Background

While the lungs are the primary target of COVID-19, the liver is also commonly affected [1]. Examination of liver tissue from COVID-19 patients reveals several abnormalities: congestion in blood vessels, breakdown of liver cells with areas of cell death, immune cell migration within the liver, and a moderate amount of fat accumulation within liver cells [2]. Several biological processes contribute to the development of liver complications following SARS-CoV-2 infection. These include hypoxia and circulatory changes, hepatotoxic drugs consumption, cytopathic effect via angiotensin-converting enzyme 2 (ACE2) receptors, and hyper-inflammatory reaction to COVID-19 [3]. The most frequent liver abnormality seen in COVID-19 patients is fatty liver, medically known as hepatic steatosis [4]. Furthermore, existing conditions such as metabolic-associated fatty liver disease (MAFLD) and liver fibrosis may worsen the inflammatory response in these patients [5].

C-reactive protein (CRP) and D-dimer are well-established markers for predicting the severity of illness in COVID-19 patients. Scoring systems such as FIB-4 and APRI utilize readily available blood tests to assess liver fibrosis without needing invasive procedures [6]. Recent research suggests that among these markers (D-dimer, CRP, APRI, and FIB-4), the FIB-4 index appears to be the most accurate predictor for requiring mechanical ventilation (IMV). D-dimer and CRP have also shown some predictive value in this context. Furthermore, for predicting mortality, the FIB-4 index has shown the highest level of reliability, followed by D-dimer. This study proposes that using a FIB-4 threshold of greater than or equal to 1.9 might be more effective than traditional markers such as CRP and D-dimer in anticipating the need for mechanical ventilation and mortality risk in patients with SARS-CoV-2 infection [7].

Ultrasound (US), computed tomography (CT), and magnetic resonance imaging (MRI) are established imaging modalities for liver evaluation [8]. US should be prioritized as the primary diagnostic modality for the initial assessment of the liver in patients presenting with abdominal symptoms. US is a popular tool for identifying fatty liver disease, especially in advanced cases. While it is good at distinguishing healthy livers from severely fatty ones (around 85% accurate), detecting moderate levels of fat (around 60% accurate) proves more challenging [9, 10]. Studies show that liver abnormalities are often seen on CT scans of COVID-19 patients [11, 12]. The most common finding is a decrease in liver density (26%), especially in severe cases (59%). Interestingly, measuring this density using CT scans—quantified liver/spleen attenuation—might help predict a patient’s outcome. An advantage is that since the liver is often included in routine chest CT scans for COVID-19, this information can be readily available without additional tests [13]. Also, MRI is recommended for elucidating liver abnormalities in COVID-infected patients where findings on US and CT are inconclusive [14].

In everyday clinical practice, CT scans are the most common way to image the liver. This is because they are widely available, provide detailed pictures with fast image capture, and offer the advantage of standardized analysis based on size and density measurements. Additionally, their excellent image quality makes them suitable for both routine and emergency situations [15]. Unenhanced CT, without contrast agents, is utilized to diagnose morphological traits of liver steatosis and cirrhosis. Additionally, for detecting nonspecific liver pathology, measuring Hounsfield Units (HU) values can serve as an additional method to diagnose liver injuries. HU values represent the X-ray attenuation properties of a material relative to water (0 HU) and air (− 1000 HU), obtained through a linear transformation of the measured attenuation coefficient. Normally, the liver parenchyma is homogeneous, with typical liver attenuation ranging from 50 to 60 Hus [16].

Liver density is assessed using a tube voltage of 120 kVp by calculating the average Hounsfield Units within a 1.5 cm2 circular region of interest (ROI) in four distinct regions spanning both lobes, each delineated by the hepatic veins. Spleen density, on the other hand, is derived from a 1.5 cm2 ROI positioned within the parenchyma. The regions of interest (ROIs) are strategically placed in both cases to steer clear of high-density zones (like calcifications) or low-density regions caused by vascular structures, cysts, or vessel entry points at the hila. Subsequently, the liver-to-spleen ratio (CT L/S) is computed, and steatosis is identified if the CT L/S index is equal to or less than 0.9 [17]. Assessment of hepatic steatosis (HS) through non-enhanced phase CT reveals that an ROI measurement in the right hepatic lobe below 40 HU indicates moderate hepatic steatosis with a liver fat percentage exceeding 30% [18, 19].

Chest CT is a common imaging procedure for diagnosing pneumonia and plays a crucial role in classifying COVID-19 pneumonia [20]. During CT examinations of patients with COVID-19, the upper abdomen, including the liver and spleen, is routinely visualized in the scans [21]. Therefore, evaluating liver abnormalities in the chest CT scans of COVID-19 patients can be achieved by measuring the Hounsfield Units values of the liver and spleen. This study aims to offer a comprehensive review of the CT findings related to liver injury caused by COVID-19 as reported thus far. The review specifically focuses on studies that investigated liver injury associated with changes hepatic CT attenuation values.

Methodology

Medline was searched for “SARS-CoV-2 [MESH]” and “COVID-19 [MESH]” and “computed tomography [MESH]” and “liver injury [MESH]” and “liver steatosis [MESH],” to retrieve papers that published on liver injuries related to COVID-19 in chest CT. Published papers in PubMed, ScienceDirect, and Web of Sciences were used to search for original articles, reviews, and case reports in English between 2019 and March 2024. References of the articles were screened for other papers and included in this review when considered relevant.

The inclusion criteria for this paper were published papers about examining liver injury associated with COVID-19 by CT scan 9. However, the exclusion criteria conducted by eliminating articles were ones which examined liver disorders, according to the severity of COVID-19 and its relationship with biochemical abnormalities and liver disorders caused by drug consumption. Additionally, diabetes was included in the exclusion criteria since it contributes to fatty liver, which could confound the assessment of COVID-19-related liver injury. Finally, the articles were classified based on the findings of chest CT scan imaging.

Main text

This review included nine retrospective cohort studies (Table 1). Out of the 12 studies, five divided patients into a research group (positive COVID-19) and a control group (negative COVID-19) [22,23,24,25,26]. It should be noted that the research group in the Shumskaya et al. study was divided into three groups based on the severity of COVID-19 [26]. In other studies, patients were classified into two or three groups based on severity of symptoms in patients with COVID-19. These classifications included none severe group (NSG), severe group (SG) [27,28,29], ICU froup (IG), none ICU group (NIG) [30], fatty liver group (FL), non-fatty liver group (NFL) [31], positive oxygen demand OD (+), negative oxygen demand OD (−) [32], non-prognosis group (NPG), and prognosis group (PG) [33]. The most common clinical symptoms in mentioned studies included diarrhea, anorexia, abdominal pain, nausea, and vomiting.

Table 1 Characteristics of included studies

In the study groups that compared hepatic CT attenuation in control and research groups, four of them determined that the Hounsfield Units of patients in the research groups significantly decreased compared to those in the control group [22,23,24, 26], while, the results of the Radzina et al. [25] study were the opposite, showing an increase in HU in the livers of patients in the research group. Uchida et al. study [27] evaluated hepatic attenuation values in both severe and non-severe patients with COVID-19. This study found that lower liver density readings (CT attenuation values) and a lower liver-to-spleen density ratio were linked to how severe a patient’s COVID-19 was upon admission to the hospital. However, the investigation by Chen et al. [28] failed to achieve analogous outcomes with Uchida et al., as they found no significant statistical difference in hepatic CT attenuation values and L/S ratios between severe and non-severe groups. Parlak et al. [30] divided patients with COVID-19 into an intensive care unit group (IG) and a none intensive care unit group (NIG). They found that liver density and L/S ratio were significantly lower in the IG. Additionally, the study by Fataftah et al. [31] revealed a significant decrease in hepatic CT attenuation values in fatty liver group compared to the non-fatty liver group at the time of admission.

Additionally, Nakayasu et al. assessed the risk factors associated with predicting oxygen demand in patients with COVID-19. The study involved a comprehensive evaluation of variables such as age, sex, existing health conditions, laboratory outcomes, and CT scan results, encompassing hepatic attenuation value and visceral fat. Its primary objective was to pinpoint particular factors capable of forecasting the requirement for oxygen assistance in individuals with COVID-19. While the link between liver-to-spleen size ratio and oxygen needs is not fully established, a lower L/S ratio is a reliable indicator of fatty liver disease [32]. Guler et al. [33] examined alterations in the L/S ratio throughout the progression of the COVID-19. They established a correlation between the L/S ratio and various factors, including clinical manifestations, laboratory results, and lung CT scores. While the progressive group had a slightly lower liver-to-spleen ratio (L/S) compared to the non-progressive group upon admission, this difference was not statistically significant (p-value = 0.547). Interestingly, at follow-up, the L/S ratio showed a significant difference between the two groups (p-value = 0.009).

Discussion

Generally, a CT scan is used to evaluate the severity of pneumonia and can also calculate Hounsfield Units of different tissues. Using the CT attenuation L/S ratio, obtained by the formula of mean hepatic CT attenuation divided by mean splenic CT attenuation value, can be a suitable factor for evaluating liver injuries such as hepatic steatosis and parenchymal injuries in patients with COVID-19. However, the visual representation of alterations in liver parenchyma on imaging remains uncertain. While variations in hepatic attenuation can be detected in certain diffuse liver conditions, the L/S ratio is frequently employed to evaluate the presence of liver fat [34,35,36]. In our study, the findings of hepatic CT attenuation and CT attenuation L/S ratio in COVID-19 patients were collected and analyzed. The study revealed that in most investigations evaluating the Hounsfield Units of the liver in patients with COVID-19, hepatic HU values significantly decreased. Moreover, the reduction in hepatic CT values was more pronounced in patients with severe symptoms hospitalized in the ICU compared to those with mild-to-moderate symptoms and non-ICU patients.

COVID-19, caused by the SARS-CoV-2 virus, can disrupt how the body manages fat, particularly in severely ill patients. Research suggests that people with severe COVID-19 are four to six times more likely to have a MAFLD compared to those without the disease. This suggests a significant impact of COVID-19 on metabolic dysfunction and liver health, especially in severe cases [37]. Therefore, the values ​​of hepatic CT attenuation and CT attenuation L/S ratio in these patients are lower than in patients with mild-to-moderate COVID-19. Lower liver density (measured by CT scan) and a smaller liver-to-spleen size ratio (L/S ratio) might be indicators of how severe COVID-19 is in a patient.

However, the evidence of two studies were completely contradictory. The study by Radzina et al. showed a significant increasing of hepatic HU values in research group, which could be due to the incomplete patients screening at the time of admission and during the course of treatment [25]. In addition, the study conducted by Chen et al. found a weak relationship between the severity of COVID-19 and the hepatic CT attenuation values and CT attenuation L/S ratio. This weak relationship could be attributed to the unavailability of liver CT records for some patients before admission to the hospital or errors in attenuation measurement due to the low quality of images obtained from the low-dose scanning protocol [28].

Studies have shown a link between lower liver density and higher mortality rates in COVID-19 patients. Patients with liver HU ≤ 40 had nearly twice the mortality rate compared to those with HU > 40. The significant increase in HU observed in the fatty liver (FL) group may be attributed to liver parenchymal damage, such as fibrosis or a reduction in liver fat content, leading to the resolution of liver steatosis. Interestingly, this notable HU change is not exclusive to the FL group. In the NFL group, several patients initially had HU values within the normal range (40–60) upon admission. However, after 10–14 days of COVID-19 treatment, they exhibited substantial deviations from their baseline HU levels. The alteration in liver texture density in the NFL group could also be associated with fibrosis, decreased liver fat content, and the regression of steatosis [31]. Among patient in this study, approximately one-quarter exhibited abnormal liver enzymes. Interestingly, no significant changes were observed in liver enzyme levels during hospitalization for either the FL or NFL group. This suggests that the alteration in liver parenchyma, as measured by Hounsfield Units, is unlikely to be solely attributed to liver injury or fibrosis. Notably, a study by Wu et al. found that common liver function tests, including measurements of enzymes, bilirubin, and protein levels, did not directly correlate with the severity of COVID-19 cases. Importantly, liver damage in patients with mild COVID-19 is typically temporary and often resolves without specific treatment [38, 39].

Several studies have investigated the effects of COVID-19 on liver injuries, but they were excluded from our analysis. Crisan et al. [40] examined blood tests and MAFLD in COVID-19 survivors and non-survivors. They found no significant link between fatty liver disease (liver steatosis) and either the severity (p = 0.61) or survival rate (p = 0.56) of COVID-19 patients. Guo et al. [41] evaluated the occurrence of low liver CT density in COVID-19 patients and revealed that it is more common in these patients. Their results also showed that liver injury strongly correlates with the patient’s sex, COVID-19 severity, and low liver CT density. There are a few studies that have investigated chest CT findings in COVID-19 patients, these investigations have not explained liver CT attenuation but have reported blood test and abdominal CT findings in COVID-19 patients [42,43,44].

Identification specific factors that could predict the need for oxygen support in COVID-19 patients revealed that the L/S ratio, lymphocyte count, D-dimer levels, and abdominal circumference could serve as predictive indicators for the onset of oxygen requirement. Hence, focusing on the L/S ratio along with laboratory tests and underlying conditions may aid in identifying patients with more severe disease more accurately. Patients with advancing lung CT scores demonstrated notably increased CRP levels during follow-up [32]. Studies suggest a positive correlation between elevated CRP levels and both lung involvement and disease severity [45].

To summarize, liver dysfunction linked to decreased hepatic CT attenuation values was found to be associated with disease severity in COVID-19 patients. Recognizing these connections can offer critical insights for effectively managing patients throughout the course of the illness. Studies have shown that liver hypoattenuation, characterized by reduced liver-to-spleen CT attenuation ratios, is more prevalent in severe cases of COVID-19. Radiological features of COVID-19-induced hepatitis include hepatomegaly, altered liver echogenicity on ultrasound, and hypoattenuation on CT scans. Imaging modalities like CT scans plays crucial roles in evaluating liver damage in COVID-19 patients.

This review acknowledges several limitations. Firstly, the small number of patients in some studies may have led to biased results. Secondly, most studies assessed CT images upon admission, but the reports showed changes in hepatic attenuation during the course of COVID-19 in patients. Thirdly, the absence of contrast-enhanced liver imaging is a limitation, as unenhanced chest CT scans were repeatedly used in COVID-19 cases, with a focus on examining alterations in the upper abdomen, specifically the L/S ratio.

Conclusions

The analysis of liver injuries in COVID-19 patients through hepatic CT attenuation values and CT attenuation L/S ratios reveals valuable insights into disease severity and liver health. The observed decrease in hepatic Hounsfield Units in severe cases, alongside the impact of COVID-19 on fat metabolism and the prevalence of MAFLD, underscores the intricate relationship between the virus and liver function. Despite conflicting findings in some studies, between reduced liver density and disease severity underscores the diagnostic utility of CT scans. Their ability to visualize the upper abdomen, encompassing the liver and spleen, offers a potential avenue for detecting liver damage in patients with COVID-19. The limitations of current research, such as sample sizes and imaging protocols, emphasize the need for further investigation to elucidate the role of liver imaging in COVID-19 management. Overall, understanding the implications of hepatic CT attenuation values in COVID-19 patients can aid in better patient care and treatment strategies during the course of the illness.