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. 2020 Dec 31;106(4):e1041–e1050. doi: 10.1210/clinem/dgaa955

Table 5.

Phenotype comparison between girls with CPP with and without MKRN3 mutations

MKRN3 CPP (n = 45) Idiopathic CPP (n = 156) P
Thelarche (years) 6.3 ± 1.2 6.0 ± 1.7 .38
Pubarche (years) 7.1 ± 1.2 6.8 ± 1.9 .24
First evaluation (years) 7.2 ± 1.1 8.4 ± 2.0 .001
Diagnostic delay (years) 0.8 ± 0.8 2.4 ± 2.1 <.001
BAA (years) 2.1 ± 1.6 2.6 ± 1.3 .08
Height SDS 1.2 ± 1.2 1.7 ± 1.1 .04
BMI SDS 0.9 ± 0.9 0.8 ± 0.9 .90
Basal LH (IU/L) 1.7 ± 1.8 1.3 ± 1.4 .22
Basal FSH (IU/L) 4.9 ± 2.3 3.8 ± 2.7 .03
Estradiol (ng/dL) 29.8 ± 20.8 30.1 ± 30.3 .95
LH peak (IU/L) 20.2 ± 14.4 17.3 ± 16.6 .45
FSH peak (IU/L) 16.9 ± 4.6 14.2 ± 10.2 .18

Data are shown as mean ± standard deviation. Diagnostic delay (years) was defined as the difference between the age at first evaluation and the age at fist pubertal signs.

Abbreviations: BAA, bone age advance; CPP, central precocious puberty; SDS, standard deviation score; LH, luteinizing hormone; FSH, follicle-stimulating hormone.