Exploratory Study of the Association of Genetic Factors With Recovery of Adrenal Function in Cushing Disease

Author:

Nguyen Matthew H1ORCID,Zhang Wei2ORCID,Pankratz Nathan3ORCID,Lane John3,Chitiboina Prashant4ORCID,Faucz Fabio R5ORCID,Mills James L6ORCID,Stratakis Constantine A1ORCID,Tatsi Christina1ORCID

Affiliation:

1. Unit on Hypothalamic and Pituitary Disorders , Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health, Bethesda, MD 20892 , USA

2. Academy of Mathematics and System Sciences, Chinese Academy of Sciences , Beijing 100045 , China

3. Department of Laboratory Medicine and Pathology, University of Minnesota Medical School , Minneapolis, MN 55454 , USA

4. Neurosurgery Unit for Pituitary and Inheritable Diseases, National Institute of Neurological Disorders and Stroke, National Institutes of Health , Bethesda, MD 20892 , USA

5. Molecular Genomics Core , Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892 , USA

6. Epidemiology Branch , Eunice Kennedy Shriver National Institutes of Child Health and Human Development (NICHD), National Institutes of Health, Bethesda, MD 20892 , USA

Abstract

Abstract Successful treatment of endogenous Cushing disease (CD) is often followed by a period of adrenal insufficiency (AI). We performed an exploratory study on genetic factors potentially involved in the hypothalamic-pituitary-adrenal (HPA) axis recovery in patients with CD after remission. We identified 90 patients who achieved remission after surgery and had a minimum of 3 months follow-up. Variants in a selected panel of genes that were rare in the general population and predicted as damaging in silico were retrieved from whole exome sequencing analysis. We did not identify any variant with significant correlation with recovery time after adjusting for multiple comparisons. On gene-specific analysis the BAG1 gene showed a correlation with shorter duration of postsurgical AI, but both patients with BAG1 variants later experienced a recurrence. After excluding patients with recurrence, no statistical association was recorded. To conclude, we did not identify a strong genetic modifier of HPA recovery in this exploratory study.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institutes of Health

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

Reference14 articles.

1. Recovery of hypothalamic-pituitary-adrenal axis in paediatric Cushing disease;Tatsi;Clin Endocrinol (Oxf),2021

2. The pituitary corticotroph is not the rate limiting step in the postoperative recovery of the hypothalamic-pituitary-adrenal axis in patients with Cushing syndrome;Gomez;J Clin Endocrinol Metab,1993

3. Recovery of adrenal function after pituitary surgery in patients with Cushing disease: persistent remission or recurrence?;Serban;Neuroendocrinology,2019

4. Extensive clinical experience: hypothalamic-pituitary-adrenal axis recovery after adrenalectomy for corticotropin-independent cortisol excess;Hurtado;Clin Endocrinol (Oxf),2018

5. Recovery of the hypothalamic-pituitary-adrenal axis in children and adolescents after surgical cure of Cushing's disease;Lodish;J Clin Endocrinol Metab,2012

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