Abstract

Objective: Although there have been several studies on the neuroanatomical changes in idiopathic central precocious puberty (ICPP), the association between each brain region and ICPP has not yet been clearly elucidated. This study aimed to evaluate the difference in brain structure in ICPP compared with age-matched healthy controls and normal puberty controls, and additionally the correlation between brain volume difference and the luteinizing hormone (LH). Materials and Methods: The study enrolled fifteen girls with ICPP, as well as 15 age-matched healthy girls and 15 normal puberty girls as controls. The subjects underwent a 1.5 Tesla Avanto MR Scanner. Anatomical T1-weighted images were acquired with a T1 spin-echo sequence. The volumes of total and regional brain were compared with each of the two control groups and analyzed through the paired T-test, and the brain region related to the peak LH level was also analyzed through a simple correlation test. Results: The mean age of the ICPP group, age-matched group, and puberty group were 8.0 ± 0.9 years, 7.8 ± 0.9 years, and 11.9 ± 0.9 years, respectively. In our findings, the regional cerebral volumes in ICPP were different from age-matched controls. Compared with controls, ICPP showed a significant increase in gray matter (GM) volumes (the medial prefrontal cortex, superior parietal gyrus, supramarginal gyrus, angular gyrus, postcentral gyrus, superior occipital gyrus, cuneus, hippocampus, parahippocampal gyrus, posterior cingulate gyrus (PCgG), cerebellar cortex (Cb)) and in white matter (WM) volumes (the insular, caudate, splenium of corpus callosum (p < 0.001)). Especially, the GM volumes of the PCgG (r = 0.57, p = 0.03) and Cb (r = 0.53, p = 0.04) were correlated positively with LH concentrations stimulated by the gonadotropin-releasing hormone agonist. Compared to the normal puberty control, no significant difference in GM volume was found. Conclusions: This study showed the overall brain volumetric differences between ICPP girls and age-matched controls using voxel-based morphometric analysis, and further showed the correlation between brain volume and the sex hormone in ICPP. Through a comparison between the two groups, the cerebral development pattern of ICPP is similar to that of normal puberty, and these local differences in cerebral volume may affect social and congenital changes. These findings will be useful for understanding the neuroanatomical mechanisms on the specific morphological variations associated with ICPP.

Highlights

  • Precocious puberty (PP) is defined as the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys [1]

  • Was diagnosed by a pediatrician in accordance with the following criteria as in a previous study [15]: first, objective breast budding appearing before the age of eight years; second, if advanced bone age (BA) is more than chronological age; third, luteinizing hormone (LH) stimulated by Gonadotropin-releasing hormone agonists (GnRHa)

  • The brain’s developmental morphological changes and the influence of of the LH on brain structure in idiopathic central precocious puberty (ICPP) girls were assessed by qualitative and quantitative the LH on brain structure in ICPP girls were assessed by qualitative and quantitative analyses by using a voxel-based morphometry (VBM) study based on the DARTEL algorithm and statistical approach

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Summary

Introduction

Precocious puberty (PP) is defined as the development of secondary sexual characteristics before the age of 8 years in girls and 9 years in boys [1]. Early maturation is believed to have a negative psychological impact on girls [4,5], and girls with early pubertal timing are more vulnerable to stressors [6]. In the case of the hypothalamic-pituitary-gonadal (HPG) axis active in PP, it is called true/central precocious puberty (CPP). Otherwise, it is called pseudo/peripheral precocious puberty [7,8]. The etiologies of CPP can be classified as organic or idiopathic by whether the abnormality of the central nervous system stimulating HPG is accompanied

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