İletişim:Engin ALTINTAŞ Mersin Üniversitesi Tıp Fakültesi Zeytinlibahçe Cad. Eskiotogar Yanı İç Hastalıkları A.D. 33079 Mersin, Türkiye • Tel: + 90 324 337 43 00 Fax: + 90 324 336 71 17 • E-mail: enginaltintas@mersin.edu.tr
Homocysteine (Hcy) is a sulfur-containing amino acid that is formed as an intermediary in methionine metabolism (1). Extensive evidence shows that elevated plasma Hcy concentration, a reflection of impaired cellular metabolism, can be considered as an independent risk factor for atherothrombotic vascular disease (2). This condition has been observed in 20% to 30% of patients with premature arteriosclerosis and in 21% of the general population above a certain age (3,4). Three enzymes utilize Hcy as a substrate: methionine synthase (MS) and betaine-homocysteine methyltransferase (BHMT), which convert Hcy back to methionine, and cystathionine β-synthase (CBS), the first enzyme in the transsulfuration pathway (1) (Figure 1)
Birincil Dil | İngilizce |
---|---|
Konular | Sağlık Kurumları Yönetimi |
Bölüm | Makaleler |
Yazarlar | |
Yayımlanma Tarihi | 1 Aralık 2011 |
Yayımlandığı Sayı | Yıl 2011 Cilt: 10 Sayı: 3 |
test-5