C1 esterase inhibitor test or C1-INH test is one of the tests carried out to check your complement protein levels. The complement system is part of your innate immune system. It consists of a set of nine proteins, numbered C1 through C9.They help your body recognize foreign cells that may cause disease. The C1-INH test can also be used to check causes of unexplained inflammation or swelling, known as edema and deficiency in C1 esterase inhibitor protein. The test includes functional C1 esterase inhibitor, C3 and C4 levels.
You don’t need to take special steps to prepare for a C1-INH test. The doctor should be informed if you are on any medications or have any underlying medical conditions or allergies before undergoing C1 Esterase Inhibitor. Your doctor, depending on your condition, will give specific instructions.
It is performed to confirm Congenital Inflammatory Disorder, Edema and Inflammation and also during treatment and after treatment of Congenital Inflammatory Disorder, Edema and Inflammation. It is also used in diagnosis of hereditary angioedema (HAE). Diagnosis of C1 esterase inhibitor deficiency The C1-INH test assesses you for hereditary angioedema (HAE). The C1-INH test is also used to learn how you’re responding to treatment for autoimmune diseases, such as systemic lupus erythematosus (SLE).
A blood sample is taken. This is most often taken through a vein. The procedure is called a venipuncture. A blood sample of minimum 5mL is required for this test.
Type | Gender | Age-Group | Value |
---|---|---|---|
C1 Esterase Inhibitor
|
Unisex
|
All age groups
|
16 - 33mg/dl
|
Ageing is a natural process, and as much as we don’t like it, it is inevitable. The effect of ageing is different from different organs, and with regard to the brain, dementia is one of the main effects. Dementia is not an isolated condition, but a set of symptoms that includes decreased memory and reduced thinking ability, making it difficult for the person to perform daily activities efficiently. Ageing is one of the main causes of dementia. Dementia is usually progressive, with a person beginning to forget his/her purse, taking pills, etc., and then progressing to forget more important things like close family members’ names or finding one’s way back home.
Though dementia is not reversible, it is possible to control the rate of progression and arrest symptoms if detected in the early stages. There are various reasons for dementia, with senility or ageing being one of the main reasons. Alzheimer’s, vascular dementia, hypothyroidism, depression, etc., are some of the other reasons and treating these can help control the symptoms of dementia. Treatment for dementia would include a combination of medications aimed at treating the underlying reason for dementia and supportive palliative care, which forms a huge component of the treatment, which includes the following:
In addition to the above, supportive palliative care is also very essential. The intention is not to cure, but to improve patient care by including the following:
As dementia is irreversible, the key is to detect the symptoms in their early stages. This will help in effective management by arresting the symptoms from progressing, thereby improving the quality of life. If you wish to discuss any specific problem, you can consult a psychiatrist.
Hereditary Angioedema is a rare skin related disorder and as the name suggests it is also a genetically inherited condition. This condition mainly afflicts the throat, abdomen and the limbs of the patient, with a certain kind of swelling. This swelling can become fatal if not treated on time. Here is everything you need to know about the condition and its treatment.
Causes: A rare genetic mutation of the SERPING1 gene can cause this condition. Usually, this gene is known to produce C1 esterase inhibitor, which is a kind of blood protein. This blood protein is an important element of one’s immune system and is usually involved in the biochemical reactions that control the body’s response to inflammation causing elements. This is done when the blood protein produces a hormone known as Bradykinin. If this blood protein does not function in a normal manner, then there is excessive production of this hormone, which leads to swelling and inflammation.
Type one: There are various types of Hereditary Angioedema that can affect various parts of the body. Type one is one of the most common kinds and can be found on the face, hands, abdomen, throat, as well as feet and genitals of the patient. The severity and frequency of attacks cannot really be predicted and the patient may suffer from attacks throughout his or her life. The best way to treat this type of Hereditary Angioedema is with the help of antihistamine drugs and prednisone which can fight allergic attacks.
Type two: This kind of Hereditary Angioedema has the same symptoms as type one and is caused by a malfunction of the C1 inhibitor, rather than the Bradykinin hormone as one can see in type one. This condition can also be treated with anti-allergy drugs.
Type three: This is very rare kind of Hereditary Angioedema. In fact, medical science is yet to find a conclusive body of knowledge that can point to the exact causes and symptoms of this condition. Coagulation is one of the main causes recognised so far. This condition is much more common in women than it is in men, and it usually shows up as facial swelling.
Timely treatment: While there is no cure for this condition, one can prevent a flare up of the symptoms by taking C1 inhibitors and Bradykinin receptors as well as enzyme inhibitors. It is important to get early treatment for the symptoms and to have constant access to a hospital and its emergency unit. One should also keep track of attacks and symptoms and get regular check-ups done by a doctor to detect the earliest signs of the same to avoid fatalities. If you wish to discuss about any specific problem, you can consult a dermatologist.
Post-traumatic stress disorder or PTSD is a mental health condition, which is usually triggered by an unfortunate event experienced or witnessed by the affected patient in the past. The symptoms of this condition are flashbacks, nightmares and extreme anxiety. The patient also thinks about the event in an uncontrolled manner.
PTSD is a serious mental health condition that can damage the affected person's personality to a great extent. Therefore, the person should be given proper treatment at the earliest. There are various treatment methods for PTSD that can help you in changing how you think about a traumatic event. The treatment options that can be used have been mentioned below:
Counselling:
There are different forms of counselling for treating PTSD which include:
SSRI medicine:
SSRI or Selective Serotonin Reuptake Inhibitor is a form of antidepressant medicine, which helps you with your sadness and tension. There are certain medicines that are really effective and can be prescribed by your doctor depending on the condition.
Other forms of treatment:
There are several other types of medicines and procedures that can be used for treating PTSD. They include the following:
Post-traumatic stress disorder is a serious mental health condition in which a patient suffers from continuous negative thoughts regarding a traumatic event which has happened in the past. This condition may give rise to other health problems, and immediate treatment is recommended. If you wish to discuss about any specific problem, you can consult a psychiatrist.
Allergic reactions are the body’s way of responding to foreign substances. The body recognizes these substances (be it food, pollens, insect bites, etc.) as antigens and produces antibodies. These antibodies can cause various reactions depending on the severity of the allergen, be it skin rash, hives, or angioedema. In severe cases, there could be swelling of the tongue and the respiratory tract, leading to choking of the airways.
Literally, angioedema means swelling of the blood vessels. These are located in the underlying layers of the skin and their swelling can lead to formation of giant hives, which can be extremely itchy, reddish, and oval or circular in shape. The affected area I usually warm and painful to touch.
Causes
Angioedema is caused due to the following:
Food allergies including eggs, peanuts, shellfish, milk, tree nuts, chocolates, etc.
Insect bites or stings
Pollen, latex, animal dander, poison ivy, and other common allergens
Medications like aspirin, penicillin, ibuprofen, and some blood pressure medicines
In response to blood transfusions
Auto-immune disorders like lupus
Conditions like leukemia and thyroid disorders
Infections like hepatitis, cytomegalovirus infections, Epstein-Barr infections, etc.
Weather conditions like extremes of cold, heat, or pressure
Extreme emotional stress
Genetic angioedema, passed on from parents to children, which could last forever
While hives usually develop without any warning, the following condition puts a person at risk of developing angioedema.
Predisposition to allergic reactions (highly active immune system)
Previous history of allergies
Genetic history of allergies or angioedema
Most angioedema cases are limited to the skin and hives, but there could be severe cases leading to respiratory distress.
Diagnosis
If it is the first instance of hives, the doctor would ask detailed questions about similar occurrence in the past. They would also check if there are similar hives on other parts of the body like the back, which you may have missed. If required, this examination is followed by allergy testing and blood testing. The allergy testing will help identify if you are allergic to some of the common things which cause allergy. The blood test will look for your eosinophil count, which is usually high in people prone to allergies. C1 esterase inhibitor test and complement particles also can be checked, if there is suspicion of genetic angioedema.
Treatment
This would depend on the severity of symptoms
Prevention
Once you know what caused it, avoid exposure to these substances and further attacks can be prevented. If you wish to discuss about any specific problem, you can consult a doctor.
Hereditary Angioedema is a rare skin related disorder and as the name suggests it is also a genetically inherited condition. This condition mainly afflicts the throat, abdomen and the limbs of the patient, with a certain kind of swelling. This swelling can become fatal if not treated on time. Here is everything you need to know about the condition and its treatment.
Causes: A rare genetic mutation of the SERPING1 gene can cause this condition. Usually, this gene is known to produce C1 esterase inhibitor, which is a kind of blood protein. This blood protein is an important element of one’s immune system and is usually involved in the biochemical reactions that control the body’s response to inflammation causing elements. This is done when the blood protein produces a hormone known as Bradykinin. If this blood protein does not function in a normal manner, then there is excessive production of this hormone, which leads to swelling and inflammation.
Type One: There are various types of Hereditary Angioedema that can affect various parts of the body. Type one is one of the most common kinds and can be found on the face, hands, abdomen, throat, as well as feet and genitals of the patient. The severity and frequency of attacks cannot really be predicted and the patient may suffer from attacks throughout his or her life. The best way to treat this type of Hereditary Angioedema is with the help of antihistamine drugs and prednisone which can fight allergic attacks.
Type Two: This kind of Hereditary Angioedema has the same symptoms as type one and is caused by a malfunction of the C1 inhibitor, rather than the Bradykinin hormone as one can see in type one. This condition can also be treated with anti-allergy drugs.
Type Three: This is very rare kind of Hereditary Angioedema. In fact, medical science is yet to find a conclusive body of knowledge that can point to the exact causes and symptoms of this condition. Coagulation is one of the main causes recognised so far. This condition is much more common in women than it is in men, and it usually shows up as facial swelling.
Timely Treatment: While there is no cure for this condition, one can prevent a flare up of the symptoms by taking C1 inhibitors and Bradykinin receptors as well as enzyme inhibitors. It is important to get early treatment for the symptoms and to have constant access to a hospital and its emergency unit. One should also keep track of attacks and symptoms and get regular check-ups done by a doctor to detect the earliest signs of the same to avoid fatalities.