kidney function testing dr. malik alqub md. phd
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An Introduction to the Urinary System
Produces urine
Transports urine towards bladder
Temporarily store urine
Conducts urine to exterior
The Function of Urinary System
Excretion & Elimination: removal of organic wastes products
from body fluids (urea, creatinine, uric acid)
Homeostatic regulation:
Water -Salt Balance
Acid - base Balance Enocrine function:
Hormones
A(
B(
C(
excretion of excess electrolytes, nitrogenous wastes and organic acids
The maximal excretory rate is limited or established by their plasma
concentrations and the rate of their filtration through the glomeruli
The maximal amount of substance excreted in urine does not exceed the
amount transferred through the glomeruli by ultrafiltration except in the
case of those substances capable of being secreted by the tubular cells.
The excretory functionA(
B) Homeostatic Functions
Regulate blood volume and blood pressure: by adjusting volume of water lost in urine releasing renin from the juxtraglomerular apparatus
• Regulate plasma ion concentrations:
– sodium, potassium, and chloride ions (by controlling quantities lost in urine)
– calcium ion levels
Blood volume is associated with Salt volume.
The greater the blood volume the greater the blood pressure.
Removing water lowers blood pressure
1) Water -Salt Balance
The kidneys control this by excreting H+ ions and reabsorbing HCO3 (bicarbonate).
2 (Acid-Base Balance (Help stabilize blood pH)
If plasma pH is low (acidic).
H+ secretion in the urine and HCO3¯ reabsorption back to the plasma increases thus urine becomes more acidic,and the plasma more alkaline.
If plasma pH is high (alkaline).
H+ secretion in the urine and HCO3¯ reabsorption back to the plasma decreases thus urine becomes more alkaline,and the plasma more acidic.
B) Homeostatic Functions
C) The endocrine function Kidneys have primary endocrine function since they produce hormones
(erythropoietin, renin and prostaglandin).
Erythropoietin is secreted in response to a lowered oxygen content in the
blood. It acts on bone marrow, stimulating the production of red blood cells.
Renin the primary stimuli for renin release include reduction of renal
perfusion pressure and hyponatremia. Renin release is also influenced by
angiotension II and ADH.
The kidneys are primarily responsible for producing vitamin D3
In addition, the kidneys are site of degradation for hormones such as
insulin and aldosterone,
Each kidney consists of one million functional units: Nephrone
A) Glomerulus B) Glomerular CapsuleC) Renal Tubule proximal convoluted tubule • loop of Henle • distal convoluted tubule D) Collecting Duct
Nephron structure
Blood pressure inside of the glomerulus is very high. Because of differences in the resistance between the afferent and efferent arterioles. Forces the fluids and some solids out of the blood into the glomerular capsule.
The Glomerulus
Urine formation requiers:
Urine Formation
Glomerular Filtration Due to differences in pressure water, small molecules move from the glomerulus capillaries into the glomerular capsule
Tubular reabsorption many molecules are reabsorbed from the nephron into the capillary (diffusion, facilitated diffusion, osmosis, and active transport)i.e. Glucose is actively reabsorbed with transport carriers.If the carriers are overwhelmed glucose appears in the urine indicating diabetes
Tubular secretionSubstances are actively removed from blood and added to tubular fluid (active transport)ie. H+, creatinine, and some drugs are moved by active transport from the blood into the distal convoluted tubule
a(
b(
c(
Urine Formation
Glomerular Filtration
The first step in the production of urine is called glomerular filtration.
Filtration: the forcing of fluids and dissolved substances through a membrane by pressure occurs in the renal corpuscle of the kidneys across the endothelial capsular membrane (Bowman's) capsule.
- The resulting fluid is called the filtrate.
- Filtration is a passive process.
- The total filtration rate of the kidneys is mainly determined by the difference between the blood pressure in the glomerular capillaries and the hydrostatic pressure in the lumen of the nephron
Glomerular Filtration Rate (GFR) Affected by:
1). Total filtration surface area
2). Membrane permeability
3). Net Filtration Pressure (as NFP goes up so does the GFR)
The amount of filtrate that flows out of all the renal corpuscles of both kidneys every minute
is called the glomerular filtration rate (GFR).
In the normal adult, this rate is about 120 ml/min; about 180 liters/Day
Glomerular Filtration Rate
Biochemical Tests of Renal Function
Measurement of GFR Clearance tests Plasma creatinine Urea, uric acid and β2-microglobulin
Renal tubular function tests Osmolality measurements Specific proteinurea Glycouria Aminoaciduria
Urinalysis Appearance Specific gravity and osmolality pH osmolality Glucose Protein Urinary sediments
When should you assess renal function?
Older age Family history of Chronic Kidney disease (CKD) Decreased renal mass Low birth weight Diabetes Mellitus (DM) Hypertension (HTN) Autoimmune disease Systemic infections Urinary tract infections (UTI) Nephrolithiasis Obstruction to the lower urinary tract Drug toxicity
Biochemical Tests of Renal Function
Measurement of GFR Clearance tests Plasma creatinine Urea, uric acid and β2-
microglobulin
In acute and chronic renal failure, there is effectively a loss of
function of whole nephrons
Filtration is essential to the formation of urine tests of
glomerular function are almost always required in the
investigation and management of any patient with renal disease.
The most frequently used tests are those that assess either the
GFR or the integrity of the glomerular filtration barrier.
Biochemical Tests of renal function
GFR can be estimated by measuring the urinary excretion of a substance that is completely filtered
from the blood by the glomeruli and it is not secreted, reabsorbed or metabolized by the renal
tubules.
Clearance is defined as the (hypothetical) quantity of blood or plasma completely cleared of a
substance per unit of time.
Clearance of substances that are filtered exclusively or predominantly by the glomeruli but
neither reabsorbed nor secreted by other regions of the nephron can be used to measure GFR.
Inulin
The Volume of blood from which inulin is cleared or completely removed in one minute is
known as the inulin clearance and is equal to the GFR.
Measurement of inulin clearance requires the infusion of inulin into the blood and is not
suitable for routine clinical use
GFR =(U V)
P
inulin
inulin
V is not urine volume, it is urine flow rate
Measurement of glomerular
filtration rate
Biochemical Tests of Renal Function
Measurement of GFR Clearance tests Plasma creatinine Urea, uric acid and β2-
microglobulin
1 to 2% of muscle creatine spontaneously converts to creatinine
daily and released into body fluids at a constant rate. Endogenous creatinine produced is proportional to muscle
mass, it is a function of total muscle mass the production
varies with age and sex Dietary fluctuations of creatinine intake cause only minor
variation in daily creatinine excretion of the same person. Creatinine released into body fluids at a constant rate and its
plasma levels maintained within narrow limits Creatinine
clearance may be measured as an indicator of GFR.
Creatinine
The most frequently used clearance test is based on the
measurement of creatinine.
Small quantity of creatinine is reabsorbed by the tubules and
other quantities are actively secreted by the renal tubules So
creatinine clearance is approximately 7% greater than inulin
clearance.
The difference is not significant when GFR is normal but when
the GFR is low (less 10 ml/min), tubular secretion makes the
major contribution to creatinine excretion and the creatinine
clearance significantly overestimates the GFR.
Creatinine clearance and clinical utility
An estimate of the GFR can be calculated from the creatinine content of a 24-hour
urine collection, and the plasma concentration within this period.
The volume of urine is measured, urine flow rate is calculated (ml/min) and the
assay for creatinine is performed on plasma and urine to obtain the concentration in
mg per dl or per ml.
Creatinine clearance in adults is normally about of 120 ml/min,
The accurate measurement of creatinine clearance is difficult, especially in outpatients,
since it is necessary to obtain a complete and accurately timed sample of urine
Creatinine clearance clinical utility
The 'clearance' of creatinine from plasma is directly related to the
GFR if:
The urine volume is collected accurately
There are no ketones or heavy proteinuria present to interfere
with the creatinine determination.
It should be noted that the GFR decline with age (to a greater extent
in males than in females) and this must be taken into account when
interpreting results.
Creatinine clearance and clinical
utility
Use of Formulae to Predict Clearance
• Formulae have been derived to predict Creatinine Clearance (CC) from Plasma creatinine.
• Plasma creatinine derived from muscle mass which is related to body mass, age, sex.
• Cockcroft & Gault Formula CC = k[(140-Age) x weight(Kg))] / serum Creatinine (µmol/L)
k = 1.224 for males & 1.04 for females• Modifications required for children & obese subjects
• Can be modified to use Surface area
Biochemical Tests of Renal Function
Measurement of GFR Clearance tests Plasma creatinine Urea, uric acid and β2-
microglobulin
Catabolism of proteins and nucleic acids results in formation of
so called nonprotein nitrogenous compounds.
Protein
Proteolysis, principally enzymatic
Amino acids
Transamination and oxidative deamination
Ammonia
Enzymatic synthesis in the “urea cycle”
Urea
Measurement of nonprotein
nitrogen-containing compounds
Urea is the major nitrogen-containing metabolic product of protein
catabolism in humans,
Its elimination in the urine represents the major route for nitrogen
excretion.
More than 90% of urea is excreted through the kidneys, with losses
through the GIT and skin
Urea is filtered freely by the glomeruli
Plasma urea concentration is often used as an index of renal glomerular
function
Urea production is increased by a high protein intake and it is decreased
in patients with a low protein intake or in patients with liver disease.
Plasma Urea
Many renal diseases with various glomerular, tubular, interstitial or vascular damage can
cause an increase in plasma urea concentration.
The reference interval for serum urea of healthy adults is 5-39 mg/dl. Plasma
concentrations also tend to be slightly higher in males than females. High protein diet causes
significant increases in plasma urea concentrations and urinary excretion.
Measurement of plasma creatinine provides a more accurate assessment than urea
because there are many factors that affect urea level.
Nonrenal factors can affect the urea level (normal adults is level 5-39 mg/dl) like:
Mild dehydration,
high protein diet,
increased protein catabolism, muscle wasting as in starvation,
reabsorption of blood proteins after a GIT haemorrhage,
treatment with cortisol or its synthetic analogous
Plasma Urea
Clinical Significance
States associated with elevated levels of urea in blood are referred to as uremia or azotemia.
Causes of urea plasma elevations: Prerenal: renal hypoperfusion Renal: acute tubular necrosis Postrenal: obstruction of urinary flow
In human, uric acid is the major product of the catabolism of the purine
nucleosides, adenosine and guanosine.
Purines are derived from catabolism of dietary nucleic acid (nucleated cells,
like meat) and from degradation of endogenous nucleic acids.
Overproduction of uric acid may result from increased synthesis of purine
precursors.
In humans, approximately 75% of uric acid excreted is lost in the urine;
most of the reminder is secreted into the GIT
Uric acid
Renal handling of uric acid is complex and involves four sequential steps:
Glomerular filtration of virtually all the uric acid in capillary plasma
entering the glomerulus.
Reabsorption in the proximal convoluted tubule of about 98 to 100%
of filtered uric acid.
Subsequent secretion of uric acid into the lumen of the distal portion
of the proximal tubule.
Further reabsorption in the distal tubule.
Hyperuricemia is defined by serum or plasma uric acid concentrations higher
than 7.0 mg/dl (0.42mmol/L) in men or greater than 6.0 mg/dl (0.36mmol/L)
in women
Uric acid
β2-microglobulin is a small peptide (molecular weight 11.8 kDa),
It is present on the surface of most cells and in low concentrations in the
plasma.
It is completely filtered by the glomeruli and is reabsorbed and catabolized
by proximal tubular cells.
The plasma concentration of β2-microglobulin is a good index of GFR in
normal people, being unaffected by diet or muscle mass.
It is increased in certain malignancies and inflammatory diseases.
Since it is normally reabsorbed and catabolized in the tubules, measurement
of β2-microglobulin excretion provides a sensitive method of assessing
tubular integrity.
Plasma β2-microglobulin
Biochemical Tests of Renal Function
Renal tubular function tests Osmolality measurements Specific proteinurea Glycouria Aminoaciduria
Renal tubular function tests
• To ensure that important constituents such as water, sodium, glucose and a.a. are not lost from the body, tubular reabsorption must be equally efficient
• Compared with the GFR as an assessment of glomerualr function, there are no easily performed tests which measure tubular function in quantitative manner
• Investigation of tubular function:
1. Osmolality measurements in plasma and urine; normal urine: plasma osmolality ratio is usually between 1.0-3.0
2. Specific proteinuria
3. Glycosuria
4. Aminoaciduria
Proteinuria may be due to:
1. An abnormality of the glomerular basement membrane.
2. Decreased tubular reabsorption of normal amounts of filtered proteins.
3. Increased plasma concentrations of free filtered proteins.
4. Decreased reabsorption and entry of protein into the tubules consequent to tubular epithelial
cell damage.
Measurement of individual proteins such as β2-microglobulin have been used in the early
diagnosis of tubular integrity.
With severe glomerular damage, red blood cells are detectable in the urine (haematuria), the red
cells often have an abnormal morphology in glomerular disease.
Haematuria can occur as a result of lesions anywhere in the urinary tract,
Assessment of glomerular integrity
The glomerular basement membrane does not usually allow passage of
albumin and large proteins. A small amount of albumin, usually less than 25
mg/24 hours, is found in urine.
Urinary protein excretion in the normal adult should be less than 150
mg/day.
When larger amounts, in excess of 250 mg/24 hours, are detected,
significant damage to the glomerular membrane has occurred.
Quantitative urine protein measurements should always be made on
complete 24-hour urine collections.
Albumin excretion in the range 25-300 mg/24 hours is termed
microalbuminuria
Proteinuria
Normal < 150 mg/24h. TYPES OF PROTEINURIA
Glomerular proteinuria Tubular proteinuria Overflow proteinuria
Proteinuria
Glomerular proteinuria
Glomerular proteinuria — Glomerular proteinuria is due to increased filtration of macromolecules (such as albumin) across the glomerular capillary wall. The proteinuria associated with diabetic nephropathy and other glomerular diseases, as well as more benign causes such as orthostatic or exercise-induced proteinuria fall into this category. Most patients with benign causes of isolated proteinuria excrete less than 1 to 2 g/day
Tubular proteinuria
Low molecular weight proteins — such as ß2-microglobulin, immunoglobulin light chains, retinol-binding protein, and amino acids — have a molecular weight that is generally under 25,000 in comparison to the 69,000 molecular weight of albumin. These smaller proteins can be filtered across the glomerulus and are then almost completely reabsorbed in the proximal tubule. Interference with proximal tubular reabsorption, due to a variety of tubulointerstitial diseases or even some primary glomerular diseases, can lead to increased excretion of these smaller proteins
Overflow proteinuria
Increased excretion of low molecular weight proteins can occur with marked overproduction of a particular protein, leading to increased glomerular filtration and excretion. This is almost always due to immunoglobulin light chains in multiple myeloma, but may also be due to lysozyme (in acute myelomonocytic leukemia), myoglobin (in rhabdomyolysis), or hemoglobin (in intravascular hemolysis
Biochemical Tests of Renal Function
Urinalysis Appearance Specific gravity and osmolality pH Glucose Protein Urinary sediments
Urinalysis is important in screening for disease is routine test for every patient, and not just
for the investigation of renal diseases
Urinalysis comprises a range of analyses that are usually performed at the point of care rather
than in a central laboratory.
Urinalysis is one of the commonest biochemical tests performed outside the laboratory.
Examination of a
patient's urine should not
be restricted to
biochemical tests.
Urinalysis
Biochemical testing of urine involves the use of commercially available disposable strips When the strip is manually immersed in the urine specimen, the reagents react with a specific component of urine in such a way that to form color
Colour change produced is proportional to the concentration of the component being tested for.
To test a urine sample:
fresh urine is collected into a clean dry container
the sample is not centrifuged
the disposable strip is briefly immersed in the urine specimen;
The colour of the test areas are compared with those provided on a colour chart
Urinalysis using disposable strips
Chemical AnalysisChemical Analysis
Urine DipstickUrine Dipstick
GlucoseGlucose
BilirubinBilirubin
KetonesKetones
Specific GravitySpecific Gravity
BloodBlood
pHpH
ProteinProtein
UrobilinogenUrobilinogen
NitriteNitrite
Leukocyte EsteraseLeukocyte Esterase
Fresh sample = Valid sample. fresh urine is collected into a clean dry container the sample is not centrifuged
Appearance: - Blood Colour (haemoglobin, myoglobin,) Turbidity (infection, nephrotic syndrome)
Urinalysis
Blue Green Pink-Orange-Red
Red-brown-black
Methylene Blue Haemoglobin Haemoglobin
Pseudomonas Myoglobin Myoglobin
Riboflavin Phenolpthalein Red blood cells
Porphyrins Homogentisic Acid
Rifampicin L -DOPA
Melanin
Methyldopa
– This is a semi-quantitative measure of concentration.
– A higher specific gravity indicates a more concentrated urine.
– Assessment of urinary specific gravity usually just confirms the impression gained by
visually inspecting the colour of the urine. When urine concentration needs to be
quantitated,
Urinalysis: Specific gravity
Urinalysis: Osmolality measurements in plasma and urine– Osmolality serves as general marker of tubular function. Because the ability
to concentrate the urine is highly affected by renal diseases.
– This is conveniently done by determining the osmolality, and then
comparing this to the plasma.
– If the urine osmolality is 600mosm/kg or more, tubular function is usually
regarded as intact
– When the urine osmolality does not differ greatly from plasma (urine:
plasma osmolality ratio=1), the renal tubules are not reabsorbing water
pH-Urine is usually acidic
-Measurement of urine pH is useful in suspected drug toxicity, abuse.., or where there is an unexplained metabolic acidosis (low serum bicarbonate or other causes…).
Urine sediments-Microscopic examination of sediment from freshly passed urine involves looking for
cells, casts, fat droplets
-Blood: haematuria is consistent with various possibilities ranging from malignancy through urinary tract infection to contamination from menstruation.
-Red Cell casts could indicate glomerular disease
-Crystals
-Leucocytes in the urine suggests acute inflammation and the presence of a urinary tract infection.
Urinalysis
-are cylindrical structures produced by the kidney and present in the urine in
certain disease states. - They form in the distal convoluted tubule and collecting ducts of nephrons,
then dislodge and pass into the urine, where they can be detected by
microscope.- They form via precipitation of Tamm-Hrsfall mucoprotein which is
secreted by renal tubule cells, and sometimes also by albumin.
Urinary casts
Red blood cell cast in urineWhite blood cell cast in urine
Urinary casts. (A) Hyaline cast (200 X); (B) erythrocyte cast (100 X); (C) leukocyte cast (100 X); (D) granular cast (100 X)
Urinary crystals. (A) Calcium oxalate crystals; (B) uric acid crystals (C) triple phosphate crystals with amorphous phosphates ; (D) cystine crystals.
• Crystals
- Water homeostasis is determined by several interrelated processes:
1. Water intake and water formed through oxidation of food stuffs.
2. Extra-renal water loss: insensible water loss the via faeces, and sweating.
3. A solute load to be excreted that is derived from ingested minerals and
nitrogenous substances.
4. The ability of the kidneys to produce concentrated or dilute urine.
5. Other factors such as vomiting and diarrhoea become important in various
disease states;
loss of ability to produce concentrated urine is a feature of virtually all types
of chronic renal diseases.
Urine volume
To maintain water homeostasis, the kidneys must produce urine in a volume
precisely balances water intake and production to equal water loss through extra
renal routes.
Minimum urine volume is determined by the solute load to be excreted whereas
maximum urine volume is determined by the amount of excess water that must be
excreted
Urine volume
Causes of polyurea
Increased osmotic load, e.g due to glucose
Increased water ingestion
Diabetes insipidus: - Failure of ADH production results
in marked polyuria (diabetes insipidus), which stimulates
thirst and greatly increases water intake
Nephrogenic diabetes insipidus: The kidneys’ lack of
response to ADH has similar effect ( failure of the
tubules to respond to Vassopressin (ADH
MAJOR CAUSES OF KIDNEY DISEASE The causes of acute or chronic kidney disease are
traditionally classified by that portion of the renal anatomy most affected by the disorder. Renal function is based upon four sequential steps, which are isolated to specific areas of the kidney or surrounding structures: First, blood from the renal arteries and their
subdivisions is delivered to the glomeruli. The glomeruli form an ultrafiltrate, nearly free of
protein and blood elements, which subsequently flows into the renal tubules.
The tubules reabsorb and secrete solute and/or water from the ultrafiltrate.
The final tubular fluid, the urine, leaves the kidney, draining sequentially into the renal pelvis, ureter, and bladder, from which it is excreted through the urethra.
Prerenal disease
The two major causes of reduced renal perfusion are volume depletion and/or relative hypotension. This may result from true hypoperfusion due to bleeding, gastrointestinal, urinary, or cutaneous losses, or to effective volume depletion in heart failure, shock, or cirrhosis.
Prerenal disease is most commonly associated with an acute time course. However, among patients with chronic kidney disease, the addition of a prerenal process may result in acute renal dysfunction
Glomerular disease
There are numerous idiopathic and secondary (due to neoplasia, autoimmunity, drugs, genetic abnormalities, and infections) disorders that produce glomerular disease. Two general patterns (with considerable overlap in some diseases) are seen: A nephritic pattern, which is associated with
inflammation on histologic examination and produces an active urine sediment with red cells, white cells, granular and often red cell and other cellular casts, and a variable degree of proteinuria.
A nephrotic pattern, which is not associated with inflammation on histologic examination and is associated with proteinuria, often in the nephrotic range, and an inactive urine sediment with few cells or casts.
Tubular and interstitial disease As with vascular disease, the tubular and
interstitial diseases affecting the kidney can be divided into those that produce acute and chronic disease: Hereditary, systemic, toxic, and drug-induced causes predominate. The most common acute tubulointerstitial
disorders are acute tubular necrosis, which typically occurs in hospitalized patients.
The major chronic tubulointerstitial disorders are polycystic kidney disease
Obstructive uropathy
Obstruction to the flow of urine can occur anywhere from the renal pelvis to the urethra. The development of renal insufficiency in patients without intrinsic renal disease requires bilateral obstruction (or unilateral obstruction with a single functioning kidney) and is most commonly due to prostatic disease (hyperplasia or cancer) or metastatic cancer. The time course can be acute or chronic
The nephrotic syndrome is caused by renal diseases that increase the permeability across the glomerular filtration barrier. It is classically characterized by four clinical features, but the first two are used diagnostically because the last two may not be seen in all patients: Nephrotic range proteinuria — Urinary protein
excretion greater than 50 mg/kg per day Hypoalbuminemia — Serum albumin
concentration less than 3 g/dL (30 g/L) Edema Hyperlipidemia
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