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Marie-Hélène Quentien, Brigitte Delemer, Dimitris T. Papadimitriou, Pierre-François Souchon, Roland Jaussaud, Anne Pagnier, Martine Munzer, Nicolas Jullien, Rachel Reynaud, Noémie Galon-Faure, Alain Enjalbert, Anne Barlier, Thierry Brue, Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections, The Journal of Clinical Endocrinology & Metabolism, Volume 97, Issue 1, 1 January 2012, Pages E121–E128, https://doi.org/10.1210/jc.2011-0407
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Among 22 independent patients from the GENHYPOPIT network who had ACTH deficiency and no identified mutation of TPIT, three of them (13.6%) displayed common variable immunodeficiency (CVID), characterized by defective Ig production.
Our objective was to describe an as yet unrecognized disease association.
We considered the hypothesis of ACTH deficiency being associated with antipituitary autoimmunity or lymphocytic hypophysitis. In the context of a functional network between the immune and endocrine systems, we also tested the hypothesis of a common genetic cause using a candidate gene approach.
This was a multicentric study in three academic hospitals.
We report four patients from three unrelated families presenting with ACTH deficiency and CVID.
Detection of antipituitary autoantibodies, and sequencing of candidate genes (LIF, IKAROS, EOS) were the main outcome measures.
All patients including a pedigree with two affected siblings had ACTH deficit diagnosed from 5–15 yr, with symptomatic hypoglycemia, and CVID diagnosed from 2–8 yr revealed by recurrent infections. Three of the four patients had a hypoplastic pituitary. One patient had low IGF-I and subnormal GH response to stimulation, suggesting that secretion of other pituitary hormones may also be affected. All patients proved negative for pituitary autoantibodies and had no alteration in any of the genes tested.
The remarkable association of two rare disorders affecting two functionally related systems in four patients from three independent pedigrees including a familial case provides strong evidence of the existence of a disease association: deficit in anterior pituitary function and variable immune deficiency, or DAVID.
