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Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies

Background: Primary antibody deficiencies (PADs) and anterior pituitary dysfunction are both rare conditions. However, recent studies have remarkably reported the occurrence of anterior pituitary dysfunction in PAD patients. Methods: In this cross-sectional, single-center study we evaluated the prev...

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Autores principales: Coopmans, Eva C., Chunharojrith, Paweena, Neggers, Sebastian J. C. M. M., van der Ent, Marianne W., Swagemakers, Sigrid M. A., Hollink, Iris H., Barendregt, Barbara H., van der Spek, Peter J., van der Lely, Aart-Jan, van Hagen, P. Martin, Dalm, Virgil A. S. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730260/
https://www.ncbi.nlm.nih.gov/pubmed/31543881
http://dx.doi.org/10.3389/fimmu.2019.02079
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author Coopmans, Eva C.
Chunharojrith, Paweena
Neggers, Sebastian J. C. M. M.
van der Ent, Marianne W.
Swagemakers, Sigrid M. A.
Hollink, Iris H.
Barendregt, Barbara H.
van der Spek, Peter J.
van der Lely, Aart-Jan
van Hagen, P. Martin
Dalm, Virgil A. S. H.
author_facet Coopmans, Eva C.
Chunharojrith, Paweena
Neggers, Sebastian J. C. M. M.
van der Ent, Marianne W.
Swagemakers, Sigrid M. A.
Hollink, Iris H.
Barendregt, Barbara H.
van der Spek, Peter J.
van der Lely, Aart-Jan
van Hagen, P. Martin
Dalm, Virgil A. S. H.
author_sort Coopmans, Eva C.
collection PubMed
description Background: Primary antibody deficiencies (PADs) and anterior pituitary dysfunction are both rare conditions. However, recent studies have remarkably reported the occurrence of anterior pituitary dysfunction in PAD patients. Methods: In this cross-sectional, single-center study we evaluated the prevalence of endocrine disorders in adult PAD patients. Our study focused on common variable immunodeficiency (CVID), immunoglobulin G (IgG) subclass deficiency (IgGSD), and specific anti-polysaccharide antibody deficiency (SPAD). We assessed hormone levels, performed provocative tests and genetic testing in a subset of patients by direct sequencing of the nuclear factor kappa beta subunit 2 (NFKB2) gene and primary immunodeficiency (PID) gene panel testing by whole exome sequencing (WES). Results: Our results demonstrated that one out of 24 IgGSD/SPAD patients had secondary hypothyroidism and three out of 9 men with IgGSD/SPAD had secondary hypogonadism. Premature ovarian failure was observed in four out of 9 women with CVID and primary testicular failure in one out of 15 men with CVID. In two out of 26 CVID patients we found partial adrenal insufficiency (AI) and in one out of 18 patients with IgGSD/SPAD secondary AI was found. Moreover, in one out of 23 patients with CVID and in two out of 17 patients with IgGSD/SPAD severe growth hormone deficiency (GHD) was found, while one patient with IgGSD/SPAD showed mild GHD. Combined endocrine disorders were detected in two women with CVID (either partial secondary AI or autoimmune thyroiditis with primary hypogonadism) and in three men with IgGSD/SPAD (two with either mild GHD or secondary hypothyroidism combined with secondary hypogonadism, and one man with secondary AI and severe GHD). Genetic testing in a subset of patients did not reveal pathogenic variants in NFKB2 or other known PID-associated genes. Conclusion: This is the first study to describe a high prevalence of both anterior pituitary and end-organ endocrine dysfunction in adult PAD patients. As these endocrine disorders may cause considerable health burden, assessment of endocrine axes should be considered in PAD patients.
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spelling pubmed-67302602019-09-20 Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies Coopmans, Eva C. Chunharojrith, Paweena Neggers, Sebastian J. C. M. M. van der Ent, Marianne W. Swagemakers, Sigrid M. A. Hollink, Iris H. Barendregt, Barbara H. van der Spek, Peter J. van der Lely, Aart-Jan van Hagen, P. Martin Dalm, Virgil A. S. H. Front Immunol Immunology Background: Primary antibody deficiencies (PADs) and anterior pituitary dysfunction are both rare conditions. However, recent studies have remarkably reported the occurrence of anterior pituitary dysfunction in PAD patients. Methods: In this cross-sectional, single-center study we evaluated the prevalence of endocrine disorders in adult PAD patients. Our study focused on common variable immunodeficiency (CVID), immunoglobulin G (IgG) subclass deficiency (IgGSD), and specific anti-polysaccharide antibody deficiency (SPAD). We assessed hormone levels, performed provocative tests and genetic testing in a subset of patients by direct sequencing of the nuclear factor kappa beta subunit 2 (NFKB2) gene and primary immunodeficiency (PID) gene panel testing by whole exome sequencing (WES). Results: Our results demonstrated that one out of 24 IgGSD/SPAD patients had secondary hypothyroidism and three out of 9 men with IgGSD/SPAD had secondary hypogonadism. Premature ovarian failure was observed in four out of 9 women with CVID and primary testicular failure in one out of 15 men with CVID. In two out of 26 CVID patients we found partial adrenal insufficiency (AI) and in one out of 18 patients with IgGSD/SPAD secondary AI was found. Moreover, in one out of 23 patients with CVID and in two out of 17 patients with IgGSD/SPAD severe growth hormone deficiency (GHD) was found, while one patient with IgGSD/SPAD showed mild GHD. Combined endocrine disorders were detected in two women with CVID (either partial secondary AI or autoimmune thyroiditis with primary hypogonadism) and in three men with IgGSD/SPAD (two with either mild GHD or secondary hypothyroidism combined with secondary hypogonadism, and one man with secondary AI and severe GHD). Genetic testing in a subset of patients did not reveal pathogenic variants in NFKB2 or other known PID-associated genes. Conclusion: This is the first study to describe a high prevalence of both anterior pituitary and end-organ endocrine dysfunction in adult PAD patients. As these endocrine disorders may cause considerable health burden, assessment of endocrine axes should be considered in PAD patients. Frontiers Media S.A. 2019-08-30 /pmc/articles/PMC6730260/ /pubmed/31543881 http://dx.doi.org/10.3389/fimmu.2019.02079 Text en Copyright © 2019 Coopmans, Chunharojrith, Neggers, van der Ent, Swagemakers, Hollink, Barendregt, van der Spek, van der Lely, van Hagen and Dalm. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Coopmans, Eva C.
Chunharojrith, Paweena
Neggers, Sebastian J. C. M. M.
van der Ent, Marianne W.
Swagemakers, Sigrid M. A.
Hollink, Iris H.
Barendregt, Barbara H.
van der Spek, Peter J.
van der Lely, Aart-Jan
van Hagen, P. Martin
Dalm, Virgil A. S. H.
Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies
title Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies
title_full Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies
title_fullStr Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies
title_full_unstemmed Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies
title_short Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies
title_sort endocrine disorders are prominent clinical features in patients with primary antibody deficiencies
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730260/
https://www.ncbi.nlm.nih.gov/pubmed/31543881
http://dx.doi.org/10.3389/fimmu.2019.02079
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