Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging “Mismatch Pattern”

Author:

Bianco Deborah12ORCID,Napoli Flavia2,Morana Giovanni3,Pistorio Angela4,Allegri Anna Elsa Maria2,Fava Daniela12,Schiavone Maurizio12,Thiabat Hanan F12,Crocco Marco12,Camia Tiziana12,Lezzi Marilea12,Calandrino Andrea12,Tortora Domenico5,Severino Mariasavina5ORCID,Patti Giuseppa12ORCID,Ibba Anastasia6,Rossi Andrea5,Di Iorgi Natascia12,Maghnie Mohamad12

Affiliation:

1. Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy

2. Department of Pediatrics, IRCCS Istituto Giannina Gaslini, Genova, Italy

3. Department of Neurosciences, University of Turin, Turin, Italy

4. Epidemiology and Biostatistics Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy

5. Pediatric Neuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy

6. SSD Endocrinologia Pediatrica, Azienda Ospedaliera Brotzu, SSD Endocrinologia Pediatrica, Ospedale Pediatrico Microcitemico “A. Cao”, Cagliari, Italy

Abstract

Abstract Context The etiology of central diabetes insipidus (CDI) in children is often unknown. Clinical and radiological features at disease onset do not allow discrimination between idiopathic forms and other conditions or to predict anterior pituitary dysfunction. Objective To evaluate the evolution of pituitary stalk (PS) thickening and the pattern of contrast-enhancement in relation with etiological diagnosis and pituitary function. Methods We enrolled 39 children with CDI, 29 idiopathic and 10 with Langerhans cell histiocytosis (LCH). Brain magnetic resonance images taken at admission and during follow-up (332 studies) were examined, focusing on PS thickness, contrast-enhancement pattern, and pituitary gland size; T2-DRIVE and postcontrast T1-weighted images were analyzed. Results Seventeen of 29 patients (58.6%) with idiopathic CDI displayed “mismatch pattern,” consisting in a discrepancy between PS thickness in T2-DRIVE and postcontrast T1-weighted images; neuroimaging findings became stable after its appearance, while “mismatch” appeared in LCH patients after chemotherapy. Patients with larger PS displayed mismatch more frequently (P = 0.003); in these patients, reduction of proximal and middle PS size was documented over time (P = 0.045 and P = 0.006). The pituitary gland was smaller in patients with mismatch (P < 0.0001). Patients with mismatch presented more frequently with at least one pituitary hormone defect, more often growth hormone deficiency (P = 0.033). Conclusions The PS mismatch pattern characterizes patients with CDI, reduced pituitary gland size, and anterior pituitary dysfunction. The association of mismatch pattern with specific underlying conditions needs further investigation. As patients with mismatch show stabilization of PS size, we assume a prognostic role of this peculiar pattern, which could be used to lead follow-up.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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