Serum Factor V Is a Continuous Biomarker of Graft Dysfunction and a Predictor of Graft Loss After Liver Transplantation.


Journal

Transplantation
ISSN: 1534-6080
Titre abrégé: Transplantation
Pays: United States
ID NLM: 0132144

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 22 8 2018
medline: 14 11 2019
entrez: 22 8 2018
Statut: ppublish

Résumé

Factor V has never been compared to a validated early allograft dysfunction (EAD) definition. We aimed to assess factor V as a biomarker of EAD and a predictor of graft loss after liver transplantation (LT). We retrospectively assessed the serum factor V levels on postoperative day 1 after LT. Patients were divided according to their factor V levels into the ≤36.1 U/mL and > 36.1 U/mL groups. The primary outcome was graft loss within 1, 3, and 6 months. The secondary outcome was EAD, as defined by Olthoff et al. Predictors of outcomes were identified by multivariable logistic regression. Two hundred twenty-seven patients were included in the study: 74 with factor V of 36.1 U/mL or less and 153 with factor V >36.1 U/mL. EAD was diagnosed in 41 (55.4%) of 74 patients with factor V of 36.1 U/mL or less and in 20/153 (13.1%) patients with factor V >36.1 U/mL (P < 0.001). According to the multivariable regression model, factor V was a continuous marker of EAD (odds ratio [OR], 0.96; 95% confidence interval [CI], 0.94-0.98 per U/mL). Among the study groups, the 1-, 3-, and 6-month graft survival rates were 82%, 74%, and 74%, respectively, for patients with factor V of 36.1 U/mL or less and 98%, 95%, and 95%, respectively, for patients with factor V >36.1 U/mL (P = 0.001). Factor V was a continuous predictor for 3- and 6-month graft losses (OR, 0.96; 95% CI, 0.94-0.99 and OR, 0.97; 95% CI, 0.94-0.99 per U/mL), whereas EAD was not significant when adjusted for factor V. Factor V is an early marker for EAD and is a continuous predictor of short-term graft loss after LT.

Sections du résumé

BACKGROUND
Factor V has never been compared to a validated early allograft dysfunction (EAD) definition. We aimed to assess factor V as a biomarker of EAD and a predictor of graft loss after liver transplantation (LT).
METHODS
We retrospectively assessed the serum factor V levels on postoperative day 1 after LT. Patients were divided according to their factor V levels into the ≤36.1 U/mL and > 36.1 U/mL groups. The primary outcome was graft loss within 1, 3, and 6 months. The secondary outcome was EAD, as defined by Olthoff et al. Predictors of outcomes were identified by multivariable logistic regression.
RESULTS
Two hundred twenty-seven patients were included in the study: 74 with factor V of 36.1 U/mL or less and 153 with factor V >36.1 U/mL. EAD was diagnosed in 41 (55.4%) of 74 patients with factor V of 36.1 U/mL or less and in 20/153 (13.1%) patients with factor V >36.1 U/mL (P < 0.001). According to the multivariable regression model, factor V was a continuous marker of EAD (odds ratio [OR], 0.96; 95% confidence interval [CI], 0.94-0.98 per U/mL). Among the study groups, the 1-, 3-, and 6-month graft survival rates were 82%, 74%, and 74%, respectively, for patients with factor V of 36.1 U/mL or less and 98%, 95%, and 95%, respectively, for patients with factor V >36.1 U/mL (P = 0.001). Factor V was a continuous predictor for 3- and 6-month graft losses (OR, 0.96; 95% CI, 0.94-0.99 and OR, 0.97; 95% CI, 0.94-0.99 per U/mL), whereas EAD was not significant when adjusted for factor V.
CONCLUSION
Factor V is an early marker for EAD and is a continuous predictor of short-term graft loss after LT.

Identifiants

pubmed: 30130328
doi: 10.1097/TP.0000000000002429
doi:

Substances chimiques

Biomarkers 0
Factor V 9001-24-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

944-951

Auteurs

Andre Gorgen (A)

Postgraduate Program, Surgical Sciences, Medical School, Federal University of Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Multi-Organ Transplant Program, General Surgery Department, University Health Network, Toronto General Hospital, University of Toronto, Toronto, Canada.

Carolina Prediger (C)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

João E Prediger (JE)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Marcio F Chedid (MF)

Postgraduate Program, Surgical Sciences, Medical School, Federal University of Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Ariane N Backes (AN)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Alexandre de Araujo (A)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Tomaz J M Grezzana-Filho (TJM)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Ian Leipnitz (I)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Aljamir D Chedid (AD)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Mario R Alvares-da-Silva (MR)

Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

Gonzalo Sapisochin (G)

Multi-Organ Transplant Program, General Surgery Department, University Health Network, Toronto General Hospital, University of Toronto, Toronto, Canada.

Cleber R P Kruel (CRP)

Postgraduate Program, Surgical Sciences, Medical School, Federal University of Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Liver Transplant Program, Hospital de Clinicas de Porto Alegre, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.

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