11 Februari 2013

bilirubbin

*Bilirubin* (formerly referred to as*hematoidin*) is the yellow breakdown product of normal heme
 catabolism
. Heme is found inhemoglobin
, a principal component of red blood cells
. Bilirubin is excreted in bile
 andurine
, and elevated levels may indicate certain diseases. It is responsible for the yellow color of bruises
, the background straw-yellow color of urine (via its reduced breakdown product,urobilin
 – the more obvious but variable bright yellow colour of urine is due tothiochrome, a breakdown product ofthiamine
), the brown color of feces
 (via its conversion to stercobilin
), and the yellow discoloration in jaundice
.
It has also been found in plants.[1]
HideChemistry
Bilirubin consists of an open chain of fourpyrrole
-like rings (tetrapyrrole
). In heme
, by contrast, these four rings are connected into a larger ring, called a porphyrin
 ring.
Bilirubin can be "conjugated" with a molecule of glucuronic acid
 which makes it soluble in water (see below). This is an example ofglucuronidation
.
Bilirubin is very similar to the pigment
phycobilin
 used by certain algae to capture light energy, and to the pigment phytochrome
used by plants to sense light. All of these contain an open chain of four pyrrolic rings.
Like these other pigments, some of the double-bonds in bilirubin isomerize
 when exposed to light. This is used in thephototherapy
 of jaundiced newborns: the E,Z-isomers of bilirubin formed upon light exposure are more soluble than the unilluminated Z,Z-isomer, as the possibility of intramolecular hydrogen bonding is removed.[2]
 This allows the excretion of unconjugated bilirubin in bile.
Some textbooks and research articles show the incorrect geometric isomer of bilirubin.[3]
The naturally occurring isomer is the Z,Z-isomer.Close this section
HideFunction
Bilirubin is created by the activity of biliverdin reductase
 on biliverdin
, a green tetrapyrrolic bile pigment that is also a product of heme catabolism. Bilirubin, when oxidized, reverts to become biliverdin once again. This cycle, in addition to the demonstration of the potent antioxidant activity of bilirubin,[4]
 has led to the hypothesis that bilirubin's main physiologic role is as a cellular antioxidant.[5]
[6]
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HideMetabolism
Heme metabolismUnconjugated
Erythrocytes
 (red blood cells) generated in thebone marrow
 are disposed of in the spleen
when they get old or damaged. This releaseshemoglobin
, which is broken down to heme
as the globin parts are turned into amino acids
. The heme is then turned into unconjugated bilirubin in the reticuloendothelial cells of the spleen. This unconjugated bilirubin is not soluble in water, due to intramolecular hydrogen bonding. It is then bound to albumin
 and sent to the liver
.
The measurement of direct bilirubin depends on its reaction with diazosulfanilic acid to create azobilirubin
. However, unconjugated bilirubin also reacts slowly with diazosulfanilic acid, so that the measured indirect bilirubin is an underestimate of the true unconjugated concentration.Conjugated
In the liver it is conjugated with glucuronic acid
 by the enzyme glucuronyltransferase
, making it soluble in water. Much of it goes into the bile and thus out into the small intestine. However 95% of the secreted bile is reabsorbed by the small intestine. This bile is then resecreted by the liver into the small intestine. This process is known asenterohepatic circulation
.
About half of the conjugated bilirubin remaining in the large intestine (about 5% of what was originally secreted) is metabolised by colonic bacteria to form urobilinogen
, which may be further oxidized to urobilin
 andstercobilin
. Urobilin, stercobilin and their degradation products give feces its brown color.[7]
 However, just like bile, some of the urobilinogen is reabsorbed and 95% of what is reabsorbed is resecreted in the bile which is also part of enterohepatic circulation
. A small amount of the reabsorbed urobilinogen (about 5%) is excreted in the urine following further oxidation to urobilin
 which gives urine its characteristic yellow color. This whole process results in only 1–20% of secreted bile being lost in the feces. The amount lost depends on the secretion rate of bile.
Although the terms direct and indirect bilirubin are used equivalently with conjugated and unconjugated bilirubin, this is not quantitatively correct, because the direct fraction includes both conjugated bilirubin and δ bilirubin (bilirubin covalently bound to albumin, which appears in serum when hepatic excretion of conjugated bilirubin is impaired in patients with hepatobiliary disease).[8]
 Furthermore, direct bilirubin tends to overestimate conjugated bilirubin levels due to unconjugated bilirubin that has reacted with diazosulfanilic acid, leading to increased azobilirubin levels (and increased direct bilirubin).Urine
Under normal circumstances, a tiny amount of urobilinogen, if any, is excreted in theurine
. If the liver's function is impaired or when biliary drainage is blocked, some of the conjugated bilirubin leaks out of the hepatocytes and appears in the urine, turning it dark amber. However, in disorders involvinghemolytic anemia
, an increased number of red blood cells are broken down, causing an increase in the amount of unconjugated bilirubin in the blood. Because the unconjugated bilirubin is not water-soluble, one will not see an increase in bilirubin in the urine. Because there is no problem with the liver or bile systems, this excess unconjugated bilirubin will go through all of the normal processing mechanisms that occur (e.g., conjugation, excretion in bile, metabolism to urobilinogen, reabsorption) and will show up as an increase in urine urobilinogen. This difference between increased urine bilirubin and increased urine urobilinogen helps to distinguish between various disorders in those systems.Close this section
HideToxicity
Unconjugated hyperbilirubinaemia in a new-born can lead to accumulation of bilirubin in certain brain regions (particularly the basal nuclei
) with consequent irreversible damage to these areas manifesting as various neurological deficits, seizures
, abnormalreflexes
 and eye movements. This type of neurological injury is known as kernicterus
. The neurotoxicity of neonatal hyperbilirubinemia manifests because theblood–brain barrier
 has yet to develop fully, and bilirubin can freely pass into the brain interstitium, whereas more developed individuals with increased bilirubin in the blood are protected. Aside from specific chronic medical conditions that may lead tohyperbilirubinaemia
, neonates in general are at increased risk since they lack the intestinal bacteria that facilitate the breakdown and excretion of conjugated bilirubin in the feces (this is largely why the feces of a neonate are paler than those of an adult). Instead the conjugated bilirubin is converted back into the unconjugated form by the enzyme β-glucuronidase
 and a large proportion is reabsorbed through the enterohepatic circulation
.Close this section
HideAssociated Health Benefits
Recent research has indicated that in the absence of liver disease, individuals with high levels of total bilirubin may experience various health benefits exceeding those with lower levels of bilirubin. Studies have found higher levels of bilirubin in elderly individuals are associated with higher functional independence [9]
 Studies have also revealed that levels of serum bilirubin are inversely related to risk of certain heart diseases.[10]
[11]
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HideBlood tests
Bilirubin is broken down by light. Tubes containing blood or (especially) serum to be used in bilirubin assays should be protected from illumination.
Bilirubin (in blood) is in one of two forms:*Abb.**Name(s)**Water-soluble?**Reaction*
"BC""Conjugated" or
"Direct bilirubin"Yes (bound toglucuronic acid
)Reacts quickly when dyes (diazo reagent) are added to the blood specimen to produceazobilirubin
"Direct bilirubin"
"BU""Unconjugated" or "Indirect bilirubin"NoReacts more slowly. Still produces azobilirubin. Ethanol makes all bilirubin react promptly then calc: Indirect bilirubin = Total bilirubin – Direct bilirubin

Total bilirubin ("TBIL") measures both BU and BC. Total and direct bilirubin levels can be measured from the blood, but indirect bilirubin is calculated from the total and direct bilirubin.
Indirect bilirubin is fat-soluble and direct bilirubin is water-soluble.Measurement methods
Originally the Van den Bergh reaction
 was used for a qualitative estimate of bilirubin.
This test is performed routinely in mostmedical laboratories
 and can be measured by a variety of methods.[12]

Total bilirubin is now often measured by the 2,5-dichlorophenyldiazonium (DPD) method, and direct bilirubin is often measured by the method of Jendrassik and Grof.[13]
Close this section
HideBlood levels
There are no normal levels of bilirubin as it is an excretion product, and levels found in the body reflects the balance between production and excretion. Different sources providereference ranges
 that are similar but not identical. Some examples for adults are provided below (different reference ranges are often used for newborns):*μmol/L**mg/dL*
total bilirubin5.1–17.0[14]
0.2–1.9,[15]

0.3–1.0,[14]

0.1–1.2[16]

direct bilirubin1.0–5.1[14]
0–0.3,[15]

0.1–0.3,[14]

0.1–0.4[16]

Reference ranges for blood tests
, comparing blood content of bilirubin (shown in blue near center) with other constituents.Hyperbilirubinemia
"Hyperbilirubinemia" results from a higher-than-normal level of bilirubin in the blood.
Mild rises in bilirubin may be caused by:
  * Hemolysis
 or increased breakdown of red blood cells
  * Gilbert's syndrome
 – a genetic disorder of bilirubin metabolism that can result in mild jaundice, found in about 5% of the population
  * Rotor syndrome
: non-itching jaundice, with rise of bilirubin in the patient's serum, mainly of the conjugated type.
Moderate["clarification needed
"] rise in bilirubin may be caused by:
  * Pharmaceutical drugs
 (especiallyantipsychotic
, some sex hormones
, and a wide range of other drugs)  * Sulfonamides
 are contraindicated in infants less than 2 months old (exception when used with pyrimethamine
 in treatingtoxoplasmosis
) as they increase unconjugated bilirubin leading tokernicterus
.[17]

  * Hepatitis
 (levels may be moderate or high)
  * Chemotherapy

  * Biliary stricture (benign or malignant)
Very high["clarification needed
"] levels of bilirubin may be caused by:
  * Neonatal hyperbilirubinaemia
, where the newborn's liver is not able to properly process the bilirubin causing jaundice

  * Unusually large bile duct obstruction, e.g. stone in common bile duct, tumour obstructing common bile duct etc.
  * Severe liver failure with cirrhosis
 (e.g.primary biliary cirrhosis
)
  * Crigler–Najjar syndrome

  * Dubin–Johnson syndrome

  * Choledocholithiasis
 (chronic or acute).
Cirrhosis may cause normal, moderately high or high levels of bilirubin, depending on exact features of the cirrhosis
To further elucidate the causes of jaundice or increased bilirubin, it is usually simpler to look at other liver function tests
 (especially the enzymes alanine transaminase
, aspartate transaminase
, gamma-glutamyl transpeptidase
, alkaline phosphatase
), blood film
 examination (hemolysis
, etc.) or evidence of infective hepatitis (e.g., hepatitis A, B, C, delta, E, etc.).Jaundice
Jaundice
 may be noticeable in the sclera
(white) of the eyes at levels of about 2 to 3 mg/dL (34 to 51 μmol/L),[18]
 and in the skin at higher levels. For conversion, 1 mg/dL = 17.1 µmol/L.[19]

Jaundice is classified depending upon whether the bilirubin is free or conjugated toglucuronic acid
 into conjugated jaundice or unconjugated jaundice.["citation needed
"] .Close this section
HideUrine tests
Urine levels of bilirubin may also be clinically significant.[20]
Close this section

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