dc.description.abstract | <b>Objective:</b> The epidemiology of hypoparathyroidism (HP) is largely unknown. We aimed to determine
prevalence, etiologies, health related quality of life (HRQOL) and treatment pattern of HP.<br>
<b>Methods:</b> Patients with HP and 22q11 deletion syndrome (DiGeorge syndrome) were identified in
electronic hospital registries. All identified patients were invited to participate in a survey. Among
patients who responded, HRQOL was determined by Short Form 36 and Hospital Anxiety and
Depression scale. Autoantibodies were measured and candidate genes (CaSR, AIRE, GATA3, and
22q11-deletion) were sequenced for classification of etiology.<br>
<b>Results:</b> We identified 522 patients (511 alive) and estimated overall prevalence at 102 per million
divided among postsurgical HP (64 per million), nonsurgical HP (30 per million), and pseudo-HP (8
per million). Nonsurgical HP comprised autosomal dominant hypocalcemia (21%), autoimmune
polyendocrine syndrome type 1 (17%), DiGeorge/22q11 deletion syndrome (15%), idiopathic HP
(44%), and others (4%). Among the 283 respondents (median age, 53 years [range, 9 – 89], 75%
females), seven formerly classified as idiopathic were reclassified after genetic and immunological
analyses, whereas 26 (37% of nonsurgical HP) remained idiopathic.Most were treated with vitamin
D (94%) and calcium (70%), and 10 received PTH. HP patients scored significantly worse than the
normative population on Short Form 36 and Hospital Anxiety and Depression scale; patients with
postsurgical scored worse than those with nonsurgical HP and pseudo-HP, especially on physical
health.
<br><b>Conclusions:</b> We found higher prevalence of nonsurgical HP in Norway than reported elsewhere.
Genetic testing and autoimmunity screening of idiopathic HP identified a specific cause in 21%.
Further research is necessary to unravel the causes of idiopathic HP and to improve the reduced
HRQOL reported by HP patientss. (J Clin Endocrinol Metab 101: 3045–3053, 2016) | en_US |