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围生期感染人类免疫缺陷病毒(HIV)和未感染 HIV 的儿童和青少年在 Tanner 分期的全身和脊柱骨密度。

Total body and spinal bone mineral density across Tanner stage in perinatally HIV-infected and uninfected children and youth in PACTG 1045.

机构信息

Center for Biostatistics in AIDS Research, Harvard School of Public Health, Boston, USA.

出版信息

AIDS. 2010 Mar 13;24(5):687-96. doi: 10.1097/QAD.0b013e328336095d.

Abstract

OBJECTIVE

To characterize total body bone mineral content (BMC) and total body and spinal bone mineral density (BMD) in perinatally HIV-infected and uninfected children/youth across puberty.

DESIGN

HIV-infected (7-24 years) were randomly selected from six strata based on Tanner stage/protease inhibitor use. HIV-uninfected were frequency-matched by Tanner group and sociodemographic background to the HIV-infected.

METHODS

Dual-energy X-ray absorptiometry (DXA) measured BMC and BMD. Linear regression models tested differences in bone outcomes by HIV and the interaction of HIV by Tanner group (1-2, 3-4, 5). Models were performed separately by sex and adjusted for DXA scanner, race/ethnicity, height, age and lean body mass.

RESULTS

HIV-infected (N = 236) and uninfected (N = 143) were comparable on sex and race/ethnicity. HIV-infected were slightly older (median 12.6 versus 11.9 years). In adjusted models, HIV-infected males had significantly lower total body BMC and total body and spinal BMD at Tanner 5, lower BMC at Tanner 3-4 and similar BMC and BMD at Tanner 1-2, compared to HIV-uninfected males. HIV-infected and uninfected girls did not differ significantly on any bone outcome, but there was a marginally significant interaction of HIV and Tanner group for spinal BMD. Kaletra/ritonavir was associated with lower BMC and total body BMD and nevirapine was associated with higher spinal BMD in a model with all HIV-infected.

CONCLUSIONS

Perinatally HIV-infected males showed more evidence of lower bone density especially in the final stage of pubertal development than HIV-infected girls and they may be at increased risk for bone disease during adulthood.

摘要

目的

描述围生期感染人类免疫缺陷病毒(HIV)和未感染 HIV 的儿童/青少年在整个青春期的全身骨矿物质含量(BMC)和全身及脊柱骨矿物质密度(BMD)。

设计

根据青春期分期/蛋白酶抑制剂的使用,从六个分层中随机选择 7-24 岁的 HIV 感染者。根据青春期分期组和社会人口统计学背景,将 HIV 未感染者与 HIV 感染者相匹配。

方法

双能 X 线吸收法(DXA)测量 BMC 和 BMD。线性回归模型检测了 HIV 对骨结局的影响,以及 HIV 与青春期分期组(1-2、3-4、5)之间的相互作用。模型分别根据性别和 DXA 扫描仪、种族/民族、身高、年龄和瘦体重进行调整。

结果

HIV 感染者(N=236)和未感染者(N=143)在性别和种族/民族方面相似。HIV 感染者年龄稍大(中位数 12.6 岁比 11.9 岁)。在调整后的模型中,与 HIV 未感染者相比,HIV 感染男性在青春期 5 期的全身 BMC 和全身及脊柱 BMD 明显较低,在青春期 3-4 期的 BMC 较低,在青春期 1-2 期的 BMC 和 BMD 相似。HIV 感染和未感染的女孩在任何骨结局上均无显著差异,但在包括所有 HIV 感染者的模型中,HIV 和青春期分期组之间存在脊柱 BMD 的边缘显著相互作用。在包含所有 HIV 感染者的模型中,洛匹那韦/利托那韦与 BMC 和全身 BMD 降低有关,奈韦拉平与脊柱 BMD 升高有关。

结论

与 HIV 感染女孩相比,围生期感染 HIV 的男性在青春期最后阶段表现出更多的骨密度降低证据,他们在成年期可能面临更高的骨病风险。

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