Gertner J M, Kaufman F R, Donfield S M, Sleeper L A, Shapiro A D, Howard C, Gomperts E D, Hilgartner M W
Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021.
J Pediatr. 1994 Jun;124(6):896-902. doi: 10.1016/s0022-3476(05)83177-4.
As part of the Hemophilia Growth and Development Study, we investigated the impact of human immunodeficiency virus (HIV) infection on statural growth, weight gain, and skeletal and sexual maturity in more than 300 boys with moderate to severe hemophilia, of whom 62% were infected with HIV. Age-adjusted height and weight were reduced in the HIV-infected subjects (p < 0.001). However, mean weight for height and triceps skin-fold thickness of the infected-boys closely resembled those of the uninfected group. In HIV-infected boys, height for age was positively related to the CD4+ lymphocyte count when the count was < 200 cells/mm3. Age-adjusted serum testosterone levels did not differ by HIV status, but in the infected participants the mean age-adjusted bone age was significantly reduced (p = 0.038) and the distribution of Tanner stages, adjusted for age, differed significantly (p = 0.003). The probability of advancing one or more Tanner stages in the first study year was significantly slowed in HIV-infected boys more than 14 years of age (p = 0.0003). We conclude that linear growth was significantly impaired in boys with hemophilia and HIV infection, but the wasting of malnutrition was not found. The delays in bone age and pubertal maturation strongly suggest that part of the growth failure seen in acquired immunodeficiency syndrome can be attributed to pubertal delay. We speculate that the lack of demonstrable difference in age-adjusted testosterone concentrations might reflect subtle differences in the pattern of secretion of testosterone or in the concentration of sex-hormone binding globulin.
作为血友病生长与发育研究的一部分,我们调查了人类免疫缺陷病毒(HIV)感染对300多名中重度血友病男孩的身高增长、体重增加以及骨骼和性成熟的影响,其中62%的男孩感染了HIV。HIV感染组经年龄调整后的身高和体重降低(p<0.001)。然而,感染男孩的身高体重比和肱三头肌皮褶厚度与未感染组相近。在HIV感染男孩中,当CD4+淋巴细胞计数<200个细胞/mm3时,年龄别身高与CD4+淋巴细胞计数呈正相关。经年龄调整后的血清睾酮水平在HIV感染状态不同的组间无差异,但在感染参与者中,经年龄调整后的平均骨龄显著降低(p=0.038),且经年龄调整后的坦纳分期分布存在显著差异(p=0.003)。14岁以上HIV感染男孩在第一个研究年度进入一个或多个坦纳分期的概率显著降低(p=0.0003)。我们得出结论,血友病合并HIV感染的男孩线性生长显著受损,但未发现营养不良性消瘦。骨龄延迟和青春期成熟延迟强烈提示,获得性免疫缺陷综合征中出现的部分生长发育迟缓可归因于青春期延迟。我们推测,经年龄调整后的睾酮浓度未显示出明显差异,可能反映了睾酮分泌模式或性激素结合球蛋白浓度的细微差异。