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December 10, 2025Journal of the Endocrine Society2 citationsOpen Access

Age-specific contributions to height in boys with Klinefelter Syndrome: Analysis of Growth using the QEPS-model

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AHAnton HolmgrenANAimon NiklassonLGLars Gelander

Key Points

  • To delineate the growth patterns and contributions to adult height in boys with Klinefelter syndrome.
  • Analyzed longitudinal growth data from 55 boys with Klinefelter syndrome.
  • Compared growth metrics with the GrowUp1974Gothenburg cohort.
  • Utilized the QEPS statistical growth model with four mathematical functions.
  • Subgroup analysis included 35 boys, 34 of whom were on testosterone replacement therapy.
  • Shorter infant growth period and lower height gain compared to the reference group.
  • Increased height gain during childhood growth phase, indicating enhanced growth.
  • Earlier onset of pubertal growth compared to reference population.
  • Higher total pubertal height gain leading to taller adult height at 184.6 cm.

Abstract

Abstract Context Increased height is a characteristic of Klinefelter syndrome (KS). Detailed evaluation of growth patterns in boys and adolescents carrying a 47,XXY karyotype is lacking. Objective To delineate detailed growth patterns during the different growth phases and their contribution to the increased adult height in boys with KS. Methods Longitudinal data on growth from 55 boys with KS were compared with a reference from GrowUp1974Gothenburg cohort using a statistical growth model using four mathematical functions; the QEPS-model. A subgroup of 35 boys out of whom 34 were on testosterone replacement therapy (TRT) reached final height. Results The infant growth period was shorter with a lower height gain (Emax, 63.3 vs 65.1 cm, p0.001) in boys with KS. The boys gained more height during the childhood growth phase, (Qmax, 110.9 vs 104.1 cm, p0.001), and onset of pubertal growth was earlier as compared with the reference (11.3 vs 11.8 years, p0.001). The total pubertal height gain was higher (32.9 vs 30.6 cm, p0.001), due to more basic growth, the specific pubertal growth, was equal resulting in a taller adult height (184.6 vs 180.5 cm, p0.001). Conclusion The boys with KS exhibited a different growth pattern as compared with a healthy reference population, with less and shorter growth in infant life and more basic growth during childhood and the pubertal years (the Q-function growth by the QEPS model), resulting in taller adult height.

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Cite This Study

Holmgren et al. (2025) studied this question.

synapsesocial.com/papers/6941aaf00f5af7fd17df5c41https://doi.org/10.1210/jendso/bvaf206
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