Systemic Management of Graves Disease. Robert James Graves, M.D., FRCS ( ) Graves Disease: Endocrinopathy or Ophthalmopathy?

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Systemic Management of Graves Disease Rona Z. Silkiss, M.D., FACS Associate Clinical Professor, UCSF Chief, Division of Ophthalmic Plastic and Orbital Surgery California Pacific Medical Center No financial disclosures. www.eyework.com Graves Disease: Endocrinopathy or Ophthalmopathy? Robert James Graves, M.D., FRCS (1796-1853) Eminent Irish Surgeon President of the Royal College of Physicians of Ireland Fellow of the Royal Society of London Founder of the Dublin Journal of Medical Science The uncredited inventor of the second hand on watches.

Graves Endocrinopathy Most common cause of hyperthyroidism Affects 2% of female population Female : male 5-10:1 25-30% of patients with endocrinopathy develop ophthalmopathy (thyroid eye disease) Thyroid Eye Disease (TED) Graves ophthalmopathy (TED) is the most common cause of unilateral or bilateral proptosis 6X more common in women than in men Associated with hyperthyroidism (90%), euthyroidism (6%), hypothyroidism (4%) Associated with severe psychosocial stress Associated with elevated TSH-R stimulating auto antibodies (TRAb) Clinical Features of TED Eyelid retraction - most common Lid lag Conjunctival injection, chemosis Proptosis Restrictive extraocular myopathy-strabismus Optic neuropathy

Treatment of Graves Endocrinopathy Antithyroid drugs Steroids Biologics RAI Surgery Thionamidesintroduced in the 1940s Methimazole- Tapazole (USA) Propylthiouracil (USA)- risk of liver failure Carbimazole- pro drug of MMI (UK) Antithyroid Drugs Mechanism of Action of Thionamides Inhibit thyroid hormone synthesis by interfering with thyroid peroxidase mediated iodination of tyrosine residues in thyroglobulin PTU blocks conversion of T4 T3 Possible immune suppression with TSHRAb, IL2, IL 6 HLA class II expression

MMI x PTU x PTU x Characteristic Methimazole Propylthiouracil Relative potency 10-50 1 Administration Oral Oral Absorption Nearly complete Nearly complete Binding to serum proteins Negligible 80-90% Serum half-life (hr) 4-6 1-2 Vol of distrib (L) 40 20 Inhib T4 T3 No Yes Dosing 10-40 mg 1-2 times/d 300-600 mg 2-3 times/d Characteristic Methimazole Propylthiouracil Met during liver ds Decreased Normal Met during renal ds Normal Transplacental pass Low Levels in breast milk Low Normal Even lower Even lower Indications for Use of Thionamides To achieve a euthyroid state Pre intervention control ( I 131, surgery) Treatment of choice in pregnancy, childhood, adolescence, presence of ophthalmopathy I 131 exacerbates eye disease, requires steroid cover

Methodologies for Administration Dose titration Block and replace ATD and Levothyroxine replacement Treatment duration - 14-18 months Recurrence rate - 50-60% within 3-6 months of discontinuing ATD May require long term low dose tx Factors Associated with Relapse Severe hyperthyroidism High serum T3/T4 ratio High TSHRAb levels initially or at end of therapy Young age Male sex Smoking Presence of ophthalmopathy Factors Associated with Relapse Family history of autoimmune disease Certain genetic markers Large initial goiter Increasing goiter size during tx Thyroid nodularity, hypoechogenicity by imaging High intrathyroidal blood flow at end of ATD tx Long delay from start of symptoms to initiation of tx Problems in coping with daily life Side Effects of Thionamides Incidence 5% MMI dose related, PTU less so Ok to switch meds, 50% cross over Urticaria, pruritis, arthralgia, fever-rx antihistamine Gastrointestinal complaints, abnormalities of taste and smell Arthritis Transient granulocytopenia

Serious Side Effects Agranulocytosis - 0.35% Equal frequency MMI-PTU Risk of pseudomonas aeruginosa sepsis Hepatotoxicity - 0.1-0.2% Vasculitis (PTU>MMI)- lupus like Hypoprothrombinemia Hypoglycemia Pancreatitis β-adrenergic Antagonist Drugs Ameliorate symptoms - sweating, anxiety, tremor, palpitation, tachycardia Mildly inhibits the conversion of T4 to T3 Avoid in patients with COPD Propranolol MMI somewhat better side effect profile than PTU Inorganic Iodide Decreases T4 and T3 synthesis by inhibiting iodide oxidation and organification (Wolff- Chaikoff effect). Blocks the release of T4 and T3 by inhibiting thyroglobulin proteolysis. Lugol s solution (8 mg iodide per drop) Saturated solution of potassium iodide (SSKI 50 mg iodide per drop) Dose : 24-50 mg/day Glucocorticoids Blocks the conversion of T4 to T3 in a similar fashion to beta-blockers Use only in patients with ophthalmopathy due to side effects

Supplementary Agents Oral cholecystographic agents (e.g., sodium iopanoate, sodium ipodate) inhibit T4- deiodinase activity. Acutely lower serum T3 levels. Potassium perchlorate is a competitive inhibitor of iodide transport. Lithium acts by inhibiting T4 and T3 release from the thyroid. Dose - 900 mg q d Novel Biologics Rituximab - more later anti-b-cell maturation factor anti-b-cell maturation antigen receptor (anti-baff) anti-b-cell maturation antigen (anti-bcma) blockade of the CD40-CD154 (CD40- ligand) abatacept (CTLA-4/Ig); Radioactive Iodine (RAI) Introduced in the 1940s (MIT, Berkeley) I 131 concentrated, oxidized, organified by follicular thyroid cells Ionizing effect of β particles (path length of 1 to 2 mm) destroys thyroid follicular cells and promotes vascular occlusion Induces hypothyroidism

I 131 131 Dosing No consensus induce hypothyroidism or retreat Incidence of hypothyroidism independent of dose: 2-3% annually Dose (mci) = 80-200 microci I 131 /g thyroid x estimated thyroid gland weight (g)/24hour radioiodine uptake Typical activities - 5 to 15 mci I 131 Corresponds to 185-555 MBq = absorbed radiation dose of 50 to 100 Gy. Becquerel The becquerel (Bq) is the SI derived unit of radioactivity. One Bq is defined as the activity of a quantity of radioactive material in which one nucleus decays per second. The Bq unit is therefore equivalent to s-1. The becquerel is named for Henri Becquerel, who shared a Nobel Prize with Pierre and Marie Curie for their work in discovering radioactivity. Scan of thyroid 24 h after intake of I 131 I 131 Influence on Thyroid Function 50-70% euthyroid within 6-8 weeks 10 to15 mci (370 555 MBq) range, 80% to 90% of patients become euthyroid or hypothyroid after one dose of I 131. 10-20% require a second dose

Carcinogenicity Avoid use of I 131 in children and adolescents Avoid use in pregnant or breastfeeding women Factors that Increase Risk of TED Smoking High levels of pretreatment serum T3 (twice the upper limit of normal) A high TSH-receptor antibody titer RAI and TED RAI is associated with increased risk of ophthalmopathy compared with antithyroid drugs. The risk of developing new or worsening ophthalmopathy is ~ 20% after radioiodine and ~ 5% after antithyroid drugs. Post radioiodine hypothyroidism risk of TED Post radioiodine hypothyroidism should be treated promptly. Patients with mild pre-existing ophthalmopathy, should be pretreated with prednisone to prevent progression. Routine use of prophylactic steroids in all RAI pts is not indicated at present- but should be considered in pts at higher risk of TED (e.g. smokers).

Surgery Children, adolescents, pregnant women Large goiters (pressure symptoms, cosmesis) Suspicion of thyroid malignancy Graves ophthalmopathy especially those not responsive to ATD. Complications of Thyroidectomy Permanent damage to the recurrent laryngeal nerve and hypoparathyroidism - (1-2% up to 5-10%) Transient hypocalcemia, bleeding, wound infections, keloids. Hypothyroidism (12-80% during the first year and at a rate of 1-3% annually) Subtotal thyroidectomy associated with recurrent hyperthyroidism in 5-15%

Choices? Preference for ATD, I 131 or surgery should be discussed with patient and endocrinologist on an individualized level. Stop smoking! References Hegedus, L, Treatment of Graves Hyperthyroidism: Evidence based and emerging modalities, Endo Metab Clin North Am 38(2):355-71, 2009. Acharya, SH, et al. RAI for GD and the Effect on Ophthalmopathy, Clin Endo 69, 943-50, 2008. Ponto, K, The Tale of Radioiodine and Graves Orbitopathy, Thyroid, 20(7), 2010 Stallberg, P, Surgical Treatment of Graves Disease: Evidence Based Approach, World J of Surg 32:1269-1277, 2008. Clark, O, The Treatment of Graves Disease - The Advantages of Surgery, Endo and Metab Clinics, 29(2), 2000. Thank you