Clinical features and autoimmune associations in patients presenting with Idiopathic Isolated ACTH deficiency

Abstract

Objective

Idiopathic Isolated ATCH deficiency (IIAD) is a rare cause of secondary adrenal insufficiency. As the condition is rare, and the diagnostic criteria ill-defined, there are few good clinical descriptions in the literature. We have described presenting features, autoimmune associations, natural history and responses to CRF, in a large case series of patients presenting with IIAD.

Design

This is a retrospective case note analysis with data derived from the recently commenced National Pituitary Database of Ireland.

Patients

23 patients with isolated ACTH deficiency were identified. A thorough chart and biochemistry review was performed.

Results

23 patients were examined (18 women and 5 men). Age at presentation ranged from 17 to 88 years, (median 48 years). Most patients complained of fatigue; 9 patients presented with hyponatraemia, 13 had autoimmune illnesses (primary hypothyroidism, n = 9). CRF stimulation testing was available in 12 of the 23 patients, 5 of whom demonstrated a rise in plasma ACTH concentrations, indicating hypothalamic, rather than pituitary aetiology. 2 patients recovered ACTH secretion and 2 patients progressed to have other pituitary hormone deficiencies.

Conclusions

IIAD typically presents with insidious symptoms. Euvolaemic hyponatraemia is common at diagnosis. It is associated with autoimmune diseases, particularly primary hypothyroidism. As two patients recovered ACTH secretion, and two progressed to other pituitary hormone deficits, repeat pituitary testing should be considered, to identify recovery of function, or progression to other hormone deficits

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