PLoS ONE (Jan 2018)

Evolution of platelet functions in cirrhotic patients undergoing liver transplantation: A prospective exploration over a month.

  • Daniel Eyraud,
  • Ludovic Suner,
  • Axelle Dupont,
  • Christilla Bachelot-Loza,
  • David M Smadja,
  • Dominique Helley,
  • Sébastien Bertil,
  • Ovidiu Gostian,
  • Jean Szymezak,
  • Yann Loncar,
  • Louis Puybasset,
  • Pascal Lebray,
  • Corinne Vezinet,
  • Jean-Christophe Vaillant,
  • Benjamin Granger,
  • Pascale Gaussem

DOI
https://doi.org/10.1371/journal.pone.0200364
Journal volume & issue
Vol. 13, no. 8
p. e0200364

Abstract

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This prospective observational study was designed to analyze platelet functions across time in 50 patients scheduled for liver transplantation (LT) secondary to decompensated cirrhosis or hepatocellular carcinoma. Platelet functions were assessed before LT (pre-LT), one week (D7) and 1 month (D28) after LT. Platelet count significantly increased from pre-LT time to day 28 as well as circulating CD34+hematopoietic stem cells. To avoid any influence of platelet count on assays, platelet function was evaluated on platelet-rich-plasma adjusted to pre-LT platelet count. Although platelet secretion potential did not differ between time-points, as evaluated by the expression of CD62P upon strong activation, platelet aggregation in response to various agonists significantly increased along time, however with no concomitant increase of circulating markers of platelet activation: platelet microvesicles, platelet-leukocyte complexes, soluble CD40L and soluble CD62P. In the multivariate analysis, hepatic function was associated with platelet count and function. A lower platelet aggregation recovery was correlated with Child C score. History of thrombosis or bleeding was associated with respective higher or lower values of platelet aggregation. This longitudinal analysis of platelet functions in LT patients showed an improvement of platelet functions along time together with platelet count increase, with no evidence of platelet hyperactivation at any time-point.