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      The Addition of C‐Reactive Protein and von Willebrand Factor to Model for End‐Stage Liver Disease‐Sodium Improves Prediction of Waitlist Mortality

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          Abstract

          Background and Aims

          Patients with cirrhosis on the liver transplant (LT) waiting list may die or be removed because of complications of portal hypertension (PH) or infections. von Willebrand factor antigen (vWF‐Ag) and C‐reactive protein (CRP) are simple, broadly available markers of these processes.

          Approach and Results

          We determined whether addition of vWF‐Ag and CRP to the Model for End‐Stage Liver Disease‐Sodium (MELD‐Na) score improves risk stratification of patients awaiting LT. CRP and vWF‐Ag at LT listing were assessed in two independent cohorts (Medical University of Vienna [exploration cohort] and Mayo Clinic Rochester [validation cohort]). Clinical characteristics, MELD‐Na, and mortality on the waiting list were recorded. Prediction of 3‐month waiting list mortality was assessed by receiver operating characteristics curve (ROC‐AUC). In order to explore potential mechanisms underlying the prognostic utility of vWF‐Ag and CRP in this setting, we evaluated their association with PH, bacterial translocation, systemic inflammation, and circulatory dysfunction. In the exploration cohort (n = 269) vWF‐Ag and CRP both improved the predictive value of MELD‐Na for 3‐month waitlist mortality and showed the highest predictive value when combined (AUC: MELD‐Na, 0.764; MELD‐Na + CRP, 0.790; MELD‐Na + vWF, 0.803; MELD‐Na + CRP + vWF‐Ag, 0.824). Results were confirmed in an independent validation cohort (n = 129; AUC: MELD‐Na, 0.677; MELD‐Na + CRP + vWF‐Ag, 0.882). vWF‐Ag was independently associated with PH and inflammatory biomarkers, whereas CRP closely, and MELD independently, correlated with biomarkers of bacterial translocation/inflammation.

          Conclusions

          The addition of vWF‐Ag and CRP—reflecting central pathophysiological mechanisms of PH, bacterial translocation, and inflammation, that are all drivers of mortality on the waiting list for LT—to the MELD‐Na score improves prediction of waitlist mortality. Using the vWFAg‐CRP‐MELD‐Na model for prioritizing organ allocation may improve prediction of waitlist mortality and decrease waitlist mortality.

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          Most cited references49

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          Hyponatremia and mortality among patients on the liver-transplant waiting list.

          Under the current liver-transplantation policy, donor organs are offered to patients with the highest risk of death. Using data derived from all adult candidates for primary liver transplantation who were registered with the Organ Procurement and Transplantation Network in 2005 and 2006, we developed and validated a multivariable survival model to predict mortality at 90 days after registration. The predictor variable was the Model for End-Stage Liver Disease (MELD) score with and without the addition of the serum sodium concentration. The MELD score (on a scale of 6 to 40, with higher values indicating more severe disease) is calculated on the basis of the serum bilirubin and creatinine concentrations and the international normalized ratio for the prothrombin time. In 2005, there were 6769 registrants, including 1781 who underwent liver transplantation and 422 who died within 90 days after registration on the waiting list. Both the MELD score and the serum sodium concentration were significantly associated with mortality (hazard ratio for death, 1.21 per MELD point and 1.05 per 1-unit decrease in the serum sodium concentration for values between 125 and 140 mmol per liter; P<0.001 for both variables). Furthermore, a significant interaction was found between the MELD score and the serum sodium concentration, indicating that the effect of the serum sodium concentration was greater in patients with a low MELD score. When applied to the data from 2006, when 477 patients died within 3 months after registration on the waiting list, the combination of the MELD score and the serum sodium concentration was considerably higher than the MELD score alone in 32 patients who died (7%). Thus, assignment of priority according to the MELD score combined with the serum sodium concentration might have resulted in transplantation and prevented death. This population-wide study shows that the MELD score and the serum sodium concentration are important predictors of survival among candidates for liver transplantation. 2008 Massachusetts Medical Society
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            Model for end-stage liver disease (MELD) and allocation of donor livers.

            A consensus has been reached that liver donor allocation should be based primarily on liver disease severity and that waiting time should not be a major determining factor. Our aim was to assess the capability of the Model for End-Stage Liver Disease (MELD) score to correctly rank potential liver recipients according to their severity of liver disease and mortality risk on the OPTN liver waiting list. The MELD model predicts liver disease severity based on serum creatinine, serum total bilirubin, and INR and has been shown to be useful in predicting mortality in patients with compensated and decompensated cirrhosis. In this study, we prospectively applied the MELD score to estimate 3-month mortality to 3437 adult liver transplant candidates with chronic liver disease who were added to the OPTN waiting list at 2A or 2B status between November, 1999, and December, 2001. In this study cohort with chronic liver disease, 412 (12%) died during the 3-month follow-up period. Waiting list mortality increased directly in proportion to the listing MELD score. Patients having a MELD score or =40 had a mortality rate of 71.3%. Using the c-statistic with 3-month mortality as the end point, the area under the receiver operating characteristic (ROC) curve for the MELD score was 0.83 compared with 0.76 for the Child-Turcotte-Pugh (CTP) score (P < 0.001). These data suggest that the MELD score is able to accurately predict 3-month mortality among patients with chronic liver disease on the liver waiting list and can be applied for allocation of donor livers.
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              Acute-on-Chronic Liver Failure

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                Author and article information

                Contributors
                starlinger.patrick@mayo.edu
                Journal
                Hepatology
                Hepatology
                10.1002/(ISSN)1527-3350
                HEP
                Hepatology (Baltimore, Md.)
                John Wiley and Sons Inc. (Hoboken )
                0270-9139
                1527-3350
                29 August 2021
                September 2021
                : 74
                : 3 ( doiID: 10.1002/hep.v74.3 )
                : 1533-1545
                Affiliations
                [ 1 ] Department of Surgery Division of Hepatobiliary and Pancreas Surgery Mayo Clinic Rochester MN
                [ 2 ] Department of Surgery Division of General Surgery Medical University of Vienna General Hospital Vienna Vienna Austria
                [ 3 ] Division of Gastroenterology and Hepatology Mayo Clinic Rochester MN
                [ 4 ] Department of Health Sciences Research Mayo Clinic Rochester MN
                [ 5 ] Division of Transplantation Department of Surgery Medical University of Vienna General Hospital Vienna Vienna Austria
                [ 6 ] Institute of Bioinformatics Biocenter Medical University of Innsbruck Innsbruck Austria
                [ 7 ] Division of Gastroenterology and Hepatology Department of Medicine III Medical University of Vienna Vienna Austria
                [ 8 ] Vienna Hepatic Hemodynamic Lab Medical University of Vienna Vienna Austria
                [ 9 ] Christian Doppler Laboratory for Portal Hypertension and Liver Fibrosis Medical University of Vienna Vienna Austria
                [ 10 ] Department of Surgery Division of Transplantation Surgery Mayo Clinic Rochester MN
                Author notes
                [*] [* ] ADDRESS CORRESPONDENCE AND REPRINT REQUESTS TO:

                Patrick Starlinger, M.D., Ph.D.

                Department of Surgery, Division of Hepatobiliary and Pancreas Surgery, Mayo Clinic 200 First Street Southwest

                Rochester, MN 55905

                E‐mail: starlinger.patrick@ 123456mayo.edu

                Tel.: +1‐507‐284‐2511

                Author information
                https://orcid.org/0000-0002-4666-5337
                https://orcid.org/0000-0002-0863-2876
                https://orcid.org/0000-0001-6700-9163
                https://orcid.org/0000-0002-4590-3583
                https://orcid.org/0000-0003-2330-0017
                Article
                HEP31838
                10.1002/hep.31838
                8518408
                33786862
                4bf3200b-61ca-462c-9b6c-783614c8144e
                © 2021 The Authors. Hepatology published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 09 February 2021
                : 06 October 2020
                : 14 March 2021
                Page count
                Figures: 4, Tables: 3, Pages: 13, Words: 8242
                Categories
                Original Article
                Original Articles
                Liver Failure/Cirrhosis/ Portal Hypertension
                Custom metadata
                2.0
                September 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.8 mode:remove_FC converted:15.10.2021

                Gastroenterology & Hepatology
                Gastroenterology & Hepatology

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