BMJ - The Ultimate Tissue Support

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BMJ - The Ultimate Tissue Support

The BMJ Formula

an easy way to effectively support

bone, joints, connective tissue and

neuromuscular function.


This is what Robert S. Hoffman, M.D. says about the BMJ:

I take the BMJ formula myself, and I recommend it to my patients.

The BMJ provides multiple nutrients in a very bioavailable form with benefits documented by research.

Included is a patented dicalcium malate for improved calcium bioavailability. See comparison graph. (Blue-Dicalcium Malate, Red-Calcium Carbonate)

Excerpted and summarized from the full study entitled “Comparison of calcium Absorption from various calcium- containing products in Healthy Human Adults: A Bioavailability study”. Copyrights, Albion International, Inc. November, 2005

Calcium is important, but it is not necessary to take high amounts according to research. When a two year study compared perimenopausal women who took either 1000 mg or 2000 mg of calcium daily with a placebo group, the groups taking calcium increased their bone density by 1.6%. No difference was found between the groups taking 1000 mg or 2000 mg indicating there is no reason to take high amounts (Elders PJ, et al. 1994).

Bone also needs other important nutrients. Magnesium has shown to prevent fractures and increase bone density (Sojka JE, Weaver CM. 1995, Stendig-Lindberg G, et al. 1993).

Bone density has been found to be significantly better when the minerals zinc, copper, manganese, and potassium were added to calcium (Strause L, et al. 1994). Zinc intake and plasma zinc concentrations have been documented to be lower in men with osteoporosis, this has also been reported for women (Hyun TH, et al. 2004).

Minerals in the form of amino acid chelates have documented better bioavailability when compared with other forms of minerals. As an example, when an amino acid chelate of zinc was compared with zinc gluconate, the amino acid chelate increased the bioavailability of zinc by 43.4% (Gandia P, et al. 2007).

Magnesium, copper, zinc and manganese are included in the BMJ as patented amino acid chelates.

Vitamin D is important for many reasons and it is very common to be deficient or marginally deficient in this vitamin. Vitamin D has been documented to reduce the fracture risk in elderly persons (Bischoff-Ferrari HA, et al. 2009, Bischoff-Ferrari HA, et al. 2005).

Vitamin D3 (cholecalciferol) is more efficient in sustaining vitamin D levels. Vitamin D2 potency is less than one third that of vitamin D3 and has much shorter duration of action compared to vitamin D3 (Armas LA, et al. 2004).

The BMJ contains 1500 mg of glucoseamine sulfate in a daily serving which numerous studies have shown to be safe and effective in decreasing osteoarthritis pain (Reginster JY, et al. 2001, Pavelka K, et al. 2002, da Camara CC, et al. 1998, Foster PK, et al. 1995, Pujalte JM, et al. 1980, Drovanti A, et al. 1980, D’Ambrosio E, et al. 1981, Lopes VA, et al. 1982.)

The graph below shows research comparing glucosamine sulfate with Ibuprofen for eight weeks (Vaz AL. 1982).


After four weeks the glucosamine sulfate produced more pain relief than the Ibuprofen. 

Two studies conducted over three years documented that cartilage degeneration stopped in the treatment group taking glucoseamine sulfate while the control group experienced further degeneration (Reginster JY. 2001, Pavelka K, et al. 2002). 
Research has documented that glucoseamine sulfate supplies cartilage with building materials. Glucosamine sulfate caused a significant stimulation of proteoglycan production by chondrocytes (cartilage cells) in samples obtained from human osteoarthritic cartilage (Basleer C, et al, 1998).
Another study showed that treatment of osteoarthritic chondrocytes with glucosamine sulfate resulted in an increased cell-mediated GAG (glycosaminoglycans) content (Dodge GR, Jimenez SA, 2003). GAG is a common building block both for cartilage, ligaments, and tendons.

Free radicals are also a factor involved in cartilage degeneration. Patients with osteoarthritis had approximately a four fold lower level of extra cellular SOD, the body’s own antioxidant enzymes a constituent of cartilage (Regan E, et al. 2005).

Zinc, copper, and manganese are necessary for the formation of SOD. That is one of the reasons these minerals are included in the BMJ.

Vitamin D is also important for joints. An increased risk for osteoarthritis of the hip and knee has been documented in people with low risk levels of vitamin D (Bergink AP, et al. 2009, Lane NE, et al. 1999). Osteoarthritis of the knee and hip progress more rapidly in patients with low vitamin D (McAlindon TE, et al. 1996, Lane NE, et al. 1999).

A high percentage of patients with non-traumatic persistent, musculoskeletal pain have been found to be vitamin D deficient (Plotnikoff GA, et al. 2003).

Research also shows that support of bone metabolism is important for cartilage integrity. Higher baseline serum osteocalcin, a marker of bone metabolism, has been found to be associated with a decreased rate of cartilage loss (Wang Y, et al. 2005).

The BMJ includes important nutrients for both bone and joint metabolism.

Vitamin B6 is included in the BMJ because it has shown to help prevent kidney stones when taken with magnesium (Prien E, et al. 1974, Gershoffs, et al. 1967).





The BMJ is now in Vegetable Capsules! 

Suggested Use: Take 8 capsules in divided doses daily.




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Bergink AP1, Uitterlinden AG, Van Leeuwen JP, Buurman CJ, Hofman A, Verhaar JA, Pols HA. Vitamin D status, bone mineral density, and the development of radiographic osteoarthritis of the knee: The Rotterdam Study. J Clin Rheumatol. 2009 Aug;15(5):230-7. doi: 10.1097/RHU.0b013e3181b08f20.
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Bischoff-Ferrari HA1, Dawson-Hughes B, Staehelin HB, Orav JE, Stuck AE, Theiler R, Wong JB, Egli A, Kiel DP, Henschkowski J. Fall prevention with supplemental and active forms of vitamin D: a meta-analysis of randomised controlled trials. BMJ. 2009 Oct 1;339:b3692. doi: 10.1136/bmj.b3692.
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Gandia P, Bour D, Maurette JM, Donazzolo Y, Duchène P, Béjot M, Houin G. A bioavailability study comparing two oral formulations containing zinc (Zn bis-glycinate vs. Zn gluconate) after a single administration to twelve healthy female volunteers. Int J Vitam Nutr Res. 2007 Jul;77(4):243-8.
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Lane NE, Gore LR, et al. Serum vitamin D levels and incident changes of radiographic hip osteoarthritis: a longitudinal study. Arthritis Rheum. 1999;42(5):854-860.
Largo R1, Alvarez-Soria MA, Díez-Ortego I, Calvo E, Sánchez-Pernaute O, Egido J, Herrero-Beaumont G. Glucosamine inhibits IL-1beta-induced NFkappaB activation in human osteoarthritic chondrocytes. Osteoarthritis Cartilage. 2003 Apr;11(4):290-8.
Lopes Vaz A. Double-blind clinical evaluation of the relative efficacy of ibuprofen and glucosamine sulphate in the management of osteoarthrosis of the knee in out-patients. Curr Med Res Opin. 1982;8(3):145-9.
Louvet L1, Büchel J, Steppan S, Passlick-Deetjen J, Massy ZA. Magnesium prevents phosphate-induced calcification in human aortic vascular smooth muscle cells. Nephrol Dial Transplant. 2013 Apr;28(4):869-78. doi: 10.1093/ndt/gfs520. Epub 2012 Dec 9.
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Stendig-Lindberg G, et al. Trabecular bone density in a two year controlled trial of peroral magnesium in osteoporosis. Magnes Res. 1993 Jun;6(2):155-63.
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