Kandji Pape Matar
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
LiveDNA: 221.37708
Barry Nene Oumou Kesso
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
Thioune Ndeye Mareme
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
Saida Elbouzidi
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
Djite Moustapha
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
LiveDNA: 221.31153
Mbacke Ndoumbé Mame
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
Diagne Binta
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
Ndour El Hadji Malick
Laboratory of Pharmaceutical Biochemistry, Faculty of Medicine, Pharmacy, Cheikh Anta Diop University, Dakar, Senegal
Gueye- Tall Fatou
Laboratory of Pharmaceutical Biochemistry, Faculty of Medicine, Pharmacy, Cheikh Anta Diop University, Dakar, Senegal
Lopez- Sall Philomene
Laboratory of Pharmaceutical Biochemistry, Faculty of Medicine, Pharmacy, Cheikh Anta Diop University, Dakar, Senegal
Gueye Papa Madieye
Laboratory of Biochemistry and Hematology, National University Hospital of Fann, Dakar, Senegal
Asian Journal of Biochemistry
Year: 2022 | Volume: 17 | Issue: 1 | Page No.: 1-6
DOI: 10.3923/ajb.2022.1.6
ABSTRACT
Background and Objective: SARS-CoV-2 infection is the cause of many complications that can affect many organs, hepatic manifestations have been described due to the existence of hepatic tropism. The objective of this study was to assess the markers of liver damage in patients infected with SARS-CoV-2 monitored at the epidemiological treatment centre of fann. Materials and Methods: This is a prospective analytical study. Were included 202 subjects infected with SARS-CoV-2. The parameters studied were on the one hand age and sex and on the other hand transaminases (ALT, AST), GGT (gamma GT), PAL (alkaline phosphatase), serum albumin, total and direct bilirubin. Parameter assays were performed with the A15 Chemistry Analyzer. The statistical test used for data processing is the Chi. A p<0.05 was considered significant. Results: The average age was 60 years with a sex ratio of 1.12. The analysis of the biological parameters in the patients shows an increase in the activity of the hepatic enzymes in 38.12 and 48.02% of the patients, respectively for ALT and AST. PAL and GGT activity was increased, respectively in 25.25 and 61.88% of patients. Hypoalbuminemia was found in 61.88% of patients and an increase in total and direct bilirubin, respectively in 14.36 and 39.60% of patients. The analysis of the results according to the syndrome markers had shown in the patient's frequencies of 44, 28 and 18%, respectively for cholestasis, cytolysis and mixed damage. Conclusion: Liver disturbances could be used as markers to dictate the prognosis of COVID-19 severity.
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Kandji Pape Matar, Barry Nene Oumou Kesso, Thioune Ndeye Mareme, Saida Elbouzidi, Djite Moustapha, Mbacke Ndoumbé Mame, Diagne Binta, Ndour El Hadji Malick, Gueye- Tall Fatou, Lopez- Sall Philomene and Gueye Papa Madieye, 2022. Evaluation of Markers of Liver Damage in Patients Infected with SARS-CoV2. Asian Journal of Biochemistry, 17: 1-6.
DOI: 10.3923/ajb.2022.1.6
URL: https://scialert.net/abstract/?doi=ajb.2022.1.6
DOI: 10.3923/ajb.2022.1.6
URL: https://scialert.net/abstract/?doi=ajb.2022.1.6
INTRODUCTION
The coronavirus family is responsible for respiratory infections in mammals and birds. These are RNA viruses, grouped into four subfamilies, two of which are responsible for severe and potentially fatal pathologies: SARS-CoV-1 and MERS-CoV, identified, respectively in 2003 and 20121. In December, 2019, the appearance of several cases of pneumonia of unknown origin in the province of Hubei in China, led to the identification, in January, 2020, of a new coronavirus, called SARS-CoV-2 by the group Coronavirus Working Group of the International Committee on Taxonomy of Viruses. SARS-CoV-2 causes a sometimes severe respiratory disease, named COVID-19 by the World Health Organization2. Covid-19 is associated with many biological complications affecting many organs and tissues due to their expression of the ACE2 receptor3,4. First known by its clinical manifestations such as fever and respiratory symptoms, COVID-19 disease can be revealed by extra-pulmonary signs, including gastrointestinal and hepatic manifestations raising the potential tropism of SARS-CoV-2 for the digestive tract, numerous studies show that liver disturbances are common in patients with COVID-19, which should be of concern2,5. Thus, the objective of this work was to evaluate the markers of liver damage in patients infected with SARS-CoV-2 followed at the Epidemiological Treatment Centre of the National University Hospital of Fann.
MATERIALS AND METHODS
This was a prospective analytical study carried out during the period from June-September, 2021. The patients recruited were followed at the level of the infectiology Departments of the epidemiological treatment centre and in whom the diagnosis of COVID-19 was confirmed by RT-PCR, the study did not concern suspected patients with a negative RT-PCR and patients with a history of liver damage. Blood samples were taken from the subjects by venipuncture at the elbow crease with a tourniquet. The blood was collected in a dry tube centrifuged at 3500 rpm for 5 min. Biochemical parameter assays were performed with the A15 Chemistry Analyzer, BioSystems (Spain, Barcelona). In this study, liver damage was classified according to syndrome markers in cytolysis, cholestasis or mixed damage:
| • | Cytolysis if ALT and/or AST >2× upper limit of normal (ULN) |
| • | Cholestasis if PAL and/or GGT and BILT (total bilirubin) or BILD (direct bilirubin) >2× ULN |
| • | Mixed if the combination of ALAT and/or ASAT >2× LSN and PAL and/or GGT and BILT or BILD >2× ULN |
The recording of the data and the exploitation of the results were made by the Excel 2016 software, which had allowed us to calculate the descriptive data. The statistical test used for data processing is the Chi-square test, this test was performed by the GraphPad Prism 8.0.2 software (GraphPad Software Inc, San Diego, CA, USA). A p<0.05 was considered significant.
RESULTS
The current study population consisted of 202 subjects with COVID-19. The average age of our subjects was 60 years old with extremes of 23 and 96 years old. The sex ratio was 1.12. Liver test abnormalities were defined according to the standards of the reference interval of the laboratory in Fann: ALT >41, AST >40, PAL >270, GGT: Man >86 and Woman >48 IU L–1, BILT >1 mg dL–1, BILD >0.25 mg dL–1 and Albumin <38 g L–1. As part of our study, we considered abnormal liver function tests if at least one of the liver parameters studied was above the upper limit of normal (ULN) mentioned above. The analysis of the distribution of the results showed a disturbance of the liver balance sheet in 67.33% of the patients while 32.67% had a normal liver balance sheet (Fig. 1).
The distribution of hepatic abnormalities according to age groups shows a prevalence of 86.36% of disturbances in liver function tests in the age group (77-96 years) (Fig. 2).
Analysis of the distribution of hepatic abnormalities by sex showed a male predominance (74.77%) against 58.95% in women (Fig. 3).
The determination of the averages of the biochemical parameters studied in the patients showed enzymatic activities of the order of 47.56, 52.81, 209.4 and 111.5 UI L–1, respectively for ALT, AST, PAL and GGT. Levels of 0.71, 0.25 mg dL–1 and 36.43 g L–1 were found for BILT, BILD and albumin, respectively (Table 1).
 |
| Fig. 1: | Distribution of patients according to the presence or absence of liver abnormalities p<0.05 |
 |
| Fig. 2: | Frequency of liver abnormalities by age |
 |
| Fig. 3: | Frequency of liver abnormalities by sex p = 0.039 |
| Table 1: | Means of biological parameters in our study population | |||
Minimum | Average | Maximum | Common values | |
| ALT | 12 | 47.56 | 385 | <41 IU L–1 |
| AST | 11 | 52.81 | 340 | <40 IU L–1 |
| PAL | 65 | 209.4 | 704 | 98-270 IU L–1 |
| GGT | 19 | 111.5 | 474 | M: 16-86 IU L–1 |
W: 12-48 IU L–1 | ||||
| BILT | 0.15 | 0.71 | 6.62 | <1 mg dL–1 |
| BILD | 0.01 | 0.25 | 1.26 | <0.25 mg dL–1 |
| Albumin | 5.09 | 36.43 | 50.71 | 38-44 g L–1 |
| Table 2: | Distribution of disturbances according to the type of liver damage according to age and sex | ||||
Frequency according to gender (%) | Frequency by age (%) | ||||
| Disturbances | Frequency in the population (%) | H | F | <50 years old | >50 years |
| Cytolysis | 28 | 65.79 | 34.21 | 21.05 | 78.95 |
| Cholestasis | 44 | 41.67 | 58.33 | 18.33 | 81.67 |
| Mixed damage | 18 | 64 | 36 | 28 | 72 |
The analysis of the distribution of the parameters showed increased enzymatic activities of ALAT, ASAT, PAL and GGT, respectively in 38.12, 48.02, 25.25 and 61.88% of the patients. An increase in total and direct bilirubin levels was observed, respectively in 14.36 and 39.60% of patients and a decrease in albumin in 61.88% of patients. (Fig. 4).
Analysis of the results showed frequencies of 44, 28 and 18%, respectively for cholestasis, cytolysis and mixed damage. Breaking down the type of liver damage by gender, 65.79% of men had cytolysis and 58.33% of women presented with cholestasis syndrome. Analysis of the results according to age showed a predominance of hepatic disturbances in subjects over 50 years of age (Table 2).
 |
| Fig. 4: | Distribution of the biological parameters studied in our study population according to the reference values |
DISCUSSION
SARS-CoV-2 infection, called COVID-19, causes life-threatening pneumonia6. Additionally, there is a growing body of literature showing that liver damage is common in patients with COVID-19, which should be of concern7,8. It is in this context that we have set ourselves the objective of evaluating markers of liver damage in patients with COVID 19. The exploitation of these results made it possible to show that the average age of our population was 60 years, with extremes of 23 and 96 years and a sex ratio of 1.12. The predominance of the male sex in patients infected with SARS-CoV-2 has already been reported by several studies such as Hwaiz et al.9, Xu et al.10, this may be linked to a higher expression of the ACE2 receptor in men compared to women11. Other studies have attributed it to the hormonal difference indeed female sex hormones (estrogen, progesterone) have an anti-inflammatory role and influence immune cells (production of antibodies)12. Evaluation of biochemical parameters in our population showed averages of 47.56, 52.81, 209.4 and 111.5 UI L–1, respectively for ALT, AST, PAL and GGT. The means obtained for BILT, BILD and albumin were, respectively 0.71 and 0.25 mg dL–1 and 36.43 g L–1. Altaf et al.13 in a study conducted in Pakistan had found higher averages10. Analysis of the distribution of parameters showed an increase in liver enzyme activity in 38.12 and 48.02% of patients respectively for ALAT and ASAT. PAL and GGT activity was increased, respectively in 25.25 and 61.88% of patients. Hypoalbuminemia was found in 61.88% of patients and an increase in total and direct bilirubin respectively in 14.36 and 39.60% of patients. The frequencies found in this work were higher than those obtained by Fan et al.14 and Hundt et al.15, however, the frequencies obtained for transaminases and PAL in our study were close to those obtained in Iraq by Hwaiz et al.9 and Kumar et al.16 had found in a meta-analysis frequency for total bilirubin and albumin similar to our results. Many factors can lead to impaired liver function tests during COVID-19 including immune-mediated inflammatory response, drug-induced liver injury, hepatic congestion and direct viral toxicity17. A significant increase in liver enzyme activities in men (74.77%) compared to women (58.95%) was observed. Moreover, there was a direct positive correlation between these hepatic enzyme disturbances with age (p<0.05), this result was similar to that of Saini et al.18. Analysis of the results according to the type of liver damage showed frequencies of 44, 28 and 18%, respectively for cholestasis, cytolysis and mixed damage. In a study carried out in India frequencies of 53.48, 27.9 and 18.6%, respectively for cytolysis, cholestasis and mixed involvement were found18. The results obtained were following the literature, in fact, the angiotensin-2 converting enzyme receptor, which is the target of SARS-CoV-2, is strongly expressed in the epithelial cells of the bile ducts19. Breaking down by sex, no significant difference was found in the incidence of a type of liver injury in men and women (p>0.05). Analysis of the results by age showed a predominance of hepatic abnormalities in subjects over 50 years old (p<0.05). The underlying reason for liver injury during COVID-19 is still unclear and several mechanisms are discussed in the literature20. These mechanisms are related to direct cytotoxicity resulting from active viral replication in liver cells expressing the receptor ACE221. Other hypotheses are mentioned, in particular the reactivation of pre-existing liver disease but also patients with pre-existing chronic liver disease are predisposed to liver damage induced by SARS-CoV-2 infection22. A cause of drug origin has been reported, indeed the acetaminophen (antipyretic) used in the therapeutic management of patients with COVID-19 could cause liver damage22 but also other substances such as oseltamivir, abidol or lopinavir, may have hepatotoxic effects23.
CONCLUSION
The current study showed the existence of liver damage in patients with COVID-19. The degree of liver damage reflects the severity and increased mortality, liver disturbances could be used as markers to dictate the prognosis of the severity of COVID-19. However, it might be better to test the effect of drugs and the duration of drug administration on liver enzyme activities. further studies are needed to better explore the mechanisms of COVID-19-induced liver injury.
SIGNIFICANCE STATEMENT
The COVID-19 pandemic has caused many deaths with an impact on the global economy, this study is part of the proper management of patients infected with SARS-CoV-2 and the response to the pandemic. Our experience feedback in the management of the COVID-19 pandemic has shown the existence of liver lesions in patients infected with SARS-CoV-2. These disturbances can be used in the evaluation of the prognosis and ensure better patient care.
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