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Transcript of Interpretation of renal biochemistry Doc. Dr. Mine KUCUR.
![Page 1: Interpretation of renal biochemistry Doc. Dr. Mine KUCUR.](https://reader036.fdocuments.net/reader036/viewer/2022062715/56649d875503460f94a6c2a9/html5/thumbnails/1.jpg)
Interpretation of renal biochemistry
Doc. Dr. Mine KUCUR
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Overview
Renal function tests Tests for GFR Urinalysis Tests for Renal Tubular Acidosis Tests of Kidney Concentrating Ability
Summary
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Detect renal damage
Monitor functional damage
Help determine etiology
Renal function tests
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glomerular filtration rate (GFR)
plasma creatinine plasma urea urine volume urine urea minerals in urine
urine protein urine glucose hematuria osmolality
Laboratory tests of renal function
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glomerular filtration rate=GFR
plasma creatinine= Pcr
plasma urea-Purea
urine volume= V urine urea- Uurea
cystatin C in plasma?
urine protein urine glucose hematuria osmolality
Tests of renal function
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Tests of Glomerular FiltrationRate Urea Creatinine Creatinine Clearance eGFR Cystatin C
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Glomerular Filtration Rate (GFR)
Volume of blood filtered across glomerulus per unit time
Best single measure of kidney function
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GFR
Normally 100-130 ml/min Determined by:
• Net filtration pressure across glomerular basement membrane
• Permeability and surface area of glomerular basement membrane
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GFR
Patient’s remain asymptomatic until there has been a significant decline in GFR
Can be very accurately measured using “goldstandard” technique
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GFR
Ideal Marker Produced normally by the body Produced at a constant rate Filtered across glomerular membrane Removed from the body only by the kidney
filtered only, not reabsorbed or secreted
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Candidate markers for GFR
Inulin+ Filtered only– Not made by body; must be injected
Creatinine
+ An endogenous product of muscle metabolism; near-constant production
– Filtered, but a bit secreted
Urea
+ An endogenous product of protein intake– Filtered and absorbed; synthesis varies with diet0
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Urea
Used historically as marker of GFR Freely filtered but both re-absorbed and
excreted into the urine Re-absorption into blood increased with
volume depletion; therefore GFR underestimated
Diet, drugs, disease all significantly effect Urea production
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Urea
Product of protein catabolism
Filtered
Reabsorbed in proximal tubule
If sodium is avidly reabsorbed, so is urea
Serum urea concentration measured as “Blood Urea Nitrogen (BUN)”
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Urea
Increase Volume depletion Dietary protein Corticosteroids Tetracyclines Blood in G-I tract
Decrease Volume Expansion Liver disease Severe malnutrition
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Why does BUN increase?
GFR, but also:
Increased renal reabsorption:
ECV depletion
Increased hepatic urea synthesis High protein feeding Corticosteroid treatment (Prednisone, etc.) GI blood absorption
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Proximal tubule Na and urea reabsorption!
BUN: Uses
Imperfect marker of GFR Marker for adequacy of protein intake Marker for presence of uremic toxins in
chronic renal failure BUN:Cr ratio reflects ECV volume status:
10:1 = normal >20:1 if ECV contracted. Why???
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Creatinine
Product of muscle metabolism Some creatinine is of dietary origin Freely filtered, but also actively secreted into
urine Secretion is affected by several drugs
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Serum Creatinine
Increase Male Meat in diet Muscular body type Cimetidine & some
other medications
Decrease Age Female Malnutrition Muscle wasting Amputation
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Serum Creatinine Concentration
Normally 0.7-1.4 mg/dl, depending on muscle mass
Inversely proportional to GFR
Good way to follow changes in GFR
BUT also elevated by muscle mass, tubular secretion
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Creatinine Clearance
Measure serum and urine creatinine levels and urine volume and calculate serum volume cleared of creatinine
Same issues as with serum creatinine, except muscle mass
Requirements for 24 hour urine collection adds variability and inconvenience
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Creatinine Clearance
serum
urine
serum Cr
VCr
Cr
timeunitexcretedcreatinineCrCl
][
][
][
/
Therefore, it represents the volume of serum completely cleared of creatinine per unit time
Since virtually all creatinine is cleared via glomerular filtration, it closely approximates the GFR
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Creatinine Clearance
min/ml50hourmin/60day/hrs24dl/mg0.2
day/ml2000dl/mg72CrCl
UCr = 72 mg/dlSCr = 2.0 mg/dlV = 2 literstime = 24 hours
EXAMPLE:
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Limitations of Creatinine Clearance
Only valid at steady state—[Cr]serum must be stable
Trimethoprim, cimetidine lower tubular Cr secretion and lower CrCl without changing GFR:
Becomes more inaccurate at low GFR
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Another Problem with Creatinine Clearance
Must be done on a properly collected, timed urine sample--patient error
How can we check accuracy of any timed urine collection?
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Creatinine Excretion
The amount of creatinine excreted per day is stable for a given patient
It is function of muscle mass: generally higher in men vs. women, youth vs. elderly
expressed per kg lean body mass as the creatinine index
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Quick formulae for estimating GFR
Include some combination of sex, weight, serum creatinine, race, and age. Use only at steady state (stable SCr) Useful screens for decreased GFR, esp. in elderly and small people, where errors in drug dosing may be major
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Creatinine Test Summary
Effect ofTest Use GFR muscle
mass
SCr Follow GFR
CrClearance Estimate GFR
Cr IndexDetermine
adequacy ofcollection
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Cystatin C
Cystatin C is a 13 KD protein produced by all cells at a constant rate
Freely filtered Re-absorbed and catabolized by the kidney
and does not appear in the urine
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eGFR
Increasing requirements for dialysis and transplant (8 – 10% per year)
Shortage of transplantable kidneys Large number at risk
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eGFR
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eGFR
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Problem
Need an easy test to screen for early decreases in GFR that you can apply to a large, at-risk population
Can serum creatinine be made more sensitive by adding more information?
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eGFR by MDRD Formula
Mathematically modified serum creatinine with additional information from patients age, sex and ethnicity
eGFR = 30849.2 x (serum creatinine)-1.154 x (age)-0.203
(if female x (0.742))
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eGFR
eGFR calculation has been recommended by National Kidney Foundation whenever a serum creatinine is performed in adults
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Screen High Risk Groups
eGFR Urinalysis Albumin / Creatinine Ratio
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Tests that predict kidney disease
eGFR Albumin Creatinine Ratio
(aka ACR or Microalbumin)
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Proteinuria
In health: High molecular weight proteins are retained
in the circulation by the glomerular filter (Albumin, Immunoglobulins)
Low molecular weight proteins are filtered then reabsorbed by renal tubular cells
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Proteinuria
Glomerular: Mostly albumin, because of its high
concentration and therefore high filtered load Tubular:
Low molecular weight proteins not reabsorbed by tubular cells (e.g. alpha-1 microglobulin)
Overflow: Excessive filtration of one protein exceeds
reabsorbtive capacity (Bence-Jones, myoglobin)
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Albumin Creatinine Ratio (Microalbumin) Normal albumin molecule In health, there is very little or no albumin in
the urine Most dip sticks report albumin at greater than
150 mg/L
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Urinary Albumin
Detection of low levels of albumin (even if below dipstick cut-off) is predictive of future kidney disease with diabetes
Very significant biologic variation usually requires repeat collections
Treatment usually based on timed urine albumin collections
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Follow-up based on Screen Results
Kidney Ultrasound Specialist Referral Cardiovascular Risk Assessment Diabetes Control Smoking cessation Hepatitis / Influenza Management
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Creatinine Standardization inBritish Columbia Based on Isotope dilution /mass spectrometry
measurements of creatinine standards Permits estimation and correction of
creatinine and eGFR bias at the laboratory level
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Importance of Standardization
Low bias creatinine: Causes inappropriately increased eGFR Patients will not receive the benefits of more
intensive investigation of treatment High bias creatinine:
Causes inappropriately decreased eGFR Patients receive investigations and treatment
which is not required. Wastes time, resources and increases anxiety.
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Poor Creatinine Precision
Incorrect categorization of patients with both “normal” and decreased eGFR.
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Total Error
TE = % bias + 1.96 CV Goal is <10% (requires bias ≤ 4% and CV ≤
3%)
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Kidney Functions
Selectively secretes into or re-absorbs from the filtrate to maintain Water Balance
Tests: specific gravity, osmolarity, water deprivation testing, Antidiuretic hormone
Retention of nutrients Tests: proteins, sugar, amino acids, phosphate
Secretes waste products Tests: urate, oxalate, bile salts
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Kidney Functions
Selectively secretes into or re-absorbs from the filtrate to maintain Salt Balance
Tests: Na+, Cl-, K+ Aldosterone, Renin Acid Base Balance
Tests: pH, HCO3-, NH4+ Acid loading, Urinary Anion Gap
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Kidney Functions
Target organ Parathyroid hormone (Ca++, Mg++) Aldosterone (salt balance) ADH (water balance)
Production Erythropoietin 1, 25 dihydroxycholecalciferol
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Urinalysis
Dipstick Protein
Useful screening test Dipstick more sensitive to albumin than other
proteins Large biologic variation
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Urinalysis
Dipstick – cont’d Hemoglobin
Glomerular, tubular or post-renal source Reasonably sensitive Positive dipstick and negative microscopy with
lysed red cells
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Urinalysis
Dipstick – cont’d Glucose
Reasonable technically, however screening and monitoring programs for diabetes are now done by blood and Point-of-Care devices
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Specific Gravity
Approximate only Measurement of osmolarity preferred when
concentrating ability being assessed
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pH
pH changes with time in a collected urine Calculations to determine urine ammonium
levels and response to acid-loading generally required to assess for renal tubular acidosis
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Microscopic Urinalysis
Epithelial Cells Squamous, Transitional, Renal
All may be present in small numbers Important to recognize possible malignancy Comment on unusual numbers
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Renal Tubular Epithelial
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Red Cells
May originate in any part of the urinary tract Small numbers may be normal There is provincial protocol for the
investigation of persistent hematuria
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White Blood Cells
Neutrophils often present in small numbers Lymphocytes and moncytes less often Marker for infection or inflammation
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Casts
Hyaline and granular casts not always pathologic, clinical correlation required
Red cell casts always significant, usually glomerular injury
WBC casts also always significant, usually infection, sometimes inflammation
Bacterial casts only found in pyelonephritis Waxy casts found in significant kidney
disease
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Tests for Renal Tubular Acidosis
Urinary Anion Gap
(Na+ + K+) – Cl- In acidosis the kidney should excrete NH4+
and the gap will be negative
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RTA
If NH4 + is not present (or if HCO3 - is present) the gap will be neutral or positive, implying impaired kidney handling of acid load.
Urine Anion Gap = (Na+ + K+) –Cl-
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RTA
Ammonium Chloride Loading Load with ammonium chloride Hourly measurements of urine pH Normal at least one pH below 5.5
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Tests of Kidney Concentrating Ability
To differentiate Psychogenic polydipsia Central diabetes insipidus Nephrogenic diabetes insipidus
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Overnight Water Deprivation Testing
(Serum osmolarity <295 monitor patient weight hourly)
Collect urine hourly from 0600 for osmolarity Baseline serum osmolarity, Na+, ADH When osmolarity plateaus repeat above tests
and administer ADH
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Interpretation
If urine concentrates (osmolarity >600 and serum osmolarity below <295)
Normal physiology (? Psychogenic polydipsia)
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No Urine ConcentrationNo Response to ADH Nephrogenic diabetes insipidus
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No Urine Concentration
Positive response to ADH Central diabetes insipidus
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To summarize:
1. Use the Creatinine Clearance as the best estimate of GFR
2. Use the Serum Creatinine to follow renal function over time
3. Use the Creatinine Index to check the adequacy of a urine collection
4. Use the BUN to help assess GFR, volume status, and protein intake