Abstract

Background5α-reductase type 2 deficiency (5αRD) is an autosomal recessive hereditary disease of the group of 46, XY disorders of sex development (DSD).ObjectiveTo study the growth pattern in Chinese pediatric patients with 5αRD.SubjectsData were obtained from 141 patients with 5αRD (age: 0–16 years old) who visited eight pediatric endocrine centers from January 2010 to December 2017.MethodsIn this retrospective cohort study, height, weight, and other relevant data were collected from the multicenter hospital registration database. Baseline luteinizing hormone (LH), follicle stimulating hormone (FSH), testosterone (T), and dihydrotestosterone (DHT) after human chorionic gonadotropin (HCG) stimulation test were measured by enzyme enhanced chemiluminescence assay. Bone age (BA) was assessed using the Greulich-Pyle (G-P) atlas. Growth curve was constructed based on λ-median-coefficient of variation method (LMS).ResultsThe height standard deviation scores (HtSDS) and weight standard deviation scores (WtSDS) in 5αRD children were in the normal range as compared to normal boys. Significantly higher HtSDS was observed in patients with 5αRD who were <1 year old (t = 3.658, 2.103, P = 0.002, 0.048, respectively), and higher WtSDS in those <6 months old (t = 2.756, P = 0.012). Then HtSDS and WtSDS decreased gradually and fluctuated near the median of the same age until 13 years. WtSDS in 5αRD children from northern China were significantly higher than those from the south (Z = -2.670, P = 0.008). The variation tendency of HtSDS in Chinese 5αRDs was consistent with the trend of stimulating T. HtSDS and stimulating T in the external masculinization score (EMS) <7 group were slightly higher than those in EMS ≥ 7 group without significant difference. Additionally, the ratio of BA over chronological age (BA/CA) was significantly <1 in children with 5αRD.ConclusionChildren with 5αRD had a special growth pattern that was affected by high levels of T, while DHT played a very small role in it. Their growth accelerated at age <1 year, followed by slowing growth and fluctuating height near normal median boys’ height. The BA was delayed in 5αRD children. Androgen treatment, which may be considered anyway for male 5αRD patients with a micropenis, may also be beneficial for growth.

Highlights

  • Sex hormones are synthesized in the gonads and adrenal glands (Shen, 2016) and have bioactivity within bone and other target tissues (Vanderschueren et al, 2014)

  • The height standard deviation scores (HtSDS) and weight standard deviation scores (WtSDS) in 5α-reductase type deficiency (5αRD) children were in the normal range as compared to normal boys

  • Higher HtSDS was observed in patients with 5αRD who were

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Summary

Introduction

Sex hormones are synthesized in the gonads and adrenal glands (Shen, 2016) and have bioactivity within bone and other target tissues (Vanderschueren et al, 2014). Their biological effects on bone are mediated by different cell types and mechanisms (Almeida et al, 2017) and controlled by gonadotropins via hypothalamic-pituitary feedback. Longitudinal bone growth shows no significant sex differences (Nishiyama et al, 2012). Whether androgen receptor in chondrocytes contributes to sex differences in longitudinal growth remains unclear. Sex hormones have an essential role for male and female growth

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