Non-Protein Nitrogen Flashcards
Non-protein nitrogen sources
- urea
- amino acids
- uric acid
- creatinine
- ammonia
Blood Urea Nitrogen (BUN)
- ammonia from the breakdown of protein
- urea formed in liver from ammonia (high NH4 levels cause brain damage)
- urea is main NPN compound
- filtered by renal tubules and partially reabsorped
- excreted by kidneys in urine
BUN concentration
- depends on renal function, perfusion of kidney, protein content of diet and rate of protein catabolism
- increases with kidney damage because it can’t leave kidney
- decreases in people who don’t eat protein
Azotemia
- increased BUN related to BUN abnormalities
- Pre-renal, Renal or Post-renal conditions
Pre-renal conditions
- increased protein degradation (increase AA’s) due to diet, stress, fever, cortisol
- decreased blood flow thru kidney due to CHF, shock, hemmorrhage, dehydration, etc.
Renal conditions
- kidney diseases, inflammation
- ineffective filtering by kidney
Post-renal conditions
- blockages, obstructions
- calculi or severe kidney infection
- bladder or prostate tumor that blocks tubules
BUN decreases
- not very often/significant
- low protein intake
- severe liver disease
- late in pregnancy, infancy (making more protein)
BUN:Creatinine
- normal ratio is 10-20
- pre-renal: increased (elevated BUN, normal creatinine)
- renal: normal (both elevated but ratio is normal)
- post-renal: increased (both elevated, but especially BUN)
- low-protein diet: decreased (BUN low compared to creatinine)
Methods for BUN analysis
- Coupled enzymatic method
- Electrochemical method
Coupled enzymatic method
- NAD is one product of reaction
- NAD is measured at 340nm to get the BUN concentration
Electrochemical method
- urease breaks down urea to ammonia
- ammonia ions change conductivity of electrode
- meter reads change in potential between standard and patient sample
BUN specimens
- no ammonia, Na-citrate, Na-fluoride in samples
- don’t need fasting specimen
- avoid contamination
- plasma or serum, urine needs to be diluted
Uric acid
- product of purine (A,G) breakdown
- secreted through kidney tubule, but 98% reabsorbed
- 70% excreted by kidneys, 30% by GI (of the 2%)
Hyperuricemia
- Gout (inflammation of joints by uric acid crystals)
- increased in leukemia, G-6-PD deficiency, F-1-PA, Lactic acidosis
- Lesch-Nyhan syndrome (defect in HGPRT - enzyme that breaks down amino acids for recycling)
- chronic renal disease
Hypouricemia
- Fanconi’s syndrome (tubule defect, don’t reabsorb uric acid)
- severe liver disease
- drugs (interfere with degradation)
Methods for Uric Acid
- Enzymatic method
- uses uricase, produces peroxide
- use peroxidase + dye to make a color rxn
Uric acid specimens
- heparinized plasma or serum
- NO EDTA
High uric acid values can result from method susceptibility to
drugs like aspirin and thiazides
Low uric acid value can result from method susceptibility to
- gross lipemia, high bilirubin, hemolysis, glutathione release
- interfere with perioxidase
- lipemia interferes with absorbance
Creatinine
- produced from creatine degradation (in muscle tissue)
- levels depend on muscle mass
- plasma creatinine is inversely proportional to GFR
- filtered by kidney, some reabsorbed, some excreted in urine
- Creatinine Clearance is a measure of GFR
eGFR
measure of GFR that accounts for age, gender and ethnicity
High Creatinine Levels associated with
- decreased GFR
- not sensitive enough to predict glomerulus damage until 50% kidney loss
- can be due to high protein diet
Creatinine methods
- Kinetic Jaffe rxn
- Colorimetric Jaffe rxn
- enzymatic method (with creatininase)
- Isotope Dilution Mass Spectroscopy (IDMS)
Creatinine specimens
- plasma, serum, urine
- no hemolysis, lipemia, or icteric specimens
- fasting not required
- refrigerate urine
Creatinine sources of error
- ascorbate, glucose, alpha-keto acids and uric acid
- bilirubin gives negative bias in rxns
- ascorbate and peroxidase rxns
- cephalosporin antibiotics
- dopamine and lidocaine
Ammonia
- formed form the deamination of amino acids
- most processed into urea by liver, but some travels through blood and is excreted by the kidneys
- levels increase in liver failure, Reye’s syndrome and enzyme deficiencies in the urea cycle
- neurotoxic: can lead to encephalopathy
Ammonia methods
- ion-selective electrode (measures pH change)
- enzymatic method (read absorbance)
Ammonia specimens
- heparin or EDTA tube
- no hemolysis
- no smoking before specimen collection
- higher levels in kids