Quote:
Originally Posted by RobLL
My concern is that the studies supporting just about all supplements for preventative use are not well done studies. they are seldom (never?) double blind, and so often later better studies discovers no benefits, or worse -bad side effects.
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I search PUBMED for studies on supplements. Then I analyze the study based on what I know and have researched about those supplements.
There ARE plenty of double blind studies on vitamin D.
IMO, the studies you have to look out for are the FUD studies. Those are studies paid for by the pharmaceutical industry, deliberately designed for a negative outcome, and to sow Fear, Uncertainty, and Doubt about supplements. A sicker population is a cash cow for pharmaceutical companies.
One FUD study on vitamin D I particulary remember was a so called double blind study on vitamin D that showed no benefit in vitamin D supplementation over the control group.
It had these, IMO, deliberate weaknesses.
1. The vitamin D dose given was too small to be effective or pharmacological despite countless other studies proving the minimum dose needed to be effective.
2. Vitamin D cofactors such as magnesium, and vitamin K were not given; calcium was given in too small an amount to be effective.
3. The control group was not screened for vitamin D use nor prohibited from taking vitamin D during the study.
So, of course, the study found no benefit for vitamin D supplementation.
Or
The FDA not allowing verified, long-recognized vitamin D experts to testify at the hearing to decide whether vitamin D levels should be raised.
Instead they determined based on one study on vitamin D that vitamin D was only important for bone health and had no other role in human health.
The vitamin D expert they selected to speak supported the above position and suggested that 400 IU/day of vitamin D3 was more than adequate and should be reduced.
Consequently the FDA dropped the RDA of vitamin D3 from 400 IU to 200 IU/day.
The problem with the basis on which they made their decision
1. No other vitamin D experts were allowed to testify though these experts filed a brief and recommended a list of experts to speak.
2. The study the FDA based its decision on was over 40 years old. They ignored reams of much more recent studies.
3. The expert they allowed to speak who stated that vitamin D3 had no other role than for bone health and recommended lowering the RDA of vitamin D3 holds over 200 patents on vitamin D3 analogs for treating cancer.
4. A good portion of the FDA panel, including the chairman had recent ties to or came from the pharmaceutical industry.
I do my own research.