• ]]>Urinary Tract Infections]]>
Mannose is a “six-carbon-sugar,” as are the better known and closely related substances glucose and fructose. Relying on evidence that is both exceedingly preliminary and highly inconsistent, some alternative medicine practitioners have popularized mannose as a treatment for urinary tract infections.
Mannose plays an important role in human physiology. However, there is no nutritional need for this substance, as the body can easily produce it from glucose. Nonetheless, significant quantities of it can be found in many fruits and vegetables, including peaches, apples, blueberries, green beans, cabbage, and tomatoes.
A typical recommended dose of mannose for the treatment or prevention of bladder infections is 1.5 g daily, often divided into three doses of 500 mg each.
The idea that mannose supplements can help prevent or treat bladder infections derives from a property of the E. coli bacteria. E. coli is one of the common causes of bladder infections. Many, though not all, strains of E. coli have the ability to attach to the mannose present in the wall of the bladder by means of thread-like structures called pili. This process of attachment allows them to initiate the process of infection.
Reasoning from this fact of basic science, medical researchers in the 1980s hypothesized that consumption of mannose as a supplement will increase levels of mannose in the urine to such an extent that this free mannose will saturate the E. coli’s mannose-binding pili and thereby make the bacteria unable to grapple onto the cells of the bladder wall.
It is essentially this reasoning that is restated by proponents of mannose for bladder infections. However, the argument has at least four problems. First, one of the main ways that the body’s white blood cells recognize and kill E. coli is via these mannose-sensitive pili. 1]]> When these pili are saturated by mannose, white blood cells (specifically, macrophages) are less able to consume the E. coli bacteria. ]]>2]]> Second, many species of E. coli , including some of the most dangerous, do not have mannose-sensitive pili at all. ]]>3-4]]> Third, there are numerous other bacteria that cause bladder infections, and these are not known or suspected to have mannose-sensitive pili.
But perhaps the most important point is that the use of mannose for preventing or treating bladder infections has never undergone any meaningful scientific study in human beings. There is a bit of evidence from animal studies performed in the 1980s, ]]>5]]> but it is a long way from animal studies to efficacy in humans. Proponents of mannose also cite numerous testimonials, but the placebo effect and related ]]>confounding factors]]> are quite sufficient to produce numerous testimonials for any treatment. Only ]]>double-blind, placebo-controlled studies]]> can actually prove a treatment effective, and none have been performed on mannose.
The bottom line: There is no meaningful scientific reason to believe that mannose is useful for the prevention or treatment of bladder infections.
As a sugar widely present in foods, mannose is assumed to be safe. However, the maximum safe dosage has not been established in healthy adults, nor in pregnant or nursing women or young children. Very weak evidence from test tube studies hints that consumption of gigantic amounts of mannose by pregnant women could conceivably increase risk of birth defects in their offspring. 6-8]]>
1. Blumenstock E, Jann K. Adhesion of piliated Escherichia coli strains to phagocytes: differences between bacteria with mannose-sensitive pili and those with mannose-resistant pili. Infect Immun. 1982;35:264-269.
3. van der Bosch JF, Verboom-Sohmer U, Postma P, et al. Mannose-sensitive and mannose-resistant adherence to human uroepithelial cells and urinary virulence of Escherichia coli . Infect Immun. 1980;29:226-233.
4. Vaisanen V, Elo J, Tallgren LG, et al. Mannose-resistant haemagglutination and P antigen recognition are characteristic of Escherichia coli causing primary pyelonephritis. Lancet. 1981;2:1366-1369.
Last reviewed April 2009 by EBSCO CAM Review Board]]>
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