Servei de Bioquímica, Hospital de la Santa Creu i Sant Pau i Institut d'Investigació Biomèdica Sant Pau, Barcelona, Spain.
Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Barcelona, Spain.
Front Endocrinol (Lausanne). 2022 Jan 31;12:815565. doi: 10.3389/fendo.2021.815565. eCollection 2021.
Depleted nicotinamide adenine dinucleotide (NAD+) is a common hallmark of metabolic disorders. Therefore, NAD+-increasing strategies have evolved as a potential therapeutic venue to combat cardiometabolic diseases. Several forms of vitamin B3, i.e., nicotinamide and nicotinamide mononucleotide, and especially nicotinamide riboside, have attracted most interest as potentially safe and efficacious candidates for NAD+ restoration. Herein, we dissected the characteristics of the latest clinical trials testing the therapeutic potential of different vitamin B3 molecules to improve cardiometabolic health, with a special focus on randomized, placebo-controlled clinical trials performed in the context of obesity or other pathologies, mainly linked to cardiovascular system and skeletal muscle functionality. The favorable outcomes NAD+-increasing strategies found in the different studies were quite heterogeneous. NAD+-increasing interventions improved capacity to exercise, decreased blood pressure, increased the anti-inflammatory profile and insulin-stimulated glucose disposal, and reduced the fat-free mass. Except for the decreased blood pressure, the significant results did not include many hard clinical end points, such as decreases in weight, BMI, fasting glucose, or HbA1c percentage. However, the analyzed trials were short-term interventions. Overall, the accumulated clinical data can be interpreted as moderately promising. Additional and long-term studies will be needed to directly compare the doses and duration of treatments among different vitamin B3 regimes, as well as to define the type of patients, if any, that could benefit from these treatments. In this context, a major point of advancement in delineating future clinical trials would be to identify subjects with a recognized NAD+ deficiency using novel, appropriate biomarkers. Also, confirmation of gender-specific effect of NAD+-increasing treatments would be needed.
消耗的烟酰胺腺嘌呤二核苷酸 (NAD+) 是代谢紊乱的常见标志。因此,NAD+ 增加策略已成为治疗心脏代谢疾病的潜在治疗方法。几种形式的维生素 B3,即烟酰胺和烟酰胺单核核苷酸,尤其是烟酰胺核苷,作为潜在安全有效的 NAD+ 恢复候选物引起了最大的兴趣。在此,我们剖析了测试不同维生素 B3 分子治疗心脏代谢健康的潜在作用的最新临床试验的特征,特别关注在肥胖或其他病理学背景下进行的、以随机、安慰剂对照临床试验,主要与心血管系统和骨骼肌功能有关。不同研究中发现的 NAD+ 增加策略的有利结果相当多样化。NAD+ 增加干预措施提高了运动能力,降低了血压,增加了抗炎谱和胰岛素刺激的葡萄糖摄取,并减少了无脂肪质量。除了降低血压外,显著的结果并不包括许多重要的临床终点,如体重、BMI、空腹血糖或 HbA1c 百分比的降低。然而,分析的试验是短期干预。总的来说,累积的临床数据可以被解释为有一定的希望。需要进行更多和长期的研究,以直接比较不同维生素 B3 方案之间的治疗剂量和持续时间,并确定是否有任何类型的患者可以从这些治疗中受益。在这种情况下,确定未来临床试验的一个主要进展点将是使用新的适当生物标志物来识别具有公认的 NAD+ 缺乏的受试者。还需要确认 NAD+ 增加治疗的性别特异性作用。