Early onset of puberty during COVID-19 pandemic lockdown: experience from two Pediatric Endocrinology Italian Centers
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Martina Goffredo
, Alba Pilotta
Abstract
Objectives
During COVID-19 pandemic lockdown, reports of evaluations for suspected precocious puberty significantly raised. We aimed to assess the increase of precocious puberty in patients referred to Pediatric Endocrinology Units of Brescia (Italy), to determine clinical characteristics of patients undergoing a GnRH stimulation test before and during lockdown and evaluate the role of environmental factors in pubertal development.
Methods
Clinical and biochemical data of patients undergoing GnRH stimulation test were collected and stratified in two groups: March 2019 – February 2020 (Period 1) and March 2020 – February 2021 (Period 2).
Results
A total number of 391 evaluations for suspected precocious puberty were identified in the two study periods: 183 (46.8%) first visits during Period 1, and 208 (53.2%) in Period 2. Sixty-one patients underwent a GnRH stimulation test (4.1% of first consultations) before the SARS-CoV2 pandemic, and 93 children (8.7%) after the lockdown. Thirty-four new diagnoses of central precocious puberty were registered during Period 1 (2.3%), vs. 45 new cases (4.2%) in Period 2. During lockdown patients evaluated for suspected precocious puberty underwent a stimulation test at younger age than those evaluated before pandemic (median age of 8.2 years vs. 8.4, p=0.04). In Period 2, children showed a median bone age advancement of 0.61 years vs. 1.06 of Period 1 (p=0.03).
Conclusions
During the COVID-19 pandemic, we observed an increased proportion of consultations for suspected precocious puberty. These children showed lower bone age advancement than observed in pre-lockdown suggesting the influence of pandemic-related lifestyle changes on pubertal development.
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Research funding: None declared.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: Informed consent was obtained from all individuals included in this study.
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Ethical approval: The local Institutional Review Board deemed the study exempt from review.
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Supplementary Material
This article contains supplementary material (https://doi.org/10.1515/jpem-2022-0492).
© 2022 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Editorial
- Thyroid – what is a healthy thyroid function test?
- Review
- Thyroid storm in pediatrics: a systematic review
- Opinion Paper
- DSD/intersex: historical context and current perspectives
- Original Articles
- Predictive value of 6 h postoperative parathyroid hormone level on permanent hypoparathyroidism in pediatric total thyroidectomy: a pilot study
- Evaluation of a nurse-led counselling intervention on selected outcome variables for parents of children with congenital adrenal hyperplasia
- The relationship between estrogen and subsequent growth restriction among adolescents with heavy menstrual bleeding at menarche
- An open-label extension of a phase 2 dose-finding study of once-weekly somatrogon vs. once-daily Genotropin in children with short stature due to growth hormone deficiency: results following 5 years of treatment
- Normal bone density but altered geometry in girls with Turner syndrome
- Newborn screening for inborn errors of metabolism in a northern Chinese population
- Evaluation of serum telomerase activity in normal-weight young girls with polycystic ovary syndrome and its relation to metabolic parameters
- Early onset of puberty during COVID-19 pandemic lockdown: experience from two Pediatric Endocrinology Italian Centers
- Using change in predicted adult height during GnRH agonist treatment for individualized treatment decisions in girls with central precocious puberty
- Short Communications
- Long-term experience with the use of a single histrelin implant beyond one year in patients with central precocious puberty
- Relationships among biochemical measures in children with diabetic ketoacidosis
- Case Reports
- Hyperthyroidism in McCune–Albright Syndrome – a case report
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