Lactate Dehydrogenase (LDH)
I have my 2nd apt with my MPN specialist tomorrow, I'm hopefully for lower platelets as I'm 47 and my last blood draw was 900, I just noticed my doctor had a 3rd test for tomorrow that I haven't had yet called lactate dehydrogenase (LDH), is this common for ET patients?
Hi Renee I have my LDH each time I have a blood draw. Sitting at 480. Which is high but it is to do with tissue damage with cancer. I have ET
Hello Renee,
I'm not sure how common this test is for ET patients (like me), but my Stanford hematologist orders it every time I see him. As I understand it, LDH can help differentiate between essential thrombocythemia and myelofibrosis.
My original diagnosis was ET but my hematologist at the time never checked my LDH. When I suspected I had progressed to MF, I went to a mpn specialist and she tested my LDH. That was in 2019. My numbers were in the 400’s and she diagnosed me with MF intermediate 1. I am now intermediate 2/high risk and my LDH hovers between 1000 and 1200. I still don’t really understand what it all means. She doesn’t really address it.
Follow Up Tests
LDH Levels
Has Anyone Been Suggested To Try Low Dose Naltrexone To Help Manage ET ? .. My GP Who Is Very Integrative Has Suggested This.