Publication Type:

Journal Article

Source:

Indian Journal of Clinical Biochemistry, Volume 19, Number 2, p.36-44 (2004)

URL:

http://www.scopus.com/inward/record.url?eid=2-s2.0-3943099389&partnerID=40&md5=2bef1a9809c1f4b23c570b0035d433e9

Keywords:

alcohol, Alcohol abuse, alcohol consumption, article, assay, carbohydrate deficient transferrin, contraception, contraceptive agent, diagnostic accuracy, disease marker, enzyme induction, enzyme inhibition, gender, hormone response, human, iron, iron balance, menopause, menstrual cycle, Pregnancy, protein metabolism, protein processing, protein transport, sex hormone, sialidase, sialyltransferase, Transferrin

Abstract:

Carbohydrate deficient transferrin (CDT) is one of the conventional markers for chronic alcohol consumption, is used by researchers and clinicians. A number of enzymes are affected by ethanol intake. The induction or inhibition of sialyl transferase and plasma sialidase may be involved in the CDT level elevation. An alteration of protein transport during post-translational modification could be a primary mechanism in the impairment of protein metabolism associated with chronic alcohol abuse. Transferrin being a steroid responsive protein, sex-based hormonal variations might contribute to the lower sensitivity of CDT. Varying hormonal statuses such as pregnancy, use of contraceptives, menopause/ menstrual cycle can alter iron homeostasis in women. CDT levels are markedly affected by iron homeostasis. Several CDT assay methods appeared promising, but it is not readily apparent which technique is the most accurate. Moreover, false-positive results of CDT have been reported in non-alcohol related hepatic failure and in rare conditions. Therefore clinical interpretation of CDT needs careful assessment in patients with alcohol-related or non-alcohol-related health disorders.

Notes:

cited By 4

Cite this Research Publication

S. K. Das and Vasudevan, D. M., “Should we use carbohydrate deficient transferrin as a marker for alcohol abusers?”, Indian Journal of Clinical Biochemistry, vol. 19, pp. 36-44, 2004.

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