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ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.
- Source :
-
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2013 Feb; Vol. 15 (2), pp. 153-6. Date of Electronic Publication: 2013 Jan 03. - Publication Year :
- 2013
-
Abstract
- MTHFR polymorphism testing is frequently ordered by physicians as part of the clinical evaluation for thrombophilia. It was previously hypothesized that reduced enzyme activity of MTHFR led to mild hyperhomocysteinemia which led to an increased risk for venous thromboembolism, coronary heart disease, and recurrent pregnancy loss. Recent meta-analyses have disproven an association between hyperhomocysteinemia and risk for coronary heart disease and between MTHFR polymorphism status and risk for venous t-hromboembolism. There is growing evidence that MTHFR polymorphism testing has minimal clinical utility and, therefore should not be ordered as a part of a routine evaluation for thrombophilia.
- Subjects :
- Coronary Disease diagnosis
Coronary Disease genetics
Genetic Predisposition to Disease genetics
Genetics, Medical methods
Genetics, Medical organization & administration
Genomics methods
Genomics organization & administration
Humans
Hyperhomocysteinemia diagnosis
Hyperhomocysteinemia genetics
Methylenetetrahydrofolate Reductase (NADPH2) genetics
Polymorphism, Genetic
Risk Factors
Thrombophilia diagnosis
Thrombophilia genetics
United States
Venous Thromboembolism diagnosis
Venous Thromboembolism genetics
Genetic Testing standards
Genetics, Medical standards
Genomics standards
Practice Guidelines as Topic
Subjects
Details
- Language :
- English
- ISSN :
- 1530-0366
- Volume :
- 15
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Genetics in medicine : official journal of the American College of Medical Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 23288205
- Full Text :
- https://doi.org/10.1038/gim.2012.165