Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Horm Res Paediatr. 2018;90(2):102-108. doi: 10.1159/000491793. Epub 2018 Aug 21.
BACKGROUND/AIMS: To compare racial/ethnic proportions of subjects receiving growth hormone (GH) treatment to the expected proportions, and secondarily, to assess racial/ethnic differences in subject characteristics at GH treatment initiation.
Race/ethnicity-based expected frequencies of height <-2.25 SD were determined by applying relative risks for short stature, calculated from a regional population of 189,280 pediatric primary care patients, to US census data, and compared to racial/ethnic proportions of US subjects enrolled in the Pfizer International Growth Study (KIGS) using the χ2 test. Characteristics of white and black subjects at GH treatment initiation were presented as medians and compared by the Wilcoxon rank sum test (significant p < 0.01).
White subjects exceeded the expected frequency (63%) for all indications (83%) and each separately, ranging from 73% for congenital GH deficiency (GHD) to 85% for idiopathic short stature (p < 0.001). Compared to white subjects, black subjects treated for idiopathic GHD had greater height deficits relative both to the population (-2.97 vs. -2.56 SD) and to their mid-parental heights (-2.47 vs. -1.89 SD), lower stimulated GH peak levels (4.9 vs. 6.0 ng/mL), and lower birth weights (-0.86 vs. -0.48 SD). Black subjects with congenital GHD had lower stimulated GH peaks (2.1 vs. 3.2 ng/mL) and started GH treatment at younger ages (2.9 vs. 4.8 years), while those with acquired GHD had lower birth weights (-1.12 vs. -0.08 SD). Male predominance did not differ by race for any or all indications.
Overrepresentation of white children among those receiving GH treatment in the US KIGS registry reflects racial/ethnic treatment biases, not just differences in growth rates.
背景/目的:比较接受生长激素(GH)治疗的患者的种族/民族比例与预期比例,其次评估 GH 治疗开始时患者特征的种族/民族差异。
根据矮身材的相对风险(从 189280 名儿科初级保健患者的区域人群中计算得出),应用于美国人口普查数据,确定种族/民族为身高 <-2.25 SD 的预期频率,并通过 χ2 检验比较 Pfizer 国际生长研究(KIGS)中美国患者的种族/民族比例。用 Wilcoxon 秩和检验(显著 p < 0.01)比较 GH 治疗开始时白人和黑人患者的特征,以中位数表示。
白人患者的所有适应症(83%)和单独适应症(73%用于先天性 GH 缺乏症(GHD),85%用于特发性身材矮小)的频率均超过预期(63%)。与白人患者相比,接受特发性 GHD 治疗的黑人患者的身高缺陷相对人群(-2.97 对 -2.56 SD)和中亲身高(-2.47 对 -1.89 SD)更大,GH 激发峰值水平更低(4.9 对 6.0 ng/mL),出生体重更低(-0.86 对 -0.48 SD)。先天性 GHD 的黑人患者的 GH 激发峰值较低(2.1 对 3.2 ng/mL),开始 GH 治疗的年龄较小(2.9 对 4.8 岁),而获得性 GHD 的患者出生体重较低(-1.12 对 -0.08 SD)。任何或所有适应症的男性优势均不因种族而有所不同。
美国 KIGS 登记处接受 GH 治疗的白人儿童比例过高,反映了种族/民族治疗偏见,而不仅仅是生长速度的差异。