BIG NEWS! Results from the 2014 Dysautonomia International Conference POTS Antibody Study, our very first conference study, have finally published! And what the researchers found is super important to advancing our understanding of autoimmunity in POTS.
It's a very technical journal article, but to summarize the key points...
1. People with POTS tend to have higher than normal levels of norepineprhine (NE) in their blood, which is a catecholamine that activates the sympathetic nervous system. We already knew this from prior research, but what we didn't have clear evidence of until this study is that NE can cause false positives on adrenergic receptor antibody tests. This makes sense, because NE binds to adrenergic receptors, similar to the way an antibody binds to the receptor.
2. Researchers have always assumed that NE degrades quickly if you don't carefully preserve the blood sample. Since the researchers in this study weren't trying to preserve the NE, they initially assumed it would have degraded before they ran their antibody tests. But it didn't degrade and it messed up their first round of antibody tests (which is why it took long to finish this study, because they had to figure out what was messing up the antibody assays, and how to fix the problem). Finding that NE doesn't degrade as quickly in blood samples as previously thought is really important for POTS research, but is also an important finding that will impact research on other diseases too, because NE and its effect on adrenergic receptors is studied in a lot of other diseases: other forms of dysautonomia, heart rhythm disorders, asthma and allergic disorders, anxiety, PTSD, Parkinson's, etc.
3. After the researchers figured out the NE was messing up the antibody results, they had to develop a way to remove NE from the blood/serum samples before running the antibody test without removing antibodies that may be present. They did this by "washing out" the NE with monoamine oxidase, and enzyme that breaks down NE.
4. After they washed out the NE from the blood/serum samples, they found that a majority of POTS patients had antibodies to one or both of the adrenergic receptors they explored in this study (alpha1 and beta1 adrenergic receptors). This is the largest cohort of POTS patients to date that have been tested for these antibodies (37 patients). Prior smaller cohort studies have found these antibodies in a majority of POTS patients too. And if you have been following our page, you know that other antibodies have also been found in a majority of POTS patients, like angiotensin receptor antibodies.
5. Most people with POTS (and people with related disorders like OI, AAG, NCS, etc.) want to know if they have these antibodies, but to date we haven't had a reliable way to test for these antibodies on a large scale, because the testing done in prior research studies was very expensive, time consuming, and labor intensive. For a test to be widely available on a commercial scale, it has to be accurate, economical and not very labor intensive. The new testing approach developed by the University of Oklahoma lays the groundwork for eventually commercializing this antibody assay and making it available to patients around the world. There will be more research required before that happens, but we are on the right path and making good progress in our quest to identify biomarkers in POTS!
You can find the full journal article here:
http://bit.ly/2KFBT9u.
Tremendous thanks to all of the donors and study volunteers who made this possible, and the researchers who worked tirelessly on this project for the past five years! You can help Dysautonomia International advance POTS research even further by making a contribution at CurePOTS.org.