Katana VentraIP

Pernicious anemia

Pernicious anemia is a disease where not enough red blood cells are produced due to a deficiency of vitamin B12.[5] Those affected often have a gradual onset.[5] The most common initial symptoms are feeling tired and weak.[4] Other symptoms may include shortness of breath, feeling faint, a smooth red tongue, pale skin, chest pain, nausea and vomiting, loss of appetite, heartburn, numbness in the hands and feet, difficulty walking, memory loss, muscle weakness, poor reflexes, blurred vision, clumsiness, depression, and confusion.[4] Without treatment, some of these problems may become permanent.[5]

"Addison's anaemia" redirects here. For the disease affecting the adrenal glands, see Addison's disease.

Pernicious anemia

Vitamin B12 deficiency anemia, Biermer's anemia,[1] Addison's anemia,[2] Addison–Biermer anemia[3]

Feeling tired, shortness of breath, pale skin, numbness in the hands and feet, confusion, poor reflexes[4]

Any age, particularly those over 60 years old[1]

Not enough intrinsic factor[5]

Vitamin B12 injections[7]

With treatment a normal life[5]

1 per 1000 people[8]

Pernicious anemia refers to a type of vitamin B12 deficiency anemia that results from lack of intrinsic factor.[5] Lack of intrinsic factor is most commonly due to an autoimmune attack on the cells that create it in the stomach.[9] It can also occur following the surgical removal of all or part of the stomach or small intestine; from an inherited disorder or illnesses that damage the stomach lining.[9] When suspected, diagnosis is made by blood tests initially a complete blood count, and occasionally, bone marrow tests.[6] Blood tests may show fewer but larger red blood cells, low numbers of young red blood cells, low levels of vitamin B12, and antibodies to intrinsic factor.[6] Diagnosis is not always straightforward and can be challenging.[10]


Because pernicious anemia is due to a lack of intrinsic factor, it is not preventable.[11] Pernicious anemia can be treated with injections of vitamin B12.[7] If the symptoms are serious, frequent injections are typically recommended initially.[7] There are not enough studies that pills are effective in improving or eliminating symptoms.[12] Often, treatment may be needed for life.[13]


Pernicious anemia is the most common cause of clinically evident vitamin B12 deficiency worldwide.[14] Pernicious anemia due to autoimmune problems occurs in about one per 1000 people in the US. Among those over the age of 60, about 2% have the condition.[8] It more commonly affects people of northern European descent.[2] Women are more commonly affected than men.[15] With proper treatment, most people live normal lives.[5] Due to a higher risk of stomach cancer, those with pernicious anemia should be checked regularly for this.[13] The first clear description was by Thomas Addison in 1849.[16][17] The term "pernicious" means "deadly", and this term came into use because, before the availability of treatment, the disease was often fatal.[5][18]

Signs and symptoms[edit]

Pernicious anemia often presents slowly, and can cause harm insidiously and unnoticeably. Untreated, it can lead to neurological complications, and in serious cases, death.[19] The onset may be vague and slow and the condition can be confused with other conditions, and there may be few to many symptoms without anemia.[20] Pernicious anemia may be present without a person experiencing symptoms at first, over time, feeling tired and weak, lightheadedness, dizziness, headaches, rapid or irregular heartbeat, breathlessness, glossitis (a sore red tongue), poor ability to exercise, low blood pressure, cold hands and feet, pale or yellow skin, easy bruising and bleeding, low-grade fevers, tremor, cold sensitivity, chest pain, upset stomach, nausea, loss of appetite, heartburn, weight loss, diarrhea, constipation, severe joint pain, feeling abnormal sensations including tingling or numbness to the fingers and toes (pins and needles), and tinnitus, may occur.[21][22][23][24][25] Anemia may present with a number of further common symptoms,[21][26] including hair thinning and loss, early greying of the hair, mouth ulcers, bleeding gums,[22] angular cheilitis, a look of exhaustion with pale and dehydrated or cracked lips and dark circles around the eyes, as well as brittle nails.[23]


In more severe or prolonged cases of pernicious anemia, nerve cell damage may occur. This is may result in sense loss, difficulty in proprioception, neuropathic pain, difficulty walking, poor balance, loss of sensation in the feet, muscle weakness, blurred vision (either due to retinopathy[27] or optic neuropathy[28]), impaired urination, fertility problems, decreased sense of taste and smell, decreased level of consciousness, changes in reflexes, memory loss, mood swings, depression, irritability, cognitive impairment, confusion, anxiety, clumsiness, psychosis, and, in more severe cases, dementia.[21][22][23][24][25][29][30] Anemia may also lead to cardiac murmurs[24][23] and/or altered blood pressure (low or high). The deficiency may also present with thyroid disorders.[21] In severe cases, the anemia may cause congestive heart failure.[26] A complication of severe chronic PA is subacute combined degeneration of spinal cord, which leads to distal sensory loss (posterior column), absent ankle reflex, increased knee reflex response, and extensor plantar response.[31] Other than anemia, hematological symptoms may include cytopenias, intramedullary hemolysis, and pseudothrombotic microangiopathy.[1] Vitamin B12 deficiency, which is reversible, is occasionally confused with acute myeloid leukemia, which is an irreversible condition presenting with some of the same hematological symptoms, including hypercellular bone marrow with blastic differentiation and hypersegmented neutrophils.[32] Pernicious anemia can cause osteoporosis and may lead to bone fractures.[33] Pernicious anemia can contribute to a delay in physical growth in children, and may also be a cause for delay in puberty for adolescents.[5]

Pathophysiology[edit]

Although the healthy body stores three to five years' worth of B12 in the liver, the usually undetected autoimmune activity in one's gut over a prolonged period of time leads to B12 depletion and the resulting anemia; pernicious anemia refers to one of the hematologic manifestations of chronic auto-immune gastritis, in which the immune system targets the parietal cells of the stomach or intrinsic factor itself, leading to decreased absorption of vitamin B12. The body needs enough intrinsic factor to absorb and reabsorb vitamin B12 from the bile, in which reduces the time needed to develop a deficiency.[49]


B12 is required by enzymes for two reactions: the conversion of methylmalonyl-CoA to succinyl-CoA, and the conversion of homocysteine to methionine. In the latter reaction, the methyl group of levomefolic acid is transferred to homocysteine to produce tetrahydrofolate and methionine. This reaction is catalyzed by the enzyme methionine synthase with B12 as an essential cofactor. During B12 deficiency, this reaction cannot proceed, which leads to the accumulation of levomefolic acid. This accumulation depletes the other types of folate required for purine and thymidylate synthesis, which are required for the synthesis of DNA. Inhibition of DNA replication in maturing red blood cells results in the formation of large, fragile megaloblastic erythrocytes. The neurological aspects of the disease are thought to arise from the accumulation of methylmalonyl- CoA due to the requirement of B12 as a cofactor to the enzyme methylmalonyl-CoA mutase.[50][51][52][53]

Prognosis[edit]

A person with well-treated PA can live a healthy life. Failure to diagnose and treat in time, however, may result in permanent neurological damage, excessive fatigue, depression, memory loss, and other complications. In severe cases, the neurological complications of pernicious anemia can lead to death – hence the name, "pernicious", meaning deadly.


There is an increased risk of gastric cancer in those with pernicious anemia linked to the common feature of atrophic gastritis.[67][68]

Epidemiology[edit]

PA is estimated to affect 0.1% of the general population and 1.9% of those over 60, accounting for 20–50% of B12 deficiency in adults.[1] A review of literature shows that the prevalence of PA is higher in Northern Europe, especially in Scandinavian countries, and among people of African descent, and that increased awareness of the disease and better diagnostic tools might play a role in apparently higher rates of incidence.[69]

Research[edit]

Permeation enhancers[edit]

Treatment using oral drugs is an easier option in management but the bioavailabity of B12 is low. This is due to low absorption in the intestine, and breakdown by enzyme activity. Research continues to focus on the use of permeation enhancers or permeation absorbers in combination with the treatment. One of the better performing enhancers studied is salcoprozate sodium (SNAC).[79][80] SNAC is able to form a noncovalent complex with cobalamin while preserving its chemical integrity and protect B12 from gastric acidity.[81] This complex is much more lipophilic than the water-soluble vitamin B12, so is able to pass through cellular membranes with greater ease. Molecular dynamics are used in experiments to gain an understanding of the molecular interactions involved in the different molecules used and the degree of ease achieved in absorption across the gastric epithelium.[79]

at Curlie

Pernicious anemia