Takayasus Arteritis
Anyone on this group have Takayasus Arteritis?
I’m just wondering if anyone has become anemic
From this disease
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
Anyone on this group have Takayasus Arteritis?
I’m just wondering if anyone has become anemic
From this disease
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
I have Giant Cell Arteritis, and I was anemic when I was diagnosed. I was retested a couple of months ago after 5 months of treatment, and my numbers all looked good.
Hello @brandyruby1234, I would like to add my welcome along with @jeff97 and others. There are few members who have posted in other discussions on Takayasus Arteritis. Here's a link that shows the discussions and comments - https://connect.mayoclinic.org/search/?search=Takayasus+Arteritis.
While you wait for others to respond, here are a couple of research articles I found if you haven't already seen them.
-- Anemia in patients with Takayasu arteritis: prevalence, clinical features, and treatment:
https://pmc.ncbi.nlm.nih.gov/articles/PMC6790956/
-- Anaemia can be improved by controlling the disease activity of Takayasu's arteritis without iron administration: https://pubmed.ncbi.nlm.nih.gov/36117441/
An interesting side note related to your question - I was watching a video about GCA from 6 years ago, and it mentioned that having anemia at the time of diagnosis for GCA was one of the predictors for relapse, along with fever greater than 38 C and severe inflammation with the biopsy. Things might be different now with the use of the biologic medications.