Hepatitis D

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Hepatitis D
File:Hepatitis-d-virion-Pathogens-04-00046-g001-1024.png
Synonyms Hepatitis delta
Pronounce N/A
Specialty N/A
Symptoms Jaundice, fatigue, abdominal pain, nausea, vomiting
Complications Cirrhosis, liver failure, hepatocellular carcinoma
Onset Typically 2 to 8 weeks after exposure
Duration Acute or chronic
Types N/A
Causes Hepatitis D virus (HDV) infection
Risks Hepatitis B infection, intravenous drug use, unprotected sex
Diagnosis Serology, liver function tests, HDV RNA detection
Differential diagnosis Hepatitis B, Hepatitis C, Hepatitis E
Prevention Hepatitis B vaccination, avoiding risk factors
Treatment Antiviral drugs, interferon therapy, liver transplant
Medication N/A
Prognosis Variable; worse with co-infection or superinfection
Frequency Approximately 15-20 million people worldwide
Deaths N/A


Hepatitis D is a form of hepatitis that only causes symptoms when the individual is already infected with hepatitis B

Other names[edit]

Hepatitis D is also known as “delta hepatitis and is caused by hepatitis D virus.

Summary[edit]

  • Hepatitis D is a liver infection caused by the hepatitis D virus (HDV).
  • Hepatitis D only occurs in people who are also infected with the hepatitis B virus.
  • Hepatitis D is spread when blood or other body fluids from a person infected with the virus enters the body of someone who is not infected. Hepatitis D can be an acute, short-term infection or become a long-term, chronic infection.
  • Hepatitis D can cause severe symptoms and serious illness that can lead to life-long liver damage and even death.
  • People can become infected with both hepatitis B and hepatitis D viruses at the same time (known as ‚Äúcoinfection‚Äù) or get hepatitis D after first being infected with the hepatitis B virus (known as ‚Äúsuperinfection‚Äù).
  • There is no vaccine to prevent hepatitis D.
  • Prevention of hepatitis B with hepatitis B vaccine also protects against future hepatitis D infection.
Hepatitis viruses A,E,B,C,D.
Hepatitis viruses A,E,B,C,D.

Coinfection and superinfection[edit]

  • HBV/HDV coinfection occurs when a person simultaneously becomes infected with both HBV and HDV, whereas HDV superinfection occurs when a person who is already chronically infected with HBV acquires HDV.
  • Although acute HBV/HDV coinfections can resolve, HDV superinfection can lead to rapid progression of the already present HBV infection, resulting in liver cirrhosis and liver failure.
  • These outcomes occur within 5–10 years in 70%–80% and within 1–2 years in 15% of people with chronic HBV/HDV infection.

Incidence[edit]

HDV infection is uncommon in the United States, where most cases occur among people who migrate or travel to the United States from countries with high HDV endemicity. Hepatitis D is most common in Eastern Europe, Southern Europe, the Mediterranean region, the Middle East, West and Central Africa, East Asia, and the Amazon Basin in South America.

Genotypes[edit]

  • Eight different HDV genotypes can be found across the globe, all of which share the same transmission routes and risk groups.
  • HDV genotype 1 circulates mainly in North America, Europe, the Middle East, and North Africa.
  • HDV genotypes 2 and 4 can be found in East Asia; genotype 3 is found exclusively in the Amazon Basin in South America, and
  • HDV genotypes 5, 6, 7, and 8 are found in West and Central Africa.
Histopathology of acute hepatitis
Histopathology of acute hepatitis

Transmission and Exposure[edit]

HDV is mainly transmitted through activities that involve percutaneous (i.e., puncture through the skin) and to a lesser extent through mucosal contact with infectious blood or body fluids (e.g., semen and saliva), including

  • sex with an infected partner;
  • injection-drug use that involves sharing needles, syringes, or drug-preparation equipment;
  • birth to an infected mother (rare);
  • contact with blood from or the open sores of an infected person;
  • needle sticks or exposures to sharp instruments; and
  • sharing items (e.g., razors and toothbrushes) with an infected person.
  • HDV is not spread through food or water, sharing eating utensils, breastfeeding, hugging, kissing, hand holding, coughing, or sneezing.

Risk groups[edit]

The following populations are at increased risk for becoming infected with HDV:

  • People chronically infected with HBV
  • Infants born to mothers infected with HDV
  • Sex partners of persons infected with HDV
  • Men who have sex with men
  • People who inject drugs
  • Household contacts of people with HDV infection
  • Health care and public safety workers at risk for occupational exposure to blood or blood-contaminated body fluids
  • Hemodialysis patients

Signs and Symptoms[edit]

HDV causes infection and clinical illness only in HBV-infected people. These include:

  • Fever
  • Fatigue
  • Loss of appetite
  • Nausea
  • Vomiting
  • Abdominal pain
  • Dark urine
  • Clay-colored bowel movements
  • Joint pain
  • Jaundice

These signs and symptoms typically appear 3–7 weeks after initial infection.

Interface hepatitis -- very high mag
Interface hepatitis -- very high mag

Clinical course and complications[edit]

Chronic HDV generally causes a more aggressive and rapid progression of liver disease than chronic HBV infection alone. This is especially evident in patients infected with genotype HDV-3, which is common in the Amazon Basin Of people with chronic HDV superinfection, cirrhosis and liver failure occur within 5–10 years in 70%–80% and within 1–2 years in 15%. Comparatively, the mean age of onset of cirrhosis for people who acquire chronic hepatitis B in childhood is 40 years.

Diagnosis[edit]

  • Because cases of hepatitis D are not clinically distinguishable from other types of acute viral hepatitis, diagnosis can be confirmed only by testing for the presence of antibodies against HDV and/or HDV RNA.
  • HDV infection should be considered in any person with a positive hepatitis B surface antigen (HBsAg) who has severe symptoms of hepatitis or acute exacerbations.

Treatment[edit]

  • No treatment is available for HDV infection specifically.
  • Pegylated interferon alpha has shown some efficacy, but the sustained virologic response rate (a measure of viral clearance) is low (25%).
  • In cases of fulminant hepatitis and end-stage liver disease, liver transplantation may be considered.

Prevention[edit]

Although no vaccine is available for hepatitis D, vaccination with the hepatitis B vaccine can protect people from HDV infection.