Hyperhomocysteinaemia: Physiophatology and medical implications.

Citation
At. Delgadillo et al., Hyperhomocysteinaemia: Physiophatology and medical implications., REV INV CLI, 52(5), 2000, pp. 557-564
Citations number
63
Categorie Soggetti
General & Internal Medicine
Journal title
REVISTA DE INVESTIGACION CLINICA
ISSN journal
00348376 → ACNP
Volume
52
Issue
5
Year of publication
2000
Pages
557 - 564
Database
ISI
SICI code
0034-8376(200009/10)52:5<557:HPAMI>2.0.ZU;2-8
Abstract
Homocysteine is an intermediate aminoacid result of the conversion of methi onine to cysteine. Homocystinuria or the hyperhomocysteinaemia are the most frequently related disorders of this aminoacid, being the former an. autos omic recessive alteration, whereas the latter is conditioned by multiple fa ctors, being the most important the genetic and nutritional factors. In the last years this alteration has regained special interest because of its increasing role in the thrombotic pathologies and the identification th at hyperhomocysteinaemia represents art independent risk factor for the acc elerated atherogenesis of multiple diseases. In this review physiopathologi cal aspects and clinical implications of hyperhomocysteinaemia are mentione d as well as its diagnoses and treatment.