Nicotinamide Adenine Dinucleotide Augmentation in Overweight or Obese Middle-Aged and Older Adults: A Physiologic Study

被引:24
|
作者
Pencina, Karol Mateusz [1 ]
Valderrabano, Rodrigo [1 ]
Wipper, Benjamin [1 ]
Orkaby, Ariela R. [2 ]
Reid, Kieran F. [1 ]
Storer, Thomas [1 ]
Lin, Alexander P. [3 ]
Merugumala, Sai [3 ]
Wilson, Lauren [1 ]
Latham, Nancy [1 ]
Ghattas-Puylara, Catherine [1 ]
Ozimek, Noelle E. [1 ]
Cheng, Ming [1 ]
Bhargava, Avantika [1 ]
Memish-Beleva, Yusnie [1 ]
Lawney, Brian [4 ]
Lavu, Siva [5 ]
Swain, Pamela M. [5 ]
Apte, Rajendra S. [5 ,6 ,7 ,8 ]
Sinclair, David A. [5 ,9 ]
Livingston, David [5 ]
Bhasin, Shalender [1 ]
机构
[1] Brigham & Womens Hosp, Boston Claude D Pepper Older Amer Independence Ct, Harvard Med Sch, Res Program Mens Hlth Aging & Metab, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Harvard Med Sch, Div Aging, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[4] Dana Faber Canc Ctr, Boston, MA 02115 USA
[5] Metro Int Biotech, Worcester, MA 01606 USA
[6] Washington Univ Sch Med, Dept Ophthalmol & Visual Sci, St Louis, MO 63110 USA
[7] Washington Univ Sch Med, Dept Med, St Louis, MO 63110 USA
[8] Washington Univ Sch Med, Dept Dev Biol, St Louis, MO 63110 USA
[9] Blavatnik Inst, Paul F Glenn Ctr Biol Aging Res, Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
来源
关键词
beta-nicotinamide mononucleotide; lipids; blood pressure; geroscience; physical function; muscle bioenergetics; metabolic effects; LIFE-SPAN; NAD(+) METABOLISM; CELL FUNCTION; MITOCHONDRIAL; HOMEOSTASIS; RIBOSIDE; MUSCLE; SIRT1; STATE; MONONUCLEOTIDE;
D O I
10.1210/clinem/dgad027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Nicotinamide adenine dinucleotide (NAD) levels decline with aging and age-related decline in NAD has been postulated to contribute to age-related diseases. Objective: We evaluated the safety and physiologic effects of NAD augmentation by administering its precursor, f3-nicotinamide mononucleotide (MIB-626, Metro International Biotech, Worcester, MA), in adults at risk for age-related conditions. Methods: Thirty overweight or obese adults, >= 45 years, were randomized in a 2:1 ratio to 2 MIB-626 tablets each containing 500 mg of microcrystalline f3-nicotinamide mononucleotide or placebo twice daily for 28 days. Study outcomes included safety; NAD and its metabolome; body weight; liver, muscle, and intra-abdominal fat; insulin sensitivity; blood pressure; lipids; physical performance, and muscle bioenergetics. Results: Adverse events were similar between groups. MIB-626 treatment substantially increased circulating concentrations of NAD and its metabolites. Body weight (difference -1.9 [-3.3, -0.5] kg, P = .008); diastolic blood pressure (difference -7.01 [-13.44, -0.59] mmHg, P = .034); total cholesterol (difference -26.89 [-44.34, -9.44] mg/dL, P = .004), low-density lipoprotein (LDL) cholesterol (-18.73 [-31.85, -5.60] mg/dL, P = .007), and nonhigh-density lipoprotein cholesterol decreased significantly more in the MIB-626 group than placebo. Changes in muscle strength, muscle fatigability, aerobic capacity, and stair-climbing power did not differ significantly between groups. Insulin sensitivity and hepatic and intra-abdominal fat did not change in either group.Conclusions: MIB-626 administration in overweight or obese, middle-aged and older adults safely increased circulating NAD levels, and significantly reduced total LDL and non-HDL cholesterol, body weight, and diastolic blood pressure. These data provide the rationale for larger trials to assess the efficacy of NAD augmentation in improving cardiometabolic outcomes in older adults.
引用
收藏
页码:1968 / 1980
页数:13
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