Clinical research

Effect of short-term GnRH pulse therapy on pituitary-testicular function in adolescent male patients with congenital hypogonadotropic hypogonadism

  • Fei WANG ,
  • Yan GONG ,
  • Liya XU ,
  • Qingxu LIU ,
  • Yan LI ,
  • Sheng GUO ,
  • Pin LI
Expand
  • Department of Endocrinology, Shanghai Children's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200062, China
LI Pin,E-mail: lipin21@126.com.

Received date: 2022-07-18

  Accepted date: 2022-11-09

  Online published: 2022-12-20

Supported by

Medical Innovation Research Special Project in "Science and Technology Innovation Action Plan" of Shanghai(21Y21901000);Precise Diagnosis and Treatment Project for Difficult Diseases in "Three-year Action Plan for Promoting Clinical Skills and Innovation Capacity of Municipal Hospitals" of Shanghai(SHDC2020CR2058B)

Abstract

Objective ·To investigate the effect of short-term gonadotropin-releasing hormone (GnRH) pulse therapy on pituitary and testicular function in the adolescent male patients with congenital hypogonadotropic hypogonadism (CHH). Methods ·A retrospective study was conducted on 20 adolescent male patients with CHH who received GnRH pulse therapy from January 2016 to June 2021, and their clinical data were collected. They were treated with subcutaneous continuous pulsed administration of gonadorelin by the pump for 1 week (20 cases), of which 5 cases were treated for 3 months. The dose was 8?10 μg per pulse, and the pulse interval was 90 min. The levels of luteinizing hormone (LH), follicle stimulating hormone (FSH) and testosterone were measured before GnRH pulse therapy at 1 week, 1 month and 3 months after treatment. After 3 months of treatment, the testicular volume was measured. All 20 patients with CHH underwent whole exome sequencing. Results ·The age of 20 CHH patients was 14.35 (14.08, 15.31) years old. The clinical manifestations were infantile testis (20/20) and micropenis (20/20), followed by obesity (12/20), dysosmia (9/20), insulin resistance (4/20), cryptorchidism (4/20), and short stature (3/20). The patients' height was 161.79 (154.90, 173.25) cm, body mass index was 23.80 (20.51, 27.46) kg/m2, and testicular volume was 0.91 (0.55, 1.25) mL. Inhibin B was 39.67 (11.29, 64.97) pg/mL; the base values of LH, FSH and testosterone before therapy were 0.20 (0.10, 0.30) IU/L, 0.87 (0.23, 0.89) IU/L, and 0.92 (0.38, 1.49) nmol/L, respectively. After 1 week of continuous GnRH pulse therapy, the base and peak values of LH and FSH and the peak value of testosterone in the 20 patients significantly increased (all P<0.05). In the 5 patients treated for 3 months, the base values and peak values of LH and FSH gradually increased with the prolongation of treatment time. After 3 months of treatment, the base values and peak values of LH and FSH, and the peak value of testosterone were significantly higher than those before treatment (all P<0.05), and the testicular volume was also significantly increased (P=0.004). Gene mutations were detected in only 14 of 20 patients, including fibroblast growth factor receptor 1 (FGFR1) mutations in 7 cases, anosmin 1 (ANOS1) mutations in 4 cases, prokineticin receptor 2 (PROKR2) mutations in 2 cases, and a prokineticin 2 (PROK2) mutation in 1 case. There was no significant difference of the effect of GnRH pulse therapy for 1 week on pituitary-testicular function between the patients with FGFR1 mutations and ANOS1 mutations. Conclusion ·The continuous GnRH pulse therapy for 1 week can make pituitary-testicular function respond in adolescent male CHH patients; the treatment for 3 months helps to induce the secondary sexual characteristics of puberty.

Cite this article

Fei WANG , Yan GONG , Liya XU , Qingxu LIU , Yan LI , Sheng GUO , Pin LI . Effect of short-term GnRH pulse therapy on pituitary-testicular function in adolescent male patients with congenital hypogonadotropic hypogonadism[J]. Journal of Shanghai Jiao Tong University (Medical Science), 2023 , 43(1) : 36 -43 . DOI: 10.3969/j.issn.1674-8115.2023.01.005

References

1 CANGIANO B, SWEE D S, QUINTON R, et al. Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease[J]. Hum Genet, 2021, 140(1): 77-111.
2 BIANCO S D C, KAISER U B. The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism[J]. Nat Rev Endocrinol, 2009, 5(10): 569-576.
3 SWEE D S, QUINTON R. Current concepts surrounding neonatal hormone therapy for boys with congenital hypogonadotropic hypogonadism[J]. Expert Rev Endocrinol Metab, 2022, 17(1): 47-61.
4 HAO M, NIE M, YU B Q, et al. Gonadotropin treatment for male partial congenital hypogonadotropic hypogonadism in Chinese patients[J]. Asian J Androl, 2020, 22(4): 390-395.
5 GONG C X, LIU Y, QIN M, et al. Pulsatile GnRH is superior to hCG in therapeutic efficacy in adolescent boys with hypogonadotropic hypogonadodism[J]. J Clin Endocrinol Metab, 2015, 100(7): 2793-2799.
6 YOUNG J, XU C, PAPADAKIS G E, et al. Clinical management of congenital hypogonadotropic hypogonadism[J]. Endocr Rev, 2019, 40(2): 669-710.
7 孙首悦, 王卫庆, 蒋怡然, 等. 微量泵脉冲输注戈那瑞林治疗特发性低促性腺激素性性腺功能减退症[J]. 中华内分泌代谢杂志, 2011, 27(8): 654-658.
7 SUN S Y, WANG W Q, JIANG Y R, et al. Treatment of idiopathic hypogonadotropic hypogonadism with pulse infusion of gonadorelin via micro pump[J]. Chinese Journal of Endocrinology and Metabolism, 2011, 27(8): 654-658.
8 GACH A, PINKIER I, SA?ACI?SKA K, et al. Identification of gene variants in a cohort of hypogonadotropic hypogonadism: diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease[J]. Mol Cell Endocrinol, 2020, 517: 110968.
9 WANG Y, GONG C X, QIN M, et al. Clinical and genetic features of 64 young male paediatric patients with congenital hypogonadotropic hypogonadism[J]. Clin Endocrinol (Oxf), 2017, 87(6): 757-766.
10 MAIONE L, DWYER A A, FRANCOU B, et al. Genetics in endocrinology: genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing[J]. Eur J Endocrinol, 2018, 178(3): R55-R80.
11 AMATO L G L, MONTENEGRO L R, LERARIO A M, et al. New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism[J]. Eur J Endocrinol, 2019, 181(2): 103-119.
12 GACH A, PINKIER I, SZARRAS-CZAPNIK M, et al. Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes[J]. Reprod Biol Endocrinol, 2020, 18(1): 8.
13 LIU Q X, YIN X Q, LI P. Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism[J]. BMC Endocr Disord, 2022, 22(1): 30.
14 FESTA A, UMANO G R, MIRAGLIA DEL GIUDICE E, et al. Genetic evaluation of patients with delayed puberty and congenital hypogonadotropic hypogonadism: is it worthy of consideration?[J]. Front Endocrinol (Lausanne), 2020, 11: 253.
15 KIM J H, SEO G H, KIM G H, et al. Targeted gene panel sequencing for molecular diagnosis of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism[J]. Exp Clin Endocrinol Diabetes, 2019, 127(8): 538-544.
16 WANG Y, QIN M, FAN L J, et al. Correlation analysis of genotypes and phenotypes in Chinese male pediatric patients with congenital hypogonadotropic hypogonadism[J]. Front Endocrinol (Lausanne), 2022, 13: 846801.
17 LI S Y, ZHAO Y L, NIE M, et al. Clinical characteristics and spermatogenesis in patients with congenital hypogonadotropic hypogonadism caused by FGFR1 mutations[J]. Int J Endocrinol, 2020, 2020: 8873532.
18 NEOCLEOUS V, FANIS P, TOUMBA M, et al. GnRH deficient patients with congenital hypogonadotropic hypogonadism: novel genetic findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A genes in a case series and review of the literature[J]. Front Endocrinol (Lausanne), 2020, 11: 626.
19 MOSBAH H, BOUVATTIER C, MAIONE L, et al. GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty[J]. Hum Reprod, 2020, 35(10): 2312-2322.
20 SEGAL T Y, MEHTA A, ANAZODO A, et al. Role of gonadotropin-releasing hormone and human chorionic gonadotropin stimulation tests in differentiating patients with hypogonadotropic hypogonadism from those with constitutional delay of growth and puberty[J]. J Clin Endocrinol Metab, 2009, 94(3): 780-785.
21 BINDER G, SCHWEIZER R, BLUMENSTOCK G, et al. Inhibin B plus LH vs GnRH agonist test for distinguishing constitutional delay of growth and puberty from isolated hypogonadotropic hypogonadism in boys[J]. Clin Endocrinol (Oxf), 2015, 82(1): 100-105.
22 GAO Y T, DU Q, LIU L Y, et al. Serum inhibin B for differentiating between congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty: a systematic review and meta-analysis[J]. Endocrine, 2021, 72(3): 633-643.
23 VARIMO T, MIETTINEN P J, K?NS?KOSKI J, et al. Congenital hypogonadotropic hypogonadism, functional hypogonadotropism or constitutional delay of growth and puberty? An analysis of a large patient series from a single tertiary center[J]. Hum Reprod, 2017, 32(1): 147-153.
24 中华医学会内分泌学分会性腺学组. 特发性低促性腺激素性性腺功能减退症诊治专家共识[J]. 中华内科杂志, 2015, 54(8): 739-744.
24 Division of Gonadal Disease, Chinese Society of Endocrinology. Expert consensus on the diagnosis and treatment of idiopathic hypogonadotropic hypogonadism[J]. Chinese Journal of Internal Medicine, 2015, 54(8): 739-744.
25 SHAH R, PATIL V, SARATHI V, et al. Prior testosterone replacement therapy may impact spermatogenic response to combined gonadotropin therapy in severe congenital hypogonadotropic hypogonadism[J]. Pituitary, 2021, 24(3): 326-333.
26 中华医学会儿科学分会内分泌遗传代谢学组. 性发育异常的儿科内分泌诊断与治疗共识[J]. 中华儿科杂志, 2019, 57(6): 410-418.
26 The Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, the Society of Pediatrics, Chinese Medical Association. Consensus statement on the diagnosis and endocrine treatment of children with disorder of sex development[J]. Chinese Journal of Pediatrics, 2019, 57(6): 410-418.
27 LIU Y, REN X Y, PENG Y G, et al. Efficacy and safety of human chorionic gonadotropin combined with human menopausal gonadotropin and a gonadotropin-releasing hormone pump for male adolescents with congenital hypogonadotropic hypogonadism[J]. Chin Med J (Engl), 2021, 134(10): 1152-1159.
Outlines

/