Diagnostic Delays are Common for this Rare Disease (Acromegaly) скачать в хорошем качестве

Diagnostic Delays are Common for this Rare Disease (Acromegaly)

Patrick Lewis, PharmD, Senior Director, Medical Affairs at Amryt Pharma provides an overview of acromegaly and why it is often difficult to diagnose quickly. Acromegaly is a rare endocrine disorder caused by excess levels of growth hormone (GH) in the body. In many cases, the excess of GH is caused by a benign tumor on the pituitary gland which can signal the liver to overproduce insulin-like growth factor 1 (IGF1). Common symptoms include subtle skeletal overgrowth; soft tissue swelling (tongue, heart, kidney, colon, and vocal cords); unusually prominent forehead and heavy brow ridge; protruding lower jaw; overbite; skin thickening; increased shoe and ring size; hypertension; increased perspiration; headaches; paresthesia; and sexual dysfunction. As noted by Dr. Lewis, the insidious nature at which acromegaly symptoms develop means there is an average diagnostic delay of several years. There are currently four orphan drugs approved to treat acromegaly. They either stimulate somatostatin receptors (octreotide, octreotide-oral, pasireotide) or inhibit GH receptors (pegvisomant). At ENDO 2023, new data was presented that can help predict treatment response to oral octreotide.