SAMe (S-Adenosylmethionine)

Published on 23/06/2015 by admin

Filed under Complementary Medicine

Last modified 23/06/2015

Print this page

rate 1 star rate 2 star rate 3 star rate 4 star rate 5 star
Your rating: none, Average: 2 (3 votes)

This article have been viewed 1946 times

Chapter 120 SAMe (S-Adenosylmethionine)

image Clinical Indications

The five principal uses of SAMe are for depression, osteoarthritis, fibromyalgia, liver disorders, and migraine headaches.


SAMe is necessary in the manufacture of important brain compounds, such as neurotransmitters and phospholipids like phosphatidylcholine and phosphatidylserine. Adding SAMe to the diet of depressed patients raises levels of serotonin, dopamine, and phosphatidylserine and improves binding of neurotransmitters to receptor sites, resulting in increased serotonin and dopamine activity and better brain-cell membrane fluidity, leading to significant clinical improvement.24

The antidepressant effects of folic acid (see Chapter 142) are mild compared with the effects noted in clinical trials of SAMe. On the basis of results from a number of clinical studies, it appears that SAMe is perhaps the most effective natural antidepressant (although a strong argument could be made for the extract of St. John’s wort standardized to contain 0.3% hypericin).511

Although most of the early studies used injectable SAMe, the later studies have used an oral dose of 400 mg four times daily (1600 mg total) and have demonstrated that SAMe is just as effective given orally as when it is given intravenously.4,1015 That is not surprising, because there are no significant differences in the pharmacokinetic parameters of SAMe 1000 mg administered orally or intravenously.16

Several studies have compared SAMe with tricyclic antidepressants. Before the rise of selective serotonin reuptake inhibitors (SSRIs), tricyclics were the mainstay pharmaceutical treatment for depression. A 2002 review concluded that “at doses of 200 to 1600 mg/day, SAMe is superior to placebo and is as effective as tricyclic antidepressants in alleviating depression, although some individuals may require higher doses.”10 The reviewers found six of eight placebo-controlled studies, featuring anywhere from 40 to 100 participants, demonstrating that SAMe was superior to placebo; moreover, six of eight comparison studies showed that SAMe was just as effective as tricyclic antidepressants. These studies have shown that SAMe is better tolerated than the tricyclics and has a quicker onset of antidepressant action.11

In one study comparing SAMe with desipramine, in addition to determining the clinical response, the blood level of SAMe was determined in both groups. At the end of the 4-week trial, 62% of the patients treated with SAMe and 50% of those treated with desipramine had significantly improved. Regardless of the type of treatment, patients with a 50% decrease in scores on the Hamilton Depression Scale showed a significant rise in plasma SAMe concentration. These results suggest that one of the ways in which tricyclic antidepressant agents exert their antidepressant effects is by raising SAMe levels.17

In two separate double-blind studies, SAMe was given orally (1600 mg daily) or intramuscularly (400 mg daily) and compared with 150 mg of imipramine given orally daily. In both studies, the results of SAMe and imipramine treatment did not differ significantly for any efficacy measure. However, significantly fewer adverse events were observed in the patients treated with SAMe. The researchers concluded that the antidepressant efficacy of 1600 mg SAMe orally and 400 mg SAMe intramuscularly is comparable with that of 150 mg of imipramine but that SAMe is significantly better tolerated.18

In a double-blind, randomized clinical trial lasting 6 weeks, 73 depressed patients who were unresponsive to SSRI medications alone were given 800 mg of SAMe or placebo twice daily along with their SSRIs.19 The response and remission rates according to the Hamilton Depression Scale were higher for patients treated with adjunctive SAMe (36.1% and 25.8%, respectively) than adjunctive placebo (17.6% versus 11.7%, respectively). These results indicate that SAMe can be used safely with SSRIs and may have a synergistic effect.

In a study on 20 HIV-seropositive individuals with depression, SAMe as a sole antidepressant medication showed significant effect. There was a significant reduction in acute depressive symptomatology, reaching the defined clinical treatment response threshold of a greater than 50% reduction in symptom scores. The researchers also noted that SAMe had a rapid effect as early as after only 1 week, with progressive decreases in symptom scores throughout the study.20

SAMe has also been shown to produce significant effects in other conditions associated with depression, as during the postpartum period and in drug rehabilitation. SAMe’s benefits in these conditions are probably due to a combination of its effects on brain chemistry and liver function (discussed later). In the study in postpartum depression, the administration of SAMe (1600 mg/day) was associated with significantly better mood scores compared with placebo.21 In another study, SAMe (1200 mg/day) was shown to significantly reduce psychological distress (chiefly anxiety and depression) in the detoxification and rehabilitation of opiate abusers.22

SAMe may also be helpful in managing the symptomatology of schizophrenia. In one double-blind study, 18 patients with chronic schizophrenia were randomly assigned to receive either SAMe (800 mg) or placebo for 8 weeks. Results indicated some reduction in aggressive behavior and improved quality of life following SAMe administration. Female patients showed improvement of depressive symptoms, whereas male patients showed no change compared with placebo. Blood dopamine levels increased in women, but decreased in men receiving SAMe. Clinical improvement did not correlate with serum SAMe levels. Two patients receiving SAMe exhibited some exacerbation of irritability; therefore, it should be used with caution in these patients.23

Detailed clinical evaluations using electroencephalography, event-related potentials, and low-resolution brain electromagnetic tomography have clearly indicated a central nervous system antidepressant action of SAMe.18


SAMe has also demonstrated impressive results in the treatment of osteoarthritis.2426 A deficiency of SAMe in the joint tissue, just like a deficiency of glucosamine, leads to loss of the gel-like nature and shock-absorbing qualities of cartilage. As a result, osteoarthritis can develop.

In vitro studies have shown that SAMe exerts a number of effects that appear to be highly relevant in the treatment of osteoarthritis. First, the agent has been shown to be very important in the manufacture of cartilage components.27 This effect has been demonstrated very well in humans. In one double-blind study conducted in Germany, the 14 patients with osteoarthritis of the hands who were given SAMe showed greater cartilage formation on magnetic resonance imaging.28 These results indicate that SAMe is capable of improving the structure and function of cartilage in joints affected by osteoarthritis. Second, SAMe has shown some mild pain-relieving and anti-inflammatory effects in animal studies.1 All of these effects combine to produce exceptional clinical benefits.

In double-blind trials, SAMe has demonstrated similar reductions in pain scores and clinical symptoms to those produced by nonsteroidal antiinflammatory drugs (NSAIDs) like ibuprofen, indomethacin, naproxen, nabumetone, celecoxib, and piroxicam. In one double-blind study, SAMe was compared with ibuprofen.29 The 36 subjects with osteoarthritis of the knee, hip, and/or spine received a daily oral dose of 1200 mg of SAMe or 1200 mg of ibuprofen for 4 weeks. Morning stiffness, pain at rest, pain on motion, crepitation (crackling noise upon movement of a joint), swelling, and limitation of motion of the affected joints were assessed before and after treatment. The total score obtained by evaluating all the individual clinical parameters improved to the same extent in patients treated with SAMe and in those treated with ibuprofen. In two other studies, SAMe was actually shown to produce slightly better results.30,31

SAMe has also been compared with naproxen (Naprosyn). In one double-blind study, 20 patients with osteoarthritis of the knee were given either SAMe or naproxen for 6 weeks.32

Buy Membership for Complementary Medicine Category to continue reading. Learn more here