shirkavand A. Association of Two Single-Nucleotide Polymorphisms (rs1805087 and rs1801131) with Coronary Artery Disease in Golestan Population. Ann Mil Health Sci Res. 2017;15(1):e11473. doi: https://doi.org/10.5812/amh.11473

More by these authors

Rafael CastilloPubMedScholar
Rafael de la RosaPubMedScholar
Susana DuranPubMedScholar
Yolanda BacaPubMedScholar
Ruth GallegosPubMedScholar
Margarita MartnezPubMedScholar
Fernando PernPubMedScholar
Susana PedrinaciPubMedScholar
Juan BravoPubMedScholar
Share
Cited by
Metrics