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美国儿科生长激素治疗中的性别偏见。

Gender Bias in U.S. Pediatric Growth Hormone Treatment.

作者信息

Grimberg Adda, Huerta-Saenz Lina, Grundmeier Robert, Ramos Mark Jason, Pati Susmita, Cucchiara Andrew J, Stallings Virginia A

机构信息

1] Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA [2] Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA [3] Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia, PA.

Department of Pediatrics, Albert Einstein Medical Center, Philadelphia, PA.

出版信息

Sci Rep. 2015 Jun 9;5:11099. doi: 10.1038/srep11099.

Abstract

Growth hormone (GH) treatment of idiopathic short stature (ISS), defined as height <-2.25 standard deviations (SD), is approved by U.S. FDA. This study determined the gender-specific prevalence of height <-2.25 SD in a pediatric primary care population, and compared it to demographics of U.S. pediatric GH recipients. Data were extracted from health records of all patients age 0.5-20 years with ≥ 1 recorded height measurement in 28 regional primary care practices and from the four U.S. GH registries. Height <-2.25 SD was modeled by multivariable logistic regression against gender and other characteristics. Of the 189,280 subjects, 2073 (1.1%) had height <-2.25 SD. No gender differences in prevalence of height <-2.25 SD or distribution of height Z-scores were found. In contrast, males comprised 74% of GH recipients for ISS and 66% for all indications. Short stature was associated (P < 0.0001) with history of prematurity, race/ethnicity, age and Medicaid insurance, and inversely related (P < 0.0001) with BMI Z-score. In conclusion, males outnumbered females almost 3:1 for ISS and 2:1 for all indications in U.S. pediatric GH registries despite no gender difference in height <-2.25 SD in a large primary care population. Treatment and/or referral bias was the likely cause of male predominance among GH recipients.

摘要

生长激素(GH)治疗特发性矮小症(ISS,定义为身高低于-2.25标准差(SD))已获美国食品药品监督管理局(FDA)批准。本研究确定了儿科初级保健人群中身高低于-2.25 SD的性别特异性患病率,并将其与美国接受生长激素治疗的儿科患者的人口统计学特征进行比较。数据从28个地区初级保健机构中所有年龄在0.5至20岁且有≥1次身高测量记录的患者的健康记录以及美国四个生长激素注册机构中提取。通过多变量逻辑回归对身高低于-2.25 SD与性别及其他特征进行建模。在189,280名受试者中,2073人(1.1%)身高低于-2.25 SD。未发现身高低于-2.25 SD的患病率或身高Z评分分布存在性别差异。相比之下,在接受生长激素治疗的特发性矮小症患者中,男性占74%,在所有适应症患者中占66%。矮小症与早产史、种族/民族、年龄和医疗补助保险相关(P<0.0001),与BMI Z评分呈负相关(P<0.0001)。总之,在美国儿科生长激素注册机构中,尽管在大量初级保健人群中身高低于-2.25 SD不存在性别差异,但在特发性矮小症患者中男性数量几乎是女性的3倍,在所有适应症患者中男性数量是女性的2倍。治疗和/或转诊偏倚可能是生长激素治疗患者中男性占主导的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea78/4650610/32dce8d642ac/srep11099-f1.jpg

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