Study summary · research use only
NAD(+) precursor supplementation in human ageing: clinical evidence and challenges
Plain-language summary
Paraphrased from the published abstract below — not a verdict on whether anything works.
This review discusses clinical evidence for NAD+ precursor supplementation in human ageing. It notes that an age-related decline in NAD+ levels in humans has been consistently observed in only a limited number of studies, and that although preclinical studies support NAD+ precursor supplementation as a strategy related to healthy ageing, human clinical trials have shown limited effects. The review evaluates tissue-specific effects of NAD+ precursor supplementation and states that published data on NAD+ dynamics in human tissues remain sparse, with extrapolation from rodent studies not straightforward, underscoring a need for more clinical studies of systemic and tissue-specific NAD+ metabolism.
Abstract
Nicotinamide adenine dinucleotide (NAD+) is an essential molecule involved in cellular metabolism, and its decline has been implicated in ageing and age-related disorders. However, evidence for an age-related decline in NAD+ levels in humans has been consistently observed only in a limited number of studies. Similarly, although preclinical studies support the idea that supplementation with NAD+ precursors is a promising therapeutic strategy to promote healthy ageing, human clinical trials have shown limited efficacy. Therefore, an increasing understanding of how NAD+ metabolism is affected in different tissues during disease and following NAD+ precursor supplementation is crucial to defining the therapeutic value of NAD+-targeted therapies. In this Review, we evaluate the clinical evidence supporting the notion that NAD+ levels decline with age, as well as the tissue-specific effects of NAD+ precursor supplementation. Viewed in perspective, the published body of data on NAD+ dynamics in human tissues remains sparse, and the extrapolation of rodent-based data is not straightforward, underscoring the need for more clinical studies to gain deeper insights into systemic and tissue-specific NAD+ metabolism.
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