Methotrexate- has any one else noticed a rapid increase in deformed joints since taking methotrexate, six months in and I am noticing my joints are becoming deformed at a rapid rate, is this a side efffect of the drug or am I just getting osteoarthritis at a rapid rate.
Thanks in advance
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Oneta
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Hello Oneta, Sounds more to me that the mtx isn't working as it should. You talked about cutting down your dose recently. Did you have a talk about it with your doc? What dose are you on at the present?
Talk to your rheum team as sounds like your treatment plan might need tweaking. The only times I've picked up erosions has been when I reduced drugs....
Will discuss it with my doctor on my next visit, I like to do lots of research and get a bit informed before I approach a doctor as I feel a bit rushed in a surgery
Hiya Oneta. As MTX is prescribed to help stop joint deformity in the form (very concisely) of reducing the inflammation that causes them to become damaged then no, you shouldn't be noticing any. As long as your dose is correct & your blood tests & examinations (DAS 28 score) show you're controlled then all should be well other than the most common issues such as fatigue.
As it isn't I wonder if you also have OA. MTX will do nothing for OA progression... it would be helpful to know which joints are being so noticeably affected. I have both RD & OA, recently halted my NSAID & my distal interphalangeal (DIP) joints nearest the nail & trapeziometacarpal (basilar joint) at the base of the thumb/wrist are very quickly being affected. I have heberden's nodes on fingers that were spared until halting my NSAID, my thumb, index finger & little fingers had them but now all my fingers are affected. The intention was to wait until my next appointment to review restarting my NSAID but it's clear something has to be done before then, mid Sept.
Don't know if any of this helps or sounds familiar?
Sounds a bit like me; I must agree as I reckon it is OA in my joints, I suppose what surprise is how quickly the joint deforminity is appearing. Six months ago there was nothing now it is progressing rapidly and I wonder why the rapid progression.
Hello Oneta I saw a Rhematologist last September. I was referred to him with ?Sjogren's Syndrome. He took one loook at my hands & told me I had RA. I developed a rheumatoid nodule about a year or so ago & asked the junior doctor about it. She just waffled! I looked at the NRAS website
I found this passage interesting [from my point of view] but it may go some way to answering your question
There is a suggestion that the incidence of rheumatoid nodules is falling (possibly due to the reducing severity of rheumatoid arthritis) but nowadays they are most commonly seen in patients commenced on methotrexate therapy in whom the nodules that develop tend to be small and multiple (micro nodules) most commonly around the finger joints. About 8% of patients on methotrexate develop micro-nodules and we don’t really know why. The image with this article shows a severe case of rheumatoid nodules. Micro-nodules are normally slightly smaller, at around 0.5cm across.
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I should have said I took MTX for 2 years & stopped in 2014. I am taking Pred & have been on that non stop since 2011 or 12, I forget now
Oneta, are you using your joints more because you are generally better when taking Mtx? You do still have to protect those joints even though they're feeling OK. I've had damaged joints over the years even though on Mtx but I'm rubbish at protecting them. When I feel well I just get on a do stuff and b..... the consequences.
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