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Nicotinamide Mononucleotide (NMN): Difference between revisions
Nicotinamide Mononucleotide (NMN) (view source)
Revision as of 19:39, 2 November 2023
, 2 November 2023→Clinical Trials
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!Outcome | !Outcome | ||
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|{{ | |{{pmid_text:31685720}} | ||
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* singe admission of up to 500 mg | * singe admission of up to 500 mg | ||
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* admission was safe and well-tolerated | * admission was safe and well-tolerated | ||
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|{{ | |{{pmid_text:33888596}} | ||
|[[RCT]], 10 weeks | |[[RCT]], 10 weeks | ||
* placebo (n=12) | * placebo (n=12) | ||
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* improvement in muscle insulin sensitivity is clinically relevant and is similar to the improvement observed after ~10% weight loss | * improvement in muscle insulin sensitivity is clinically relevant and is similar to the improvement observed after ~10% weight loss | ||
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|{{ | |{{pmid_text:34238308}} | ||
|[[RCT]], 6 weeks | |[[RCT]], 6 weeks | ||
* placebo (n=12) | * placebo (n=12) | ||
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* The improvement is muscle, not cardiac, related. | * The improvement is muscle, not cardiac, related. | ||
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| {{ | | {{pmid_text:36002548}} | ||
|[[RCT]], 4 weeks | |[[RCT]], 4 weeks | ||
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* Results indicate that NMN can be administered orally to humans at doses 1250 mg once daily for up to 4 weeks without causing hepatotoxicity and vasodilative flushing, and is believed to have a higher upper tolerable limit compared to NAM and NA. | * Results indicate that NMN can be administered orally to humans at doses 1250 mg once daily for up to 4 weeks without causing hepatotoxicity and vasodilative flushing, and is believed to have a higher upper tolerable limit compared to NAM and NA. | ||
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| {{ | | {{pmid_text:36482258}} | ||
|[[RCT]], 8.5 weeks (60 days) | |[[RCT]], 8.5 weeks (60 days) | ||
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* 900 mg/day oral dose did not give significantly better efficacy than 600 mg/day dose | * 900 mg/day oral dose did not give significantly better efficacy than 600 mg/day dose | ||
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| {{ | | {{pmid_text:35215405}} | ||
|[[RCT]], 12 weeks | |[[RCT]], 12 weeks | ||