Week 3: Thyroid physiology and thyroid function tests Flashcards

1
Q

Thyroid hormone biosynthesis

A
  1. Iodide metabolism: need ~150ug iodide from diet daily. Large reserve in colloid
  2. Iodide transport: by Na/I symporter on basolateral membrane of follicular cell
    - TSH and Iodide deficiency augments uptake
  3. Thyroglobulin biosynthesis
    - Tg made on rER/golgi, transported to apical side for iodination and transfer to colloid for storage
  4. Iodination of Tg: catalyzed by thyroid peroxidase (TPO) on apical membrane.
    - forms DIT and MIT, which combine to form T3 (DIT+MIT) and T4 (DIT+DIT)
  5. thyroid hormone release: Tg from colloid resorbed via micropinocytosis and fuses with lysosomes. Transported to basolateral side. hydrolysis frees T4 and T3.
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2
Q

thyroxine binding globulin (TBG)

A
  • most of thyroid hormone bound to TBG, which has 10x affinity for T4 than T3
    1. Causes of elevated TBG levels
  • high estrogen stages in pregnancy and with OCPs
  • drugs: heroin, methadone, clofibrate, 5-FU, nicotinic acid
  • diseases: liver disease
    2. causes of reductions in circulating TBGs
  • acute and chronic non thyroidal illness
  • nephrotic syndrome due to tubular leak
  • glucocorticoid, androgen abuse, anabolic steroids
  • congenital deficiency
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3
Q

T3 and rT3

A
  • T3 has much lower serum concentration than T4. TBG has lower affinity to T3, so most of body’s stores of T3 are in intracellular compartment
  • rT3: produced in peripheral tissues. Primarily a disposal pathway in peripheral metabolism of T4
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4
Q

Iodothyronine deiodinases

A
  1. Type 1: 5” deiodinase
    - located in liver, kidney, thyroid gland
    - inhibited by propylthiouracil (PTU)
    - prefers rT3 substrate, can convert T4 to T3
    - converts rT3 to T2
  2. Type 2 5’-deiodinase
    - CNS, placenta, heart, thyroid, pituitary gland
    - prefers T4 as substrate
    - responsible for most of circulating T3
  3. Type 3 5-Deiodinase
    - CNS, skin, placenta
    - T4 and T3 preferred substrates
    - responsible for generation of rT3 from T4
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5
Q

mechanism of action of Thyroid hormone

A
  • hormones enter target cell via MCT8 protein (transporter)
  • effects of T3 mediated by T3 receptors in nucleus of the cell
  • act in dominant negative manner: when receptor has no ligand bound, it represses that particular transcription. When ligand binds, transcription occurs.
  • beta2 receptor: inhibitory and provides negative feedback regulation of TSH. Transcription is active when no T3 bound
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6
Q

Changes in thyroid hormone metabolism with illness

A
  • initial: fall in serum T3->low T3 state
  • rise in rT3 values
  • may result from inhibition of Type 1 and Type 3 enzyme activity
  • low T3-low T4 state: decline in serum T4, due to change in affinity of TBG for T4
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7
Q

Free T4/TSH relationship

A
  • TSH levels regulated by balance between TRH stimulation and negative feedback by T4 (sensed by conversion locally to T3)
  • senses small changes in free T4 levels and alters TSH synthesis accordingly
    1. amplification: a 2fold change in free T4 produces a 100 fold change in TSH
    2. individual Set point
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8
Q

Three conditions in which TSH does not accurately reflect thyroid status of patient

A
  1. presence of hypothalamic or pituitary disease
  2. treatment of chronic thyroid hormone excess or deficiency
    - there is a lag of TSH because thyroid becomes hypo/hyperplastic and needs time to respond to therapies
  3. the superimposition of non thyroidal illness
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9
Q

Summary of thyroid function tests

A
  • serum T4 level: function of thyroid gland
  • serum T3 level: metabolic status of patient
  • TU and T3U: serum binding proteins
  • Free T4 estimate: T4/TU or T4xT3U; free T4 levels
  • Serum TSH level: readout of the endogenous free T4 value
  • anti-TPO titer: immune state of the thyroid gland
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