A. Cunha, A. Cunha, D. Solla, R. Chaves, B. G. C. Filho, R. Nascimento
{"title":"Active cytomegalovirus (CMV) infection in liver recipients in a high CMV seroprevalence region - outcomes and the use of antigenemia","authors":"A. Cunha, A. Cunha, D. Solla, R. Chaves, B. G. C. Filho, R. Nascimento","doi":"10.17525/vrrjournal.v18i1-2.89","DOIUrl":null,"url":null,"abstract":"Cytomegalovirus (CMV) is the most frequent viral infection in liver recipients, acting as immunomodulatory factor for \nother opportunistic infections and rejection. We assessed the outcomes of CMV infection in liver recipients in a high \nCMV seroprevalence region and the use of antigenemia for the diagnosis of CMV syndrome. Between March 2007 \nand April 2009, 44 liver recipients collected 344 samples for CMV antigenemia. Defi nition of active CMV infections \nused literature criteria. Recipients’ outcomes [CMV syndrome, Hepatitis C Virus (HCV) recurrence, rejection and \nmortality] were analyzed. Performance of antigenemia for the diagnosis of CMV syndrome was assessed by the area \nunder the Receiver Operating Curve (AUROC) of 52 positive samples, representing 24 recipients. CMV serology was \npositive (R+) in 90.9% of liver recipients. CMV syndrome occurred in 18 (40.9%) recipients. CMV negative serology \n(R-) recipients had lower disease-free time, as well as lower one-year and four-year survival rates (p = 0.022 and p = \n0.004, respectively). HCV+ recipients presented CMV-associated indirect eff ects and had a tendency to lower fouryear \nsurvival rate (p=0.089). Th e AUROC for CMV syndrome was 0.745 (95% CI 0.606 to 0.856, p = 0.006), with a \ncut-off of more than 8 positive cells/200,000 leukocytes, (sensitivity of 88.9% and specifi city of 74.4%). CMV infection \nis associated to morbidity and lower survival rates in liver recipients in a high CMV seroprevalence region. Using \nantigenemia, the cut-off for diagnosing CMV syndrome was higher than 8 positive cells/200,000 leukocytes, with an \nappropriated performance through its accuracy.","PeriodicalId":30621,"journal":{"name":"Virus Reviews Research","volume":"18 1","pages":"6"},"PeriodicalIF":0.0000,"publicationDate":"2013-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus Reviews Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17525/vrrjournal.v18i1-2.89","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Cytomegalovirus (CMV) is the most frequent viral infection in liver recipients, acting as immunomodulatory factor for
other opportunistic infections and rejection. We assessed the outcomes of CMV infection in liver recipients in a high
CMV seroprevalence region and the use of antigenemia for the diagnosis of CMV syndrome. Between March 2007
and April 2009, 44 liver recipients collected 344 samples for CMV antigenemia. Defi nition of active CMV infections
used literature criteria. Recipients’ outcomes [CMV syndrome, Hepatitis C Virus (HCV) recurrence, rejection and
mortality] were analyzed. Performance of antigenemia for the diagnosis of CMV syndrome was assessed by the area
under the Receiver Operating Curve (AUROC) of 52 positive samples, representing 24 recipients. CMV serology was
positive (R+) in 90.9% of liver recipients. CMV syndrome occurred in 18 (40.9%) recipients. CMV negative serology
(R-) recipients had lower disease-free time, as well as lower one-year and four-year survival rates (p = 0.022 and p =
0.004, respectively). HCV+ recipients presented CMV-associated indirect eff ects and had a tendency to lower fouryear
survival rate (p=0.089). Th e AUROC for CMV syndrome was 0.745 (95% CI 0.606 to 0.856, p = 0.006), with a
cut-off of more than 8 positive cells/200,000 leukocytes, (sensitivity of 88.9% and specifi city of 74.4%). CMV infection
is associated to morbidity and lower survival rates in liver recipients in a high CMV seroprevalence region. Using
antigenemia, the cut-off for diagnosing CMV syndrome was higher than 8 positive cells/200,000 leukocytes, with an
appropriated performance through its accuracy.