Prevalence of methylenetetrahydrofolate gene (MTHFR) C677T polymorphism among chronic hemodialysis patients and its association with cardiovascular disease: a cross-sectional analysis. (Q45998264)

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scientific article published on 26 May 2009

Language	Label	Description	Also known as
English	Prevalence of methylenetetrahydrofolate gene (MTHFR) C677T polymorphism among chronic hemodialysis patients and its association with cardiovascular disease: a cross-sectional analysis.	scientific article published on 26 May 2009

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

Prevalence of methylenetetrahydrofolate gene (MTHFR) C677T polymorphism among chronic hemodialysis patients and its association with cardiovascular disease: a cross-sectional analysis. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

cardiovascular disease

1 reference

based on heuristic

author name string

Salwa Ibrahim

1

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

Ola El Dessokiy

2

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

publication date

26 May 2009

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

Clinical and experimental nephrology

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

13

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

5

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

501-507

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

https://scigraph.springernature.com/pub.10.1007/s10157-009-0194-2

0 references

Polymorphism in methylenetetrahydrofolate reductase gene: its impact on plasma homocysteine levels and carotid atherosclerosis in ESRD patients receiving hemodialysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic factors in end-stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atherosclerotic cardiovascular disease risks in chronic hemodialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of MTHFR C677T genotype on survival in type 2 diabetes patients with end-stage diabetic nephropathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vitamin B12 decreases, but does not normalize, homocysteine and methylmalonic acid in end-stage renal disease: a link with glycine metabolism and possible explanation of hyperhomocysteinemia in end-stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association between end-stage diabetic nephropathy and methylenetetrahydrofolate reductase genotype with macroangiopathy in type 2 diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mortality risk factors in patients treated by chronic hemodialysis. Report of the Diaphane collaborative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

End-stage renal disease--not an equal opportunity disease: the role of genetic polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical epidemiology of cardiovascular disease in chronic renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma sulfur amino acids in relation to cardiovascular disease, nutritional status, and diabetes mellitus in patients with chronic renal failure at start of dialysis therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common mutation in the methylenetetrahydrofolate reductase gene offers no support for mild hyperhomocysteinemia being a causal risk factor for cardiovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia and polymorphisms of the methylenetetrahydrofolate gene in hemodialysis and peritoneal dialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocyst(e)inemia and the prevalence of atherosclerotic vascular disease in patients with end-stage renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The C677T methylenetetrahydrofolate reductase gene mutation and nephropathy in type 2 diabetes mellitus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia is related to residual glomerular filtration and folate, but not to methylenetetrahydrofolate-reductase and methionine synthase polymorphisms, in supplemented end-stage renal disease patients undergoing hemodialysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase gene polymorphism and plasma homocysteine levels in hemodialysing patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Some aspects of homocysteine metabolism in hemodialysis patients]

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An MTHFR variant, homocysteine, and cardiovascular comorbidity in renal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The C677T methylenetetrahydrofolate reductase gene mutation does not influence cardiovascular risk in the dialysis population: results of a multicentre prospective study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia in hemodialysis patients: effects of 12-month supplementation with hydrosoluble vitamins

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia is associated with atherosclerotic occlusive arterial accidents in predialysis chronic renal failure patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective homocysteine metabolism as a risk factor for diabetic retinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia, nutritional status, and cardiovascular disease in hemodialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low diastolic blood pressure, hypoalbuminemia, and risk of death in a cohort of chronic hemodialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The methylentetrahydrofolate reductase C677T point mutation is a risk factor for vascular access thrombosis in hemodialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia predicts cardiovascular outcomes in hemodialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reverse epidemiology of cardiovascular risk factors in maintenance dialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fully automated assay for total homocysteine, cysteine, cysteinylglycine, glutathione, cysteamine, and 2-mercaptopropionylglycine in plasma and urine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Death risk in hemodialysis patients: the predictive value of commonly measured variables and an evaluation of death rate differences between facilities

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase gene C677T polymorphism, plasma homocysteine and folate in end-stage renal disease dialysis and non-dialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase gene polymorphisms in essential hypertension relation: with the development of hypertensive end-stage renal disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MTHFR 677TT and 677CT/1298AC genotypes in Cypriot patients may be predisposing to hypertensive nephrosclerosis and chronic renal failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/19466593

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10157-009-0194-2

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19466593

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