Asialotransferrin discriminating excessive, subacute and chronic active alcohol consumption. Clinical usefulness in hepatic disease.

Authors

  • J A Peneda Hospital St. A. Capuchos (H.C.L.) Dep. Biologia Médica, Lisboa.
  • A Fonseca
  • M Neves
  • P Ribeiro
  • M Alves
  • I Redondo
  • F Calinas
  • M C Martins

DOI:

https://doi.org/10.20344/amp.2561

Abstract

The determination of serum levels of carbohydrate deficient transferrin (CDT) and transferrin ratio in the persistent abusive alcohol consumer arises with promising utility in the study of alcohol related disorders. This series shows the excellent specificity (97%), though poor sensitivity (52%), for CDT. However the CDT/Tft ratio affords a higher sensitivity, reaching 74%, maintaining the high specificity. In persistent abusive consumers (> 70 g/day) this index, which is positively correlated with serum transferrin, is capable of defining these amounts of alcohol per capita with a high frequency and provides independent information since it is not significantly correlated with the levels of traditional biological markers (AST, ALT, GGT, AGV). Although with defined methodological limitations, these indexes denote, with the improvement of technical accessibility, a practical applicability in the screening of chronic abusive consumers. In the field of hepatology the behaviour of CDT and the transferrin ratio is capable of showing the involvement of ethanol in the study of the nature of a chronic hepatic disease with a high frequency. However, the degree of liver lesion show by the PGA hepatic index, has no significant influence on the serum levels of CDT and the transferrin ratio. In this series, the circumstances and conditions of alcohol consumption seem to be the independent determinant of the informative character which these indexes reveal.

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How to Cite

1.
Peneda JA, Fonseca A, Neves M, Ribeiro P, Alves M, Redondo I, Calinas F, Martins MC. Asialotransferrin discriminating excessive, subacute and chronic active alcohol consumption. Clinical usefulness in hepatic disease. Acta Med Port [Internet]. 1996 Mar. 30 [cited 2024 Nov. 13];9(2-3):103-11. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/2561

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Arquivo Histórico