Liver diseases can develop through several mechanisms:
DNA damage One general mechanism, increased
DNA damage, is shared by some of the major liver diseases, including infection by
hepatitis B virus or
hepatitis C virus,
heavy alcohol consumption, and
obesity. Viral infection by the hepatitis B virus, or hepatitis C virus, causes an increase in
reactive oxygen species. The increase in
intracellular reactive oxygen species is about 10,000-fold with chronic hepatitis B virus infection and 100,000-fold following hepatitis C virus infection. In addition, activation of neutrophils in alcoholic liver disease contributes to the pathogenesis of hepatocellular damage by releasing reactive oxygen species (which can damage DNA). The level of oxidative stress and acetaldehyde-induced DNA adducts due to alcohol consumption does not appear sufficient to cause increased mutagenesis.
Obesity is associated with a higher risk of primary liver cancer. As shown with mice, obese mice are prone to liver cancer, likely due to two factors. Obese mice have increased pro-inflammatory cytokines. Obese mice also have higher levels of deoxycholic acid, a product of
bile acid alteration by certain gut microbes, and these microbes are increased with obesity. The excess
deoxycholic acid causes DNA damage and inflammation in the liver, which, in turn, can lead to liver cancer.
Other relevant aspects Viral infections cause some forms of liver disease.
Viral hepatitides such as
Hepatitis B virus and
Hepatitis C virus can be vertically transmitted during birth via contact with infected blood. According to a 2012
NICE publication, "about 85% of hepatitis B infections in newborns become chronic". In occult cases, Hepatitis B virus is present by hepatitis B virus
DNA, but testing for
HBsAg is negative. High consumption of
alcohol can lead to several forms of liver disease including
alcoholic hepatitis,
alcoholic fatty liver disease,
cirrhosis, and
liver cancer. In the earlier stages of alcoholic liver disease,
fat builds up in the liver's cells due to increased
creation of triglycerides and
fatty acids and a decreased ability to
break down fatty acids. Progression of the disease can lead to
liver inflammation from the excess fat in the liver.
Scarring in the liver often occurs as the body attempts to heal, and extensive scarring can lead to the development of cirrhosis in more advanced stages of the disease. Insight into the exact causes and mechanisms mediating pathophysiology of the liver is quickly progressing due to the introduction new technological approaches like
Single cell sequencing and kinome profiling
Air pollutants Particulate matter or carbon black are common pollutants. They have a direct toxic effect on the liver; cause
inflammation of the liver, caused by and thereby impacting lipid metabolism and fatty liver disease; and can translocate from the lungs to the liver. Because particulate matter and carbon black are very diverse and each has different toxicodynamics, the detailed mechanisms of translocation are unclear. Water-soluble fractions of particulate matter are the most important part of translocation to the liver through extrapulmonary circulation. When particulate matter gets into the bloodstream, it combines with immune cells and stimulates innate immune responses.
Pro-inflammatory cytokines are released and cause disease progression. ==Diagnosis==