Cytomegalovirus (CMV) viraemia detected by polymerase chain reaction identifies a group of HIV-positive patients at high risk of CMV disease

被引:120
作者
Bowen, EF
Sabin, CA
Wilson, P
Griffiths, PD
Davey, CC
Johnson, MA
Emery, VC
机构
[1] ROYAL FREE HOSP,DEPT VIROL,LONDON NW3 2QG,ENGLAND
[2] ROYAL FREE HOSP,DEPT THORAC HIV MED,LONDON NW3 2QG,ENGLAND
[3] ROYAL FREE HOSP,DEPT PRIMARY CARE & POPULAT SCI,LONDON NW3 2QG,ENGLAND
[4] ROYAL FREE HOSP,DEPT OPHTHALMOL,LONDON NW3 2QG,ENGLAND
[5] UNIV LONDON SCH MED,LONDON NW3 2QG,ENGLAND
关键词
pre-emptive therapy; viral load; retinitis;
D O I
10.1097/00002030-199707000-00008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Cytomegalovirus (CMV) disease is a major cause of morbidity in patients with HIV infection. Despite treatment, CMV retinitis causes substantial visual loss, especially in patients with CD4 cell counts below 50 x 10(6)/l. Although routine ophthalmological screening of these patients has been recommended, no controlled trials have evaluated how frequently it should be performed. The aim of this study was to assess whether CMV polymerase chain reaction (PCR) results could direct ophthalmological screening to patients at high risk of CMV retinitis. Methods: In a prospective study of HIV-positive patients with CD4 cell counts below 50 x 10(6)/l, CMV viraemia was detected by qualitative PCR of whole blood. Patients who were CMV PCR-viraemic were allocated to monthly virological and ophthalmological follow-up; patients who were PCR-negative received 3-monthly virological and ophthalmological follow-up. CMV viral load was determined in all CMV-positive samples using a quantitative competitive PCR. Results: Nineteen out of 97 patients developed CMV disease over the first 12 months of the study. Sixteen (59%) out of 27 patients who were CMV-positive developed disease compared with three (4%) out of 70 of patients who were PCR-negative (P = 0.0001). A positive CMV PCR result was significantly associated with the development of disease (P = 0.0001), with a relative hazard of 20.15 [95% confidence interval (CI), 5.80-69.98]. Median CMV viral toad was significantly higher in those individuals who went on to develop CMV disease (P = 0.02). In PCR-positive patients, each 0.25 log,, increase in viral load increased the risk of disease (relative hazard, 1.37; 95% CI, 1.15-1.63; P = 0.0004). Conclusions: CMV PCR predicts the development of CMV disease and can be used to target ophthalmological resources to those patients at highest risk of retinitis. Asymptomatic patients who are PCR-positive represent a high-risk group in whom controlled trials of pre-emptive therapy could be conducted.
引用
收藏
页码:889 / 893
页数:5
相关论文
共 16 条
[1]  
BOECKH M, 1994, BONE MARROW TRANSPL, V14, pS66
[2]   Natural history of untreated cytomegalovirus retinitis [J].
Bowen, EF ;
Wilson, P ;
Atkins, M ;
Madge, S ;
Griffiths, PD ;
Johnson, MA ;
Emery, VC .
LANCET, 1995, 346 (8991-2) :1671-1673
[3]  
Cox D. R., 1984, ANAL SURVIVAL DATA
[4]   ORAL GANCICLOVIR AS MAINTENANCE TREATMENT FOR CYTOMEGALOVIRUS RETINITIS IN PATIENTS WITH AIDS [J].
DREW, WL ;
IVES, D ;
LALEZARI, JP ;
CRUMPACKER, C ;
FOLLANSBEE, SE ;
SPECTOR, SA ;
BENSON, CA ;
FRIEDBERG, DN ;
HUBBARD, L ;
STEMPIEN, MJ ;
SHADMAN, A ;
BUHLES, W .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (10) :615-620
[5]  
Dunn J P, 1995, AIDS Clin Rev, P99
[6]   QUANTIFICATION OF HUMAN CYTOMEGALOVIRUS DNA USING THE POLYMERASE CHAIN-REACTION [J].
FOX, JC ;
GRIFFITHS, PD ;
EMERY, VC .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :2405-2408
[7]   INCIDENCE AND NATURAL-HISTORY OF CYTOMEGALOVIRUS DISEASE IN PATIENTS WITH ADVANCED HUMAN-IMMUNODEFICIENCY-VIRUS DISEASE TREATED WITH ZIDOVUDINE [J].
GALLANT, JE ;
MOORE, RD ;
RICHMAN, DD ;
KERULY, J ;
CHAISSON, RE ;
BARTLETT, J ;
MCAVINUE, S ;
BRYSON, Y ;
COHEN, H ;
FISCHL, M ;
BOLIN, T ;
KESSLER, H ;
BURROUGH, Y ;
MILDVAN, D ;
FOX, A ;
RICHMAN, D ;
FREEMAN, B ;
SIMON, G ;
GRABOWY, KW ;
CHERNOFF, D ;
DUFF, P ;
THOMPSON, S ;
BARRETT, K ;
AWE, R ;
CHAPMAN, R ;
LEONARD, S ;
BAINES, L ;
TURNER, P ;
HAWKINS, M ;
MURRAY, H ;
BOWERS, J ;
LANE, C ;
TILSON, H ;
ANDREWS, E ;
SMILEY, L .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 (06) :1223-1227
[8]   DETECTION OF CYTOMEGALOVIRUS DNA IN SERUM CORRELATES WITH CLINICAL CYTOMEGALOVIRUS RETINITIS IN AIDS [J].
HANSEN, KK ;
RICKSTEN, A ;
HOFMANN, B ;
NORRILD, B ;
OLOFSSON, S ;
MATHIESEN, L .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (05) :1271-1274
[9]   PROVISION OF PROGNOSTIC INFORMATION IN IMMUNOCOMPROMISED PATIENTS BY ROUTINE APPLICATION OF THE POLYMERASE CHAIN-REACTION FOR CYTOMEGALOVIRUS [J].
KIDD, IM ;
FOX, JC ;
PILLAY, D ;
CHARMAN, H ;
GRIFFITHS, PD ;
EMERY, VC .
TRANSPLANTATION, 1993, 56 (04) :867-871
[10]   CORRELATION BETWEEN CD4+ COUNTS AND PREVALENCE OF CYTOMEGALOVIRUS RETINITIS AND HUMAN IMMUNODEFICIENCY VIRUS-RELATED NONINFECTIOUS RETINAL VASCULOPATHY IN PATIENTS WITH ACQUIRED-IMMUNODEFICIENCY-SYNDROME [J].
KUPPERMANN, BD ;
PETTY, JG ;
RICHMAN, DD ;
MATHEWS, WC ;
FULLERTON, SC ;
RICKMAN, LS ;
FREEMAN, WR .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1993, 115 (05) :575-582