European Journal of Clinical Investigation, volume 53, issue 12

Effects of NAD+ precursors on blood pressure, C‐reactive protein concentration and carotid intima‐media thickness: A meta‐analysis of randomized controlled trials

Langhuan Lei 1
Xiaoli Zhang 2
Jiali Lin 1
Qiuyu Liang 1
Mohammad Hassan Sohouli 3
Elma Izze Da Silva Magalhães 4
Somaye Fatahi 3
LIHUA YANG 5
Wanting Xu 6
Xingyong Wang 7
Wei Li 1, 8
Yang Jianrong 1
Show full list: 12 authors
1
 
Research Center of Health Management Guangxi Zhuang Autonomous Region People's Hospital and Guangxi Academy of Medical Sciences Nanning China
5
 
Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region Nanning China
6
 
Pediatric Department Chengdu Second People's Hospital Chengdu China
8
 
Department of Health Management Guangxi Zhuang Autonomous Region People's Hospital and Guangxi Academy of Medical Sciences Nanning China
Publication typeJournal Article
Publication date2023-08-18
scimago Q1
wos Q2
SJR1.270
CiteScore9.5
Impact factor4.4
ISSN00142972, 13652362
Biochemistry
General Medicine
Clinical Biochemistry
Abstract
Background

There are contradictory effects regarding the effect of NAD+ precursor on blood pressure and inflammation. In order to obtain a better viewpoint from them, this study aimed to comprehensively investigate the effects of NAD+ precursor supplementation on blood pressure, C‐reactive protein (CRP) and carotid intima‐media thickness (CIMT).

Methods

PubMed/MEDLINE, Web of Science, SCOPUS and Embase databases were searched using standard keywords to identify all controlled trials investigating the effects of NAD+ precursor on blood pressure, CRP and CIMT. Pooled weighted mean difference (WMD) and 95% confidence intervals (95% CI) were achieved by random‐effects model analysis for the best estimation of outcomes.

Results

Twenty‐nine articles (with 8664 participants) were included in this article. Results from meta‐analyses of RCTs from random‐effects models indicated a significant reduction in systolic (SBP) (weighted mean difference (WMD): −2.54 mmHg, p < .001) and diastolic blood pressure (DBP) (WMD: −2.15 mmHg, p < .001), as well as in CRP (WMD: −.93 mg/L, 95% CI −1.47 to −.40, p < .001) concentrations and CIMT (WMD: −.01 mm, 95% CI −.02 to −.00, p = .005) with the NAD+ precursors supplementation compared with the control group. In addition, a greater effect of supplementation with NAD+ precursors in reducing blood pressure (BP) were observed with the highest dose (≥2 g) and duration of the intervention (>12 weeks), as well as with NA supplementation when compared to NE.

Conclusions

Overall, these findings suggest that NAD+ precursor supplementation might have a beneficial effect on cardiovascular risk factors such as BP, CRP concentration and CIMT.

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