emily – LupusCorner https://lupuscorner.com Health Info on Lupus Symptoms, Treatments & Research Wed, 04 Mar 2020 20:54:09 +0000 en-US hourly 1 https://wordpress.org/?v=6.2.4 https://lupuscorner.com/wp-content/uploads/2019/07/cropped-lupuscorner-new-profLogo-nobg-32x32.png emily – LupusCorner https://lupuscorner.com 32 32 ANA Tests and Lupus https://lupuscorner.com/ana-tests-and-lupus/ https://lupuscorner.com/ana-tests-and-lupus/#comments Mon, 18 Feb 2019 17:40:52 +0000 http://goodlife.fuelthemes.net/fashion-demo/?p=314 The post ANA Tests and Lupus appeared first on LupusCorner.

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ANA tests identify autoantibodies in the body. And, they are one of the tools that clinicians use to help diagnose lupus.

Rheumatologists review laboratory tests, symptom logs, and family history before making a lupus diagnosis. This can be a long and challenging process. ANA tests are a crucial element as they offer insight into the functioning of the immune system by measuring the presence of particular proteins in the blood.

The newest criteria for determining a lupus diagnosis was established by the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR) in 2018. The first requirement of the criteria to be diagnosed is:

  • Positive ANA test with a titer of at least 80

The titer value relates to the ratio of blood serum being tested to a dilution agent. So, a titer of 80 would mean that for every 80 parts of dilution, there was one part of blood serum. The higher the dilution, the more antibodies would need to be in the blood sample to return a positive result for the test.

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What are Antinuclear Antibodies (ANA)?

Before jumping to antinuclear antibodies, we will start with antibodies. Antibodies are proteins made by your immune system that help your body recognize and fight harmful substances, such as bacteria and viruses, by activating the immune system to target them. You can think of antibodies as the soldiers that protect your body from bad, foreign invaders.

Sometimes, antibodies mistakenly attack healthy cells and tissues in the body. This is known as an autoimmune response. Antibodies that target healthy proteins specifically in the nucleus of your cells are called antinuclear antibodies (ANA). To continue the analogy from above, ANAs are rogue soldiers that misidentify the cells they are supposed to ignore, and attack them in error.

 

NOTE: Most people have some ANA, but having too many of these proteins puts you at an increased risk for developing an autoimmune disease, such as lupus.

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Who Gets ANA Tests?

Typically, an ANA test is ordered when someone has symptoms that may indicate a systemic autoimmune disease. Some examples of symptoms that may prompt a doctor to order the test include (but are not limited to):

  • low-grade fevers
  • arthritis-like pain
  • fatigue
  • weakness
  • headaches
  • rashes
  • muscle pain

Even with a positive ANA test result, it is not clear that a person has lupus. A study published in 2003 in the New England Journal of Medicine found that 88% of people (115 out of 130) eventually diagnosed with lupus had received a positive autoantibody lab result multiple years prior to the diagnosis. On average, that positive test result occurred 3.3 years before the diagnosis was confirmed.

Quick Stats on ANA Tests and Lupus

  • 97% of people with lupus will have a positive ANA test.
  • Between 5-20% of the general population will have a positive ANA test. A positive test can be a false-positive, or indicate other conditions, such as thyroid disease, certain liver conditions, or other autoimmune diseases.
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What Should I Know About ANA Tests and Lupus?

  • There is no one definitive test for lupus – an ANA test is just one tool used to help diagnose lupus.
  • The ANA test is not a specific test for lupus. This means that most people with lupus will have a positive ANA test, but not everyone with a positive ANA test has lupus.
  • Some medications can produce a positive ANA test, so be sure to tell your doctor about any prescription or over-the-counter drugs you take.
  • Test results can fluctuate over time and when they are performed at different labs. However, if you have active lupus, your ANA test will probably be positive at most labs, most of the time.

How is an ANA Test Performed?

  • An ANA test is performed in a laboratory, using a sample of your blood.
  • The test shows if your immune system is producing antinuclear antibodies. A positive ANA test means antinuclear antibodies are present.
  • The most common strategies used for detecting and measuring ANAs are indirect immunofluorescence and enzyme-linked immunosorbent assay (ELISA).
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What Should I Do if My ANA Test is Positive?

  • Your doctor will interpret your ANA test in the context of your symptoms, other lab work, and your medical history, including family history. Keeping a symptom journal or using digital tools can help you be better prepared to go over your symptoms with your doctor.
  • Remember, a single positive ANA does not mean you have an autoimmune disease. And a positive ANA test does not require immediate treatment. Your lupus treatment team will take the ANA test results in context with many other factors.

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Cutaneous Lupus Erythematosus (CLE) https://lupuscorner.com/cutaneous-lupus-erythematosus-cle/ https://lupuscorner.com/cutaneous-lupus-erythematosus-cle/#comments Mon, 13 Nov 2017 18:02:05 +0000 https://lupus-appli-1kjf77zfuvjpc-635402343.us-east-1.elb.amazonaws.com/?p=810 The post Cutaneous Lupus Erythematosus (CLE) appeared first on LupusCorner.

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Cutaneous Lupus Erythematosus is a chronic autoimmune disease and one form of lupus.

This form of lupus is limited to the skin. Approximately two-thirds of people with lupus will develop some form of CLE. Skin disease in lupus can cause rashes or sores (lesions). These symptoms typically appear on on sun-exposed areas such as the:

  • face
  • ears
  • neck
  • arms
  • legs
  • hands
Approximately two-thirds of people with lupus will develop some form of CLE

Subtypes of CLE

  1. Chronic Cutaneous Lupus (CCLE)
  2. Subacute Cutaneous Lupus (SCLE)
  3. Acute Cutaneous Lupus (ACLE)

Chronic Cutaneous Lupus (CCLE)/Discoid Lupus (DLE)

The most common form of CCLE is discoid lupus (DLE), which appears as disk-shaped, round lesions that are raised, scaly, and red. Usually they do not itch or hurt. The sores usually appear on the scalp and face but sometimes they will occur on other parts of the body as well. These lesions can produce scarring and skin discoloration (darker and/or lighter colored areas). Discoid lesions that occur on the scalp may cause hair to fall out. If the lesions form scars when they heal, hair loss may be permanent.

Discoid lupus lesions can be very sensitive to light (photosensitive), so it’s important to avoid being outside during peak sunlight hours and make sure you wear sunscreen and protective clothing if you are out in the sun.

Discoid Lupus normally occurs without systemic lupus (SLE). However, some people with SLE do get discoid lesions. About 5% of those with localized DLE (above the neck) and 20% of those with generalized DLE (above and below the neck) can get systemic symptoms.

Lupus Warriors with DLE should be evaluated regularly to make sure that SLE is not developing.

Subacute Cutaneous Lupus (SCLE)

Subacute Cutaneous Lupus lesions may appear as areas of red scaly skin with distinct edges or as red, ring-shaped lesions, most commonly on sun-exposed areas of the arms, shoulders, neck, and body. They usually do not itch or scar, but they can leave the skin discolored. Lesions are also sensitive to light, so preventive measures should be taken when spending time outdoors or under fluorescent lights. SCLE is not often associated with SLE, but it is always important to keep your doctor informed of new symptoms or changes.

Acute Cutaneous Lupus (ACLE)

Acute Cutaneous Lupus lesions occur when SLE is active. The most typical form of acute cutaneous lupus is flat red patches on the face that resemble a sunburn. When the rash appears on both cheeks and across the bridge of the nose in the shape of a butterfly, it is known as the “butterfly rash.” The rash can also appear on arms, legs, and body. Up to 65% of Lupus Warriors experience the butterfly rash.

These lesions tend to be very sensitive to light. The lesions are non-scarring but change in skin color can occur.

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Benlysta (Belimumab) for Lupus (SLE) https://lupuscorner.com/benlysta-belimumab-lupus/ https://lupuscorner.com/benlysta-belimumab-lupus/#comments Mon, 05 Jun 2017 14:56:23 +0000 https://lupus-appli-1kjf77zfuvjpc-635402343.us-east-1.elb.amazonaws.com/?p=1024 The post Benlysta (Belimumab) for Lupus (SLE) appeared first on LupusCorner.

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What is Benlysta (belimumab)?

Benlysta is the first prescription medication designed specifically to treat adults with active Systemic Lupus Erythematosus (SLE). It was approved for the treatment of Lupus by the U.S. Food and Drug Administration (FDA) on March 9, 2011. Benlysta is the first drug approved to treat lupus in over 50 years and is the first ever drug developed specifically for lupus since the disease was discovered! 

 Benlysta…

  • is given to adults with SLE who are receiving other Lupus medicines.
  • works by reducing certain cells in your immune system that can make Lupus active.
  • targets specific immune cells in your body, rather than the blanket approach of other therapies that suppress your entire immune system.
  • is a biological therapy. Biological therapy involves the use of living organisms or substances derived from living organisms to treat disease.
  • is a monoclonal antibody. A monoclonal antibody is a type of protein made in a laboratory that finds and attaches to only one type of substance in the body. It is made to target and destroy only certain cells in the body, which may help protect healthy cells from damage.

Before the development of Benlysta, most treatments (such as steroids, antimalarial medications, immunosupressive drugs, and organ-rejection drugs) were borrowed from treatment for other diseases or conditions.

Type: Biologic infusion

Benlysta is given through IV infusion, meaning it is delivered through a needle placed in a vein by a nurse or health provider. The medicine must be given slowly, so the needle will remain in place for at least 1 hour. Preparation time before the infusion and monitoring time afterwards will vary, depending on what your healthcare professional thinks is best for you.

Your doctor will prescribe a dose and schedule that is appropriate for your Lupus symptoms and your body. The most common schedule is to receive the first three infusions at two week increments, and after that to receive one infusion every four weeks.

Benlysta is a biologic, also known as a biopharmaceutical. These types of medications are synthesized from biological sources and can contain sugars, proteins, nucleic acids, or other living cells.

Take a 2 minute survey and help Lupus Warriors better understand the medications that they are taking!

Need-to-know Benlysta Info

Before you begin taking Benlysta, you should have an open and honest conversation with your doctor about all aspects of your lupus (if you haven’t already!).

It is not known if Benlysta is safe and effective in people with severe active lupus nephritis or severe active central nervous system lupus, and it has not been studied in combination with other biologics or intravenous cyclophosphamide. Use of Benlysta is not recommended in these situations.

Do not receive Benlysta if you are allergic to belimumab or to any of the ingredients in Benlysta.

Women who are pregnant, may become pregnant, or are breastfeeding should not take Benlysta as it’s not known what effect it may have on an unborn baby or on breastmilk.

The Benlysta label information from the FDA is available here.

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Side Effects of Benlysta

Call your doctor right away if you notice any of these side effects:

  • Allergic reaction: Itching or hives, swelling in your face or hands, swelling or tingling in your mouth or throat, chest tightness, trouble breathing
  • Anxiety, depression, thoughts of hurting yourself
  • Change in how much or how often you urinate, bloody or cloudy urine, pain or burning when you urinate
  • Chest pain or trouble breathing
  • Confusion, memory loss, problems with vision, speech, or walking
  • Fever, chills, cough, runny or stuffy nose, sore throat, and body aches
  • Lightheadedness, dizziness, or fainting, severe headache
  • Pain, itching, burning, swelling, bleeding, or a lump under your skin where the needle is placed

If you notice these less serious side effects, talk with your doctor:

  • Diarrhea, nausea
  • Trouble sleeping

If you notice other side effects that you think are caused by this medicine, tell your doctor.

The most commonly reported negative reactions with Benlysta are nausea, diarrhea, fever, inflammation of the nose and throat, bronchitis, insomnia, pain in extremity, depression, and migraine.

The FDA label also notes that there were more deaths reported during the clinical trial of those on Benlysta as compared to the placebo groups. In 3 clinical trials, 14 deaths occurred out of 2,133 people enrolled in the trials. 3 deaths occurred in the placebo groups while 11 occurred in the Benlysta groups (which were subdivided based on amount of medication received).

A full list of known side effects can be found here.

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Starting Benlysta

Benlysta is administered via intravenous infusion only. Additionally, it must be reconstituted and diluted prior to administration. It should not be administered as an IV push or as a bolus.

Benlysta is delivered as a lyophilized powder and needs to be reconstituted, diluted, and administered by a healthcare professional. For those interested, the directions for that process are available on the FDA label.

The dosage schedule for Benlysta traditionally is:

First 3 doses: 10 mg/kg given every 2 weeks

Subsequent doses: 10 mg/kg given ever 4 weeks

All doses should be administered over the course of roughly an hour, though the infusion rate may be slowed or stopped if there are any reactions.

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Drug interactions with Benlysta

A total of 109 drugs are known to interact with methotrexate, including 29 major drug interactions. For a full list that can be easily searched, visit drugs.com

Due to the nature of the medication, the weakened immune system may lead to increased incidence of infection. This also means that many live vaccines have an opportunity to interact with the medication and should be discussed with a doctor. This includes:

  • the flu vaccine (administered via mist or shot)
  • measles vaccine
  • mumps vaccine
  • polio virus vaccine
  • rotavirus vaccine
  • rubella vaccine
  • smallpox vaccine
  • typhoid vaccine

With regard to medications, there are a number of relatively common medications that people with lupus and other autoimmune diseases should be aware of. The following medications are known to interact strongly with Benlysta (tell you doctor if you are taking, or have taken, any of the following):

  • Cimzia (certolizumab)
  • Enbrel (etanercept)
  • Humira (adalimumab)
  • Remicade (infliximab)
  • Renflexis (infliximab)

Cost

Benlysta is an expensive medication and is not always covered by insurance.

GoodRx makes the following price estimate for 400 mg of Benlysta:

1 400mg vial costs $1,707.

Lupus and Benlysta research

Benlysta was developed and researched specifically for people with lupus.

The initial clinical trials were able to pool the data for the trial groups because there were no differences in safety at various dosing strengths. Participants received either Benlysta or a placebo as an addition to their standard care.

The population in the initial trial was:

  • Average age: 39 years old
  • 94% Female
  • 52% Caucasian

93% of people in the Benlysta groups experienced an adverse reaction compared to 92% of people in the placebo group. The most common adverse reaction was a serious infection (6% in the Benlysta group compared to 5.2% in the placebo group).

 

3 clinical trials were used to test for the efficacy of the medication. The first helped researchers define a subpopulation, with a positive autoantibody result for whom the medication could be effective. Future studies limited enrollment to those with positive autoantibody scores and SELENA-SLEDAI scored greater than or equal to 6.

The primary endpoint (necessary measure to equal a successful trial) was a decrease of the SELENA-SLEDAI score of greater than or equal to 4 points. A significantly greater number of people in the Benlysta cohort saw this decrease in disease activity as compared to the placebo group for people taking the 10 mg/kg dose of Benlysta.

There was not a significant difference between the placebo group and the Benlysta cohort at the 76 week mark.

 

Due to lack of diversity and some variable scores, there are still outstanding questions about the efficacy of Benlysta for black or African-American people with lupus. Additional studies are underway to explore any variability in dosing or effectiveness. The FDA label notes that caution should be used when considering Benlysta as a treatment.

Additionally, the researchers noted that taking Benlysta did not significantly reduce a person’s chance of having a severe flare OR enable a person to take significantly less steroids.

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Drug-Induced Lupus Erythematosus (DIL) https://lupuscorner.com/drug-induced-lupus-erythematosus/ https://lupuscorner.com/drug-induced-lupus-erythematosus/#respond Mon, 14 Nov 2016 13:31:39 +0000 https://lupus-appli-1kjf77zfuvjpc-635402343.us-east-1.elb.amazonaws.com/?p=812 The post Drug-Induced Lupus Erythematosus (DIL) appeared first on LupusCorner.

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Lupus symptoms, and a different diagnosis known as drug-induced lupus, may develop as a result of taking certain medications.

Drug-Induced Lupus (DIL or DILE) is an autoimmune disease (similar to systemic lupus erythematosus) caused by long term and chronic use of certain prescription drugs. These drugs cause an autoimmune response. This is when your body’s antibodies attack its own healthy cells and tissue, producing symptoms similar to SLE.

The symptoms of DIL are similar to those of SLE, but it rarely affects major organs.

Of the 38 drugs known to cause DIL, 3 are most commonly connected with it:

  1. Hydralazine
    • Used to treat high blood pressure or hypertension
  2. Procainamide
    • Used to treat irregular heart rhythms
  3. Isoniazid
    • Used to treat tuberculosis

There is no one established method for diagnosing DIL. Symptoms usually overlap with SLE’s symptoms, including:

  • muscle and joint pain
  • swelling
  • fatigue
  • fever
  • inflammation around the lungs or heart that causes pain or discomfort (serositis)

The only way to know for certain that someone has DIL is if symptoms resolve and do not return after stopping the medication. Generally, lupus-like symptoms disappear between a few days to two weeks (sometimes up to six months) after you’ve stopped taking these medications.

DIL is more common in men because men take these drugs more often. Not everyone who takes these drugs will develop DIL.

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Systemic Lupus Erythematosus | Autoimmune Disease https://lupuscorner.com/systemic-lupus-erythematosus/ https://lupuscorner.com/systemic-lupus-erythematosus/#comments Thu, 03 Nov 2016 22:43:34 +0000 http://goodlife.fuelthemes.net/fashion-demo/?p=339 The post Systemic Lupus Erythematosus | Autoimmune Disease appeared first on LupusCorner.

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The most common type of lupus is Systemic Lupus Erythematosus (eh-RITH-eh-muh-TOE-sus)

It is often called SLE, or simply lupus. SLE is a chronic autoimmune disease and can range from mild to severe, with a range of effects on the body. When people talk about lupus, they are usually referring to SLE, but there are other types of lupus: Cutaneous Lupus Erythematosus, Drug-Induced Lupus, and Neonatal Lupus.

What is going on in a body with lupus?

In a properly functioning immune system, the body identifies foreign substances (such as viruses, bacteria, and germs) and creates antibodies to fight them off. With SLE and other autoimmune diseases, a body’s immune system mistakenly attacks healthy tissue, creating autoantibodies. “Auto” means self, so “autoantibodies” means that these antibodies attack the body’s own healthy cells and tissues, breaking them down and causing inflammation, damage, and pain.

SLE is a chronic disease, meaning that symptoms flare up (get worse) and then go into remission (get better). For most people, when symptoms flare up, they tend to last longer than six weeks. But because every person’s SLE is different, is important to know that everyone’s flare ups are different too. Most people with SLE will have periods of time when they feel fine (symptoms may even seem to disappear) and then periods when their disease is more active and symptoms are more severe.

 

The symptoms of lupus

The “systemic” part of Systemic Lupus Erythematosus means that the disease can affect many parts of the body. Although not every symptom needs to be present in order for someone to have SLE. Some of the most common symptoms of SLE are:

    • Extreme fatigue (tiredness)
    • Headaches
    • Joint pain
    • Swelling joints
    • Fever
    • Anemia (low numbers of red blood cells or hemoglobin, or low total blood volume)
    • Pain in chest on deep breathing (pleurisy)
    • Butterfly-shaped rash across cheeks and nose
    • Sun- or light-sensitivity (photosensitivity)
    • Hair loss
    • Blood clotting problems
    • Fingers turning white and/or blue when cold (Raynaud’s phenomenon)

SLE is not preventable with vaccines or curable with medications or treatment. The outlook for each individual depends a lot on the severity of lupus and when they begin to receive care. With increasing research and modern treatments in the last few decades, 80-90% of people with SLE live to the normal life expectancy. Getting appropriate medical care, following treatments and medications as directed, and living a healthy lifestyle are all crucial parts of living well with SLE.

SLE is not contagious or infectious, meaning you cannot “catch it” from someone. It is not a form of cancer and it is not like or related to HIV (Human Immunodeficiency Virus) or AIDS (Acquired Immune Deficiency Syndrome).

Lupus mostly affects women from 15 years old to 44 years old. However, men, children and teenagers can develop it, too. People of all races and ethnic groups can develop lupus, however women of color are 2-3 times more likely to develop SLE than white women.

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