Pos0394 nad+ Boosters Reestablish the Altered Nad+ Metabolism of Leukocytes From Rheumatoid Arthritis Patients Improving Their Oxidative, Apoptotic and Inflammatory Status

Abstract

Background:NAD+ is an important cofactor and second messenger for multiple cellular processes that exhibits antioxidant, anti-apoptotic and anti-inflammatory properties. Pre-clinical studies in animal models of Rheumatoid Arthritis (RA) have demonstrated the therapeutic potential of NAD+ boosters in the control of the disease activity. However, to date no studies have been set up to evaluate the NAD+ metabolism and the therapeutic effects of NAD+ boosters in RA patients.Objectives:1- To study the NAD+ metabolism in RA patients and its association with key clinical features. 2- To evaluate the effect of anti-TNF therapy in the NAD+ metabolism.3- To analyze the beneficial effects of NAD+ boosters in leukocytes from active RA patients.Methods:Plasma and PBMCs were purified from 100 RA patients and 50 healthy donors (HDs). Moreover, an additional cohort of 50 RA patients treated with Anti-TNF therapy was analyzed before and after 6 months of treatment. NAD+ levels were determined by using the NAD/NADH-Glo Assay. NAD+-consuming genes expression were analyzed by RT-PCR. In parallel, PBMCs from eight HDs and eight active RA patients were treated ex vivo with 1 mM of NAD+ boosters including nicotinamide (NAM), nicotinamide riboside (NR), and nicotinamide mononucleotide (NMN). After 24 hours, intracellular reactive oxygen species (ROS) levels (DFCHDA) and the percentage of apoptotic PBMCs (annnexin V/PI) were assessed by flow cytometry. Lastly, a panel of key pro-inflammatory genes were evaluated by RT-PCR.Results:NAD+ and NADH levels were significantly reduced in plasma and PBMCs of RA patients compared with HDs and directly related to disease activity (DAS28, CDAI, SDAI). Accordingly, the expression levels of genes involved in the consumption of NAD+ such as SIRT-1, CD38 and PARP-1 were found up-regulated in PBMCs from RA patients. Anti-TNF therapy for 6 months restored the altered NAD+ levels towards those showed by HDs. Furthermore, the clinical response promoted by Anti-TNF therapy (changes in DAS28) correlated with changes in NAD+ levels. The in vitro treatments of PBMCs isolated from active RA patients with NAD+ boosters significantly increased the NAD+ levels and promoted a deep reduction of intracellular ROS levels, the percentage of apoptotic cells and the expression levels of key inflammatory mediators, such as IL-6, IL-8, IL-1ß, TNF-α, CCL2, IL-23, and STAT-3.Conclusion:1. NAD+ metabolism is altered and associated with the disease activity of RA patients, involving both, reduced NAD+ levels and increased expression of NAD+-consuming genes. 2. Anti-TNF therapy restored NAD+ levels, which were directly linked to the clinical effectiveness. 3. NAD+ boosters reduced the oxidative, apoptotic and inflammatory profiles of RA leukocytes through the parallel increase of intracellular NAD+ levels. Thus, NAD+ boosters might be considered novel therapeutic tools for RA patients.Acknowledgements:Supported by PI18/00837, RIER RD16/0012/0015, RTI2018-100695-B-I00, P18-RT-4264 and CVI276, co-funded with FEDER.Disclosure of Interests:None declared

Disease-specific loss of microbial cross-feeding interactions in the human gut

“…One example is the link between rheumatoid arthritis and ribosyl nicotinamide (also known as nicotinamide riboside, or NR). This metabolite is one of the main precursors of nicotinamide adenine dinucleotide (NAD+), which has been reported to be significantly reduced in individuals with rheumatoid arthritis 36 . Administration of NR and other NAD+ precursors leads to improved clinical outcomes for rheumatoid arthritis patients 36 and for a range of other inflammatory, neurodegenerative and cardiovascular diseases 37 .…”

“…This metabolite is one of the main precursors of nicotinamide adenine dinucleotide (NAD+), which has been reported to be significantly reduced in individuals with rheumatoid arthritis 36 . Administration of NR and other NAD+ precursors leads to improved clinical outcomes for rheumatoid arthritis patients 36 and for a range of other inflammatory, neurodegenerative and cardiovascular diseases 37 . To our knowledge, this is the first reported evidence for a role of microbial NR metabolism in rheumatoid arthritis.…”

Disease-specific loss of microbial cross-feeding interactions in the human gut

“…One example is the link between rheumatoid arthritis and ribosyl nicotinamide (also known as nicotinamide riboside or NR). This metabolite is one of the main precursors of nicotinamide adenine dinucleotide (NAD + ), which has been reported to be significantly reduced in individuals with rheumatoid arthritis 37 . Administration of NR and other NAD + precursors leads to improved clinical outcomes for rheumatoid arthritis patients 37 and for a range of other inflammatory, neurodegenerative and cardiovascular diseases 38 .…”

“…This metabolite is one of the main precursors of nicotinamide adenine dinucleotide (NAD + ), which has been reported to be significantly reduced in individuals with rheumatoid arthritis 37 . Administration of NR and other NAD + precursors leads to improved clinical outcomes for rheumatoid arthritis patients 37 and for a range of other inflammatory, neurodegenerative and cardiovascular diseases 38 . To our knowledge, this is the first reported evidence for a role of microbial NR metabolism in rheumatoid arthritis.…”