Department of Preventive and Social Medicine, University of Otago, , Dunedin, New Zealand.
Sex Transm Infect. 2014 May;90(3):243-5. doi: 10.1136/sextrans-2013-051235. Epub 2013 Dec 13.
To examine herpes simplex virus type 2 (HSV-2) incidence over four periods to age 38 in a birth cohort, and to compare risks for men and women, taking into account sexual behaviour.
At ages 21, 26, 32 and 38, participants in the Dunedin Multidisciplinary Health and Development Study were invited to provide serum for HSV-2 serology, and information on sexual behaviour. HSV-2 incidence rates were calculated for four age periods, and comparisons made by sex and period, taking into account number of sexual partners.
By age 38, 17.3% of men and 26.8% of women had ever been seropositive for HSV-2. Incidence peaked for women from age 21 to 26 (19.1 per 1000 person-years) and men from age 26 to 32 (14.1 per 1000 person-years); it fell markedly for both from age 32 to 38 (5.1 and 6.8 per 1000 person-years for men and women, respectively). Overall risk was significantly higher for women: adjusted incidence rate ratio 1.9 (95% CI 1.4 to 2.7); the sex difference was most marked from age 21 to 26 (3.4, 95% CI 1.9 to 6.3).
Our findings are consistent with a greater biological susceptibility to HSV-2 among women, and with the increasing risk to the early/mid-20s for women and late 20s/early 30s for men, being driven by an increasing pool of prevalent infection. The reduced risk in the mid-30s is consistent with declining infectivity of long-term prevalent infections.
在一个出生队列中,检查四个时期至 38 岁的单纯疱疹病毒 2 型(HSV-2)发病率,并考虑性行为,比较男性和女性的风险。
在 21、26、32 和 38 岁时,邀请 Dunedin 多学科健康与发展研究的参与者提供血清进行 HSV-2 血清学检测,并提供性行为信息。计算了四个年龄期的 HSV-2 发病率,并根据性别和时期进行了比较,同时考虑了性伴侣数量。
到 38 岁时,17.3%的男性和 26.8%的女性 HSV-2 血清阳性。女性的发病率在 21 岁至 26 岁期间(19.1/1000 人年)和男性在 26 岁至 32 岁期间(14.1/1000 人年)达到峰值;此后,两者均明显下降(男性和女性分别为 5.1 和 6.8/1000 人年)。女性的总体风险明显更高:调整后的发病率比 1.9(95%CI 1.4 至 2.7);从 21 岁至 26 岁,性别差异最为显著(3.4,95%CI 1.9 至 6.3)。
我们的研究结果与女性对 HSV-2 的生物学易感性更高一致,并且与女性在 20 岁出头到中期以及男性在 20 岁后期到 30 岁初期的风险增加一致,这是由流行感染的增加所驱动。30 多岁中期风险降低与长期流行感染的传染性下降一致。