4.7 Article

Gender Bias in US Pediatric Growth Hormone Treatment

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SCIENTIFIC REPORTS
卷 5, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep11099

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  1. Genentech Center for Clinical Research in Endocrinology
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development [R01 HD057037]
  3. University of Pennsylvania Clinical and Translational Science Award (National Institutes of Health grant from National Center for Research Resources) [UL1TR000003]
  4. University of Pennsylvania Clinical and Translational Science Award (National Institutes of Health grant from National Center for Advancing Translational Sciences) [UL1TR000003]
  5. Agency for Healthcare Research and Quality

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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.

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