Variation in the WBC differential count and other factors associated with reporting of herpes labialis: A population-based study of adults

被引:3
|
作者
Parks, Christine G.
Andrew, Michael E.
Blanciforti, Laura A.
Luster, Michael I.
机构
[1] NIOSH, Hlth Effects Lab Div, Biostat & Epidemiol Branch, Morgantown, WV 26505 USA
[2] NIOSH, Hlth Effects Lab Div, Toxicol & Mol Biol Branch, Morgantown, WV 26505 USA
来源
关键词
herpes labialis/epidemiology; fever blisters; labialis virus/immunology; leukocytes;
D O I
10.1111/j.1574-695X.2007.00314.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Reactivation of latent herpes virus has been linked to triggers of mild immunosupression, such as stress or UV-exposure. Despite having predictive value in severe immunodeficiency, the white blood cell (WBC) differential count has not been examined in relation to risk of herpes reactivation in population studies. The WBC differential count and other risk factors for herpes labialis were examined in 5687 adults (ages 18-64) from the Third National Health and Nutrition Examination Survey, who had WBC 3.5-11 x 10(6) cells mL(-1) and reported no acute infections in the past month. The association between self-reported herpes labialis in the past year and the WBC differential count was modeled, adjusting for age, sex, race/ethnicity, education, smoking, upper respiratory infections (URI), and HSV-1 antibodies. Herpes labialis was significantly associated with white race/ethnicity, being a nonsmoker, and frequent URI. Compared with the highest quartile, being in the lowest quartile of granulocytes was associated with herpes labialis, adjusted odds ratio=1.82 (95% confidence interval 1.20, 2.28). At the same time, there was a trend towards an inverse association of lower lymphocyte count and herpes labialis. These findings suggest that moderate differences in the WBC differential count are related to reactivation of HSV-1. Prospective studies may help to show whether such differences indicate susceptibility to loss of latency or represent a consequence of reactivated infection.
引用
收藏
页码:336 / 343
页数:8
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