(Redirected from Bilirubin metabolism)
Jump to navigation Jump to search


WikiDoc Resources for Bilirubin


Most recent articles on Bilirubin

Most cited articles on Bilirubin

Review articles on Bilirubin

Articles on Bilirubin in N Eng J Med, Lancet, BMJ


Powerpoint slides on Bilirubin

Images of Bilirubin

Photos of Bilirubin

Podcasts & MP3s on Bilirubin

Videos on Bilirubin

Evidence Based Medicine

Cochrane Collaboration on Bilirubin

Bandolier on Bilirubin

TRIP on Bilirubin

Clinical Trials

Ongoing Trials on Bilirubin at Clinical

Trial results on Bilirubin

Clinical Trials on Bilirubin at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Bilirubin

NICE Guidance on Bilirubin


FDA on Bilirubin

CDC on Bilirubin


Books on Bilirubin


Bilirubin in the news

Be alerted to news on Bilirubin

News trends on Bilirubin


Blogs on Bilirubin


Definitions of Bilirubin

Patient Resources / Community

Patient resources on Bilirubin

Discussion groups on Bilirubin

Patient Handouts on Bilirubin

Directions to Hospitals Treating Bilirubin

Risk calculators and risk factors for Bilirubin

Healthcare Provider Resources

Symptoms of Bilirubin

Causes & Risk Factors for Bilirubin

Diagnostic studies for Bilirubin

Treatment of Bilirubin

Continuing Medical Education (CME)

CME Programs on Bilirubin


Bilirubin en Espanol

Bilirubin en Francais


Bilirubin in the Marketplace

Patents on Bilirubin

Experimental / Informatics

List of terms related to Bilirubin

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Bilirubin is a yellow breakdown product of normal heme catabolism. Its levels are elevated in certain diseases and it is responsible for the yellow colour of bruises and the brown colour of feces. Bilirubin reduction in the gut leads to a product called urobilinogen, which is excreted in urine.


Bilirubin consists of an open chain of four pyrrole-like rings (tetrapyrrole). In heme, by contrast, these four rings are connected into a larger ring, called a porphyrin.

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, bilirubin changes its conformation when exposed to light. This is used in the phototherapy of jaundiced newborns: the illuminated version of bilirubin is more soluble than the unilluminated version.

Several textbooks and research articles show incorrect chemical structures for the two isoforms of bilirubin. [1]


Bilirubin is created by the activity of biliverdin reductase on biliverdin. Bilirubin, when oxidized, reverts to become biliverdin once again. This cycle, in addition to the demonstration of the potent antioxidant activity of bilirubin, has led to the hypothesis that bilirubin's main physiologic role is as a cellular antioxidant.[2]


Erythrocytes (red blood cells) generated in the bone marrow are destroyed in the spleen when they get old or damaged. This releases hemoglobin, 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 macrophages of the spleen. It is then bound to albumin and sent to the liver.

In the liver it is conjugated with glucuronic acid, making it water soluble. Much of it goes into the bile and thus out into the small intestine. Some of the conjugated bilirubin remains in the large intestine and is metabolised by colonic bacteria to stercobilinogen and then oxidised to stercobilin.

Some is reabsorbed, and excreted in the urine as urobilinogen and the oxidised form, urobilin. If the liver’s function is impaired, or biliary drainage blocked, some of the conjugated bilirubin appears in the urine, turning it dark amber.

Bilirubin toxicity

Unconjugated hyperbilirubinaemia in the neonate can lead to accumulation of bilirubin in certain brain regions, a phenomenon known as kernicterus, with consequent irreversible damage to these areas manifesting as various neurological deficits, seizures, abnormal reflexes and eye movements. Aside from specific chronic medical conditions that may lead to hyperbilirubinaemia, 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 b-glucoronidase and a large proportion is reabsorbed through the enterohepatic circulation.

Bilirubin benefits

Reasonable levels of bilirubin can be beneficial to the organism. Evidence is accumulating that suggests bilirubin can protect tissues against oxidative damage caused by free radicals and other reactive oxygen species. Statistical analysis of people with high normal or slightly elevated bilirubin levels in blood shows that they have a lower risk of developing cardiovascular diseases.

Bilirubin blood tests

Bilirubin is in one of two forms:

Abb. Name Soluble? Reaction
"BC" conjugated or direct Yes (bound to glucuronic acid) Reacts directly when dyes are added to the blood specimen.
"BU" unconjugated or indirect No Free bilirubin does not react to the reagents until alcohol (methanol) or Caffeine is added to the solution. Therefore, the measurement of this type of bilirubin is indirect. (It is transformed into a soluble or direct form, in the liver. )

Total bilirubin 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.

To further elucidate the causes of jaundice or increased bilirubin, it is usually simpler to look at other liver function tests (especially the enzymes ALT, AST, GGT, Alk Phos), blood film examination (hemolysis, etc.) or evidence of infective hepatitis (e.g., Hepatitis A, B, C, delta E, etc).

Bilirubin is an excretion product, and the body does not control levels. Bilirubin levels reflect the balance between production and excretion. Thus, there is no "normal" level of bilirubin.

Bilirubin is broken down by light, and therefore blood collection tubes (especially serum tubes) should be protected from such exposure.


Different sources provide reference ranges which 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 bilirubin 5.1–17.0 [3] 0.2-1.9 [4], 0.2-1.0 [5], 0.3–1.0 [3], 0.1-1.2 [6]
direct bilirubin 1.0–5.1 [3] 0-0.3[4], 0.1–0.3[3], 0.1-0.4 [6]

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 which can result in mild jaundice, found in about 5% of the population.
  • Drugs: Cladribine

Moderate rise in bilirubin may be caused by

Very high levels of bilirubin may be caused by

Cirrhosis may cause normal, moderately high or high levels of bilirubin, depending on exact features of the cirrhosis

Indirect bilirubin is fat soluble and direct bilirubin is water soluble.


Jaundice may be noticeable in the sclera (white) of the eyes at levels of about 30-50 μmol/l, and in the skin at higher levels. Jaundice is classified depending upon whether the bilirubin is free or conjugated to glucuronic acid into:

  • Conjugated jaundice
  • Unconjugated jaundice

Cultural references

  • (1988) Bilirubin was used as a wordplay in the novel The Silence of the Lambs. The incarcerated psychopathic psychiatrist Hannibal Lecter assists the FBI in capturing a killer. Lecter gives the name of the killer as "Billy Rubin". After Lecter escapes from custody, they find a piece of paper in his cell on which he had written his warden's name (Chilton) and, from the C,H,N,O in the name, given the formula for bilirubin.
  • (1990) In Juan Luis Guerra's song, "Me sube la bilirrubina" on the album Bachata Rosa, the protagonist's bilirubin levels increase as a result of unrequited love.
  • (2001) German industrial band Einstürzende Neubauten have a song called "Bili Rubin", on Strategies Against Architecture III.


  1. "Bilirubin's Chemical Formula". Retrieved 2007-08-14.
  2. Baranano DE, Rao M, Ferris CD, Snyder SH (2002). "Biliverdin reductase: a major physiologic cytoprotectant". Proc. Natl. Acad. Sci. U.S.A. 99 (25): 16093–8. doi:10.1073/pnas.252626999. PMID 12456881.
  3. 3.0 3.1 3.2 3.3 "Bilirubin". Retrieved 2007-08-14.
  4. 4.0 4.1 MedlinePlus Encyclopedia 003468
  5. "Bloodindex - Haematology Reference Values". Retrieved 2007-08-14.
  6. 6.0 6.1 "Laboratory tests". Retrieved 2007-08-14.

See also

bn:বিলিরুবিন de:Bilirubin it:Bilirubina he:בילירובין lt:Bilirubinas hu:Bilirubin nl:Bilirubine sq:Bilirubina simple:Bilirubin sk:Bilirubín sl:Bilirubin fi:Bilirubiini sv:Bilirubin uk:Білірубін

Template:WikiDoc Sources