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Table 1 Basic characteristics at diagnosis of central precocious puberty of the gonadotropin releasing hormone (GnRH) analogue treated and untreated groups

From: Gonadotropin releasing hormone analogue treatment of central precocious puberty is not associated with altered prevalence of polycystic ovary syndrome: a single center cohort study

Parameter

GnRHa treatment

N = 27

No treatment

N = 24

P value

Age at diagnosis (years)

7.3 ± 0.6 (5.7–8.0)

7.6 ± 0.6 (6.0–8.0)

0.101

Bone age at diagnosis (years)

9.6 ± 1.7 (7.1–12.0)

10.7 ± 1.7 (7.1–13.0)

0.072

Advanced over chronological age (months)

16.4 ± 11.8 (0–43.0)

21.6 ± 12.0 (8.0–50.0)

0.214

Weight at diagnosis (kg)

32.9 ± 8.6 (22.0–58.0)

36.4 ± 11.7 (17.0–67.0)

0.250

Height at diagnosis (centimeters)

130.6 ± 10.4 (114–149)

135.6 ± 14.2 (98–162)

0.189

BMI percentile at diagnosis

80.5 ± 19.3 (15.2–98.9)

75.7 ± 24.9 (1.0–98.4)

0.480

Medical background

 Neurologic

3 (11.1)

5 (20.8)

0.451

 Developmental

2 (8.3)

4 (16.7)

0.402

 Fetal

  

0.175

  Small for gestational age

1 (3.7)

4 (16.7)

 

  Large for gestational age

1 (3.7)

0

 

  Prematurity (< 37 weeks)

4 (14.8)

1 (4.2)

 

 Endocrine

  

0.661

  Hypothyroidism

1 (3.7)

0

 

  NCCAH

2 (7.4)

2 (8.3)

 

  Vitamin D deficiency

0

2 (8.3)

 

  Benign premature thelarche

1 (3.7)

1 (4.2)

 

Clinical presentation at diagnosis

  

0.422

 Pubarche and thelarche

19 (70.4)

12 (57.1)

 

 Thelarche only

5 (18.5)

5 (23.8)

 

 Pubarche only

3 (11.1)

4 (19.1)

 

LH at diagnosis (IU/L)

1.9 ± 1.7 (0.1–6.2)

2.1 ± 1.6 (0.3–6.0)

0.722

FSH at diagnosis (IU/L)

3.8 ± 2.3 (1.1–9.4)

4.7 ± 1.9 (1.6–8.3)

0.200

Estradiol at diagnosis (pmol/L)

121.9 ± 56.4 (70–232)

191.2 ± 246.6 (70–1080)

0.296

LH/FSH ratio at diagnosis

0.5 ± 0.3 (0.1–1.0)

0.5 ± 0.4 (0.1–1.4)

0.446

  1. Data presented as Mean ± SD (range) or n (%)
  2. Note: SGA Small for gestational age, LGA Large for gestational age, LH Luteinizing Hormone, FSH Follicle Stimulating Hormone, BMI Body Mass Index, NCCAH Non-classical congenital adrenal hyperplasia