Adrenal Insufficiency and Cushings Flashcards

1
Q

Adrenal Gland lie in the_______ above or medial to the upper pole of the kidneys. The adrenal cortex differentiates into three adult zones: glomerulosa (______) and fasciculata/reticularis (_____and_____)

A

retroperitoneum

aldosterone

cortisol and androgens

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2
Q

The adrenal_____ is richly vascularized receiving its main arterial supply from branches of the inferior phrenic artery, the renal arteries and the aorta.

A

cortex

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3
Q

What is the difference beteween the drainage of right and left adrenal glands?

A

The right adrenal vein drains directly into the posterior aspect of the vena cava and the left adrenal vein enters the left renal vein.

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4
Q

What could cause bilateral adrenal hemorrhage?

A

a coagulopathy resulting in bilateral adrenal vein thrombosis.

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5
Q

Steroid production from the zona fasciculata and reticularis is controlled by the pituitary hormone_____ whose secretion is regulated by the hypothalamus and central nervous system via neurotransmitters and ________ and by negative feedback.

A

ACTH

corticotroph-releasing hormone [CRH and arginine vasopressin (AVP)]

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6
Q

CRH stimulates ACTH in a

A

pulsatile manner. Diurnal rhythm causes a peak before awakening and a decline as the day progresses.

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7
Q

Pathologic conditions such as Cushing’s disease (an ACTH-secreting pituitary tumor) are manifested by deregulated______ secretion since the set point for negative feedback on______ is increased

A

cortisol

ACTH

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8
Q

Adrenocorticotropin or ACTH is a 39 amino acid peptide hormonewhich is processed from a large precursor molecule, _________within the ACTH-secreting cells in the pituitary gland corticotroph.

A

pro-opiomelanocortin (POMC)

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9
Q

The cortisol synthetic pathway requires ACTH-stimulated cholesterol import into the mitochondrion, a process initiated by the action of the __________which shuttles cholesterol from the outer to the inner mitochondrial membrane.

A

steroidogenic acute regulatory (StAR) protein,

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10
Q

The majority of steroidogenic enzymes are cytochrome P450 (CYP) enzymes, which are either located in the________ (side chain cleavage enzyme, CYP11A1; 11-hydroxylase, CYP11B1; aldosterone synthase, CYP11B2) or in the_________ (17- hydroxylase, CYP17A1; 21-hydroxylase, CYP21A2)

A

mitochondrion

endoplasmic reticulum membrane

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11
Q

The cholesterol side chain cleavage enzyme CYP11A1 (P450scc) generates

A

pregnenolone

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12
Q

Glucocorticoid synthesis requires conversion of pregnenolone to progesterone by what enzyme

A

3-beta-hydroxysteroid dehydrogenase (3-βHSD2)

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13
Q

Cortisol binds to plasma proteins on entering the circulation. At physiological concentrations, cortisol circulates in the plasma bound mainly to _______, and to a much lesser extent to albumin.

A

corticosteroid-binding globulin (CBG

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14
Q

The measurement of this free cortisol can be done in

A

saliva and is independent of salivary flow rates.

used clinical application for the assessment of the hypothalamic-pituitary-adrenal axis particularly in states of suspected hypercortisolism.

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15
Q

Cortisol is metabolized to biologically inert steroid cortisone by the enzyme_______ in the kidney to protect the mineralcorticoid receptor as cortisol has same affinity for that receptor as aldosterone

A

11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2).

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16
Q

prodigious increases in cortisol secretion may overwhelm the intrarenal metabolism of cortisol in the kidney causing significant mineralocorticoid effects such as

A

hypertension and hypokalemia

seen in pts with Cushings

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17
Q

how does the liver handle cortisone?

A

uses 11B-HSD1 takes it to cortisol

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18
Q

What are the two mechanisms of action of cortisol?

A

GR Transrepression (depresses genes that work in inflammation)

GR Transactivation

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19
Q

Utilization of a glucocorticoid receptor antagonist,________, has emerged as an effective therapy for the treatment of endogenous hypercortisolism

A

mifepristone

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20
Q

The progesterone compound,____________ may be used to actually stimulate appetite in cancer patients and has been shown to cause suppression of ACTH and cortisol

A

megestrol acetate,

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21
Q

What are the main targets and actions of clucocorticoids and consequences of hypercortisolism and hypocortisolism

A

Intermediary metabolism, calcium homeostais, other endocrine systmes, immune system, skin and CT, CV system, Na+, K+ and ECF volume and pysch

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22
Q

Inadequate production of cortisol from the adrenal cortex may be caused by either a disease process in the adrenal gland :_________or due to diseases of the pituitary gland :__________ or hypothalamus __________

A

(primary adrenal insufficiency)

(secondary adrenal insufficiency)

(tertiary adrenal insufficiency)

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23
Q

Secondary and tertiary cortisol deficiency are clinically and biochemically similar:____ cortisol and _________ACTH levels

(remember in states of hypocortisolism, ACTH levels should increase).

A

low

low or inappropriately normal

24
Q

Primary adrenal insufficiency differs clinically since_______ is also absent (hypotension is more common and hyperkalemia may be present).

A

aldosterone

25
Plasma\_\_\_\_\_ levels are always elevated in untreated primary adrenal insufficiency.
ACTH
26
Signs and symptoms of Adrenal Insufficiency
Signs and Symptoms Fatigue, malaise, lack of energy GI: nausea, vomiting, anorexiaÆwt loss HypotensionÆdizziness, orthostasis Increased skin pigmentation, salt craving (primary)
27
Key lab abnormalities in adrenal insufficiency
Hyponatremia Hyperkalemia (primary) Hypercalcemia, hypoglycemia (rare in adults) Lymphocytosis
28
What do we call it when ther is something intrinsically wrong with the adnreal gland and have elevated ACTH and CRH to activate but no Aldosterone
Primary adnreal insufficiency
29
What are some causes of seconeary adrenal insufficiency?
pituitary tumor/infection/hemmorhage decrease ACTH thus decrease in cortisol and aldosterone will be normal ACTH has permissive and not big effect on aldosterone production in this case
30
Imaging abnormality seen with adrenal insufficiency
Bilateral adrenal enlargement Pituitary mass
31
These drugs cause adnreal insufficiency Adrenostatic/lytic: Glucocorticoid receptor antagonist:
ketoconazole, etomidate, mitotane mifepristone
32
What concurrent Medical Problems do we see with adnreal insufficiency
Severe critical illness w/ hypotension, Pituitary disease, Traumatic brain injury, Brain radiation
33
Genetic causes of Adrenal insufficiency
Congenital Adrenal Hyperplasia Adrenoleukodystrophy (X-linked disorder w/accumulation of very long chain fatty acids in adrenal glands and the brain)
34
Patient comes in with recent unintientional weight loss, posterula hypotension and HYPOnatremia, what screening do you order?
Get plasma cortisol level, suspicious for adrenal insufficiency
35
What test can you order if you suspect adrenal insufficiency?
plasma cortisol or Cosyntropin stimulation test; evals maximum adrenocortical secreatory capacity and tests for adrenal destruction or adrenal atrophy
36
You can confirmed your patient has low cortisol levels, what is the next step?
Get pts ACTH, plasma renin and serum aldosterone levels to find out if it's primary (elevated ACTH) or 2/3
37
Your pt has low cortisol levles and high ACTH levels = Primary adrenal insufficiency, what is the next step?
Provide pt with Glucocorticoid AND mineralcorticoid replacement and get Adrenal Autoantibody test
38
Pt tests positive for adrenal autoantibodies in what type of adrenal disease?
primary adrenal insufficiency d/t autoimmune adrenaliatis--\> you can still have this even if autoantibodies come back negative
39
Your pt has primary adrenal insufficiency, you order autoimmune antibodies and test comes bck negative, what's the next step?
Get a chest xray (+ means infiltration, infection, hemorrhage, hyperplasia) If - can gets for long chain fatty acids for VLCFA which may be high in men with adrenoleukodystrophy
40
What do we see for serum levels of cortisol, ACTH and remin in secondary adrenal insufficiency?
see low cortisol low or no elevated ACTH
41
What tx do you offer for patients with secondary adrenal insufficiency?
Glucocorticoids ONLY
42
You have a pt with secondary adrenal insufficiency, what test do you need to order?
MRI of the pituitiary look for hypothalamic pituitary mass
43
Pt has secondary adrenal insufficiency but pituitary MRI is negative, what else could cuase this problem?
history of exogenous glucocorticoid tx head trauma isolated ACTH deficiency
44
Critically or chronically ill patients may have low binding proteins (i.e., CBG), and the total cortisol concentration may be low and the “free” or biologically active cortisol may actually be normal thus how do we assess free cortisol levels?
Assessment of “free” cortisol can be done in saliva, plasma, or by formula calculation if the concentration of CBG is known.
45
patients receiving medications (such as estrogen—e.g., oral contraceptives) will have a significant increase in\_\_\_\_\_levels that reflect an increase in CBG rather than any alteration of adrenal function.
total cortisol
46
Measurement of __________ is sensitive marker of adrenal reserve: a normal level is very unusual in patients with any type of adrenal insufficiency
adrenal androgen production (i.e., DHEAS)
47
Plasma ACTH is always _____ in pts with primary adrenal insufficiency and may be ______ in pts with secondary adrenal insufficiency
Increased! (loss of neg feedback) low or normal (innappropriately NOT increased)
48
If the peak cortisol response to ACTH is _____ or the basal morning cortisol is _____ a plasma ACTH measurement should be performed to distinguish primary from secondary adrenal insufficiency.
\< 18 µg/dL \<5 µg/dL,
49
Causes of primary adrenal insufficiency
Autoimmune: Autoimmune polyglandular syndromes Malignancy :Metastatic (lung, breast, melanoma, GI) or primary adrenal lymphoma Adrenal Hemorrhage: (bilateral) Associated with coagulopathies (anticoagulation therapy, antiphospholipid syndrome, heparin-induced thrombocytopenia) and usually due to bilateral adrenal vein thrombosis Infectious :Tuberculosis, fungi (histoplasmosis, coccidiomycosis), HIV Genetic: Congenital Adrenal Hyperplasia Familial glucocorticoid deficiency Adrenoleukodystrophy Infiltrative Disorders: Amyloidosis, hemochromatosis Drugs: Ketoconazole, metyrapone, mitotane, etomidate
50
Causes of SEcondary Adrenal insufficiency
** (Withdrawal from) exogenous corticosteroid therapy**: dose/duration dependent, but variable from patient to patient Pituitary/Hypothalamic Disease Especially hypophysitis [autoimmune, granulomatosis, drug-induced (**ipilimumab**)] may cause isolated ACTH deficiency
51
What two drugs can we give for pts with adrenal insufficiency and how are they different?
**Hydrocortisone**: give 10-15mg in AM and 5-10 in the afternoon and monitor plasma ACTH, wellbeing while **Fludrocortisone** is 50-100mcg daily \*monitory electrolyte compostion and plasma renin
52
What is important for pts on hydrocorisone for adnreal insufficiency when they are sick?
Sick day management: 3 x 3 Æ triple the dose for three days or until illness resolves
53
What tx do we give for secondary adrenal insufficiency?
Hydrocortisone 7.5-15 mg daily in divided doses. Lower doses needed than in primary adrenal insufficiency (there is usually still some cortisol secretion from the adrenals) Mineralocorticoid replacement NOT needed
54
What do pts with primary and secondary adrenal insufficiency on medication need to do for surgery?
Correct electrolytes, blood pressure, hydration if necessary Give hydrocortisone 100 mg IM or IV on call to OR Hydrocortisone 50 mg every 6-8 hours for 24 hours and then taper judiciously to maintenance
55
evaluates maximum adrenocortical secreatory capacity and tests for adrenal destruction (primary adrenal insufficiency) or adrenal atrophy (secondary adrenal insufficiency)
Cosyntropin
56
\_\_\_\_ and ____ are elevated in primary AI bc of loss of cortisol and angio II negative feedback
Plasma ACTHand PRA