Homocysteine (Hcy) is a sulfhydryl amino acid derived from the metabolic conversion of methionine, which is dependent on vitamins (folic acid, B12 and B6) as cofactors or cosubstrates. Severe hyperhomocysteinemia (homocystinuria), due to inherited metabolic defects of Hcy metab., is assocd. with very high risk of venous thromboembolism (VTE); treatment with vitamins is assocd. with dramatic decrease of VTE risk. Several case-control and prospective studies showed that also mild/moderate hyperhomocysteinemia (which is caused by the interaction of environmental factors with mild genetic abnormalities of Hcy metab.) is assocd. with heightened risk of VTE; however, it is uncertain whether treatment with vitamins also decreases the VTE risk in these patients. [on SciFinder (R)]
Hyperhomocysteinemia and venous thromboembolism / M. Cattaneo. - In: SEMINARS IN THROMBOSIS AND HEMOSTASIS. - ISSN 0094-6176. - 32:7(2006), pp. 716-723.
Hyperhomocysteinemia and venous thromboembolism
M. CattaneoPrimo
2006
Abstract
Homocysteine (Hcy) is a sulfhydryl amino acid derived from the metabolic conversion of methionine, which is dependent on vitamins (folic acid, B12 and B6) as cofactors or cosubstrates. Severe hyperhomocysteinemia (homocystinuria), due to inherited metabolic defects of Hcy metab., is assocd. with very high risk of venous thromboembolism (VTE); treatment with vitamins is assocd. with dramatic decrease of VTE risk. Several case-control and prospective studies showed that also mild/moderate hyperhomocysteinemia (which is caused by the interaction of environmental factors with mild genetic abnormalities of Hcy metab.) is assocd. with heightened risk of VTE; however, it is uncertain whether treatment with vitamins also decreases the VTE risk in these patients. [on SciFinder (R)]Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.