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Perfusion of glucose, sucrose, galactose, maltose, 3- O -methylglucose, and a - or B -methylglucoside significantly stimulate GIP secretion, while mannose, 6-deoxygalactose, 2-deoxyglucose, myoinositol, fructose or lactose do not (Sykes et al., 1980)

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[26] The same critics claimed that previous controlled trials "found no evidence that chelation is superior to placebo for treatment of CAD [Coronary Artery Disease] or PVD [Peripheral Vascular Disease]," making the trial "unethical, dangerous, pointless, and wasteful." [3] Evidence of insurance fraud and other felony convictions among (chelation proponent) investigators further undermined the credibility of the trial