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125 Cards in this Set

  • Front
  • Back
Case control study measures...? ("What happened?")
Odds Ratio (OR)
Cohort Study measures...? ("What will happen?")
Relative Risk (RR)
Cross sectional study measures...? (Observational)
Disease prevalance
Prevalence =
= total cases in a pop at a given time/ total pop at risk

= incidence x dz duration
Incidence =
new cases in a pop over a given time/ tot pop at risk during that time
Sensitivity =
= a/ (a+c)

= SNOUT (low false neg rate; rules out dz)
Specificity =
= d/ (d+b)

= SPIN (low false positive; rules in dz)
PPV =
= a/(a+b)

= prob of having dz given pos result
NPV =
= c/ (c+d)

= prob of being dz free given a neg test
Odds ratio =
= ad/bc

=odds of having dz in exposed group / odds of dz in unexposed group
Sensitivity =
= a/ (a+c)

= SNOUT (low false neg rate; rules out dz)
Specificity =
= d/ (d+b)

= SPIN (low false positive; rules in dz)
PPV =
= a/(a+b)

= prob of having dz given pos result
NPV =
= c/ (c+d)

= prob of being dz free given a neg test
Odds ratio =
= ad/bc

=odds of having dz in exposed group / odds of dz in unexposed group
Relative risk =
= [a/(a+b)] / [c/(c+d)]

= percent with dz in exposed group divided by percent with dz in unexposed group
Random error causes...
reduced precision in a test
Systematic error causes...
reduced accuracy
The statistical distribution of a positive skew is...
Mean > Median > Mode

Asymmetry with tail on right
The statistical distribution of a negative skew is...
Mean < Median < Mode

Asymmetry with tail on left
Null Hypothesis =
hypothesis of NO DIFFERENCE
Type I error =
stating that there is a difference or effect when in fact, there is NO difference
Type II error =
Stating that there is no difference or effect when there really IS A Difference or effect
p < 0.5 means that...
there is a < 5% chance that the data will show something that is not really there
Power =
= (1- beta) = (1 - type II error)
To increase power, you can?
Increase sample size
t-test checks the difference between?
the means of 2 groups
ANOVA checks the difference between?
the means of 3 or more groups
Chi squared checks the difference between?
2 or more % or proportions of categorical outcomes (NOT mean values)
Primary Dz Prevention means...
prevent dz occurrence (ex. vaccination)
Secondary prevention means...
early dz detection (ex. pap smear)
Tertiary prevention means...
preenting dz progression (insulin for diabetics)
Reportable Diseases are:
Hep A, B, C; HIV; Salmonella; Shigella; Syphilis; Measles; Mumps; AIDS; Rubella; TB; Chickenpox; Gonorrhea
Top 3 causes of death in ages 1-14 year olds:
1. Accidents 2. Cancer 3. Cong anomalies
Top 3 causes of death in 15-24 year olds:
1. Accidents 2. Homicide 3. Suicide
Top 3 causes of death in 25-64 year olds:
1. Cancer 2. Heart Dz 3. Accidents
Top 3 causes of death in 65+:
1. Heart dz 2. Cancer 3. Stroke
APGAR Scoring
Appearance (Blue, peripheral cyanosis, all pink)

Pulse (none, <100, >100)

Grimace (None, grimace, grimace + cough)

Activity (Limp, Some, active)

Respiration (None, Irregular, Regular)
Low Birth weight =
<2500 g
Sleep Stage and EEG Waveform:

Stage I:
Beta (high freq, low amp)
Sleep Stage and EEG Waveform:

Stage II:
Alpha
Sleep Stage and EEG Waveform:

Stage 3-4:
Deepest sleep: Delta (low freq, high amp)
Stage of sleep when sleepwalking, night terrors, and bedwettting occurs:
Stage 3-4
Sleep Stage and EEG Waveform:

REM:
Beta (high freq, low amp)
Effect of benzos on stages of sleep:
Shorten stage 4 sleep (and useful for night terrors, sleepwalking)
Drug of choice to treat bedwetting:
Imipramine (shortens stage 4)
Principal neurotransmitter involved in REM sleep:
ACh
Neonate becomes mentally retarded, hyperactive, and has musty odor. Dx?
PKU
Rapid consumption of alcohol before dinner causes hypoglycemia how?
incr. NADH prevents gluconeogenesis by shunting pyruvate and oxaloacetate to lactate and malate
Alcoholic develops rash, diarrhea, and altered MS. Vitamin deficiency?
Vit B3 (pellagra)
urine turns black upon standing. Dx?
Alkaptonuria
25 year old has chest pain, xanthomas on acchilles. Dx and site of defect?
Familial Hypercholesterolemia. --> LDL receptor
Dark urine and muscle cramps after exercise. Dx?
McArdles Dz
Child has weakness and big calves. Dx and inheritance?
Duchenne's MD, X-linked recessive
Sxs of Deficiency--

Vitamin A:
Night blindness, Dry skin
Sxs of Deficiency--

Vitamin B1 (Thiamine)
Beriberi and Wernicke-Korsakoff syndrome (alcoholism and malnutrition)
Dry BeriBeri =
polyneuritis, symmetric muscle wasting
Wet BeriBeri =
high output cardiac failure (dilated cardiomyopathy), edema
Sxs of Deficiency--

Vit B2 (Riboflavin)
Cheilosis (imflamm of lips) and Corneal vascularization (2 C's)
Sxs of Deficiency--

Vit B3 (Niacin)
Pellagra (3 D's): Diarrhea, Dermatitis, Dementia and beefy glossitis
tryptophan + B6 =
Niacin (Vit B3)
Sxs of Deficiency--

Vit B5 (pantothenate)
dermatitis, enteritis, alopecia, adrenal insufficiency
Sxs of Deficiency--

Vit B6 (pyroxidine)
Convulsions, hyperirritability, peripheral neuropathy
Vit B6 deficiency can be induced by?
INH or
Oral Contraceptives
Sxs of deficiency of:

Vit B12 (cobalamin)
Macrocytic, megaloblastic anemia, neuro sxs (differentiate if from folate def), glossitis
Reasons for Vit 12 deficiency:
1. Malabsorption
2. Lack of Intrinsic factor (pernicious anemia)
3. Ansence of terminal ileum (Crohn's)
which is stored longer:
B12 or folate?
B12!
Where can you get B12? Folate?
B12: Only in animal products;
Folate: green leafy veggies
Sxs of Deficiency--

Biotin
Dermatitis, enteritis
Causes for Biotin deficiency:
1. Abx
2. Excessive ingestion of raw eggs
Sxs of deficiency:

Vit C (ascorbic Acid)
Scurvy (swollen gums, bruising, anemia, poor wound healing)
Sxs of deficiency:

Vit D
Rickets (kids)--bending bones;
Osteomalacia (adults)--soft bones, hypocalcemic tetany
Vit D2 comes from?
Milk (ergocalciferol)
Vit D3 comes from?
sun-exposed skin (cholecalciferol)
Fcn of Vit D:
Increases intestinal absorption of calcium and phosphate
Storage form of Vit D:
25-OH D3
Active Form of Vit D:
1,25 (OH)2 D3
Sxs of excess Vit D:
Hypercalcemia, loss of appetite, stupor
One cause of excess vit D:
Sarcoidosis (epithelioid macrophages convert Vit D to active form)
Sxs of deficiency:

Vit E:
increases frag of erythrocytes, neuerodysfunction
Fcn of Vit E:
Antioxidant (protects erythrocytes from hemolysis)
Sxs of Deficiency:

Vit K
neonatal hemorrhage with Incr. PT and PTT, nml bldg time (neonates are given Vit K injection)
Vit K dependant clotting factors:
II, VII, IX, X, protein C and S
Mechanism of action of Warfarin:
Vit K antagonist
Sxs of deficiency:

Zinc
delayed wound healing, hypogonadism, Decreased adult hair
Mechanism of action:

Antabuse (Disulfiram)
Inhibits acetaldehyde dehydrogenase (acetaldehyde accumulation gives hangover sxs)
Purines =
A, G (PURe As Gold: PURINES)
Pyrimidines =
C, T, U (CUT the PY: PYrimidines)
Which bond is stronger? G-C or A-T?
G-C (3 H bonds)
DNA Mutations Definitions--

silent:
Same aa
DNA Mutations Definitions--

Missense:
Changed aa, but new aa is similar in chemical structure to original
DNA Mutations Definitions--

Nonsense:
Change results in Early STOP codon ("stop the nonsense!)
DNA Mutations Definitions--

Frame Shift:
change results in misreading of all nucleotides downstream (truncated protein)
Put these mutations in order of severity:
silent, missense, nonsense
Nonsense > Missense > Silent
Site of action of fluouroquinolones:
DNA gyrase

(gyrase is specific prokaryoptic topoisomerase)
Role of DNA polymerase III:
elongates DNA chain by addine deoxynucleotides to the 3' end (leading strand)
Progression of enzymes in DNA replication:
1. Helicase--> unwinds DNA template at replication fork

2. DNA Topoisomerase--> creates a nick in helix to relieve supercoils

3. Primase--> Makes an RNA primer on which DNA poly III can initiate replication

4. DNA PolIII--> elongates chain

5. Exonuclease--> proofreads each added nucleotide

6. DNA PolI--> degrades RNA primer and fills in gap with DNA

7. Ligase--> Seals
Direction of DNA replication:
5' --> 3'
Mutation in Hereditary nonpolyposis colorectal cancer:
Mismatch repair (unmethylated string is recognized, nuc removed and gap refilled)
Mutation in xeroderma pigmentosum:
Nucleotide excision repair (oligonucleotide with damaged bases is removed)
Start codon:
AUG (AUG inAUGurates protein synthesis)
Stop codons:
UGA (U Go Away)
UAA (U Are Away)
UAG (U Are Gone)
Function of rough ER (RER):
synthesis of secretory (exported) proteins and of N-linked oligosaccharide addition to proteins
Function of Nissl bodies:
(In neurons) -->synthesize enzymes and peptide neurotransmitters
Function of free ribosomes:
unattached to membrane--> synthesis of cytosolic and organellar proteins
Function of Smooth ER (SER):
site of steroid synthesis and detoxification of drugs and poisons
What modification in the golgi targets proteins to the lysosome?
Mannose-6-phosphate
Failure of the addition of mannose-6-phosphate to proteins causes?
I-cell disease (enzymes are secreted outside of the cell rather than targeted to the lysosome)
5 Drugs that act on microtubules:
1. Mebendazole (antihelminthic)
2.Paclitaxel (anti-breast cancer)
3. Griseofulvin (antifungal)
4. Vincristine/vinbalstine (anti-cancer)
5. Colchicine (anti-gout)
What is Kartagener's syndrome?
Immotile cilia due to defect in dynein (ATPase causes bending of cilia).

Results in male/female fertility, bronchiectasis, recurrent sinusitis.

associated with situs inversus
The cytoskeletal element found in: Microvilli
Actin and myosin
The cytoskeletal element found in: Cilia
Microtubule
The cytoskeletal element found in: Flagella
microtubule
Type of collagen found in: Bone
Type I
Type of collagen found in: Cartilage
Type II
Type of collagen found in: skin, blood vessels, uterus, granulation tissue
Type III (reticulin)
Type of collagen found in: Basement membrane
Type IV
Type of collagen found in: Skin
Type I
Type of collagen found in: Tendon
Type I
Type of collagen found in: Nucleus pulposus
Type II
Site in collagen synthesis which requires Vitamin C, and the dz that results when there is a deficiency:
Step II (Hydroxylation of residues in alpha chain or preprocollagen)--> Scurvy
Step of collagen synthesis disrupted in osteogenesis imperfecta:
Step III, Glycosylation (formatgion of procollagen-->triple helix of alpha chains)
Clinical Manifestations of ehlers-danlos and most commonly type of collagen affected:
Type III

1. hyperextensible skin
2. easy bruising/bleeding
3. Hypermobile joints
(assoc with berry aneurysms)
Disease of blue sclera and multiple fractures with little trauma:
OI (osteogenesis imperfecta)
Type of collagen typically affected in OI:
Type I