Literature DB >> 25501964

Pregnancy may favour the development of severe autoimmune central diabetes insipidus in women with vasopressin cell antibodies: description of two cases.

Giuseppe Bellastella1, Antonio Bizzarro1, Ernesto Aitella1, Mariluce Barrasso1, Domenico Cozzolino1, Sergio Di Martino1, Katherine Esposito1, Annamaria De Bellis2.   

Abstract

Recently, an increased incidence of central diabetes insipidus (CDI) in pregnancy, and less frequently in the post partum period, has been reported, most probably favoured by some conditions occurring in pregnancy. This study was aimed at investigating the influence of pregnancy on a pre-existing potential/subclinical hypothalamic autoimmunity. We studied the longitudinal behaviour of arginine-vasopressin cell antibodies (AVPcAbs) and post-pituitary function in two young women with a positive history of autoimmune disease and presence of AVPcAbs, but without clinical CDI, and who became pregnant 5 and 7 months after our first observation. The behaviour of post-pituitary function and AVPcAbs (by immunofluorescence) was evaluated at baseline, during pregnancy and for 2 years after delivery. AVPcAbs, present at low/middle titres at baseline in both patients, showed a titre increase during pregnancy in one patient and after delivery in the other patient, with development of clinically overt CDI. Therapy with 1-deamino-8-d-arginine vasopressin (DDAVP) caused a prompt clinical remission. After a first unsuccessful attempt of withdrawal, the therapy was definitively stopped at the 6th and the 7th month of post partum period respectively, when AVPcAbs disappeared, accompanied by post-pituitary function recovery, persisting until the end of the follow-up. The determination of AVPcAbs is advisable in patients with autoimmune diseases planning their pregnancy, because they could be considered good predictive markers of gestational or post partum autoimmune CDI. The monitoring of AVPcAb titres and post-pituitary function during pregnancy in these patients may allow for an early diagnosis and an early replacement therapy, which could induce the disappearance of these antibodies with consequent complete remission of CDI.
© 2015 European Society of Endocrinology.

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Year:  2014        PMID: 25501964     DOI: 10.1530/EJE-14-0762

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  5 in total

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4.  Common variable immune deficiency, central diabetes insipidus, and anemia.

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Review 5.  Revisitation of autoimmune hypophysitis: knowledge and uncertainties on pathophysiological and clinical aspects.

Authors:  Giuseppe Bellastella; Maria Ida Maiorino; Antonio Bizzarro; Dario Giugliano; Katherine Esposito; Antonio Bellastella; Annamaria De Bellis
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  5 in total

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