A 10-pound weight loss reduces pain by 50 percent
By David Dunaief, M.D.
Over 27 million people in the U.S. suffer from osteoarthritis (OA) (1). Osteoarthritis is insidious, developing over a long period of time. By nature, it is chronic. It is also a top cause of disability (2). What can we do about it?
It turns out that OA is not just caused by friction or age-related mechanical breakdown, but rather by a multitude of factors. These include friction, but also local inflammation, genes and metabolic processes at the cellular level (3). This means that we may be able to prevent and treat it better than we thought by using exercise, diet, medication, injections and possibly even supplements. Let’s look at some of the research.
How can exercise be beneficial?
In an older study, results showed that even a small 10-pound weight loss could result in an impressive 50 percent reduction of symptomatic knee OA over a 10-year period (4).
Most of us either tolerate or actually enjoy walking. We have heard that walking can exacerbate OA symptoms; the pounding can be harsh on our joints, especially our knees. Well, maybe not. Walking actually may have benefits.
In the Multicenter Osteoarthritis Study (MOST), results showed that walking may indeed be useful to prevent functional decline (5). The patients in this study were a mean age of 67 and were obese, with a mean body mass index (BMI) of 31 kg/m2, and either had or were at risk for knee arthritis. In fact, the most interesting part of this study was that the researchers quantified the amount of walking needed to see a positive effect.
The least amount of walking to see a benefit was between 3,250 and 3,750 steps per day, measured by an ankle pedometer. The best results were seen in those walking more than 6,000 steps per day, a relatively modest amount. This was random, unstructured exercise. In addition, for every 1,000 extra steps per day, there was a 16 to 18 percent reduced risk of functional decline two years later.
Acetaminophen may not live up to its popularity
Acetaminophen (e.g., Tylenol) is a popular initial go-to drug for osteoarthritis treatment, but what does research tell us about its effectiveness?
Although acetaminophen doesn’t have anti-inflammatory properties, it does have analgesic properties. However, in a meta-analysis (involving 137 studies), acetaminophen did not reduce pain for OA patients (7).
In this study, all other oral treatments were significantly better than acetaminophen, including diclofenac, naproxen and ibuprofen, as well as intra-articular (in the joint) injectables, such as hyaluronic acid and corticosteroids. The exception was an oral Cox-2 inhibitor, celecoxib, which was only marginally better.
What about NSAIDs?
NSAIDs (nonsteroidal anti-inflammatory drugs) help to reduce inflammation, by definition. However, they have side effects that may include gastrointestinal bleed, and they have a black box warning for heart attacks. Risk tends to escalate with a rise in dose. Interestingly, a newer formulation of diclofenac (Zorvolex) uses submicron particles, which are roughly 20 times smaller than the older version. This allows it to dissolve faster, so it requires a lower dosage.
The approved dosage for OA treatment is 35 mg, three times a day. In a 602-patient, one-year duration, open-label randomized controlled trial (RCT), the newer formulation of diclofenac demonstrated improvement in pain, functionality and quality of life (7). The adverse effects, or side effects, were similar to the placebo. The only caveat is that there was a high dropout rate in the treatment group; only 40 percent completed the trial when they were dosed three times daily.
Don’t forget about glucosamine and chondroitin
Study results for this supplement combination or its individual components for the treatment of OA have been mixed. In a double-blind RCT, the combination supplement improved joint space, narrowing and reducing the pain of knee OA over two years. However, pain was reduced no more than was seen in the placebo group (8).
In a Cochrane meta-analysis review study of 43 RCTs, results showed that chondroitin, with or without glucosamine, reduced the symptom of pain modestly compared to placebo in short-term studies (9). Yet, the researchers stipulate that most of the studies were of low quality.
So, think twice before reaching for the Tylenol. If you are having symptomatic OA pain, NSAIDs such as diclofenac may be a better choice, especially with SoluMatrix fine-particle technology that uses a lower dose, hopefully meaning fewer side effects.
Even though results are mixed, there is no significant downside to giving glucosamine-chondroitin supplements a chance. However, if it does not work after 12 weeks, it is unlikely to have a significant effect. Also, try increasing your walking step count gradually; this could reduce your risk of functional decline. And above all else, if you need to lose weight and do, you will reduce your risk of OA significantly.
(1) Arthritis Rheum. 2008;58:26-35. (2) Popul Health Metr. 2006;4:11. (3) Lancet. 1997;350(9076):503. (4) Ann Intern Med.1992;116:535-539. (5) Arthritis Care Res (Hoboken). 2014;66(9):1328-1336. (6) Ann Intern Med. 2015;162:46-54. (7) ACR 2014 Annual Meeting: Abstract 249. (8) Ann Rheum Dis. Online Jan 6, 2014. (9) Cochrane Database Syst Rev. 2015 Jan 28;1:CD005614.
Dr. Dunaief is a speaker, author and local lifestyle medicine physician focusing on the integration of medicine, nutrition, fitness and stress management. For further information, visit www.medicalcompassmd.com or consult your personal physician.