aCenter for Biostatistics in AIDS Research bDepartment of Biostatistics, Harvard School of Public Health, Boston, Massachusetts cDepartment of Pediatrics (Infectious Diseases), University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, Colorado dTulane University School of Medicine, New Orleans, Louisiana eEunice Kennedy Shriver National Institute of Child Health & Human Development, Bethesda, Maryland fDepartment of Epidemiology, Harvard School of Public Health, Boston, Massachusetts gSection of Pediatric Endocrinology, Indiana University School of Medicine, Indianapolis, Indiana hDepartment of Pediatrics, University of Colorado School of Medicine, Denver, Colorado iNew York University School of Medicine, New York jDepartment of Pediatrics, New Jersey Medical School, Newark, New Jersey kSaban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.
AIDS. 2013 Jul 31;27(12):1959-70. doi: 10.1097/QAD.0b013e328361195b.
To evaluate associations of perinatal HIV infection, HIV disease severity, and combination antiretroviral treatment with age at pubertal onset.
Analysis of data from two US longitudinal cohort studies (IMPAACT 219C and PHACS AMP), conducted during 2000-2012, including perinatally HIV-infected (PHIV) and HIV-exposed but uninfected (HEU) youth. Tanner stage assessments of pubertal status (breast and pubic hair in girls; genitalia and pubic hair in boys) were conducted annually.
We compared the timing of pubertal onset (Tanner stage ≥2) between PHIV and HEU youth using interval-censored models. For PHIV youth, we evaluated associations of HIV disease severity and combination antiretroviral treatment with age at pubertal onset, adjusting for race/ethnicity and birth cohort.
The mean age at pubertal onset was significantly later for the 2086 PHIV youth compared to the 453 HEU children (10.3 vs. 9.6, 10.5 vs. 10.0, 11.3 vs. 10.4, and 11.5 vs. 10.7 years according to female breast, female pubic hair, male genitalia, and male pubic hair staging, respectively, all P < 0.001). PHIV youth with HIV-1 RNA viral load above 10, 000 copies/ml (vs. ≤10, 000 copies/ml) or CD4% below 15% (vs. ≥15%) had significantly later pubertal onset (by 4-13 months). Each additional year of combination antiretroviral treatment was associated with a 0.6-1.2-month earlier mean age at pubertal onset, but this trend did not persist after adjustment for birth cohort.
Pubertal onset occurs significantly later in PHIV than in HEU youth, especially among those with more severe HIV disease. However, in the current era, combination antiretroviral treatment may result in more normal timing of pubertal onset.
评估围产期 HIV 感染、HIV 疾病严重程度和联合抗逆转录病毒治疗与青春期开始年龄的关联。
对 2000-2012 年期间进行的两项美国纵向队列研究(IMPAACT 219C 和 PHACS AMP)的数据进行分析,包括围产期 HIV 感染(PHIV)和 HIV 暴露但未感染(HEU)的年轻人。每年进行一次青春期状态的 Tanner 分期评估(女孩的乳房和阴毛;男孩的生殖器和阴毛)。
我们使用间隔censored 模型比较 PHIV 和 HEU 年轻人青春期开始的时间(Tanner 分期≥2)。对于 PHIV 年轻人,我们评估了 HIV 疾病严重程度和联合抗逆转录病毒治疗与青春期开始年龄的关联,调整了种族/民族和出生队列。
与 453 名 HEU 儿童相比,2086 名 PHIV 年轻人的青春期开始年龄明显较晚(女性乳房、女性阴毛、男性生殖器和男性阴毛分期分别为 10.3 岁 vs. 9.6 岁、10.5 岁 vs. 10.0 岁、11.3 岁 vs. 10.4 岁和 11.5 岁 vs. 10.7 岁,均 P<0.001)。HIV-1 RNA 病毒载量高于 10,000 拷贝/ml(vs. ≤10,000 拷贝/ml)或 CD4%低于 15%(vs. ≥15%)的 PHIV 年轻人青春期开始的时间明显较晚(晚 4-13 个月)。每增加一年联合抗逆转录病毒治疗与青春期开始年龄平均提前 0.6-1.2 个月,但在调整出生队列后,这种趋势并未持续。
PHIV 年轻人的青春期开始年龄明显晚于 HEU 年轻人,尤其是在 HIV 疾病更严重的年轻人中。然而,在当前时代,联合抗逆转录病毒治疗可能导致青春期开始时间更正常。