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. Author manuscript; available in PMC: 2019 Mar 6.
Published in final edited form as: Cell Metab. 2017 Dec 14;27(3):513–528. doi: 10.1016/j.cmet.2017.11.002

Table 3.

Conditions in which NAD+ decline has been documented

Disease/Condition Tissue NAD+ concentration (% of normal) Ref
Aging Muscle ~30–35% (22 mo), ~40–45% (30 mo), (Gomes et al., 2013)
~60–65% (32 mo) (Camacho-Pereira et al., 2016)
~80–85% (25–31 mo) (Yoshino et al., 2011)
~65–70% (24 mo) (Frederick et al., 2016)
~50% (24 mo) (Mouchiroud et al., 2013)
Liver ~85–90% (25–31 mo) (Yoshino et al., 2011)
~85–90% (12 mo), ~75–80% (20 mo), ~70–75% (<45 vs. >60 humans) (Zhou et al., 2016)
unchanged (12 mo), ~40–50% (24 mo) (Braidy et al., 2011)
55–60% (32 mo) (Camacho-Pereira et al., 2016)
~60% (24 mo) (Mouchiroud et al., 2013)
Adipose 55–60% (32 mo) (Camacho-Pereira et al., 2016)
70–75% (25–31 mo) (Yoshino et al., 2011)
Brain 63–66% (12 mo), ~90% (at age 70 vs. 20 based on regression) (Stein and Imai, 2014; Zhu et al., 2015)
Pancreas ~80–85% (Yoshino et al., 2011)
Spleen 35–40% (32 mo) (Camacho-Pereira et al., 2016)
Heart unchanged (12 mo), ~30–40% (24 mo) (Braidy et al., 2011)
Kidney unchanged (12 mo), ~15–20% (24 mo) (Braidy et al., 2011)
Lung unchanged (12 mo), ~20–25% (24 mo) (Braidy et al., 2011)
CSF ~91% (<45 vs. >=45 humans) (Guest et al., 2014)
Obesity Liver ~50–60% (Wang et al., 2017)
unchanged (Escande et al., 2010)
~30–35% (Gariani et al., 2016)
~80–85%, (Trammell et al., 2016b)
~50–55% (Yoshino et al., 2011)
Adipose ~15–20% (Yoshino et al., 2011)
Muscle unchanged (Yoshino et al., 2011)
~80–85% (Frederick et al., 2015)
mdx (Duchenne muscular dystrophy model) Muscle ~70–75% (Chalkiadaki et al., 2014)
~45–50% (Ryu et al., 2016)
hURI overexpression (Oncogenic transgene that leads to spontaneous hepatocellular carcinoma) Liver ~25% (Tummala et al., 2014)
Noise injury Cochlea ~40–50% (Brown et al., 2014)
Liver regeneration Liver ~60–70% (Mukherjee et al., 2017)
Atm mutant mice (Ataxia telangiectasia model) Cerebellum ~40% (Fang et al., 2016)

Values are estimated from graphs when not stated in the cited reference. In most cases, a decrease in NAD+ cannot be distinguished from a shift in the NAD+/NADH ratio, and in at least some cases, the effect of a redox shift appears to be important (e.g., in the age-related changes reported by Braidy et al. (Braidy et al., 2011) and in the NAD+ decline in human brain (Zhu et al., 2015).