Clinical Chemistry Flashcards

1
Q

Where is the thyroid gland and what is its function?

A

butterfly shape organ located in the neck, responsible for the secretion of thyroid hormones

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2
Q

Where is the parathyroid and what is it’s function?

A

4 yellowish organ located within the thyroid gland, primary responsibility in maintaining calcium levels

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3
Q

What is thyroglobulin?

A

main storage site of thyroid hormones and is the precursor to thyroid hormones

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4
Q

What is regulated by the thyroid hormones and secreted from the pituitary gland?

A

Thyrotropin (TSH)

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5
Q

What are the two major thyroid hormones?

A

T3 (thriiodothyronine) and T4 (thyroxine)

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6
Q

What is the function of T3?

A

regulates metabolism, growth and development

  • 20% of T3 is derived from the thyroid gland
  • most comes from de-iodinzation of T4 from liver, kidney and muscle
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7
Q

What is the function of T4?

A

major hormone secreted from the thyroid gland

-most is bound by TBG FT4, only the unbound fraction is biologically active

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8
Q

What are the additional biologically inactive forms of T4?

A

rT3, MIT and DIT

-MIT and DIT are precursors to T3 and T4

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9
Q

What is the function of calcitonin?

A
  • not much is known about physiological role in humans
  • release is stimulated by increasing circulating calcium levels in the blood
  • serves as an antagonist to PTH-inhibits osteoclastic bone activity
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10
Q

How is thyroid hormone synthesized in the thyroid gland? (5 steps)

A
  1. Iodine is ingested in food and water, concentrated in thyroid gland
  2. Incorporated into the amino acid tyrosine (Thyroglobulin)
  3. Concentrated iodine is oxidized and bound to tyrosyl residues on thyroglobulin-catalyzed by thyroid peroxidase (TPO)
  4. MIT and DIT are formed as a result
  5. TSH stimulates lysosomes to cleave T3 and T4 and release into blood stream
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11
Q

TSH is released in a ____nature and is _____?

A

pulsating and diurnal

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12
Q

Who am I?

more loosely bound to carrier protein, more metabolically active, 99.7% bound to TBG and 0.3% free form

A

T3

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13
Q

Who am I?
70 times more in circulating in peripheral blood, strongly bound to carrier protein: 70-75% to TBG, 15-20% to TBPA and 10% albumin

A

T4

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14
Q

Common Lab tests

A

TSH, FT4 and FT3

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15
Q

Which factors serve as markers for thyroid tumors?

A

Thyroglobulin or Calcitonin

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16
Q

Can a goiter be present in both hyper and hypothyroidism?

A

yes

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17
Q

Causes for hypothyroidism

A

autoimmune, iodine deficiency and radioactive iodine treatment

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18
Q

primary dysfunction

A

thyroid is the site of defect

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19
Q

secondary dysfunction

A

pituitary is the site of defect

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20
Q

tertiary dysfunction

A

hypothalamus is site of defect

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21
Q

What is another word used for hyperthyroidism?

A

thyrotoxicosis

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22
Q

What disease am I?
autoimmune disorder, 80% of all hyperthyroidism
TSH decreased
FT4 increaseed

A

Graves disease

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23
Q

What am I?
FT4 decreased
TSH increased

A

hypothyrodism

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24
Q

Causes of hypothyroidism

A

radioactive treatments or ablation, low iodine intake, certain foods or meds

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25
Q

What is the treatment for hypothyroidism?

A

levothyroxine (synthetic thyroid hormone)

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26
Q

Hashimoto’s Thyroiditis

A
  • autoimmune condition commonly associated with permanent hypothyroidism
  • is a primary hypothyroidism resulting in insufficient T4 available to tissues
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27
Q

Graves disease

A
  • autoimmune disorder characterized by diffuse, toxic hyperplasia
  • caused by IgG antibody vs Thyroid TSH receptor=overproduction of thyroid hormones
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28
Q

Euthyroid Sick Syndrome

A

TSH or thyroid hormones may be abnormal but the thyroid gland is functioning normally, often stimulated hypothyroidism
-FT4 remains normal

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29
Q

definition of ischemia

A

local, temporary lack of blood supply due to obstruction

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30
Q

What is the most common cause of atherosclerosis?

A

acute coronary syndrome

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31
Q

What are the lab markers for an MI?

A

LDH (flip), troponin, CK, CKMB ratio, myoglobin, AST, homocysteine, hsCRP and CHF=BNP

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32
Q

CK

A

used as a general screen but not very specific, increase in 6 hours, back to normal in 3 days

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33
Q

CKMB

A

rise 4-6 hours
peak 12-24 hours
normal 2-3 days post onset

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34
Q

CKMB/CK index

A

<3 muscle and >6 MI

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35
Q

LD1/LD2 flip

A

LD1>LD2 peak at 48 hours, back to normal within ten days

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36
Q

Troponin (Gold Standard)

A
binds calcium and regulates muscle contraction
rise: 4-6 hours
peak: 12-18 hours
normal: 4-10 days
normal level: 0.1 ng/mL
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37
Q

Myoglobin

A

O2 binding heme protein found in cardiac and skeletal muscle

rise: 1-3 hours
peak: 6-9 hours
normal: 18-24 hours

38
Q

CRP

A

acute phase protein produced by liver in response to infection, injury and inflammation, non specific marker for inflammation

39
Q

hsCRP

A
  • more cardiac specific, small changes can be seen earlier

- higher hsCRP associated with higher risk of future cardiac related morbidity and mortality

40
Q

homocysteine

A

-amino acid found in the blood

41
Q

hyperhomcyteniemia is related to increased risk of

A

CHD, stroke and peripheral vascular disease

42
Q

What are natriuretic peptides?

A

hormones that play an important role in cardiac homeostasis

43
Q

What are the natriuretic peptides that are markers for CHF?

A

ANP, BNP, CNP and DNP

44
Q

Name the five enzymes that are used to assess liver function plus a sixth extra parameter

A

ALT, AST, ALKP, GGT and LDH

5 prime nucleotidase

45
Q

Where is ALT found and how long does it stay elevated?

A
  • found in hepatocytes (specific to liver)

- stays elevated longer than AST

46
Q

Where is AST found and what do values greater than 400 mean?

A
  • found in many sources (not as specific)

- values over 400 suggest acute viral hepatitis

47
Q

ALT>AST

A

hepatitis, most liver disease

48
Q

AST>ALT

49
Q

Where is ALKP found and what do elevated levels mean?

A
  • found in many sources throughout the body
  • highest amounts found in obstruction (can help differentiate from hepatocellular injury)
  • mild elevation in cirrhosis or hepatitis
50
Q

What is GGT and where is it found?

A
  • membrane enzyme that helps amino acid cross cell membrane
  • found in liver cells and bile duct walls
  • sensitive marker for obstructive cholestasis and ETOH intoxication
51
Q

What if ALKP is high and GGT is normal

A

probably not liver

52
Q

Where is LDH found and when are levels elevated?

A
  • widely distributed in body (high amount in RBC)
  • not found in bone
  • moderate elevation: hepatobiliary disease
  • slight elevation: biliary tract disease
  • high elevation: hepatic carcinoma
53
Q

5’ Nucleiotidase

A
  • widely distributed in cells

- no bone source

54
Q

both______&______with be increased in liver disease but only _____will be elevated in bone disease

A

5’ nucleosidase and ALKP

ALKP

55
Q

5 additional tests for liver function

A

ammonia, albumin, immunoglobulins, protime and AFP

56
Q

Ammonia is normally converted to____ by the _____

A

urea by the liver

-reflects the liver’s ability to convert ammonia to urea

57
Q

When will ammonia levels be increased?

A

liver failure, hepatic carcinoma or in Reye Syndrome

58
Q

Methods to test ammonia

A

Caraway, Nessler’s and enzymatic reaction

59
Q

Normal reference range for ammonia

A

20-50umol/L

>100 is critical

60
Q

Where is albumin synthesized?

61
Q

IgG and IgM may both be elevated in…

A

chronic active hepatitis

62
Q

IgM may be elevated in…

A

primary biliary cirrhosis

63
Q

IgA may be elevated in…

A

alcoholic cirrhosis

64
Q

If patient has liver damage the protime will be…

A

prolonged because clotting factors are synthesized in the liver

65
Q

What is a common tumor maker of the liver?

66
Q

Bu-unconjugated bilirubin (indirect)

A

bound to albumin, insoluble in water, NOT filtered and excreted by kidney

67
Q

Bc-conjugated bilirubin (direct)

A

water soluble and can be filtered and excreted

68
Q

Total bilirubin=

69
Q

What is delta bilirubin?

A

conjugated bilirubin that is bound to albumin. Can occur when liver is conjugating effectively but it cannot be excreted from the liver. Only seen in significant obstruction

70
Q

What is urobilinogen?

A

derived from bilirubin in GI tract, oxidized by intestinal bacteria to form urobilin, adds color to stool

71
Q

Is urobilinogen present in obstruction?

A

no it is absent

72
Q

When is urobilinogen increased?

A

hemolytic disease, defective liver cell function and hapatitis

73
Q

What causes neonatal jaundice?

A

-an enzyme deficiency of glucoronyl transferase (one of the last enzymes to be activated in prenatal life)

74
Q

What is kernicterus?

A

bilirubin deposited in nuclei of brain and nerve cells, is life threatening, may require exchange transfusion

75
Q

What is ascites fluid?

A

presence of free fluid in the peritoneal cavity

commonly seen in: cirrhosis due to alcoholism, hepatitis and hepatic vein obstruction

76
Q

Pre hepatic jaundice bilirubin values

A

Total: increased
Unconjugated: increased
Conjugated: normal

77
Q

Pre hepatic jaundice what will be seen in the toilet?

A
  • Bilirubin will NOT be seen in UA
  • Urobilinogen is seen in urine as a result of increased bilirubin being conjugated
  • Stool will be dark brown
78
Q

Hepatic Jaundice bilirubin values

A

Total: increased
Unconjugated: variable
Conjugated: variable

79
Q

Hepatic Jaundice can be one of two problems

A

biliary metabolism or transport
In biliary increase in unconjugated bilirubin
In transport increase in conjugated bilirubin

80
Q

Disorders of unconjugated hyperbilirubinemia

A

Gilberts Disease, Criggler-Najjar, and Neonatal Jaundice

81
Q

Disorders of conjugated hyperbilirubinemia

A

Dubin-Johnson syndrome and Rotor Syndrome

82
Q

What is Gilbert’s Disease?

A

inherited disease, problem with encoding of enzyme that catalyzes bilirubin conjugation

83
Q

What is Criggler Najjar?

A

inherited disease, similar to Gilbert’s but more severe

84
Q

What is Dubin-Johnson disease?

A

rare inherited disorder causing a deficiency in a transport protein, problem is in transporting bilirubin out of the cells to be excreted in bile

85
Q

What is Rotor Syndrome?

A

clinically similar to Dubin-Johnson, defect is not known, dark granules no seen on biopsy

86
Q

Post hepatic jaundice bilirubin values

A

all elevated

87
Q

What will you see in the toilet for post hepatic jaundice?

A

no urobilinogen in the urine, stool with no color

88
Q

What are the methods for measuring bilirubin?

A

Ehrlich’s method, Van Den Bergh, Malloy and Evelyn and Jendrassik and Grof

89
Q

Which bilirubin detection test measures total bilirubin and the Bu

A

Jendrassik and Grof

90
Q

What is cholestasis?

A

stoppage of bile flow, commonly due to bile duct obstruction

91
Q

Endocrine function of the pancreas

A

release hormones: alpha cells (glucagon) and beta cells (insulin), somatostatin and pancreatic polypeptide

92
Q

Exocrine function of the pancreas

A

release AMY and Lipase