Minocin/Minocycline Studies | Arthritis Information

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Since Lev opened the door...lol...and Reader wanted some also...here is the first foray into the Minocin Studies I have.  This is the correct versions to the NLM and PubMed versions of what is on the Roadback.  If a link doesn't work, let me know and I'll repost the correct one. 

 
I also have a ton of other studies I'll post as time goes on as you all know I'm redoing my filing cabinet.  I tend to file them by disease or body part studied.  For example, I have a study on how Mino stops joint damage and how doxy (earlier generation tetracycline) works in OA.  Also mino in eye disease etc.  Basically, if it effects us somehow, I saved it.  If it even could possibly effect us...I saved it.  I now have over 1000 studies alone related to our disease and how the cells work in relation to our disease.
 
This will start us for tonight.  Then every day I'll post another few. 
 
Pip
 
1. http://www.annals.org/cgi/content/full/122/2/81
Tilley MIRA 48 wks minocycline vs placebo, 1995

2. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10446869&dopt=Abstract
O’Dell 4 year Minocycline vs placebo, early-onset RA, 1999

3. http://www.rheumatology.org/public/factsheets/minocycline.asp
ACR on Minocycline, updated 2006; “Minocycline is prescribed for patients with symptoms of mild rheumatoid arthritis, sometimes in combination with other medications to treat patients with persistent symptoms of this form of arthritis.”

4. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16447240&dopt=Abstract
Doxycycline + MTX vs MTX alone, no previous DMARD, <1 year with RA, 2006

5. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11273473&dopt=Abstract
India study, 6 months, Doxycycline vs MTX 6 months, 2000

6.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11665963&dopt=Abstract
Minocycline vs Plaquenil O’Dell 2001

7. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9592865&dopt=Abstract
Chinese, Minocycline + unspecified DMARD, DMARD resistant before study, 1998

8.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=10047718&dopt=Abstract
Japanese study, DMARD resistant, 6 mos, 1 yr, minocycline only, 1998

9.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1334514&dopt=Abstract
Israeli study, DMARD resistant, 48 weeks, minocycline only. Limited data, 1992

10. http://www.jrheum.com/abstracts/abstracts06/224.html
London study. Tetracycline plus clindamycin vs no treatment, 1 year, DMARD resistant, 2006

 
So, Lev, keep your pants on - I'll get to the current studies - I have only 500 of those.
 
Pip
Thanks, Pip. I was irritated Lev was demanding studies , which he won't read yet again, and if he did read might not understand, since links to these studies have been posted on AI ad naseum, but I was going to do it anyway for reader, so I did, but you have way good piles of studies and a fresh, dedictaed thread was a great idea.

Rock on.

Hope these help you, reader!

If you have irritation Gimpy, they have medicines for that. I'm patient, I'm waiting for those multiple clinical trials. I'm glad that yous are going to post some clinical trials with-in the past few years because these that you posted aren't worth but a couple of bottles of ibuprophin. Looking forward to some better information. Please post some clinical trials that compare AP to biologics rather than to mtx or plaquinal and post clinical trials that address bone and joint damage prevention, you know whether AP prevents damage as does the biologics and dmards. Thanks in advance. There has to be standard clinical trials, right?

LEV

First - the neurodegenerative studies I offered to get for a different thread.
 
Mino in neurodegenative diseases -
 
http://www.jleukbio.org/cgi/content/abstract/78/1/135
 
Mino to be studied in MS - newspaper report - not a study.
 
http://www.canada.com/vancouversun/news/story.html?id=0ff4e564-96bd-4915-8438-e6cf7734a2f2&k=77334
 
Mino in neurology -
 
http://www.thelancet.com/journals/laneur/article/PIIS1474442204009378/abstract
 
Mino in stroke -
 
http://www.medscape.com/viewarticle/563619
 
Thats it for today - 4.
 
Lev - thank you for your patience.
 
Pip
 
 
Pip,
 
I'm patient but c'mon, lets get to the meat and potatoes. It seems that those multiple clinical trials would be at the top of the lists. It's well and good that minocin is being studied for other diseases just as the new biologics have been tested and proven through federal clinical trials and being used for so many other diseases besides RHEUMATOID ARTHRITIS and are in gov't approved clinical trials for many others. When I asked that you start a thread and post the multiple clinical trials I asked that you call the thread Minocin trials for RHEUMATOID ARTHRITIS. That way we wouldn't have to go thru all the gobblty-goop and save you all the time and energy posting about what hasn't been asked for rather than just posting the multiple clinical trials. How long do you think that it will take you to finally get to the multiple clinical trials. Certainly you aren't going to waste web space on 400 studies not concerned with the multiple clinical trials are you? I don't mind you taking the time needed but it seems like you are stalling or beating around the bush posting about minocin for other diseases when you could be posting what yous claim. Are you just building us up for the big moment when you post the multiple clinical trials? If you don't have them, just say you don't have them. If you have them, just post them.
 
LEV
Lev -
 
Just shut up and read.  If you're going to allow that biologics have been approved for other diseases than RA - then of course you want the 'equal time' for Mino.  And frankly, this is more for the people that asked for this info than for you.  I doubt you even read these. 
 
And no - it's not just clinical trials - it's studies in peer reviewed journals.  If its not a study then I clearly mark it so.  I do not use 'press releases' as most are hogwash. 
 
Finally, how many times have I mentioned that I'm redoing my filing system and going over to a new one?  That involves a lot of work moving one study/article to another and making them capatible as well as re-titling them so I can find them much more easily.  As we have seen, I'm only in December of my online subscriptions - this is really taking a bite out of my day - so, by basic logic - one would assume I'm only in December of my filing system.  And that's only the 'new' material.  I have 2 years and over 12000 emails I saved to hard drive involving studies. 
 
Therefore, take your backside over to the Chicken Lev thread and await my slam that I will post as soon as I deal with the 'real people'.  This thread is not for debate; it's for info and you will not be answered if you are hostile.  Debate/arguing will remain on the Chicken Lev thread.
 
Pip
They are clinical trials. And there are multiple ones of them.Hey,
 
Okay, don't get mad because I'm asking for just the facts, mam, just the facts. The truth, the whole truth and nothing but the truth. But if you say that the reason you can't post the clinical trials is because your filing system is being re-organized, I am going to certainly give you the benifit of the doubt and will just wait for you to find the multiple clinical trials. I just thought you were beating around the bush rather than admitting you had no multiple clinical trials. But now that I know that they are just lost in your files, I will continue to wait knowing that you have them and that they are just somewhere in your 12000 emails. Thanks again in advance for the multiple clinical trials.
 
LEV
levlarry2008-09-17 10:48:18So anyway Pip and Gimpy,
 
You actualy posted a study from this decade, one study from this decade. And here is the conclusion:
 
CONCLUSION: In patients with early seropositive RA, initial therapy with MTX plus doxycycline was superior (based on an ACR50 response) to treatment with MTX alone. The therapeutic responses to low-dose and high-dose doxycycline were similar, suggesting that the antimetalloproteinase effects were more important than the antibacterial effects. Further studies to evaluate the mechanism of action of tetracyclines in RA are indicated.
Even without a study I can honestly say that Methotreaxate along with Advil is more affective than Methotrexate alone. This isn't even a good study.
 
LEV
Mino + calcium as a neuroprotective
 
http://www.ncbi.nlm.nih.gov/pubmed/15964487?ordinalpos=37&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum
 
Neuro mechanism identified - may explain why men usually respond quicker to AP than women - 
 
http://www.whatsnextnetwork.com/health/index.php/2006/06/22/p3182#more3182
 
That's it for today -
 
Pip
Well Pip and Gimpy,
 
Just as I figured, no multiple clinical trials. What's wrong with just being honest? Now quit telling everyone that there are multiple clinical trials, you can't post them here so quit saying it. It's just that simple.
 
LEV
Are you in denial? Or does the phrase "multiple clinical trials" mean something different to you than it does to most people?

There are multiple clinical trials showing the efficacy of minocycline and doxycycline on rheumatoid arthritis linked on the first post of this thread.Gimpy, post them in there entirety along with the dates, what's so hard about it? Your smoke and mirrors are harder than that. Why are yous beating around the bushes? Are the studies that you are trying to pass off as clinical trials those that are dated from the 1990's? Yes or no. Yes or no, Gimpy?
 
LEV
??????

Why? Do the links not work for you? THEY'RE THERE. Is the idea you need people working around the clock posting stuff for you in response to your anger? You're just trying to start and prolong another senseless argument to get attention.


The links are there. The links work. The links take you to pages showing the full studies, the dates, the people who worked on them. They are published in publications such as the "American College of Rheumatology".

So what if some were done in the '90's? Are they supposed to do them again to get the same results in the '00's? That doesn't even make any sense. People do studies, collect the data and use it. they don't repeat them over and over. You obviously have never done even cursory medical research or you would know that.

Yes Larry, even though no one has posted several pages of studies for you because you don't know how to use a link, there are multiple clinical trials showing AP works.

And what do you care anyway? You don't want to do AP? Don't. No one cares.Yous are pathetic.
 
If I had a miracle cure for arthritis that all of the world has been trying to keep from the world, I would shout it from the mountain tops. I would post it in it's entirity right here. Right here, got it? Shame on yous. Absolutely shame on yous. Why are you so shamed of your studies that you refuse to post them in their entirety? I have given you such a wonderful opportunity for yous to show everyone here at this rheumatoid arthritis forum the clinical trials to prove that what yous have been spewing is good medical fact and yet given such a glorious opportunity, yous spend all of your time runninfg around bushes. Yous are pathetic for abusing those of us with ra with untruths about cures. Shame on yous.
 
LEV
So first they don't exist, then they do exist bu they're too old, and now they do exist, they're not oo old, but they're not a cure.

To quote Lynne49:

Whatever.LevLarry's "arguments" reminded me of an incident I think would be worthwhile to add to this thread, for people who don't understand the adverse medical politics surrounding AP, and why gathering inofmration on the therapy is slow (but still going on, and not just for RA). Here is an article outlining an incident which occurred a few years ago:



Drug Company Denies Harvard Rheumatoid Arthritis Researcher


By Alice Dembner

Dr. David Trentham is the chairman of the Department of Rheumatology at Harvard. He has used the antibiotic Minocin for successfully for many with rheumatoid arthritis and scleroderma. He decided to study the drug in those ages 6 to 14 and asked drug maker Wyeth for a donation of ,000 worth of the antibiotic. Wyeth, which made billion last year in total sales of drugs and other products, had acquired a small company that supported Trentham's previous studies of minocycline in animals and in adults. But this time, the answer was an unequivocal no.

''While scientifically interesting, the concept and design is not consistent with our current business objectives,'' wrote a company official in a letter that Trentham said stunned him.

While company officials later said patient safety was the reason for the denial - the antibiotic can cause some side effects, such as discoloration of the teeth - Trentham believes the letter gave far more insight into the company's reasoning.

Trentham's translation of the letter: If minocyline worked, it might compete with a blockbuster drug called Enbrel that Wyeth now markets for both adult and juvenile rheumatoid arthritis. Enbrel costs ,300 per month for adults and has life-threatening side effects, while Wyeth's brand of minocycline, called Minocin, costs only 0 for an adult monthly dose, Trentham said. And unlike Enbrel, minocycline is no longer under patent, so many companies could benefit from the drug's success.

As rheumatologist Trentham put it, ''It's a commercial decision, and it's unfortunate for the patients.''

Trentham said it was the first time in his career that a drug company had turned down his request for support of a study. But other researchers said denials are becoming more common as the drug market becomes ever more competitive.

''It happens all the time,'' said Dr. Raymond Woosley, a prominent drug researcher who is vice president of health sciences at the University of Arizona. ''They don't want you to study their drug because of what you might find or how your finding might affect another drug they're marketing. They want to control the data on their drug.''

While companies have no legal obligation to support research by doctors who don't work for them, many scientists believe they have a moral responsibility to society.

''When a company refuses to allow someone to do legitimate research on their drugs, we all lose out,'' said Sheldon Krimsky, a Tufts University professor who has studied relationships between academic researchers and drug companies. ''Their interest is in their market share, not in public well-being.''

A spokeswoman for Wyeth, however, said economics played no role in the company's decision. ''The decision was made primarily on safety,'' said Natalie de Vane. ''The company felt there were newer medications that could be studied that didn't have the side effects that this particular drug has. Minocin is contraindicated in young children and there were very young children in this proposal.''

While minocycline carries an FDA warning against use in children under 8 because of possible permanent discoloration of teeth, Trentham said that is a far cry from the warning on Enbrel, of serious and sometimes fatal infection or sepsis. Nonetheless, Enbrel was approved by the FDA in 1999 for use in juvenile rheumatoid arthritis for those patients who fail other treatments.

Despite the rejection by Wyeth, Trentham is forging ahead. He secured a ,000 grant from a small private foundation, the Road Back Foundation, to fund lab fees for the six-month study and will buy Minocin from Wyeth, and then charge study participants or their insurers for the drug. But he said he worries that that will make it much harder to recruit participants and will delay the study, now scheduled to begin this summer. He plans to recruit patients across the country who are not currently taking Enbrel or another treatment, methotrexate.

''It's terribly important to get to the bottom of whether Minocin works in children with juvenile rheumatoid arthritis because of the benign nature of Minocin,'' said Trentham, who is known as an antibiotic enthusiast.

Juvenile rheumatoid arthritis affects up to 50,000 children in the United States, causing painful swelling, stiffness and deformity of joints and sometimes stunting growth. While some children outgrow it, others fight the disease their whole lives. Doctors believe it is caused by a malfunction of the immune system and typically treat children with anti-inflammatory drugs starting with ibuprofen and moving to more potent drugs.

If minocycline works consistently in children, Trentham said, it would also be a safer alternative to two other common treatments for JRA - steroids and methotrexate. Steroids can stunt a child's growth, and methotrexate, often used to treat cancer, can be toxic to the liver and it can harm the immune system when given in higher doses than usually given in children.

Some pediatric rheumatologists said, however, that methotrexate is not as risky and minocycline is not as safe for children as Trentham suggests. A cousin of tetracycline, it commonly is used to treat severe acne. But it can discolor teeth and skin, irritate the stomach, and, in rare instances, it can cause liver or kidney damage and has been associated with lupus.

''We're able to control a large number of our patients with currently available drugs,'' said Edward Giannini of Cincinnati Children's Hospital, a senior scientist with an international consortium that studies pediatric rheumatology treatments and helped test Enbrel and methotrexate. ''I don't see much of a need to look at this drug, because we feel it's only partly effective in adults. But there's no harm in studying it.''

Concern about side effects of methotrexate led Melanie Masala to bring her daughter, Gloria, to Boston for treatment with minocycline. ''I was wondering which was worse, the disease or the cure,'' she said.

With minocycline, Marsala said, Gloria's transformation was ''incredible.'' As Gloria said: ''Before, not many people liked to play with me because I couldn't do the things they wanted to do. Now, I ride my bike, I rollerskate, I can jump, I can even climb a little.'' And Trentham said she is growing again, catching up to her classmates, without any medication side effects.

Scientists do not understand why minocycline appears to help some arthritis patients. A national study of 219 adults with rheumatoid arthritis, supported by the National Institutes of Health and published in 1995, found, however, that minocycline significantly reduced joint swelling and tenderness in more than half of patients, although a dummy pill caused similar improvement in about 40 percent. Lederle Laboratories, which then made Minocin, provided the drug and placebo free for the study. Wyeth subsequently bought Lederle and helped market Enbrel, which chalked up 0 million in sales last year.

Trentham, who was one of several investigators for the NIH study, chose to use Minocin for his new study for consistency, rather than other generic versions of the antibiotic made by other drug companies.

Getting free drugs for research is ''especially a problem when the company has a competing drug,'' said Woosley, a professor of pharmacology and medicine. He and colleagues were thwarted a few years ago, he said, when they wanted to study the side effects of an older synthetic estrogen replacement. The company, which he declined to name, refused because officials were worried the study would focus attention on the side effects of a new drug they were developing.

''From a business point of view, it makes sense. Why should they get involved in anything that might harm them?'' said a Boston-area researcher, who requested anonymity because he feared alienating companies from which he regularly seeks support. ''But the research community is trying to find out the truth, about mechanisms and side effects of drugs and how they are best used clinically. And the drug companies' posture impedes that. It's gotten worse year by year and the last two years have been impossible.''

Boston Globe June 25, 2002


Gimpy,
 
Isn't it shameful that you post smack against wyeth and yet you don't mention that previously wyeth did donate big money for minocin or roadback and what they did was use a large part of the money to fund that phoney Harris Poll that yous and they tried to pass off as medical fact when in fact it was actually a paid off marketing group using people for the fake study supllied by those that paid for the study, roadback. If you want, I will post the garbage poll and rub your nose in it. You and pip used to constantly refer to the  Harris study ubtil I showed everyone that it was a paid marketing study, certainly nothing near medical fact. Wyeth previously donated monies and are and were certainly under no obligation to do so and all the people that benifited from the money did was bad mouth wyeth just like you are still doing. Can't you at least say thanks before you trash them? I love this part of your post:
[BEGIN QUOTE]Trentham's translation of the letter: If minocyline worked, it might compete with a blockbuster drug called Enbrel that Wyeth now markets for both adult and juvenile rheumatoid arthritis. Enbrel costs ,300 per month for adults and has life-threatening side effects, while Wyeth's brand of minocycline, called Minocin, costs only 0 for an adult monthly dose, Trentham said. And unlike Enbrel, minocycline is no longer under patent, so many companies could benefit from the drug's success.[END] His translation is of course more honest then the words sent, right? Isn't Trentham associated with roadback? Why shouldn't roadback do the funding? Isn't Trentham a professor at Harvard? Seems to me that if he had good medical proof it would be easy to get funding, seems even from Harvard. Such a miracle drug should easily be funded. Are they planning on hiring the Harris group again? It's pretty wild that you can post this great big garbage can of garbage but you can't bring yourself to post one clinical trial in it's entirety. That speaks volumes of your honesty. C'mon, post just the best one in it's entirety for stoopid people like me that can't click on a link, duh. Okay, I'll beg, please post just the best clinical trial of the multiple clinical trials in it's entirety, please? Do you want me to start posting them along with the date? I can do that even in my stoopidity, duh.

LEV


Oh yeah Gimpy,
 
I like the part where Trentham say "if it works". Maybe you and Pip should send him all of your clinical trials.
 
LEV
Larry is right. So why don't you try something new. MTX always works better with an additional DMRAD even the mild ones (like mino, like azulafdine). Why aren't you still posting the study with doxy or mino against MTX where is doesn't mention the MTX dose and I think it was 25 people.

Since AP has been around since at least the 40's, if it really worked don't you think doctors would be prescribing it? All my doctors knew all about it but only recommend it for mild RA. Do you really think 90% of doctors don't recommend it for most situations because they are all paid by the drug companies. Really? How come most of the very few AP doctors now recommend Enbrel too.

What amazes me is how scared the people are where AP failed to acknowledged in a public forum. They are afraid of attacks because of the cult like behavior. There are three here I that I know of, how many more? Its like the "tapers off MTX" that never happen.From the American College of Rheumatology:
 
http://www.rheumatology.org/search/search.asp?templ=home&aud=home
 
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13 total documents matching the search string "minocin"
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1)   Patient Education - Minocycline
  ACR. MINOCYCLINE (Minocin). Description. Side Effects. Uses. Points to remember. How it works. Drug interactions. Dosing. For More Information. Time to effect. Minocycline (Minocin) is a member of the tetracycline group of antibiotics. Although rheumatoid arthritis is not an infection, minocycline may improve

size 13.1 KB - Tuesday, May 20, 2008 at 11:04:44 PM GMT
 
2)   Patient Education - Minocycline
  ACR. MINOCYCLINE (Minocin). Description. Minocycline (Minocin) is a member of the tetracycline group of antibiotics. Although rheumatoid arthritis is not an infection, minocycline may improve the signs and symptoms of this disease. There is evidence minocycline may slow the progression of joint damage in arthritis

size 13.3 KB - Monday, September 29, 2008 at 2:55:47 PM GMT
 
3)   Patient Education
  ACR. Patient Education. The ACR and ARHP have prepared information for patients about. 28 rheumatic diseases. about the caregivers who treat patients with arthritis, and about several. common medications. used to treat rheumatic diseases.. Disease-Specific Information:. Listed below are some of

size 17.6 KB - Monday, August 18, 2008 at 3:06:21 PM GMT
 
4)   Patient Education
  ACR. Patient Education. The ACR and ARHP have prepared information for patients about. 28 rheumatic diseases. about the caregivers who treat patients with arthritis, and about several. common medications. used to treat rheumatic diseases.. Disease-Specific Information:. Listed below are some of

size 17.6 KB - Monday, September 29, 2008 at 2:55:46 PM GMT
 
5)   Patient Education - Medications
  ACR. Patient Education - Medications. The ACR and ARHP have prepared information for patients about. 28 rheumatic diseases. about the. caregivers. who treat patients with arthritis, and about several common medications. used to treat rheumatic diseases.. Information About Medications. This new information for

size 18.7 KB - Monday, September 29, 2008 at 2:55:49 PM GMT
 
6)   Patient Education - Medications
  ACR. Patient Education - Medications. The ACR and ARHP have prepared information for patients about. 30 rheumatic diseases and 12 rheumatic conditions. about the. caregivers. who treat patients with arthritis, and about several common medications. used to treat rheumatic diseases.. Information About Medications.

size 18.9 KB - Monday, September 29, 2008 at 2:55:47 PM GMT
 
7)   Patient Education - Rheumatoid Arthritis
  ACR. RHEUMATOID ARTHRITIS. For Español. click here. The outlook has dramatically improved for many people newly diagnosed with rheumatoid arthritis (RA) long feared as one of the most disabling types of arthritis. RA remains a serious disease, and one that can vary widely in symptoms and outcomes. Eve

size 24.1 KB - Thursday, May 22, 2008 at 2:49:33 AM GMT
 
8)   Patient Education - Rheumatoid Arthritis
  ACR. RHEUMATOID ARTHRITIS. For Español. click here. While rheumatoid arthritis (RA) has long been feared as one of the most disabling types of arthritis, the outlook has dramatically improved for many newly diagnosed patients. Certainly RA remains a serious disease, and one that can vary widely in sym

size 23.2 KB - Friday, August 15, 2008 at 2:16:37 PM GMT
 
9)   Patient Education - Rheumatoid Arthritis
  ACR. RHEUMATOID ARTHRITIS. For Español. click here. The outlook has dramatically improved for many people newly diagnosed with rheumatoid arthritis (RA) long feared as one of the most disabling types of arthritis. RA remains a serious disease, and one that can vary widely in symptoms and outcomes. Eve

size 24.1 KB - Monday, September 29, 2008 at 2:55:49 PM GMT
 
10)   Patient Education - Rheumatoid Arthritis
  ACR. RHEUMATOID ARTHRITIS. For Español. click here. The outlook has dramatically improved for many people newly diagnosed with rheumatoid arthritis (RA) long feared as one of the most disabling types of arthritis. RA remains a serious disease, and one that can vary widely in symptoms and outcomes. Eve

size 24.1 KB - Monday, September 29, 2008 at 2:55:49 PM GMT
 
11)   Patient Education - Rheumatoid Arthritis
  ACR. RHEUMATOID ARTHRITIS. Para Español. haga clic aquí. While rheumatoid arthritis (RA) has long been feared as one of the most disabling types of arthritis, the outlook has dramatically improved for many newly diagnosed patients. Certainly RA remains a serious disease, and one that can vary widely in sym

size 28 KB - Friday, October 10, 2008 at 3:46:21 PM GMT
 
12)   Educación al Paciente - artritis reumatoidea
  ACR, artritis reumatoidea. ARTRITIS REUMATOIDEA. El panorama ha mejorado drásticamente para muchas personas a quienes recientemente se les diagnosticó artritis reumatoidea (AR) una afección temida, durante mucho tiempo, por ser uno de los tipos de artritis más incapacitantes. La artritis reumatoide

size 26 KB - Thursday, May 22, 2008 at 4:52:36 PM GMT
 
13)   Educación al Paciente - artritis reumatoidea
  ACR, artritis reumatoidea. ARTRITIS REUMATOIDEA. El panorama ha mejorado drásticamente para muchas personas a quienes recientemente se les diagnosticó artritis reumatoidea (AR) una afección temida, durante mucho tiempo, por ser uno de los tipos de artritis más incapacitantes. La artritis reumatoide

size 27.9 KB - Monday, September 29, 2008 at 2:55:44 PM GMT
 
justsaynoemore2008-10-13 17:46:35Part II, from the American College of Rheumatology:
 
http://www.rheumatology.org/public/factsheets_original/minocycline.asp
 

MINOCYCLINE (Minocin)

+ Description + Side Effects
+ Uses + Points to remember
+ How it works + Drug interactions
+ Dosing + For More Information
+ Time to effect  

Description

Minocycline (Minocin) is a member of the tetracycline group of antibiotics. Although rheumatoid arthritis is not an infection, minocycline may improve the signs and symptoms of this disease. There is evidence minocycline may slow the progression of joint damage in arthritis and prevent disability like other drugs in the class known as DMARDs (disease-modifying antirheumatic drugs).

Uses

Minocycline is prescribed for patients with symptoms of mild rheumatoid arthritis, sometimes in combination with other medications to treat patients with persistent symptoms of this form of arthritis.   (Persistent symptoms of RA?  Doesn't that mean EVERY person with RA could be treated with minocin, along with other DMARDS?) JSNM

How it works

Minocycline is an antibiotic, which means it helps neutralize or kill bacteria that cause infections. When used to treat rheumatoid arthritis, however, minocycline works through a different mechanism to control inflammation. Minocycline decreases the production of substances causing inflammation, such as prostaglandins and leukotrienes, while increasing production of interleukin-10, a substance that reduces inflammation.

Dosing

Minocycline usually is given as a 100 milligram (mg) capsule twice a day. It may be taken with food, although it should not be taken with other medications such as antacids or iron tablets.

Time to effect

It may take 2 to 3 months before any improvement in arthritis symptoms is experienced and up to a year before maximum benefits are realized.

Side Effects

The most common side effects from this medicine are gastrointestinal symptoms, dizziness and skin rash. Patients who take this medication for a long time may notice changes in their skin color, but this usually resolves after stopping the medication.

Some women who take minocycline develop vaginal yeast infections. While this can occur with other antibiotics, it seems more prevalent with minocycline and other tetracyclines. It is thought minocycline kills bacteria normally present in the body which protect against yeast infections.

Minocycline may increase sensitivity to sunlight, resulting in more frequent sunburns or the development of rashes following sun exposure. It is recommended patients apply sunscreen (SPF 15 or greater) before outdoor activities or avoid prolonged exposure to the sun while taking minocycline.

More rarely, minocycline can affect the kidneys or liver. Doctors may recommend periodic blood tests for long-term users to check liver and kidney function. In equally rare cases, minocycline can induce lupus, but this condition usually improves after stopping the medication.

Points to remember

Before taking minocycline, tell your doctor if you have ever had any unusual or allergic reaction to any other tetracycline antibiotic.

Minocyline use during pregnancy can slow the growth of teeth or bones in infants after birth as well as cause discoloration of the newborn’s teeth when taken during the last half of pregnancy. Because minocycline may decrease the effectiveness of some birth control pills, talk with your doctor about other contraception options while taking minocycline.

Minocycline is passed into breast milk, so mothers should avoid breast-feeding to prevent delayed development of teeth and bones in their infants. Minocycline can increase a nursing infant’s risk of fungal infections or dizziness in the newborn. Because minocycline may cause discoloration of teeth and problems with bone growth in young children, it is recommended that those younger than 8 years old not take this medication. This is not a problem in older children and adults.

Drug interactions

Be sure to tell your doctor about all of the medications you are taking, including over-the-counter drugs and natural remedies. Possible interactions with minocycline may occur when taking warfarin (Coumadin), antacids containing calcium, aluminum or magnesium (such as Tums, Rolaids, Maalox, or Mylanta), iron tablets and oral contraceptives (birth control pills).

For more information

The American College of Rheumatology has compiled this list to give you a starting point for your own additional research. The ACR does not endorse or maintain these Web sites, and is not responsible for any information or claims provided on them. It is always best to talk with your rheumatologist for more information and before making any decisions about your care.

National Institutes of Health Medline Plus link

http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a682101.html

Updated June 2006.

justsaynoemore2008-10-13 17:53:27So, the American College of Rheumatology is lying?  If we cannot trust them, who do we turn for advice about rheumatoid arthritis?Yes. What's astounding is how vitriolic people get over this therapy with relatively benign side-effects. If they don't want to use it that's their choice, but why do they get their shorts in a knot that other people use it?

As to how long it takes to taper off MTX, that's a go nowhere argument. It takes as long as it takes. Every time I decrease my MTX it takes a long time to stabalise, but the fact is I have gone from 20mg to 7.5 with no detectable damage and a lot of painfree days. I lived this summer for 4 months in a camper van. I ran, I swam, I biked around. I can do everything I could do before RA.

I could probably go completely off MTX all at once, but why should I have a serious herx if I don't have to, just to prove something to some ignorant bozos, or these fine forum mates here?

My Rheumatologist and I are happy with the results of my drug therapy. No one elses opinion really matters.

It is unfortunate, and cruel, that some would try to steer RA sufferers away from this viable therapy, but anyone who knows the history of AP knows that's nothing new, and they will have to answer to thier own conscience, or maker, if that's what they believe.

If anyopne is really interested in the questions they asked, all the answers can be found in a book called "Why Arthritis".

[QUOTE=levlarry] Oh yeah Gimpy,



[/QUOTE]

He's a doctor trying to conduct a clinical study. The whole point of a clinical study is to show if it works or not. If he claims it works before he does the study, what does that do for his professional credibility? He's obviously pretty convinced it would work or he wouldn't want to conduct the study.

Lev, you're really not much of a thinker.

Justsaynoemore,
 
I've never accused the American College of Rheumatology of lying. I have probably accused you and Pip and Gimpy of lying but none the less you must be aware that the American College of Rheumatology just updated their 2002 guidelines for Rheumatoid arthritis therapy, right? Guess what? They have lowered their recommendations in the use of minocin or other antibiotics for rheumatoid arthritis from the previous recomendations in 2002 which was for mild only. Anyway, like you say, if you can't believe the American College of Rheumatology, who can you trust? Certainly not you, Pip or Gimpy so with that absolute fact, here is the facts straight from guess who? The American College of Rheumatology. They now recomend antibiotics for only the most minor of the mild rheumatoid arthritis at early onset. Who ya gonna believe?
 

June 5, 2008 —The American College of Rheumatology (ACR) has updated its 2002 guidelines on the use of nonbiologic disease-modifying antirheumatic drugs (DMARDs) for rheumatoid arthritis (RA), which now include data on the use of biologic agents as well. The updated recommendations are reported in the June 15 issue of Arthritis Care and Research.

These guidelines were developed following the principles set forth by the Appraisal of Guidelines for Research and Evaluation Collaboration. A systematic review of scientific evidence was conducted to create an evidence report and draft guidelines addressing 5 domains prespecified by the ACR: (1) indications for use, (2) screening for tuberculosis (TB; for biologic DMARDs only), (3) monitoring for adverse effects, (4) evaluating clinical response, and (5) the roles of cost and patient preferences in decision making (for biologic DMARDs only).

A Task Force Panel that critiqued and rated proposed recommendations included internationally recognized clinicians, methodologists, and patient representatives with broad expertise in the use of nonbiologic and biologic DMARDs, evidence-based medicine, patient preference, and healthcare economics.

Indications for starting or resuming a nonbiologic or biologic DMARD highlight the use of these agents on the background of optimal and appropriate use of nonmedical therapy such as physical and occupational therapy as well as the use of nonsteroidal anti-inflammatory drugs and intraarticular and oral glucocorticoids.

Biologic DMARDs should be used only after failure of nonbiologic DMARDs. Patients with RA should be seen regularly to evaluate disease activity and severity and to determine whether alternative therapies should be used.

The only nonbiologic agents included in these recommendations are hydroxychloroquine, leflunomide, methotrexate, minocycline, and sulfasalazine, and the only biologics included are abatacept, adalimumab, etanercept, infliximab, and rituximab. The remaining DMARDs were not included because of very infrequent use, the high incidence of adverse events, or both.

Nonbiologic DMARD combinations best supported by evidence and used most commonly are methotrexate plus hydroxychloroquine, methotrexate plus sulfasalazine, methotrexate plus leflunomide, sulfasalazine plus hydroxychloroquine, and sulfasalazine plus hydroxychloroquine followed by methotrexate.

Methotrexate or leflunomide monotherapy should be started for patients with all disease durations and for all degrees of disease activity irrespective of poor prognostic features.

Hydroxychloroquine monotherapy is recommended for patients without poor prognostic features, with low disease activity, and with disease duration not greater than 24 months.

Minocycline monotherapy is recommended for patients without poor prognostic features, with low disease activity, and with short disease duration.

Sulfasalazine monotherapy is recommended for patients with all disease durations and without poor prognostic features and includes those with all degrees of disease activity.

Methotrexate plus hydroxychloroquine is recommended for patients with moderate to high disease activity regardless of disease duration or poor prognostic features.

Methotrexate plus leflunomide is recommended for patients with intermediate or longer disease duration (≥ 6 months), with high disease activity irrespective of prognostic features.

Methotrexate plus sulfasalazine is recommended in patients with all disease durations provided they have high disease activity and poor prognostic features.

Hydroxychloroquine plus sulfasalazine is recommended only for patients with intermediate disease duration (6 - 24 months) and high disease activity but without poor prognostic features.

The triple DMARD combination of sulfasalazine, hydroxychloroquine, and methotrexate is recommended for all patients with poor prognostic features and moderate or high levels of disease activity, regardless of disease duration.

Recommendations for the use of biologic DMARDs are separated according to disease duration (< 6 months and ≥ 6 months). The use of antitumor necrosis factor–alpha (TNFα) agents (etanercept, infliximab, and adalimumab) is stratified for durations of 3 months or longer or 3 to 6 months. Anti-TNFα agents can be used interchangeably with methotrexate in patients with early RA who have never received DMARDs and have high disease activity. Patients with early RA and only low or moderate disease activity are not considered candidates for biologic therapy.

An anti-TNFα agent plus methotrexate is recommended for patients with high disease activity for 3 months or longer with poor prognosis and no barriers related to treatment cost and no insurance restrictions to accessing medical care.

In intermediate-duration and longer-duration RA, the anti-TNFα agents can be used interchangeably in patients with inadequate response to prior methotrexate monotherapy, moderate disease activity, and features of a poor prognosis as well as for patients with high disease activity, regardless of prognostic features.

Anti-TNFα agents can also be used interchangeably in patients with inadequate response and at least moderate residual disease activity after previous therapy with methotrexate in combination or with sequential administration of other nonbiologic DMARDs, regardless of prognostic features.

Contraindications to the use of nonbiologic and biologic DMARDs may include infectious disease or pneumonitis, or both; and hematologic, oncologic, cardiac, liver, renal, neurologic, and pregnancy and breast-feeding contraindications.

"Using a formal group process and the scientific evidence as much as possible, we provide recommendations for the use of nonbiologic and biologic therapies in patients with RA when starting or resuming these therapies," the guidelines authors conclude. "These recommendations are not meant to take the place of personalized patient care and are intended to help guide therapy rather than proscribe appropriate therapies. The recommendations are extensive but not comprehensive, and it is intended that they will be regularly updated to reflect the rapidly growing scientific evidence in this area along with changing practice patterns in rheumatology." [END]

So now, no one has ever disagreed that minocin may be helpful in very mild cases of rheumatoid arthritis and now the ACR has recomended it for only the most minor of the  "mild" RA patients. Nobody has ever argued with that. The biggest arguments is that Pip trys to push minocin down our RA throats claiming that she is being healed by minocin but keeping secret that she doesn't have rheumatoid arthritis. So now maybe with this new ACR recomendations you three will realize why studys that yous post links to snippets dated from the 1990s are outdated even if they were indeed actual clinical trials, even the ACR says so. And if you can't trust the ACR, who can you/we trust? Tada.
 
LEV
My RA was moderate to severe and minocycline works on me.Perhaps that's because you are doing triple DMARD therapy............. [QUOTE=Lynn49]Perhaps that's because you are doing triple DMARD therapy.............[/QUOTE]
Yeah Gimpy,
 
I'm not much of a thinker but I think that you also take plaquinal and for some roadback reason you never seem to mention the effects of the plaquinal, why is that? And that you say your ra was moderate to severe means nothing. Your word is about as good as Pips. Your moral fiber is lacking, it's just that simple. Have you read the 2008 American College Of Rheumatology's ra therapy recomendations? Who we gonna trust? You, Pip (who doesn't even have ra) and justsaynoemore or should we trust the American College of Rheumatology. I'm not much of a thinker, duh, but me thinks I'll believe the ACR, no offense.
 
LEV
Lev, you liar.Gimpy,
 
Gosh, now you've gone and hurt my delicate feelings. Did you read the 2008 updated American College of Rheumatology recomendations for RA therapies? Don't ya just love it? Now who are we gonna believe? You, Pip (who by the way, doesn't even have rheumatoid arthritis) and justsaynoemore or should we believe the American College of Rheumatology? Who would you believe, Gimpy? I'm sure that you will somehow find a link between the ACR and Wyeth or yous will try to convince everyone that even the ACR has been paid off. Good grief Gimp, good grief.
 
LEV
Boy, somebody should write a quick note to the American College of Rheumatology and tell them their website is out of date. [QUOTE=Gimpy-a-gogo]




"If minocycline works consistently in children, Trentham said, it would also be a safer alternative to two other common treatments for JRA - steroids and methotrexate. Steroids can stunt a child's growth, and methotrexate, often used to treat cancer, can be toxic to the liver and it can harm the immune system when given in higher doses than usually given in children.

Some pediatric rheumatologists said, however, that methotrexate is not as risky and minocycline is not as safe for children as Trentham suggests. A cousin of tetracycline, it commonly is used to treat severe acne. But it can discolor teeth and skin, irritate the stomach, and, in rare instances, it can cause liver or kidney damage and has been associated with lupus."

 


Boston Globe June 25, 2002


[/QUOTE]

Trentham made the comment 'if it works' about children.  He wanted to study it in children.  As our internal med friend says, "Peds is not just adult medicine divided by four."

(Funny how my then three yr. old was on the same or higher mtx dose than many of you adults...but I digress.)

This was also reported in 2002.   Look what they say about biologics in children/young adults now.  Adult are not growing and developing and won't have the same issues. 

As for my little Study of One, on Zithromax we don't have to worry about  discolored teeth.  No more Prevacid because it was just the NSAIDS tearing up her stomach. 

Find me a child on mtx and/or Enbrel not also on NSAIDS.........which, besides stomach damage, can also screw up your liver, and the PPIs you need when you are on them have been linked to fractures, right?.....

And I have to ASK to get labs done!  Ped rheum and ped say the zith dose isn't high enough to worry about her liver/kidney function.   Only the AP dr. wants that checked.

I pray that the day will come when Zithromax is studied for children.   I don't get what they are afraid of.  The ACR needs to give children an option for a mild DMARD, too.  They need it the most, don't they?

 
Suzanne2008-10-14 07:22:35If I were lying about AP, why would I cop to using other DMARDS?

I actually never lie as a rule, because I have good self-esteem.

How's your girlfriend, Cindy, LevLarry? She must not be giving you much attention for you to be so ornery.Suzanne,
 
I am not against any medical study. I am against those that instead of figuring a way to make the study happen, continue to say bad things against wyeth because Wyeth will not fund a study. Wyeth is under no obligation to anyone to fund anything, period. It makes Trentham look bad when he makes false statements against Wyeths reply. He sounds like someone that would take the money and put it toward a study like the Harris Poll. Certainly you don't believe that the paid for Harris Poll is a legitimate medical study do you? It was a paid by roadback marketing poll, just like large corporations pay marketing firms to come up with good looking statistics, no matter how altered. If Trentham had such good proof that there was good reason for his study, money would be easy to come by. It was just a ploy to extort more money from Wyeth. Good for Wyeth for saying no this time. The money would probably be wasted again and they would still keep a negative campaign against wyeth and enbrel going. Oh, and by the way, minocin can even cause liver death. Minocin can destroy the digestive system. Minocin can absolutely leave women with terrible vaginal diseases that soon won't be able to be destroyed because of the overuse of antibiotics. In short, this is all moot because the safe effective cure for ra is just around the corner. These biologics that you and the others constantly rag on may someday be the medicines that allow your daughter to live a fairly normal life. At that time you will have a much more favorable opinion of the biologics and be very thankful to the big bad Wyeth.
 
LEV
GoGo, JSNM, Suzanne and any other reasonable people reading this thread.  Let's get real here.  Lev is jealous that people, such as myself, who went on to develop RA from PRA and reversed on AP, or GoGo, who can do all she did before, as well as JSNM and Suzanne's baby, has obviously progressed in his disease because he is too damaged to do anything anymore.  We've all seen the pictures.  Lev needs our sympathy and pity - and we know he's no intellectual scholar.  He wouldn't be this wound up if he was happy with the road he chose. 
 
So - let's ignore him, as usual. 
 
OK, now for the good news.  I had to go thru ministry training at my church last weekend.  By some miracle I was seated next to this wonderful woman who is in communications area there.  I don't even know how the conversation started, but I blathered on about my undone filing cabinet.  She volunteered to help me rebuild it!  OMG!  Is that the most fantastic thing ever!  She's going to put multiple tags on everything so I can find it when I need it.  We start this Saturday!
 
So, hang on, I found more Mino studies.  Anna should love some of them.  There were a few on AS.
 
What I've decided to do, should this person think it's feasible, is every time I take something off the computer and transfer it to the new filing system, I'll post the Mino ones here at the same time.  That should avoid double posting of the same studies.  And, when AOL is empty - its gone too. 
 
Hugs,
 
Pip
Wow! How serendipitous.

Go, Pip!Yeah, I'm pretty stoked.  I shouldn't have started emptying it before I had a place to put it.  And amazingly, all the downloads from PubMed had something like 9u757w0476 in the descriptor.  LOL  Yeah, that makes it hard to find.  JSNM is the one that taught me to change the title of the study to the file name, but that was only a yea