hypothyroidism Flashcards

1
Q

describe the hypathalamo-pituitary thyroid axis

A

hypothalamus is at the top of the control chain - secretes TRH hormones these cause the ant pit to produce TSH these act on the thyroid gland causing it to release T3 and T4

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2
Q

draw the hypathalamo-pituitary thyroid axis

A
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3
Q

what is the general function of thyroid hormones

A

control every cell in the body determining the basal metabolic rate

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4
Q

what does TSH control in thyroid hormone production

A

iodine entry into cells and the enzyme that releases thyroxine from the cell (if the thyroid gland is over active there is more enzyme that releases thyroxine from the cell)

stimulate the release of stored thyroxine

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5
Q

where is thyroxine stored

A

in colloid which also contains thyroglobulin colloid is in the middle of the follicle, and is surrounded by cells there is enough stored thyroid for 1 month [IMAGE OF FOLLICLE]

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6
Q

what is myxoedema *

A

primary thyroid failure

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7
Q

what are the causes of myxoedema *

A

autoimmune damage - Ab attack thyroid and wipe it out - this is Hashimoto’s thyroiditis (chronic autoimmune thyroiditis which is characterised by lymphocytic invasion of the thyroid gland and anti-thyroid peroxidase (TPO) antibodies)

iatrogenic - post-thyroidectomy, post radioactive iodine

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8
Q

signs of myxoedema *

A

thyroxine levels decline TSH rises because there is no -ve feedback

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9
Q

symptoms of myxoedema *

A

hair dry and brittle LETHARGY memory impairment, slow cerebration oedema of face and eyelids thick tongue, slow speecg DEEP COURSE VOICE COLD diminished perspiration heart enlarged poor heart sounds pericardial pain hypertension skin course, dry, scaling PULSE SLOW BRADYCARDDIA ascites amenorrhoea weakness prolonged reflexes DEPRESSION TIREDNESS WEIGHT GAIN WITH REDUCED APPETITE CONSTIPATION EVENTUAL MYXOEDEMA COMA

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10
Q

describe thyroid hormones

A

healthy adult thyroid secretes T4 and T3 T4 (tetraiodothyronine) is a prohormone - converted to T3 by deiodination enzymes in the target cell 80% T3 is from T4 deiodination 20% is from direct thyroidal secretion T3 is the most metabolically active and provides most of the activity in target cells

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11
Q

describe the mechanism of action of the thyroid hormones

A

T4 and T3 enter target cell T4 converted to T3 by deiodination reaction T3 form heterodimer with RXR (retenoid x receptor) and TR (thyroid hormone receptor) heterodimer binds to part of DNA - thyroid response element (TRE) and alters gene expression

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12
Q

how would you treat primary thyroidism *

A

thyroid replacement therapy

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13
Q

hormones used for thyroid replacement therapy *

A

levothyroxine sodium, thyroxine Na, thyroxine - all mean salt of thyroxine (T4) - this will be converted to T3 to make the biological effects liothyronine Na, triiodothyronine - T3 less commonly used

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14
Q

describe the clinical use of levothyroxine *

A

treats primary hypothyroidism oral admin the aim is to normalise TSH levels -the levothyroxine provides -ve feedback for TSH - TSH level is used for guidance for treatment, when it is in the normal range that is the correct levothyroxine dose for that patient it is converted to T3 to have an effect treats secondary hypothyroidism - TSH is low so free T4 (fT4) is used as the guidance for the dose - aim for middle of reference range for fT4 oral admin

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15
Q

causes of secondary hypothyroidism *

A

pituitary tumour

post-pit surgery

or radiotherapy

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16
Q

when would you replace T3 instead of T4 *

A

in myxoedema coma - severe hypothyroidism T3 given because it works quickly and is more potent given IV then switch to oral T4 when better

17
Q

is combined hormone replacement better *

A

no randomised control trial saying that T3 is better and it is more expensive NHS England wont support prescription for T3 anymore no reason because T4 is converted to T3 T3 is v potent - difficult to get dose right - end up having low TSH below reference range - have sympyoms of hyperthyroidism T3 use is complicated by symptoms of toxicity - palpitations, tremor, anxiety and irritability some patients have reported better psychological outcomes and psychometric tests on T3/4 combinations, better QOL on T3 replacements

18
Q

describe the pharmacokinetics of thyroid hormone replacement therapy *

A

active orally half life long T4 = 6 days, T3 = 2.5 days - so lack of compliance isn’t the end of the world 99.97% T4 and 99.7% T3 are bound to plasma proteins = mainly thyroxine binding globin (TBG), transthyretin and albumin - only free hormone is active this is what is measured, plasma binding proteins increase in pregnancyand on long term treatment with oestrogens and phenothiazines, fall with malnutrition (not getting proteins) and liver disease. some co-administered drugs eg salicylates compete for protein binding sites

19
Q

what are the adverse effects of thyroid hormone over-replacement *

A

usually associated with low TSH because of -ve feedback major targets of thyroid hormones are the skeleton, heart and metabolism skeletal - increased bone turnover because the osteoclastic resorption of bone is stimulated out of proportion to the osteoblastic remineralisation, also there is a reduction in bone mineral density and risk of development for osteoporosis cardiac- tachycardia, risk of dysrhythmia, particularly afib metabolism - increased energy expenditure, weight loss

increased B -adrenergic sensitivity caused by thyroxine - tremor, nervousness

20
Q

describe the production of thyroid hormones

A

TSHR on basolateral membrane stimulated by TSH

stimulates up take of iodide through the sodium iodide symporter

at the apical membrane the iodide enters the colloid

TSHRstimulate production of thyroglobulin protein

iodine is added to the AA with tyrosyl residues - iodination catalysed by TPO (thyroid peroxidase)

this forms monoiodotyrosine and diiodotyrosine

21
Q

What term is used to describe an individual who has irreversible brain damage caused by lack of thyroxine in foetal and neonatal life? *

A

cretin

22
Q

Why is treatment of hypothyroidism essential?

A

patients will die otherwise

they will perform poorly

cholesterol goes up - causing death from heart attacks and strokes

23
Q

features of cretinism *

A

slow mentation

slow growth

small height

24
Q

how do you prevent cretinism *

A

screening

heel prick test

measure TSH

at the same time as Guthrie test for phenylketonuria

given thyroxine immediately if TSH high

25
Q

what investigations would you do to diagnose hypothyroidism *

A

blood test - TSH, fT3/4 and thyroid peroxidase Ab (inhibit TPO)

TSH high

T3/4 low

26
Q

what is secondary hypothyroidism *

A

when the problem is wiyth the piuitary

the solution is to remove the pit gland

27
Q

why are females more susceptible to thyroid disease

A

the immune system attacks the thyroid - autoimmune

more mistakes like this occur in females because of response in pregnancy