Apparent diffusion coefficient (ADC) measurements and morphometric evaluation of the cranium in age-matched children

Hanife Gülden Düzkalır1, Elif Söbü2, Özge Adıgüzel Karaoysal1

  • 1Department of Radiology, Kartal Dr. Lütfi Kırdar City Hospital, Istanbul, Türkiye.

Insights

Diffusion-weighted imaging magnetic resonance imaging (DWI-MRI) apparent diffusion coefficient (ADC) values in bone marrow can help detect central precocious puberty (CPP) early. This quantitative marker may identify CPP before sphenooccipital synchondrosis changes appear.

Area of Science:

  • Pediatric Endocrinology
  • Radiology
  • Biomedical Imaging

Background:

  • Central precocious puberty (CPP) is a common pediatric endocrine referral.
  • Magnetic resonance imaging (MRI) is crucial for ruling out intracranial pathologies in CPP.
  • Limited data exists on bone marrow abnormalities via MRI in CPP.

Purpose of the Study:

  • To evaluate apparent diffusion coefficient (ADC) values in cranial bone marrow using diffusion-weighted imaging (DWI) in girls with CPP.
  • To assess the status of the sphenooccipital synchondrosis (SOS) in girls with CPP.
  • To correlate DWI-ADC values with SOS status in CPP.

Main Methods:

  • MRI data from 146 girls (79 CPP, 67 controls), aged 6-9 years, were analyzed.
  • Apparent diffusion coefficient (ADC) values were measured in the clivus, parietal bone, and occipital protuberance.
  • Anthropometric data and hormone levels (FSH, LH, oestradiol) were recorded and compared between groups.

Main Results:

  • Girls with CPP exhibited significantly lower bone marrow ADC values compared to healthy controls (p<0.05).
  • Specific SOS patterns were observed in a small percentage of the CPP group.
  • No significant correlation was found between mean ADC values (parietal, occipital, clivus) and other variables.

Conclusions:

  • Diffusion-weighted imaging (DWI) MRI ADC analysis serves as a valuable quantitative radiological marker for early CPP detection.
  • ADC values may indicate CPP even before observable changes in the sphenooccipital synchondrosis.
Abstract