Diagnosis and management of acromegaly


Table 2: Diagnostic studies in acromegaly


Screening

Oral glucose tolerance test for growth-hormone suppression (75 g glucose; growth hormone is suppressed to less than 2 µg/L throughout a 2-h test in normal subjects)

Serum or plasma measurement of insulin-like growth factor I [IGF-I] (random blood specimen; significantly elevated level for age and sex is a preferred integrated measure of excess growth hormone)


Further tests to assess the effects of a growth-hormone-producing tumour

Serum prolactin measurement

Thyrotropin-releasing hormone (TRH) or gonadotropin-releasing hormone (GnRH) stimulation test to assess paradoxical growth-hormone response

Thyroid function tests (serum thyrotropin, free thyroxine [FT4] or FT4 index tests) and possibly thyrotropin-releasing hormone (TRH) stimulation test

In men, serum total and free testosterone, follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels

In postmenopausal women, serum FSH and LH levels

In premenopausal women with secondary amenorrhea, serum 17 ß-estradiol or progestational challenge

Assessment of the integrity of the hypothalamic-pituitary-adrenal axis (insulin tolerance, metyrapone or cortrosyn stimulation test)


Radiologic studies

Magnetic resonance imaging (MRI) or computed tomography (CT) of the pituitary fossa. MRI is more sensitive in resolving small tumours and in identifying extension outside of the sella turcica and is therefore preferred

Chest radiograph (to assess cardiac size)

If a tumour is not visible on imaging of the pituitary, but GHRH levels are elevated, CT scans of the chest and abdomen should be performed to identify an ectopic source of GHRH production


Other studies

Visual fields by perimetry, to assess effect of tumour on optic chiasm

Standard biochemical studies (calcium, phosphorous, glucose, hemoglobin A1c and lipid levels)

Sleep studies to assess presence and severity of sleep apnea