Abstract

PurposeCushing’s disease (CD) is a rare disease that contributes to 70–80% hypercortisolemia, which presents similarities and differences between pediatric and adult patients, and even between male and female patients. However, the comparative study of CD between different age groups and different genders is still insufficient. The aim of the study is to make a systematic comparison to reveal the gender differences in children and adult patients of CD, helping clinicians to provide optimal treatment for different groups of patients.MethodsWe conducted a retrospective research consisting of 30 pediatric and 392 adult CD patients in a single center in Peking Union Medical College Hospital. All 422 patients showed symptoms related to hypercortisolism and received adenoma excision surgery in the department of neurosurgery between 2014 and 2020.ResultsFor the accuracy of diagnosis, the sensitivity of BIPSS at baseline in pediatric patients was lower than in adults (75 vs. 91%, P = 0.054) but increased greatly after desmopressin stimulation (94 vs. 95%). However, the accuracy of lateralization for BIPSS was not preferred for prediction. As for clinical manifestations, growth retardation, weight gain, hirsutism, and acne were more prevalent for children, while for adults, hypertension, osteopenia, glucometabolic disorder, easy bruising, hair loss, and weight loss were more frequently seen. As previously reported, we observed a significant difference between the male prevalence of pediatric and adult patients (50 vs. 17%, P < 0.001), which was possibly caused by the more severe and earlier onset of a series of symptoms. Gender-related comparison showed greater morbidity of nephrolithiasis, hypokalemia, hypertension, easy bruising, osteopenia, and striae for male patients, while irregular menses, hirsutism, and hair loss were more common for female patients. Further analysis showed that the secretory activity of the PA axis was higher for males, presenting as the more remarkable alteration of laboratory parameters and contributing to the more severe clinical manifestations. For patients treated with transsphenoidal pituitary surgery (TSS), the immediate prognosis could be predicted by operation history, invasiveness, Ki-67, and information provided by MRI, including tumor size and Knosp grading. However, we still lack methods to predict long-term prognosis.ConclusionsOur study is the first detailed and systematic comparison between pediatric and adult CD patients. Further exploration of the impact of CD on different genders reveals a more severe and probably an earlier-onset pattern of CD for male patients.

Highlights

  • Cushing’s disease (CD) is a rare disease characterized by hypercortisolemia, caused by the excess secretion of adrenocorticotrophin hormone (ACTH) by a pituitary adenoma that stimulates overproduction of cortisol from the adrenal glands (1)

  • There was no significant difference in the sensitivity of the above four investigations between pediatric and adult patients

  • Further analysis showed that lateralization accuracy of bilateral petrosal sinus sampling (BIPSS) for macroadenomas on Magnetic resonance imaging (MRI) was not higher than that for microadenomas on MRI

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Summary

Introduction

Cushing’s disease (CD) is a rare disease characterized by hypercortisolemia, caused by the excess secretion of adrenocorticotrophin hormone (ACTH) by a pituitary adenoma that stimulates overproduction of cortisol from the adrenal glands (1). Since hypercortisolemia can lead to a series of metabolic disorders and profoundly impact the quality of life, the accurate diagnosis and effective treatment can be very challenging yet critical. CD is extremely rare in the pediatric population and results in multisystem disorder, including growth retardation, delayed sexual development, obesity, hypertension, glucose intolerance, and mood changes (2). Transsphenoidal pituitary surgery (TSS) is considered as the first-line treatment for CD, but the difficulty, effectiveness, and prognosis of TSS for children may be different from adult patients (3). Detailed and systematic comparisons of diagnostic accuracy, clinical manifestations, laboratory investigations, and prognosis between pediatric and adult patients have seldom been performed. It is very meaningful to reveal the gender differences in children and adult populations on symptoms and laboratory parameters of CD, helping clinicians to accurately diagnose and provide optimal treatment for different groups of patients

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