About propionic acidemia
What is propionic acidemia?
Propionic acidemia is a rare metabolic disorder affecting from 1/20,000 to 1/250,000 individuals in various regions of the world. It is characterized by deficiency of propionyl-CoA carboxylase, an enzyme involved in the breakdown (catabolism) of the chemical “building blocks” (amino acids) of proteins. Symptoms most commonly become apparent during the first weeks of life and may include abnormally diminished muscle tone (hypotonia), poor feeding, vomiting, listlessness (lethargy), dehydration and seizures. Without appropriate treatment, coma and death may result. Rarely, the condition may become apparent later in life and may be associated with less severe symptoms and findings. Propionic acidemia is inherited in an autosomal recessive pattern. Individuals with this condition have to follow a specific diet including a low protein intake and specific food formulas (medical foods). Liver transplant is a surgical option that can help decrease the frequency of acute metabolic episodes (decompensation).
What are the symptoms for propionic acidemia?
Abnormal level of organic acid in blood symptom was found in the propionic acidemia condition
Symptoms most commonly develop during the first weeks of life and may include vomiting, listlessness (lethargy), Low muscle tone (hypotonia), failure to grow and gain weight at the expected rate (failure to thrive), and dehydration. Approximately 30% of affected infants may also develop seizures. The recurrence or worsening of symptoms may be associated with an infection, constipation, or consumption of high amounts of protein. In some affected infants, episodes of symptoms may alternate with periods of apparently normal health and development.
Without appropriate treatment, episodes of vomiting, lethargy, dehydration, and accumulation of excessive levels of acids in the blood and bodily tissues (acidosis) may lead to Coma and death [1-4].
As patients age, they can experience various symptoms affecting nearly all organ systems. These symptoms include brain damage (encephalopathy), hypotonia, intellectual disability, severe vision problems, Inflammation of the pancreas (pancreatitis), recurrent vomiting, chronic renal failure, heart failure (cardiomyopathy), heart rhythm problems (prolonged QTc interval) , and osteoporosis which can lead to fractures. Affected individuals can also have a reduced number of cells in their blood, such as reduced red blood cells (anemia), reduced white blood cells (leukopenia), reduced platelets (thrombocytopenia), or a reduced number of all cell types (pancytopenia). These blood abnormalities can cause various symptoms, such as immune deficiency or bleeding problems. Individuals with propionic acidemia are also at an increased risk of having a Stroke as early as a few weeks of age [4-10].
Less commonly, propionic acidemia may become apparent in childhood or later in life [11-13]. These affected individuals may not experience sudden, acute episodes of acidosis and tend to come to medical attention due to neurological symptoms such as Intellectual disability or cardiomyopathy.
What are the causes for propionic acidemia?
Propionic acidemia is caused by changes (mutations) in the PCCA and PCCB genes resulting in a deficiency of the enzyme propionyl-CoA carboxylase. This enzyme is required for the proper breakdown of the amino acids isoleucine, valine, threonine, and methionine. These amino acids are needed for proper growth and development. Propionyl-CoA carboxylase is also involved in the breakdown of cholesterol, certain fatty acids, and other substances (metabolites) necessary for metabolic actions or processes. Propionyl-CoA carboxylase deficiency leads to accumulation of toxic chemicals (metabolites). Some of these accumulated chemicals harm the mitochondria (power houses inside cells responsible for energy production). [16-20].
Propionic acidemia is inherited in an autosomal recessive pattern.Recessive genetic disorders occur when an individual inherits an abnormal gene from each parent. If an individual receives one normal gene and one abnormal gene for the disease, the person will be a carrier for the disease, but usually will not show symptoms. The risk for two carrier parents to both pass the abnormal gene and, therefore, have an affected child is 25% with each pregnancy. The risk to have a child who is a carrier, like the parents, is 50% with each pregnancy. The chance for a child to receive normal genes from both parents is 25%. The risk is the same for males and females.
What are the treatments for propionic acidemia?
During acute episodes, the treatment of infants with propionic acidemia may require fluid therapy; measures to provide appropriate nutritional intake (e.g., intravenous glucose, with and without intravenous lipids); administration of certain medications to prevent or treat bacterial infection; and other supportive measures as required. In infants with severe disease (e.g., severe acidosis, hyperammonemia), treatment may require procedures that remove excess waste products from the blood (hemodialysis). During hemodialysis, waste products are removed by filtering the blood through an artificial kidney machine. Peritoneal dialysis is a technique during which the peritoneum is used as a natural filtering membrane. (The peritoneum is the two-layered membrane that lines the abdominal wall and covers abdominal organs.). Injection of intravenous bicarbonate can also help reduce the acid load in the body. In addition, until the diagnosis is confirmed, physicians may completely eliminate protein from the newborn’s diet and may also administer biotin, a B complex vitamin that plays a role in the metabolism of certain fatty acids and amino acids.
Liver transplant is a potential surgical option for individuals with severe symptoms and frequent recurrent acute episodes (decompensation). Liver recipients generally have a lower risk of decompensation and hospitalization. However, lifelong immunosuppressive therapy is necessary to prevent organ rejection. All patients with propionic academia must be followed by dieticians with experience in providing care to metabolic patients.
Some children might need to be in special education classes, as intellectual disability is common with propionic academia.
Other treatment is symptomatic and supportive.
Genetic counseling is recommended for affected individuals and their families.
What are the risk factors for propionic acidemia?
Propionic acidemia (PA) is an inherited disorder that unbales a person to digest certain types of protein and fats. Moreover, this condition leads to an abnormal buildup of particular acids known as organic acid since it is regarded as an organic acid disorder. Here are some risk factors associated with Propionic acidemia:
- Inheritance: PA has been inherited in such a pattern that both copies of gene PCCA and PCCB in each cell have the mutation. However, if an infant carries mutated genes from both parents, he/she will be affected.
- Mutation: The changes in the PCCA and PCCB genes result in a deficiency of the enzyme propionyl-CoA carboxylase, which is required to digest fats and protein properly.
- Pregnancy: The mutated genes are carried along with the mother to the children or through the father’s chromosome received by the mother during intercourse. Thus both parents caries the affected genes the child will inherit and be prone to PPA.
- Age: PA can be identified at birth through expanded newborn screening by measuring levels of certain metabolites and blood samples.
Conditions
Abnormal level of organic acid in blood, urine, and tissues
Drugs
Low protein diet,Medical supplements to break down fats and protein chains,Intravenous glucose, with and without intravenous lipids,Liver transplant
Symptoms
Vomiting,Listlessness (lethargy),Low muscle tone (hypotonia),Failure to grow and gain weight at the expected rate (failure to thrive),Dehydration,Seizures
Is there a cure/medications for propionic acidemia?
Propionic acidemia (PA) is an inherited disorder that unbales a person to digest certain types of protein and fats.
- PA doesn’t have a cure because of the deficiency of beta or alpha subunits of mitochondrial enzyme propionyl-CoA carboxylase of PCCA and PCCB gene.
- However, it shows some symptoms like lethargy, vomiting, low muscle growth, and loss of appetite.
Here are some diagnoses and treatments that can lower the risk of propionic acidemia:
- Low-protein diet: The changes in the PCCA and PCCB genes result in a deficiency of the enzyme propionyl-CoA carboxylase, which is required to digest fats and protein properly. Since a low protein diet will help the patient to digest food.
- High calories diet: since the affected individual will find problems in digesting protein, he/she is also required to match daily calorie content for a living.
- Medical supplements: Cobalamine and carnitine are effective medical supplements to boost the body to break long chains of fatty acids and saturated fats.
- Organ transplants: Kidney or liver transplant will help to provide new cells to the human body that will help to break propionic acid.
- Avoid food items that contain complex proteins like isoleucine, threonine, methionine, and valine.
Conditions
Abnormal level of organic acid in blood, urine, and tissues
Drugs
Low protein diet,Medical supplements to break down fats and protein chains,Intravenous glucose, with and without intravenous lipids,Liver transplant
Symptoms
Vomiting,Listlessness (lethargy),Low muscle tone (hypotonia),Failure to grow and gain weight at the expected rate (failure to thrive),Dehydration,Seizures