Increased All-Cause and Cancer Mortality in HTLV-II Infection

被引:31
作者
Biswas, Hope H. [3 ]
Kaidarova, Zhanna [3 ]
Garratty, George [4 ]
Gibble, Joan W. [5 ]
Newman, Bruce H. [6 ]
Smith, James W. [7 ]
Ziman, Alyssa [8 ]
Fridey, Joy L. [9 ]
Sacher, Ronald A. [10 ]
Murphy, Edward L. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94118 USA
[2] Univ Calif San Francisco, Dept Epidemiol Biostat, San Francisco, CA 94118 USA
[3] Blood Syst Res Inst, San Francisco, CA 94118 USA
[4] Amer Red Cross Blood Serv, Pomona, CA USA
[5] Amer Red Cross Blood Serv, Baltimore, MD USA
[6] Amer Red Cross Blood Serv, Detroit, MI USA
[7] Oklahoma Blood Inst, Sylvan N Goldman Ctr, Oklahoma City, OK USA
[8] Univ Calif Los Angeles, Med Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90024 USA
[9] Childrens Hosp Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA 90027 USA
[10] Univ Cincinnati, Hoxworth Blood Ctr, Cincinnati, OH USA
关键词
blood donors; cohort studies; HTLV-I infections; HTLV-II infections; mortality; neoplasms; LYMPHOTROPIC VIRUS TYPE-1; DRUG-USERS; STRONGYLOIDES-STERCORALIS; DISEASE PROGRESSION; PREVALENCE; RISK; COINFECTION; POPULATION; SURVIVAL; OUTCOMES;
D O I
10.1097/QAI.0b013e3181cc5481
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: Human T-lymphotropic virus (HTLV)-I and HTLV-II cause chronic human retroviral infections, but few studies have examined the impact of either virus on survival among otherwise healthy individuals. The authors analyzed all-cause and cancer mortality in a prospective cohort of 155 HTLV-I, 387 HTLV-II, and 799 seronegative subjects. Methods: Vital status was ascertained using death certificates, the US Social Security Death Index or family report, and causes of death were grouped into 9 categories. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using Cox proportional hazards models. Results: After a median follow-up of 15.9 years, there were 105 deaths: 22 HTLV-I, 41 HTLV-II, and 42 HTLV-seronegative. Cancer was the predominant cause of death, resulting in 8 HTLV-I, 17 HTLV-II, and 15 HTLV-seronegative deaths. After adjustment for confounding, HTLV-I status was not significantly associated with increased all-cause mortality, though there was a positive trend (HR: 1.6, 95% CI: 0.8 to 3.1). HTLV-II status was strongly associated with increased all-cause (HR: 2.4, 95% CI: 1.4 to 4.4) and cancer mortality (HR: 3.8, 95% CI: 1.6 to 9.2). Conclusions: The observed associations of HTLV-II with all-cause and cancer mortality could reflect biological effects of HTLV-II infection, residual confounding by socioeconomic status or other factors, or differential access to health care and cancer screening.
引用
收藏
页码:290 / 296
页数:7
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