Interrelationships among quantity of human cytomegalovirus (HCMV) DNA in blood, donor-recipient serostatus, and administration of methylprednisolone as risk factors for HCMV disease following liver transplantation

被引:154
作者
Cope, AV
Sabin, C
Burroughs, A
Rolles, K
Griffiths, PD
Emery, VC
机构
[1] ROYAL FREE HOSP, SCH MED, DIV PATHOL & COMMUNICABLE DIS, DEPT VIROL, LONDON NW3 2PF, ENGLAND
[2] ROYAL FREE HOSP, SCH MED, DEPT PRIMARY CARE, LONDON NW3 2PF, ENGLAND
[3] ROYAL FREE HOSP, SCH MED, DEPT POPULAT SCI, LONDON NW3 2PF, ENGLAND
[4] ROYAL FREE HOSP, SCH MED, LIVER TRANSPLANT UNIT, LONDON NW3 2PF, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1086/514145
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Longitudinal analysis of 162 liver transplant recipients identified 51 patients who were viremic. Virus load was determined in 47 of these patients using quantitative-competitive polymerase chain reaction, Peak: virus load was significantly higher in 20 symptomatic patients than 27 asymptomatic patients (P < .0001), Elevated virus load, donor seropositivity, and total methylprednisolone dosage were risk factors for human cytomegalovirus (HCMV) disease (odds ratio [OR], 2.22/0.25 log(10) increase in virus load, P = .001; OR, 4.11, P = .05; OR, 130/1-g increment in methylprednisolone, P = .01), Methylprednisolone and virus load were independent risk factors in a multivariate analysis (OR, 2.70/1-g increase, P = .003; OR, 1.61/0.25 log(10) increase, P = .03, respectively). Virus loads of 10(4.75)-10(5.25) genomes/mL of blood were associated with an increased disease probability; the latter was shifted to lower virus loads with increasing quantities of methylprednisolone. These data illustrate the central role of virus load in HCMV pathogenesis.
引用
收藏
页码:1484 / 1490
页数:7
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