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Graves Disease Scott Gabbard

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B-lymphocytes from thyroid tissue secrete Thyroid Stimulating ... Emotional lability. Tremor. Diagnosis. Physical exam. Everything I was just talking about ... – PowerPoint PPT presentation

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Title: Graves Disease Scott Gabbard


1
Graves DiseaseScott Gabbard
2
Overview
  • Graves Disease is a syndrome of
  • hyperthyroidism
  • goiter
  • opthalmopathy
  • myxedema
  • Prevalence 1 in 89
  • Incidence 1 in 2000 per year

3
Pathogenesis
  • B-lymphocytes from thyroid tissue secrete Thyroid
    Stimulating Hormone Receptor Antibodies (TSHR-Ab)

4
Immunology????
  • CD4 Cells
  • Humoral Immune System stimulates B-cell
    proliferation and antibody production
  • Cytokines IL-4, 5, 6, 10
  • Activation Receptor complexes with HLA class II
    molecules and co-stimulatory molecules

5
Immunology of Graves
  • CD8 Cells
  • Cell Mediated Immunity Activation of macrophages
    and NK cells. Cytotoxic T-cells are also able to
    induce apoptosis in infected body cells.
  • Cytokines IFN-gamma and TNF-beta
  • Activation Receptor complexes with HLA class I
    molecules and co-stimulatory molecules

6
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7
Immunology
  • Graves disease is primarily a CD4-Th2 type of
    autoimmune disease (likely due to
    thyroid-specific co-stimulation molecules)
  • These cells secrete IL-4 and IL-5 --gt this
    activates antibody production by B-cells

8
Predisposing Factors
  • Genetics
  • Up to 40 concordance in monozygotic twins (lt5
    in dizygotics)
  • Sex
  • Women to men ratio is 71
  • Effects of estrogen vs. decreased testosterone?
  • Smoking
  • Relative risk 2
  • Pregnancy
  • Due to rebound from diminished T-cell and B-cell
    function during pregnancy?

9
Predisposing Factors
  • Infection
  • Yersinia
  • Serum of many patients with Graves contains
    antibodies that react with antigens derived from
    Yersinia entercolitia (molecular mimicry)
  • Subacute thyroiditis
  • Rubella
  • Stress
  • Drugs
  • Amiodarone
  • due to direct thyroid cell damage which releases
    thyroid antigens to the immune system
  • Iodine

10
Clinical Manifestations
  • Skin
  • Warm, smooth skin
  • Onycholysis (loosening of nail bed)
  • Thinning hair
  • Myxedema
  • Increased amounts of hyaluronic acid and
    chondroitin sulfate in the dermis layer

11
Myxedema
12
Graves Opthalmopathy
  • Exopthalmos/Lid lag
  • Pathogenesis
  • T-cell cytokines increase glycosaminoglycan
    secretion by fibroblasts
  • This leads to volume increases in extraocular
    muscles and retro-orbital adipose and connective
    tissue
  • Risk factors
  • Genetics
  • Smoking

13
Exophthalmos
14
Clinical manifestations
  • Metabolic
  • Weight loss
  • Hyperglycemia
  • Antagonism to peripheral action of insulin
  • Decreases in HDL and LDL
  • Respiratory
  • Respiratory muscle weakness
  • Exacerbation of reactive airways disease

15
Clinical manifestations
  • GI
  • Increased gut motility
  • Malabsorption
  • Urinary
  • Increased frequency
  • Bone
  • Increased bone resorption -gt increased porosity
    of cortical bone

16
Clinical manifestations
  • Neuropsych
  • Psychosis/agitation
  • Emotional lability
  • Tremor

17
Diagnosis
  • Physical exam
  • Everything I was just talking about
  • Goiter
  • Elderly patients will not necessarily have
    palpable thyroid
  • Thyroid function testing
  • Low TSH (lt0.05)
  • Increased T4, T3
  • Occasionally (5) patients may have normal T4
    but elevated free T3 (T3 toxicosis)

18
Diagnosis
  • Radionuclide scan
  • Normal thyroid uptake is 15-30
  • Graves disease homogenous increased uptake

19
Treatment
  • Two objectives to treatment
  • Ameliorate symptoms
  • Decrease thyroid hormone synthesis

20
Symptom alleviation
  • Beta-blockers
  • Start with atenolol (25-50mg per day)
  • Beta-1 specific
  • Single dose daily

21
Treatment
  • Thyroid specific treatment
  • Thionamides (methimazole and PTU) - reduce
    oxidation and organification of iodide (PTU also
    inhibits deiodination of T4 to T3)
  • Methimazole preferred because of longer duration
    than PTU
  • Start with 20mg PO Qday

22
Treatment
  • Radioiodine
  • 131-I administered by capsule or solution
  • Rapidly incorporated into thyroid tissue, beta
    emissions result in local tissue damage
  • Most patients (80) will become hypothyroid in
    6-18 weeks
  • Women must have negative hCG before this
    treatment
  • Radioiodine may precipitate or worsen
    opthalmopathy (controversial)
  • Steroids for three months may prevent worsening
    of opthalmopathy

23
Treatment
  • Surgery
  • Indications
  • Large obstructive goiter
  • Pregnant patients who cannot tolerate thionamides
  • Rapid restoration of euthyroidism

24
References
  • Uptodate.com
  • Davies, T. Pathogenesis of Graves Disease and
    Pathogenesis and Clinical features of Graves
    opthalmopathy
  • Ross, D. Diagnosis of hyperthyroidism and
    Overview of the clinical manifestations of
    hyperthyroidism in adults
  • Kasper et al. (2005) Harrisons Principles of
    Internal Medicine (pp 2113-2115) McGraw-Hill
  • Merckmedicus.com
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