key: cord-0979025-wgenusyf
authors: Altay, Ozlem; Arif, Muhammad; Li, Xiangyu; Yang, Hong; Aydın, Mehtap; Alkurt, Gizem; Kim, Woonghee; Akyol, Dogukan; Zhang, Cheng; Dinler‐Doganay, Gizem; Turkez, Hasan; Shoaie, Saeed; Nielsen, Jens; Borén, Jan; Olmuscelik, Oktay; Doganay, Levent; Uhlén, Mathias; Mardinoglu, Adil
title: Combined Metabolic Activators Accelerates Recovery in Mild‐to‐Moderate COVID‐19
date: 2021-06-28
journal: Adv Sci (Weinh)
DOI: 10.1002/advs.202101222
sha: 977d9bc9da56342ec0064d69026d96a4933ff0a6
doc_id: 979025
cord_uid: wgenusyf

COVID‐19 is associated with mitochondrial dysfunction and metabolic abnormalities, including the deficiencies in nicotinamide adenine dinucleotide (NAD(+)) and glutathione metabolism. Here it is investigated if administration of a mixture of combined metabolic activators (CMAs) consisting of glutathione and NAD+ precursors can restore metabolic function and thus aid the recovery of COVID‐19 patients. CMAs include l‐serine, N‐acetyl‐l‐cysteine, nicotinamide riboside, and l‐carnitine tartrate, salt form of l‐carnitine. Placebo‐controlled, open‐label phase 2 study and double‐blinded phase 3 clinical trials are conducted to investigate the time of symptom‐free recovery on ambulatory patients using CMAs. The results of both studies show that the time to complete recovery is significantly shorter in the CMA group (6.6 vs 9.3 d) in phase 2 and (5.7 vs 9.2 d) in phase 3 trials compared to placebo group. A comprehensive analysis of the plasma metabolome and proteome reveals major metabolic changes. Plasma levels of proteins and metabolites associated with inflammation and antioxidant metabolism are significantly improved in patients treated with CMAs as compared to placebo. The results show that treating patients infected with COVID‐19 with CMAs lead to a more rapid symptom‐free recovery, suggesting a role for such a therapeutic regime in the treatment of infections leading to respiratory problems.

Many patients infected with COVID-19 suffer from respiratory problems, metabolic dysfunction and exacerbated inflammation that triggers organ failure. [1] This has led to more than 3 million COVID-19 related deaths globally [2] due to severe outcomes. [3] [4] [5] [6] [7] Although new treatments regimes have been introduced, [8, 9] including Remdesivir and Favipiravir (FP), [10, 11] there is a need to complement existing therapeutic interventions with new approaches, in particular those targeting mitochondrial dysfunction and metabolic abnormalities. A potential approach is to promote metabolic functions by metabolic activators.

Metabolic abnormalities and a hyperinflammatory response are associated with the deficiencies in nicotinamide adenine dinucleotide (NAD + ) and glutathione (GSH) metabolism. [12, 13] The cellular depletion of NAD + and GSH may be primary factors related to the COVID-19 and the risk for mortality. Given the lack of targeted

We have also generated proteomics and metabolomics data for detailed characterization of the patients recruited in the phase 2 study and revealed the underlying molecular mechanisms associated with the improved patient phenotype. Based on the favorable findings from the phase-2 study, we conducted a randomized, controlled, double-blinded phase-3 study to evaluate the efficacy, tolerability, and safety of CMA in ambulatory COVID-19 patients. Here, we report the results from the phase-2 and phase-3 clinical trial, including the effect on the time to recovery which was the primary endpoint for both studies. The results are complimented with an extensive analysis of a large number of biochemical parameters, based on both protein and metabolite analysis.

In the phase-2 study, we recruited 100 adults with a confirmed positive PCR test for COVID-19. Five patients dropped out for personal reasons, and two were hospitalized before administrating the CMA. Of the 93 remaining patients, all of whom completed the study, 71 were randomly assigned to the CMA group and 22 to the placebo group ( Figure 1A , Dataset S1A, Supporting Information); all patients also received standard of care therapy (for Turkey) with hydroxychloroquine (HQ) for five d. On Days 0 and 14, we assessed the clinical variables and analyzed the differences between Day 0 and Day 14 in the CMA and placebo groups (Dataset S2A, Supporting Information).

The patients' mean age participated in the phase-2 study was 35.6 years (19-66 years), and 60% were men (Table S2 , Supporting Information). Patients had a low prevalence of coexisting conditions such as hypertension (2.1%) and type 2 diabetes mellitus (5.3%), and the mean body mass index (BMI) was 24.8 (16.8-37.8) . The most common COVID-19 symptoms were tiredness (51.6%), headache (48.3%), cough (31.1%), muscle or joint pain (60.2%), smell or taste disorder (26.8%), sore throat (23.6%), fever (20.4%), breathing issues (6.4%), nausea or vomiting (5.3%), and diarrhea (2.1%). The baseline demographic and clinical characteristics were similar in the CMA and placebo groups (Table S2 , Datasets S1A and S2A, Supporting Information). All patients who fully recovered had a negative PCR test for COVID-19 on Day 14. With regards to safety, no severe adverse events occurred and two patients in the CMA group (2.8%) reported adverse events. Both had a mild rash on the upper body and decided to complete the study (Dataset S1A, Supporting Information). Adverse effects were uncommon and self-limiting.

In the phase-2 study, we observed that the mean recovery time (the primary outcome variable) was shorter in the CMA group than in the placebo group (6.6 vs 9.3 d, p = 0.0001) ( Figure 1B) . A univariate Cox regression analysis shows that CMA was significantly associated with recovery time (p < 0.0004, hazard ratio 2.59, 95% confidence interval 1. 54-4.38) (Table S3 , Supporting Information). Multivariate Cox regression analysis analyses also confirmed that CMA independently reduced recovery time after adjustment for age, gender, other treatment histories, smoking, and alcohol consumption (p < 0.0004, hazard ratio 2.68, 95% confidence interval 1.57-4.59) ( Figure 1C ). 

In the phase-3 study, we recruited and randomly assigned 309 adult patients with a confirmed positive PCR test for COVID-19. Three patients dropped out for personal reasons, one patient in the CMA group dropped due to mild allergy, and one patient in the placebo group was hospitalized. Of the 304 remaining patients, all of whom completed the study, 229 were in the CMA group and 75 in the placebo group (Figure 2A , Dataset S2B, Supporting Information). 62 patients in the placebo group and 187 patients in the CMA group received standard therapy with HQ www.advancedsciencenews.com www.advancedscience.com for 5 d. Meanwhile, 13 patients in the placebo group and 42 patients in the CMA group received standard therapy with FP for 5 d. On Days 0 and 14, we assessed the clinical variables and analyzed the differences between Day 0 and Day 14 in the CMA and placebo groups (Dataset S2B, Supporting Information).

The mean age of the patients who participated in the phase-3 study was 36.3 years (18-66 years), and 57.6% were men (Table S2 , Supporting Information). Patients had a low prevalence of coexisting conditions such as hypertension (9.2%) and type 2 diabetes mellitus (6.2%), and the mean BMI was 26.7 (16.8-45.6) . The most common symptoms were muscle or joint pain (60.8%), tiredness (50.3%), cough (43.4%), headache (38.1%), fever (28.2%), sore throat (24%), smell or taste disorder (20.7%), breathing issues (9.2%), nausea or vomiting (7.8%), and diarrhea (3.6%). The baseline demographic and clinical characteristics were similar in the CMA and placebo groups (Table S2 , Dataset S1B, Supporting Information). Two patients in the CMA group (0.6%) reported mild rash and skin redness as adverse events, and both decided to complete the study (Dataset S1B, Supporting Information).

In the phase-3 study, we observed that the mean recovery time was shorter in the CMA group than in the placebo group (5.7 vs 9.2 d, p<0.0001) ( Figure 2B ). A univariate Cox regression analysis shows that CMA was significantly associated with recovery time (p < 2.0e-16, hazard ratio 5.63, 95% confidence interval 4.11-7.71) (Table S4 , Supporting Information). Multivariate Cox regression analysis also confirmed that CMA independently reduced recovery time after adjustment for HQ/FP treatment, age, gender, other treatment histories, smoking, and alcohol consumption (p < 2.0e-16, hazard ratio 5.77, 95% confidence interval 4.17-7.96) ( Figure 2C ).

To investigate if the administration of CMA is affected by the standard therapy with HQ and FP, we calculated the mean recovery time in the patient groups treated with HQ and FP separately. We observed that the mean recovery time was again shorter in CMA group than in placebo group (5.76 vs 9.32 d, p < 0.0001) in the patients treated with HQ only ( Figure S1A , Supporting Information) and (5.54 vs 8.77 d, p = 0.00034) in the patients treated with FP only ( Figure S1B , Supporting Information). We also compared the independent effect of the HQ and FP on COVID-19 patients and found that these two drugs had a similar efficacy on the recovery of the patients in all ( Figure S2A , Supporting Information), placebo ( Figure S2B , Supporting Information) and CMA ( Figure S2C , Supporting Information) patient groups. Hence, we observed that CMA administration accelerated the recovery of the COVID-19 patients independent of the standard therapy.

We measured clinical variables in all of the patients recruited in the phase-2 and phase-3 studies and analyzed the differences before and after the administration of CMA in the active and placebo groups ( Figure 3A) . Analysis of secondary outcome variables showed that serum alanine aminotransferase (ALT) levels were significantly (p = 0.032) lower on Day 14 versus Day 0 only in the CMA group ( Figure 3B ). We found that the lactate dehydrogenase (LDH) levels ( Figure 3C ) and creatinine levels (Figure 3D ) were significantly lower on Day 14 versus Day 0 only in the CMA group (p = 2.88 E-04 and p = 3.07 E-09), respectively. In contrast, we found that the plasma glucose level was significantly increased on Day 14 versus Day 0 only in the placebo group (Figure 3E ). Hence, we observed that the level of ALT, LDH, creatinine and glucose was significantly improved due to the administration of CMA.

We also measured the level of clinical chemistry parameters and found that their levels are significantly changed in both CMA and placebo groups. We found that the level of aspartate aminotransferase (AST) ( Figure S3A , Supporting Information) and C-reactive protein ( Figure S3B , Supporting Information) were significantly lower in both CMA and placebo groups on Day 14 versus Day 0. In contrast, we found that the levels of platelets ( Figure S3C , Supporting Information), white blood cells ( Figure S3D Figure S4C , Supporting Information) were significantly increased in both CMA and placebo groups on Day 14 versus Day 0. We observed that these differences were due to the recovery of the patients and not affected by the administration of CMA. D-dimer and Ferritin levels did not significantly differ between both groups on Day 14 versus Day 0 (p > 0.05; Figure 3A , Dataset S2C, Supporting Information). Our analysis suggested that administration of CMA improved the clinical parameters in parallel to the decrease in the recovery time.

We characterized the metabolome and inflammatory cytokine markers of 93 COVID-19 patients involved in the phase-2 study and revealed changes associated with the disease and administration of CMA at the molecular level. We analyzed the plasma level of metabolites and inflammatory protein markers on Day 0 and Day 14 in both groups. Generation of omics data may unveil the underlying molecular mechanisms associated to the differences before and after the disease as well as the differences in the placebo and CMA groups. We generated plasma metabolomics data and analyzed the plasma levels of 1021 different metabolites (Dataset S3, Supporting Information). After filtering out the metabolites with missing values in more than 50% of samples, the plasma metabolomics dataset included 928 metabolites that were subjected to statistical analysis. Significant differences in plasma metabolite levels on Day 14 versus Day 0 in both the CMA and placebo groups (Dataset S4, Supporting Information) and between the groups on Day 14 and Day 0 (Dataset S5, Supporting Information) are presented. We investigated the associations between the plasma level of all metabolites with the plasma levels of the metabolic activators (Dataset S6, Supporting Information).

We also measured the plasma levels of 96 inflammatory protein markers using an inflammation panel to quantify the plasma level of target proteins (Dataset S7, Supporting Information). After quality control and exclusion of proteins with missing values in more than 50% of samples, 72 proteins were analyzed. Significant differences in plasma protein levels between Day 14 versus Day 0 in both CMA and placebo groups (Dataset S8, Supporting www.advancedsciencenews.com www.advancedscience.com Information) and between the CMA and placebo groups on Day 14 and Day 0 (Dataset S9, Supporting Information) are presented. We investigated the associations between the plasma level of all inflammation-related proteins with the plasma levels of metabolic activators (Dataset S10, Supporting Information). The results showed that the administration of CMA effected a large number of biochemical parameters, based on both metabolomics and proteomics analysis.

We first analyzed the plasma levels of serine, carnitine, NR, and cysteine. CMA increased the plasma levels of each metabolic activator proportionally on Day 14 versus Day 0 in the CMA group ( Figure 4A , Dataset S4, Supporting Information). Moreover, the plasma levels of NR, nicotinamide, 1-methylnicotinamide and N1-methyl-2-pyridone-5-carboxamide (associated with NR and NAD + metabolism); of serine and N-acetylglycine (associated with serine and glycine metabolism); and of deoxycarnitine, acetylcarnitine, (R)-3-hydroxybutyrylcarnitine, linoleoylcarnitine (C18:2), and dihomo-linoleoylcarnitine (C20:2) (associated with carnitine metabolism) were significantly higher in the CMA group than in the placebo group on Day 14 (Dataset S5, Supporting Information).

Next, we investigated the relationship with the plasma level of administrated CMAs and other metabolites (Dataset S6, Supporting Information). We analyzed the 38 most significantly correlated plasma metabolites with serine, l-carnitine, NR, and cysteine ( Figure 4B , Dataset S6, Supporting Information) and found three clusters of metabolites which are significantly correlated with serine only, cysteine only and significantly correlated with all serine, l-carnitine, and NR. We observed that cysteine had a different dynamic compared to the other three metabolic activators. On the other hand, homostachydrine involved in xenobiotics metabolism as well as succinoyltaurine involved in methionine, cysteine, SAM, and taurine metabolism were significantly negatively correlated with serine and cysteine, respectively.

Mortality in COVID-19 patients has been strongly associated with the presence of the cytokine storm induced by the virus. Increased cytokine levels are also linked with increased viral load and the severe form of the disease. [30] To study the changes in the cytokine levels, we determined the dynamic range of 72 inflammatory proteins in plasma samples with the Olink multiplex inflammation panel (Dataset S7, Supporting Information). The plasma level of 14 proteins were significantly (false-discovery rate: FDR<0.01) changed following the recovery of the patients on Day 14 versus Day 0, in the placebo group ( Figure 5A , Dataset S8, Supporting Information). The plasma levels of nine proteins including CSF-1, CX3CL1, CXCL10, IFN-gamma, IL-18R1, MCP-2, OPG, TNF, and TRAIL were significantly (FDR<0.01) decreased, whereas the plasma level of remaining 5 proteins including Flt3L, MCP-4, TNFRSF9, TRANCE and TWEAK was slightly but significantly (log2FC<0.15 & FDR<0.01) increased after 14 d in the placebo group treated only with HQ ( Figure 5A , Dataset S8, Supporting Information).

We analyzed the effect of CMA on plasma cytokine levels and found that 36 proteins were significantly (FDR<0.01) different in the CMA group on Day 14 versus Day 0. 12 of these protein markers were significantly increased whereas 24 of these protein markers were significantly decreased on Day 14 versus Day 0. We observed that 14 of the 36 proteins were also significantly (FDR<0.01) differentially expressed in the placebo group (Figure 5 , Dataset S8, Supporting Information). After filtering out the proteins based on log2FC, we found that the plasma levels of 11 proteins including, IL6, IL10, IFN-gamma, CXCL10, CCL19, CX3CL1, CXCL11, IL-15RA, IL-17C, MCP-2 and TNF were significantly (FDR<0.01) downregulated and the plasma level of TRANCE and EN-RAGE was significantly (FDR<0.01) upregulated in the CMA group ( Figure 5 and Dataset S8, Supporting Information).

Next, we compared the differences in the decrease of the cytokine levels both in CMA and placebo groups and observed that the magnitude of the decrease in the plasma level of downregulated cytokines was greater in the CMA group compared to placebo group on Day 14 ( Figure 6 and Dataset S8, Supporting Information). Moreover, we found that the plasma levels of CSF-1, IL-15RA, IL18, MCP-1 and TNF were significantly downregulated in the CMA group compared to placebo group on Day 14, whereas there was no significant difference in the plasma level of these proteins between the groups on Day 0 (Dataset S9, Supporting Information).

We investigated the association between the plasma cytokine levels and the individual metabolic activators and found that the plasma level of most cytokine levels were significantly inversely correlated with the plasma level of serine ( Figure 5B , Dataset S10, Supporting Information). These results demonstrate that the administration of CMA significantly improved cytokine levels associated with inflammation during the recovery of the COVID-19 patients and improvement in metabolic conditions in COVID-19 patients.

We identified the significantly (FDR<0.001) different plasma metabolites on Day 14 versus Day 0 in both CMA and placebo groups. We found that the plasma levels of 122 metabolites were significantly different in both CMA and placebo groups, whereas plasma levels of 231 and 20 metabolites were specifically significantly different only in the CMA and placebo groups, respectively (FDR<0.001, Dataset S4, Supporting Information). Evaluation of plasma metabolites that differed significantly on Day 14 versus Day 0 in each group showed that larger number of metabolites related to amino acid ( Figure 6A acid metabolism, we found that plasma levels of 25 metabolites were significantly different both in the CMA and placebo group, whereas 70 and 6 were specifically significantly altered only in the CMA and placebo group, respectively (FDR<0.001, Figure 6A , Dataset S4, Supporting Information).

Increased plasma levels of metabolites in the kynurenine pathway were associated with COVID-19 severity. [31] In our study, we found that plasma levels of kynurenate and 8-methoxy kynurenate were significantly lower on Day 14 versus Day 0 in the CMA group ( Figure 6B, Dataset S4, Supporting Information) . The plasma level of kynurenine was significantly decreased on Day 14 versus Day 0 both in the CMA and placebo groups. However, the magnitude of the reduction of kynurenine was significant in the CMA versus placebo on Day 14 ( Figure 6C , Datasets S4 and S5, Supporting Information). Reduction in the plasma level of kynurenine and kynurenate was positively correlated with plasma serine (Dataset S6, Supporting Information). Kynurenine, which has a prooxidant effects, is the product of tryptophan degradation pathway. Its aerobic irradiation produces superoxide radicals and leads to cytochrome C reduction. [32] It has been reported that increased levels of kynurenine lead to cell death through the reactive oxygen species (ROS) pathway in nature killer (NK) cells [33] and lower blood pressure in systemic inflammation. [34] In our study we found that plasma levels of metabolites related to the urea cycle (3-amino-2-piperidone, N,N,N-trimethylalanyl proline betaine, homoarginine, and arginine) were significantly decreased in the CMA versus placebo group on Day 14 ( Figure 6B , Dataset S4, Supporting Information). Specifically, the plasma level of 3-amino-2-piperidone was significantly decreased in CMA group on Day 14 versus Day 0 ( Figure 6B , Dataset S4, Supporting Information) and inversely correlated with the plasma level of serine (Dataset S6, Supporting Information).

Emerging evidence indicates that kidney complications in COVID-19 patients are frequent, but the potential impact of SARS-Cov2 on the kidney is still undetermined. [35] Recent studies showed that plasma level of N,N,N-trimethyl-5-aminovalerate involved in lysine metabolism is an indicator of elevated urinary albumin excretion. [36] In our study, we found that the plasma level of N,N,N-trimethyl-5-aminovalerate was significantly increased on Day 14 versus Day 0 in the placebo group while its plasma level is significantly decreased on Day 14 versus Day 0 in the CMA group ( Figure 6B Lipids play a fundamental role in multiple stages of the virus cycle. Specific lipid species of cellular membranes (e.g., choles-terol and sphingolipids) are not only barriers but also receptors to infection initiation. [37] In our study, plasma level of 71 metabolites involved in lipid metabolism were significantly (FDR<0.001) different in both groups, whereas 102 and 5 were specifically significantly changed only in the CMA and placebo groups, respectively ( Figure S5A, Dataset S4, Supporting Information) . Plasma level of a significant number of metabolites associated with ceramides and sphingomyelins were significantly decreased on Day 14 versus Day 0 in both CMA and placebo groups (Figure S5B, Dataset S4, Supporting Information) . However, the reduction in the plasma level of metabolites involved in ceramides and sphingomyelins was more dramatic in the CMA group ( Figure S5B , Dataset S4, Supporting Information). Plasma level of metabolites associated with fatty acid metabolism (acyl carnitines) were significantly increased in the CMA group on Day 14 versus Day 0. In both groups, plasma levels of lysophospholipid, phosphatidylcholine, and androgenic steroids were significantly increased on Day 14 versus Day 0 ( Figure S5B ,C, Dataset S4, Supporting Information). These alterations were significantly positively correlated with carnitine and serine levels (Dataset S6, Supporting Information).

Ketone bodies have important signaling roles in restoring altered energy metabolism and redox state. In this study, we found that the plasma level of 2R,3R-dihydroxybutyrate was significantly decreased in the CMA group on Day 14 versus Day 0 ( Figure S5B , Dataset S4, Supporting Information). We also observed that plasma level of carnitine and serine also showed a significant inverse correlation with the plasma level of 2R,3Rdihydroxybutyrate (Dataset S6, Supporting Information). We also found that vitamins (Tocopherol, vitamin A, and riboflavin) and benzoate metabolism were significantly increased in both groups, whereas the plasma level of metabolites associated with the TCA cycle intermediate products were upregulated on Day 14 versus Day 0 in the CMA ( Figure S6 , Dataset S4, Supporting Information). Overall, these results indicate that the administration of CMA effected the global metabolism of the patients.

We have studied the associations between the significantly improved (decreased) clinical parameters including AST, ALT, LDH and TGs with the plasma level of all metabolites (Dataset S11, Supporting Information) and all inflammation proteins (Dataset S12, Supporting Information) and presented the 10 most significantly correlated metabolites ( Figure 7A ) and inflammation proteins ( Figure 7B ). The reduction in all four clinical parameters was significantly correlated with the plasma level of serine and glycine. We also found that plasma level of cysteine-glutathione disulfide was significantly inversely correlated with the level of AST ALT and TGs. Hence, we propose that serine is the key metabolic activator leading to the improvement in the clinical parameters in COVID-19 patients. We also evaluated the association of plasma proteins with the level of AST, ALT, LDH and TG and found that CDCP1 was positively correlated with all parameters ( Figure 7B , Dataset S12, Supporting Information). Plasma level of a set of inflammatory proteins (MCP-2, CXCL10, CSF-1, IL-18R1, TNF, MCP-1, CDCP1 and VEGFA) were significantly positively correlated with the level of ALT and AST ( Figure 7B ). Interestingly, we found that plasma levels of IL10, CCL19, CXCL9, CXCL1, OPG, CX3CL1, PD-L1, LIF-R, IFN-gamma and TRAIL were positively correlated and TRANCE, IL18, IL-12B, TWEAK, uPA and IL6 were inversely correlated with the level of AST, however these proteins were not significantly correlated with the level of ALT. On the other hand, the level of ALT was also significantly positively correlated with HGF and negatively correlated with CCL28 and SCF, which were not significantly correlated with the level of AST. Additionally, level of TG was positively correlated with the plasma level of TRANCE, IL-10RB, CDCP1 and HGF, however its inverse correlation was observed with the plasma level of CX3CL1 and SCF. We also found that hemoglobin levels were significantly correlated with the inflammatory proteins including EN-RAGE, DNER, IL-10RB, VEGFA, HGF, CST5 and MCP-1 (Dataset S12, Supporting Information).

Finally, we constructed a multi-omics correlation network based on clinical variables, proteomics, and metabolomics data (unfiltered network). The full network can be explored via iNet-Models (http://inetmodels.com), an open-access interactive web platform for multiomics data visualization and database. This network showed direct and indirect intra-and interomics functional relationships of different analytes. We subsequently overlaid the statistically altered analytes (clinical variables, metabolites and proteins) to the sub-network of the individual metabolic activators ( Figure 7C ). The subnetwork was built from the union of top 15 metabolite neighbors, and all protein and clinical neighbors. We identified the serine as the most connected metabolic activator to clinical variables, metabolites, and proteins. Moreover, we performed centrality analysis of the network to identify the most central inflammation protein markers, and found that MCP-4, IL-18R1, HGF, CXCL10 and CSF-1 were among top 10 most-central (degree) protein nodes which all showed significant downregulation on Day 14 versus Day 0 in the CMA group. We found that all of them, except MCP-4, were significantly inversely correlation with serine (Dataset S13, Supporting Information).

Our study shows that the combination of CMA and standard therapy significantly reduces the mean recovery time of ambulatory patients with COVID-19 as compared with placebo and standard therapy (6.6 vs 9.3 d in phase-2) and (5.7 vs 9.2 d in phase-3). Our multiomics analysis on patients recruited in phase-2 trial is consistent with the notion that CMA improves clinical outcomes in COVID-19 by improving immune response, and regulating antioxidant, amino acid and lipid metabolism. After having a positive result on the phase 2 study with 93 patients, we designed a double-blinded placebo-controlled Phase 3 study with 304 patients. We have shown that administration of the CMA accelerates the recovery of the patients independent of standard therapy. We have also shown that the clinical parameters including ALT, LDH, creatinine and glucose were significantly improved after the administration of the CMA in a total of 397 patients recruited in phase 2 and phase 3 trial. In the phase 3 trial, we also included the patients treated with FP, and again showed that CMA accelerates the recovery of the patients independent of the standard therapy. We also compared the effect of the HQ and FP in the recovery of the patients and observed no significant differences between the drugs used in the standard therapy.

Although COVID-19 primarily causes symptoms of respiratory infection, it often causes gastrointestinal and hepatic symptoms, including nausea/vomiting, diarrhea, and elevated levels of liver enzymes. [1] Some studies have reported that liver deficiencies correlate with worse outcomes, including longer hospitalization, progression to severe COVID-19, admission to the intensive care unit, and death. [38] [39] [40] [41] Mounting evidence shows that the GSH level is insufficient to maintain and regulate the thiol redox status of the liver in subjects with liver dysfunction. [26] Depleted liver GSH can be restored by administration of NAC, serine and glycine which can be synthesized through the interconversion of serine. Serine synthesis is downregulated in NAFLD patients, and administration of serine enhances homocysteine metabolism in mice and rats. [42] Two other components of CMA including carnitine and NR, which stimulate the transfer of fatty acids from the cytosol to mitochondria, are also depleted in liver diseases. [43] [44] [45] [46] Hence, we have here analyzed the effect of a mixture of CMA consisting of serine, a cysteine analogue, salt form of l-carnitine and an NAD+ precursor, administrated to COVID-19 patients to increase the GSH level in liver and other tissues.

NAD + is an essential metabolite in cellular energy generation and redox biology. Recently, it has been shown that the anti-coronaviral activities of four noncanonical PARP isozyme activities are limited by cellular NAD + status. [47] Additionally, a significant activation of kynurenine pathway in severe COVID-19 population has been reported. [31] Tryptophan is an essential amino acid that is fundamental for the biosynthesis of fundamental neuromodulators, namely serotonin and melatonin. Tryptophan catabolism through kynurenine pathway is the sole route for de novo NAD+ synthesis. In this context, CMA significantly decreased the plasma levels of metabolites involved in kynurenine pathway, and this reduction might play a crucial role in restoring the metabolic balance in COVID-19 patients.

The urea cycle is essential to humans for the elimination of nitrogen from protein metabolism. Arginine is critically important in diverse biological roles to regulate the host immune response and defenses. [48] Interestingly, arginine has also shown to be a key player in the life cycle of many viruses including Herpesviridae and Adenoviridae. [49] In parallel, arginine depletion treatment has shown to inhibit the viral replication and transmission of HSV-1. [50] Similarly, a recent study indicated antiviral activity of arginine-depleting enzymes in patients with hepatitis C virus. [51] In this manner, the role of the urea cycle and related metabolites offer targets for understanding the aspects of viral diseases and CMA might present a treatment opportunity of viral diseases including COVID-19, without serious adverse effects.

l-serine is generally classified as a non-essential amino acid, however under certain circumstances, vertebrates cannot synthesize it in sufficient quantities to meet necessary cellular demands. For instance, a recent study showed that extracellular serine is required for optimal T cell proliferation even in abundant glucose concentrations to support T cell effector function. Restricting dietary serine disturb pathogen-driven response of T cells in vivo, without altering the entire immune cell homeostasis. [14] In another study in vivo deprivation of the de novo serine synthesis impaired LPS induction of IL-1 levels and enhanced survival in an LPS-driven model of sepsis in mice, which reveals that serine metabolism is fundamental for GSH synthesis to maintain IL-1 cytokine production. [21] l-carnitine is a naturally occurring substance required in mammalian energy metabolism. It is a carrier molecule that facilitates the transport of long-chain fatty acids across the inner mitochondrial membrane, thereby delivering substrate for oxidation and subsequent energy production. l-carnitine has been reported to possess antioxidant and anti-inflammatory potency and its increase might be associated with the relatively decreased inflammatory response in the patients. [52] The results of another study using a lamb model with increased pulmonary blood flow showed that chronic l-carnitine treatment alleviates changes in lung carnitine homeostasis, reduces associated oxidative stress, and improves pulmonary mitochondrial function, NO signaling and eventually endothelial function. [53] As with all metabolomics studies, not every metabolite can be captured in a single assay. In this study, we were unable to measure plasma NAD+ in the study participants. NAD+ levels in the plasma are dynamic and are typically much lower than levels found in the cells and tissues. Unfortunately, plasma NR is not a surrogate marker for NAD+ status, and has an estimated half-life of 2.7 h and a C max of 3 h. [54] In a clinical kinetics study following 9 d of NR supplementation, NR levels still appeared to peak and trough at 3 h, however NAD+ levels were consistent across time points, having reached steady state. [54] Any correlations related to plasma NR and the up-or down-regulation of metabolites or inflammatory markers is not likely reflective of actual NAD+ status in the study participants. Future research that evaluates NAD+ levels in COVID-19 patients before and after CMA treatment, as well as treatment with the individual co-factors separately would provide further evidence of the role of NAD+ status on potential correlation (and causation) to changes in the metabolome and inflammatory markers.

In this study, patients also received HQ or FP, recommended as standard therapy in some countries. Therefore, we could not rule out possible drug interactions based on existing data. Unfortunately, due to access limitations to the patients during the study, we were unable to sample the patients directly following the end of HQ or FP treatment. An additional mid-point analysis at 7 d may have provided additional data related to the HQ metabolites in response to the inclusion of CMA.

Many COVID-19 patients are at risk for detrimental outcomes due to systemic inflammatory responses referred to as a cytokine storm, a life-threatening condition is dependent on downstream processes that lead to oxidative stress, dysregulation of iron homeostasis, hypercoagulability, and thrombocytopenia. [55, 56] Several studies have proposed that CMA components may effectively inhibit the production of proinflammatory molecules (e.g., IL-6, CCL-5, CXCL-8, and CXCL-10) and improve impaired mitochondrial functions by reducing oxidative damage, lipid peroxidation, and disturbed glucose tolerance. [47, 57] Based on integrative analysis, we observed that CMA may interrupt the overactive immune response and early treatment with CMA may reduce the risk of progression to severe respiratory distress and lung damage.

In conclusion, we evaluated the efficacy and safety of CMA in combination with HQ or FP therapy in patients with mild-tomoderate COVID-19 and observed that combination therapy is safe and beneficial in patients with mild-to-moderate COVID-19. Our analysis showed that administration of CMA is an effective and safe treatment for COVID-19 patients.

Trial Design and Oversight: Patients for this randomized, openlabel, placebo-controlled, phase-2 study and randomized, double-blinded, placebo-controlled, phase-3 study were recruited at the Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey. Written informed consent was obtained from all participants before the initiation of any trial-related procedures. The safety of the participants and the risk-benefit analysis was overseen by an independent external data-monitoring committee. The trial was conducted in accordance with Good Clinical Practice guidelines and the principles of the Declaration of Helsinki. The study was approved by the ethics committee of Istanbul Medipol University, Istanbul, Turkey, and retrospectively registered at https://clinicaltrials.gov/ with Clinical Trial ID: NCT04573153.

Participants: Patients were enrolled in the trial if they were over 18 years of age, had a PCR-confirmed COVID-19 test within the previous 24 h, and were in stable condition not requiring hospitalization. Chest tomography was done to rule out pneumonia. Patients who had a partial oxygen saturation below 93% and required hospitalization after diagnosis were excluded. The main characteristics of the patients are summarized in Table S2 (Supporting Information). The inclusion, exclusion, and randomization criteria are described in detail in the Appendix in the Supporting Information.

Randomization, Interventions, and Follow-up: Patients were randomly assigned to receive CMA or placebo (3:1) and also received standard therapy with HQ or FP. Patient information (patient number, date of birth, initials) was entered into the web-based randomization system, and the randomization codes were entered into the electronic case report form. All clinical staff were blinded to treatment, as were the participants.

Treatment started on the day of diagnosis. Both placebo and CMA were provided in powdered form in identical plastic bottles containing a single dose to be dissolved in water and taken orally one dose in the morning after breakfast and one dose in the evening after dinner. Each dose of CMA contained 3.73 g l-carnitine tartrate, 2.55 g N-acetylcysteine, 1 g nicotinamide riboside chloride, and 12.35 g serine. All participants also received oral HQ or FP for 5 d. The patients were contacted by telephone daily to assess symptoms and adverse events. All patients came for a follow-up visit on Day 14. Further information is provided in the Appendix in the Supporting Information.

Outcomes: The primary end point in the original protocol was to assess the clinical efficacy of CMA in COVID-19 patients. For the primary purpose, the proportion of patients who fully recovered from COVID-19, as demonstrated by being symptom free within the 14 d of the initial diagnosis of COVID-19, was determined. This was amended to include selfreporting of daily symptoms and clinical status using a binomial scale (present/absent) via daily telephone visits by clinical staff. The secondary aim in this study was to evaluate the safety and tolerability of CMA and HQ or FP combination. All protocol amendments were authorized and approved by the sponsor, the institutional review board or independent ethics committee, and the pertinent regulatory authorities.

Number and characteristics of adverse events, serious adverse events, and treatment discontinuation due to CMA were reported from the beginning of the study to the end of the follow-up period as key safety endpoints. The changes in vital signs (systolic and diastolic blood pressures, pulse, respiratory rate, body temperature, pulse oximetry values), baseline values, and the status of treatment were recorded at day 0 and 14. A complete list of the end points is provided in the Appendix in the Supporting Information.

Inflammatory Proteomics: Plasma levels of inflammatory proteins were determined with the Olink Inflammation panel (Olink Bioscience, Uppsala, Sweden). Briefly each sample was incubated with 92 DNAlabeled antibody pairs (proximity probes). When an antibody pair binds to its corresponding antigens, the corresponding DNA tails form an amplicon by proximity extension, which can be quantified by high-throughput, real-time PCR. Probe solution (3 µL) was mixed with 1 µL of sample and incubated overnight at 4°C. Then 96 µL of extension solution containing extension enzyme and PCR reagents for the pre-amplification step was added, and the extension products were mixed with detection reagents and primers and loaded on the chip for qPCR analysis with the BioMark HD System (Fluidigm Corporation, South San Francisco, CA).To minimize inter-and intrarun variation, the data were normalized to both an internal control and an interplate control. Normalized data were expressed in arbitrary units (Normalized Protein eXpression, NPX) on a log2 scale and linearized with the formula 2 NPX . A high NPX indicates a high protein concentration. The limit of detection, determined for each of the 92 assays, was defined as three standard deviations above the negative control (background).

Untargeted Metabolomics Analysis: Plasma samples were collected on Days 0 and 14 for nontargeted metabolite profiling by Metabolon (Durham, NC). The samples were prepared with an automated system (MicroLab STAR, Hamilton Company, Reno, NV). For quality control purposes, a recovery standard was added before the first step of the extraction. To remove protein and dissociated small molecules bound to protein or trapped in the precipitated protein matrix, and to recover chemically diverse metabolites, proteins were precipitated with methanol under vigorous shaking for 2 min (Glen Mills GenoGrinder 2000) and centrifuged. The resulting extract was divided into four fractions: one each for analysis by ultraperformance liquid chromatography-tandem mass spectroscopy (UPLC-MS/MS) with positive ion-mode electrospray ionization, UPLC-MS/MS with negative ion-mode electrospray ionization, and gas chromatography-mass spectrometry; one fraction was reserved as a backup.

Statistical Analysis: The primary outcome was the time to recovery, defined as the time from diagnosis to the first self-report of no symptom. The sample size for each group in phase 2 and phase 3 studies were detailed in Figures 1A and 2A , respectively. Recovery curves were generated with the Kaplan-Meier method. Hazard ratios and 95% confidence intervals were calculated with the Univariate and Multivariate Cox proportionalhazards regression model based on R package survival. The age, gender, other treatment history, cigarette, alcohol, and HQ/FP treatment in Multivariate Cox regression analysis were adjusted. In phase-2 study, the HQ/FP factor was excluded since all the patients received HQ treatment and none of them received FP treatment.

Differences in clinical measurements, proteomics, and metabolomics data were analyzed by t-test (paired t-test within group comparison, twosided and by omitting the pairs with missing values) and significant levels are detailed in the figure legends. The correlations for multi-omics networks were calculated using Spearman correlation and filtered with FDR < 0.05. The analyses were performed with the SciPy package in Python 3.7. Centrality analysis on the network was performed using Cytoscape 3.8.2. The script used to analyze the data can be found at https://github.com/ sysmedicine/AltayEtAll_2020_Covid_CMA

Supporting Information is available from the Wiley Online Library or from the author.

Proc. Natl. Acad. Sci

A.M., J.B., and M.U. are the founders and shareholders of ScandiBio Therapeutics and they filed a patent application on the use of CMA to treat COVID-19 patients. The other authors declare no competing interests.

The data have been included in the Supporting Information Datasets and presented at https://inetmodels.com/.Keywords combined metabolic activators, COVID-19, metabolomics, omics data, proteomics