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1.
Dis Markers ; 2021: 7686374, 2021.
Article in English | MEDLINE | ID: covidwho-1595046

ABSTRACT

OBJECTIVE: S-Adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) are indicators of global transmethylation and may play an important role as markers of severity of COVID-19. METHODS: The levels of plasma SAM and SAH were determined in patients admitted with COVID-19 (n = 56, mean age = 61). Lung injury was identified by computed tomography (CT) in accordance with the CT0-4 classification. RESULTS: SAM was found to be a potential marker of lung damage risk in COVID-19 patients (SAM > 80 nM; CT3,4 vs. CT 0-2: relative ratio (RR) was 3.0; p = 0.0029). SAM/SAH > 6.0 was also found to be a marker of lung injury (CT2-4 vs. CT0,1: RR = 3.47, p = 0.0004). There was a negative association between SAM and glutathione level (ρ = -0.343, p = 0.011). Interleukin-6 (IL-6) levels were associated with SAM (ρ = 0.44, p = 0.01) and SAH (ρ = 0.534, p = 0.001) levels. CONCLUSIONS: A high SAM level and high methylation index are associated with the risk of lung injury in patients with COVID-19. The association of SAM with IL-6 and glutathione indicates an important role of transmethylation in the development of cytokine imbalance and oxidative stress in patients with COVID-19.


Subject(s)
COVID-19/complications , Lung Injury/blood , S-Adenosylhomocysteine/blood , S-Adenosylmethionine/blood , SARS-CoV-2 , Adult , Aged , Aged, 80 and over , Atherosclerosis/epidemiology , Biomarkers , COVID-19/epidemiology , Comorbidity , Diabetes Mellitus/epidemiology , Female , Glutathione/blood , Humans , Hypertension/epidemiology , Interleukin-6/blood , Lung Injury/diagnostic imaging , Lung Injury/etiology , Male , Methylation , Middle Aged , Military Personnel , Risk , Tomography, X-Ray Computed , Young Adult
2.
Oxid Med Cell Longev ; 2021: 9221693, 2021.
Article in English | MEDLINE | ID: covidwho-1438138

ABSTRACT

OBJECTIVE: Aminothiols (glutathione (GSH), cysteinylglycine (CG)) may play an important role in the pathogenesis of coronavirus disease 2019 (COVID-19), but the possible association of these indicators with the severity of COVID-19 has not yet been investigated. METHODS: The total content (t) and reduced forms (r) of aminothiols were determined in patients with COVID-19 (n = 59) on admission. Lung injury was characterized by computed tomography (CT) findings in accordance with the CT0-4 classification. RESULTS: Low tGSH level was associated with the risk of severe COVID-19 (tGSH ≤ 1.5 µM, mild vs. moderate/severe: risk ratio (RR) = 3.09, p = 0.007) and degree of lung damage (tGSH ≤ 1.8 µM, CT < 2 vs. CT ≥ 2: RR = 2.14, p = 0.0094). The rGSH level showed a negative association with D-dimer levels (ρ = -0.599, p = 0.014). Low rCG level was also associated with the risk of lung damage (rCG ≤ 1.3 µM, CT < 2 vs. CT ≥ 2: RR = 2.28, p = 0.001). Levels of rCG (ρ = -0.339, p = 0.012) and especially tCG (ρ = -0.551, p = 0.004) were negatively associated with platelet count. In addition, a significant relationship was found between the advanced oxidation protein product level and tGSH in patients with moderate or severe but not in patients with mild COVID-19. CONCLUSION: Thus, tGSH and rCG can be seen as potential markers for the risk of severe COVID-19. GSH appears to be an important factor to oxidative damage prevention as infection progresses. This suggests the potential clinical efficacy of correcting glutathione metabolism as an adjunct therapy for COVID-19.


Subject(s)
COVID-19/diagnosis , Dipeptides/blood , Glutathione/blood , Advanced Oxidation Protein Products/blood , Aged , Amino Acids, Sulfur/blood , Biomarkers/blood , COVID-19/blood , COVID-19/pathology , Dipeptides/metabolism , Female , Glutathione/metabolism , Humans , Lung/diagnostic imaging , Lung/pathology , Male , Middle Aged , Oxidation-Reduction , SARS-CoV-2/isolation & purification , Severity of Illness Index
3.
Clin Biochem ; 92: 71-76, 2021 Jun.
Article in English | MEDLINE | ID: covidwho-1141672

ABSTRACT

Owing to their ease of use, glucose meters are frequently used in research and medicine. However, little is known of whether other non-glucose molecules, besides vitamin C, interfere with glucometry. Therefore, we sought to determine whether other antioxidants might behave like vitamin C in causing falsely elevated blood glucose levels, potentially exposing patients to glycemic mismanagement by being administered harmful doses of glucose-lowering drugs. To determine whether various antioxidants can be detected by seven commercial glucose meters, human blood samples were spiked with various antioxidants ex vivo and their effect on the glucose results were assessed by Parkes error grid analysis. Several of the glucose meters demonstrated a positive bias in the glucose measurement of blood samples spiked with vitamin C, N-acetylcysteine, and glutathione. With the most interference-sensitive glucose meter, non-blood solutions of 1 mmol/L N-acetylcysteine, glutathione, cysteine, vitamin C, dihydrolipoate, and dithiothreitol mimicked the results seen on that glucose meter for 0.7, 1.0, 1.2, 2.6, 3.7 and 5.5 mmol/L glucose solutions, respectively. Glucose meter users should be alerted that some of these devices might produce spurious glucose results not only in patients on vitamin C therapy but also in those being administered other antioxidants. As discussed herein, the clinical relevance of the data is immediate in view of the current use of antioxidant therapies for disorders such as the metabolic syndrome, diabetes, cardiovascular diseases, and coronavirus disease 2019.


Subject(s)
Antioxidants/chemistry , Blood Glucose Self-Monitoring/instrumentation , Blood Glucose/analysis , Acetylcysteine/blood , Acetylcysteine/chemistry , Antioxidants/analysis , Antioxidants/metabolism , Ascorbic Acid/analysis , Ascorbic Acid/blood , Blood Glucose/chemistry , Blood Glucose Self-Monitoring/methods , Glutathione/blood , Glutathione/chemistry , Humans , Point-of-Care Systems
4.
Med Hypotheses ; 149: 110543, 2021 Apr.
Article in English | MEDLINE | ID: covidwho-1087147

ABSTRACT

The socio-economic implications of COVID-19 are devastating. Considerable morbidity is attributed to 'long-COVID' - an increasingly recognized complication of infection. Its diverse symptoms are reminiscent of vitamin B12 deficiency, a condition in which methylation status is compromised. We suggest why SARS-CoV-2 infection likely leads to increased methyl-group requirements and other disturbances of one-carbon metabolism. We propose these might explain the varied symptoms of long-COVID. Our suggested mechanismmight also apply to similar conditions such as myalgic encephalomyelitis/chronic fatigue syndrome. The hypothesis is evaluable by detailed determination of vitamin B12and folate status, including serum formate as well as homocysteine and methylmalonic acid, and correlation with viral and host RNA methylation and symptomatology. If confirmed, methyl-group support should prove beneficial in such individuals.


Subject(s)
COVID-19/complications , Folic Acid/blood , Vitamin B 12 Deficiency/diagnosis , Adenosine/analogs & derivatives , Adenosine/chemistry , COVID-19/blood , COVID-19/physiopathology , Folic Acid Deficiency , Formates/blood , Genome, Viral , Glutathione/blood , Homocysteine/blood , Hospitalization , Humans , Methylation , Methylmalonic Acid/blood , Oxidative Stress , RNA/chemistry , Serine/blood , Vitamin B 12/blood , Post-Acute COVID-19 Syndrome
5.
ACS Infect Dis ; 6(7): 1558-1562, 2020 07 10.
Article in English | MEDLINE | ID: covidwho-401389

ABSTRACT

Higher rates of serious illness and death from coronavirus SARS-CoV-2 (COVID-19) infection among older people and those who have comorbidities suggest that age- and disease-related biological processes make such individuals more sensitive to environmental stress factors including infectious agents like coronavirus SARS-CoV-2. Specifically, impaired redox homeostasis and associated oxidative stress appear to be important biological processes that may account for increased individual susceptibility to diverse environmental insults. The aim of this Viewpoint is to justify (1) the crucial roles of glutathione in determining individual responsiveness to COVID-19 infection and disease pathogenesis and (2) the feasibility of using glutathione as a means for the treatment and prevention of COVID-19 illness. The hypothesis that glutathione deficiency is the most plausible explanation for serious manifestation and death in COVID-19 patients was proposed on the basis of an exhaustive literature analysis and observations. The hypothesis unravels the mysteries of epidemiological data on the risk factors determining serious manifestations of COVID-19 infection and the high risk of death and opens real opportunities for effective treatment and prevention of the disease.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Anticoagulants/pharmacology , Antioxidants/pharmacology , Antiviral Agents/pharmacology , Betacoronavirus/drug effects , Coronavirus Infections/mortality , Coronavirus Infections/pathology , Glutathione/deficiency , Glutathione/pharmacology , Pneumonia, Viral/mortality , Pneumonia, Viral/pathology , Adult , Anti-Inflammatory Agents/blood , Anticoagulants/blood , Antiviral Agents/blood , Betacoronavirus/physiology , COVID-19 , Coronavirus Infections/blood , Coronavirus Infections/virology , Disease Susceptibility , Feasibility Studies , Female , Glutathione/blood , Humans , Middle Aged , Oxidative Stress/drug effects , Pandemics , Pneumonia, Viral/blood , Pneumonia, Viral/virology , Prognosis , Reactive Oxygen Species/blood , Risk Factors , SARS-CoV-2 , Severity of Illness Index , Virus Replication/drug effects , Vitamin D Deficiency/complications
6.
J Clin Virol ; 128: 104431, 2020 07.
Article in English | MEDLINE | ID: covidwho-245358

ABSTRACT

BACKGROUND: Despite the death rate of COVID-19 is less than 3%, the fatality rate of severe/critical cases is high, according to World Health Organization (WHO). Thus, screening the severe/critical cases before symptom occurs effectively saves medical resources. METHODS AND MATERIALS: In this study, all 336 cases of patients infected COVID-19 in Shanghai to March 12th, were retrospectively enrolled, and divided in to training and test datasets. In addition, 220 clinical and laboratory observations/records were also collected. Clinical indicators were associated with severe/critical symptoms were identified and a model for severe/critical symptom prediction was developed. RESULTS: Totally, 36 clinical indicators significantly associated with severe/critical symptom were identified. The clinical indicators are mainly thyroxine, immune related cells and products. Support Vector Machine (SVM) and optimized combination of age, GSH, CD3 ratio and total protein has a good performance in discriminating the mild and severe/critical cases. The area under receiving operating curve (AUROC) reached 0.9996 and 0.9757 in the training and testing dataset, respectively. When the using cut-off value as 0.0667, the recall rate was 93.33 % and 100 % in the training and testing datasets, separately. Cox multivariate regression and survival analyses revealed that the model significantly discriminated the severe/critical cases and used the information of the selected clinical indicators. CONCLUSION: The model was robust and effective in predicting the severe/critical COVID cases.


Subject(s)
Coronary Disease/diagnosis , Coronavirus Infections/diagnosis , Diabetes Complications/diagnosis , Diabetes Mellitus/diagnosis , Disease Outbreaks , Hypertension/diagnosis , Pneumonia, Viral/diagnosis , Adult , Age Factors , Aged , Area Under Curve , Betacoronavirus , Biomarkers/blood , CD3 Complex/blood , COVID-19 , Cohort Studies , Coronary Disease/blood , Coronary Disease/complications , Coronary Disease/mortality , Coronavirus Infections/blood , Coronavirus Infections/complications , Coronavirus Infections/mortality , Diabetes Complications/blood , Diabetes Complications/mortality , Diabetes Mellitus/blood , Diabetes Mellitus/mortality , Female , Glutathione/blood , Humans , Hypertension/blood , Hypertension/complications , Hypertension/mortality , Male , Middle Aged , Pandemics , Pneumonia, Viral/blood , Pneumonia, Viral/complications , Pneumonia, Viral/mortality , Prognosis , ROC Curve , SARS-CoV-2 , Severity of Illness Index , Support Vector Machine , Survival Analysis , Thyroxine/blood
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